berberine has been researched along with Diabetes Mellitus, Type 2 in 99 studies
Diabetes Mellitus, Type 2: A subclass of DIABETES MELLITUS that is not INSULIN-responsive or dependent (NIDDM). It is characterized initially by INSULIN RESISTANCE and HYPERINSULINEMIA; and eventually by GLUCOSE INTOLERANCE; HYPERGLYCEMIA; and overt diabetes. Type II diabetes mellitus is no longer considered a disease exclusively found in adults. Patients seldom develop KETOSIS but often exhibit OBESITY.
Excerpt | Relevance | Reference |
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"Role of Pioglitazone and Berberine in Treatment of Non-Alcoholic Fatty Liver Disease, NCT00633282 ." | 9.41 | Gender differences in the efficacy of pioglitazone treatment in nonalcoholic fatty liver disease patients with abnormal glucose metabolism. ( Chang, X; Gao, J; Ma, S; Wang, L; Wu, W; Xia, M; Yan, H, 2021) |
"To explore the therapeutic effect and the hemorrheology change of berberine in new diagnosed patients with type 2 diabetes combining nonalcoholic fatty liver disease." | 9.15 | [Research on therapeutic effect and hemorrheology change of berberine in new diagnosed patients with type 2 diabetes combining nonalcoholic fatty liver disease]. ( Kong, H; Meng, X; Shu, X; Xie, X; Zhou, X, 2011) |
"One hundred sixteen patients with type 2 diabetes and dyslipidemia were randomly allocated to receive berberine (1." | 9.13 | Treatment of type 2 diabetes and dyslipidemia with the natural plant alkaloid berberine. ( Hong, J; Huo, L; Li, X; Liu, W; Ning, G; Ren, G; Wang, M; Wu, P; Yang, J; Zhang, Y; Zhu, N; Zou, D, 2008) |
"This study indicates that berberine has comparable therapeutic effect on type 2 DM, hyperlipidemia and hypertension with no serious side effect." | 8.91 | Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension. ( Dong, F; Fan, J; Lan, J; Sun, G; Yan, Z; Zhao, Y; Zheng, W, 2015) |
"Berberine may slow the progression of prediabetes to T2DM in ZDF rats by improving GLP-2 secretion, intestinal permeability, and the structure of the gut microbiota." | 8.02 | Berberine Slows the Progression of Prediabetes to Diabetes in Zucker Diabetic Fatty Rats by Enhancing Intestinal Secretion of Glucagon-Like Peptide-2 and Improving the Gut Microbiota. ( Jiang, Y; Kong, Y; Liu, H; Ren, H; Shan, C; Wang, J; Wang, S; Wang, Y; Yang, J; Yang, Y; Zheng, M, 2021) |
"The purpose of this study was to explore the anti-arrhythmic mechanisms of berberine in diabetic rats with myocardial infarction." | 7.77 | Berberine elicits anti-arrhythmic effects via IK1/Kir2.1 in the rat type 2 diabetic myocardial infarction model. ( Fu, Y; Li, Q; Sun, YQ; Wang, LH; Yu, CH, 2011) |
"This study will provide a high-quality synthesis of current evidence of BBR for T2DM with IR from several aspects including HOMA-IR, blood glucose levels, and adverse events." | 6.61 | Efficacy and safety of berberine in the treatment of type 2 diabetes with insulin resistance: Protocol for a systematic review. ( Li, H; Li, S; Liu, B; Wang, Y; Yan, A; Yan, Y, 2019) |
" The bioavailability of berberine is extremely low, suggesting that it may play a role in lowering blood sugar and lipid by regulating intestinal flora." | 6.55 | [Berberine regulates type 2 diabetes mellitus related with insulin resistance]. ( He, JZ; Li, C; Xu, X; Zhou, XD, 2017) |
"Berberine (BBR) is a widely used anti-diabetic agent, and liver glucokinase (GK) has been reported to be involved." | 5.51 | Berberine alleviates hyperglycemia by targeting hepatic glucokinase in diabetic db/db mice. ( Dang, Y; Ji, G; Li, M; Li, Q; Yao, Z; Zhang, L; Zhou, W; Zuo, J, 2019) |
"Treatment with berberine regulated BMP4 transcriptional pathways and brown adipose tissue transcriptional pathways and induced the gene mRNA expression of brown adipose tissue-specific genes in VWAT to develop browning gene phenotype of white adipose tissues, and then improved fat-induced insulin resistance." | 5.43 | [Regulations of berberine on gene expression of BMP4 transcriptional pathways to improve visceral white adipose tissues insulin resistance in type 2 diabetic hamsters]. ( Gao, ZN; Huang, L; Li, GS; Li, XY; Liu, XH; Liu, YL, 2016) |
"Role of Pioglitazone and Berberine in Treatment of Non-Alcoholic Fatty Liver Disease, NCT00633282 ." | 5.41 | Gender differences in the efficacy of pioglitazone treatment in nonalcoholic fatty liver disease patients with abnormal glucose metabolism. ( Chang, X; Gao, J; Ma, S; Wang, L; Wu, W; Xia, M; Yan, H, 2021) |
"Berberine has been reported to have antidiabetic properties." | 5.36 | Beneficial effect of berberine on hepatic insulin resistance in diabetic hamsters possibly involves in SREBPs, LXRα and PPARα transcriptional programs. ( Huang, L; Li, G; Liu, X; Liu, Y; Ma, C; Qin, C; Zhu, H, 2010) |
"In animal models, treatment of type 2 diabetes mellitus rats with BBR lowered fasting blood glucose and fasting serum insulin, increased insulin sensitivity, and elevated InsR mRNA as well as PKC activity in the liver." | 5.35 | Berberine reduces insulin resistance through protein kinase C-dependent up-regulation of insulin receptor expression. ( Jiang, JD; Kong, WJ; Li, ZR; Pan, HN; Shan, N; Si, SY; Song, DQ; Wang, YM; Wei, J; Xue, R; Yang, P; You, XF; Zhang, H; Zhao, LX; Zhao, W; Zhou, ZX, 2009) |
"To explore the therapeutic effect and the hemorrheology change of berberine in new diagnosed patients with type 2 diabetes combining nonalcoholic fatty liver disease." | 5.15 | [Research on therapeutic effect and hemorrheology change of berberine in new diagnosed patients with type 2 diabetes combining nonalcoholic fatty liver disease]. ( Kong, H; Meng, X; Shu, X; Xie, X; Zhou, X, 2011) |
"A comprehensive metabonomic method, in combination with fingerprint analysis and target analysis, was performed to reveal potential mechanisms of berberine action in the treatment of patients with type 2 diabetes and dyslipidemia." | 5.14 | Effect of traditional Chinese medicine berberine on type 2 diabetes based on comprehensive metabonomics. ( Chen, J; Gu, W; Gu, Y; Hong, J; Li, X; Lu, X; Ning, G; Shi, X; Xu, G; Zhang, Y, 2010) |
"One hundred sixteen patients with type 2 diabetes and dyslipidemia were randomly allocated to receive berberine (1." | 5.13 | Treatment of type 2 diabetes and dyslipidemia with the natural plant alkaloid berberine. ( Hong, J; Huo, L; Li, X; Liu, W; Ning, G; Ren, G; Wang, M; Wu, P; Yang, J; Zhang, Y; Zhu, N; Zou, D, 2008) |
" Among these compounds, berberine, an isoquinoline alkaloid derived from plants of the generis Berberis, has been recognized as being capable of decreasing oxidative stress, LDL, triglycerides, and insulin resistance and of improving the mood." | 4.91 | Potential benefits of berberine in the management of perimenopausal syndrome. ( Caliceti, C; Cicero, AF; Rizzo, P, 2015) |
"This study indicates that berberine has comparable therapeutic effect on type 2 DM, hyperlipidemia and hypertension with no serious side effect." | 4.91 | Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension. ( Dong, F; Fan, J; Lan, J; Sun, G; Yan, Z; Zhao, Y; Zheng, W, 2015) |
"Co-administration of metformin (250 mg/kg) with berberine (125 mg/kg) could not only further improve insulin sensitivity, but also demonstrate different alterations on gut microbial communities than that of their individual treatment in db/db mice." | 4.12 | Effects of combination treatment with metformin and berberine on hypoglycemic activity and gut microbiota modulation in db/db mice. ( Kong, APS; Li, D; Li, Z; Lyu, Y; Ming, X; Shaw, PC; Yuan, X; Zhang, C; Zhang, J; Zuo, Z, 2022) |
"The aim of this study was to investigate the effects of berberine on polycystic ovary syndrome (PCOS) with insulin resistance (IR)." | 4.02 | Berberine Improves the Symptoms of DHEA-Induced PCOS Rats by Regulating Gut Microbiotas and Metabolites. ( Li, XL; Shen, HR; Xu, X; Ye, D, 2021) |
"Berberine may slow the progression of prediabetes to T2DM in ZDF rats by improving GLP-2 secretion, intestinal permeability, and the structure of the gut microbiota." | 4.02 | Berberine Slows the Progression of Prediabetes to Diabetes in Zucker Diabetic Fatty Rats by Enhancing Intestinal Secretion of Glucagon-Like Peptide-2 and Improving the Gut Microbiota. ( Jiang, Y; Kong, Y; Liu, H; Ren, H; Shan, C; Wang, J; Wang, S; Wang, Y; Yang, J; Yang, Y; Zheng, M, 2021) |
"Diabetogenesis triggered by arsenic contributed to the mitochondrial ROS overproduction, impaired complex II activity, glucose homeostasis, glucose tolerance and insulin sensitivity." | 3.91 | SirT3 regulates diabetogenic effects caused by arsenic: An implication for mitochondrial complex II modification. ( Javadipour, M; Keshtzar, E; Khodayar, MJ; Rezaei, M, 2019) |
"The purpose of this study was to explore the anti-arrhythmic mechanisms of berberine in diabetic rats with myocardial infarction." | 3.77 | Berberine elicits anti-arrhythmic effects via IK1/Kir2.1 in the rat type 2 diabetic myocardial infarction model. ( Fu, Y; Li, Q; Sun, YQ; Wang, LH; Yu, CH, 2011) |
"Berberine (BBR) is an isoquinoline alkaloid extracted from plants that possess a broad array of medicinal properties, including anti-diarrheal, anti-fibrotic, antidiabetic, anti-inflammatory, anti-obesity, antihyperlipidemic, antihypertensive, antiarrhythmic, antidepressant, and anxiolytic effects, and is frequently utilized as a traditional Chinese medicine." | 2.82 | Expatiating the Pharmacological and Nanotechnological Aspects of the Alkaloidal Drug Berberine: Current and Future Trends. ( Albarrati, A; Albratty, M; Behl, T; Bungau, S; Meraya, AM; Najmi, A; Sharma, N; Singh, S; Zahoor, I, 2022) |
"Berberine has been shown to regulate glucose and lipid metabolism in vitro and in vivo." | 2.73 | Efficacy of berberine in patients with type 2 diabetes mellitus. ( Xing, H; Ye, J; Yin, J, 2008) |
"Nonalcoholic fatty liver disease (NAFLD) is the most common chronic liver disease in the world." | 2.72 | Mechanism of Natural Drugs on Nonalcoholic Fatty Liver Disease. ( Li, L; Xie, J; Zhao, L, 2021) |
"Berberine (BBR) is an isoquinoline alkaloid belonging to the structural class of protoberberines." | 2.66 | Nano-based delivery systems for berberine: A modern anti-cancer herbal medicine. ( Araj-Khodaei, M; Ezzati Nazhad Dolatabadi, J; Ghaffari, M; Hamblin, MR; Majidzadeh, H; Torbati, M, 2020) |
" Subgroup-analyses indicated that effects of Berberine on blood glucose became unremarkable as the treatment lasted more than 90 days, the daily dosage more than 2 g/d and patients aged more than 60 years." | 2.61 | Effects of berberine on blood glucose in patients with type 2 diabetes mellitus: a systematic literature review and a meta-analysis. ( Chen, R; Huang, L; Liang, Y; Ni, J; Xu, X; Yin, M; Zhang, Y, 2019) |
"This study will provide a high-quality synthesis of current evidence of BBR for T2DM with IR from several aspects including HOMA-IR, blood glucose levels, and adverse events." | 2.61 | Efficacy and safety of berberine in the treatment of type 2 diabetes with insulin resistance: Protocol for a systematic review. ( Li, H; Li, S; Liu, B; Wang, Y; Yan, A; Yan, Y, 2019) |
" The bioavailability of berberine is extremely low, suggesting that it may play a role in lowering blood sugar and lipid by regulating intestinal flora." | 2.55 | [Berberine regulates type 2 diabetes mellitus related with insulin resistance]. ( He, JZ; Li, C; Xu, X; Zhou, XD, 2017) |
"Berberine (BBR) is a type of alkaloids isolated from Coptidis Rhizoma and Phellodendri Chinensis Cortex and has been used to treat bacterial gastroenteritis, diarrhea and other digestive diseases for more than 1 000 years." | 2.52 | [Effect of berberine in treating type 2 diabetes mellitus and complications and its relevant mechanisms]. ( Chen, L; Li, Y; Zhang, Q, 2015) |
"The incidence of type 2 diabetes is increasing rapidly worldwide, and the development of novel anti-diabetic drugs is emerging." | 2.52 | Berberine as a therapy for type 2 diabetes and its complications: From mechanism of action to clinical studies. ( Chang, W; Chen, L; Hatch, GM, 2015) |
"Berberine is an alkaloid that is highly concentrated in the roots, rhizomes, and stem bark of various plants." | 2.48 | Antidiabetic properties of berberine: from cellular pharmacology to clinical effects. ( Cicero, AF; Tartagni, E, 2012) |
"Berberine has significant antimicrobial activity against several microbes through inhibiting the assembly function of FtsZ and halting the bacteria cell division." | 2.47 | Modulating gut microbiota as an anti-diabetic mechanism of berberine. ( Han, J; Huang, W; Lin, H, 2011) |
"Berberine (BBR) can ameliorate type 2 diabetes and insulin resistance in many ways." | 1.91 | Berberine Regulates GPX4 to Inhibit Ferroptosis of Islet β Cells. ( Bao, L; Han, J; Jin, Y; Qian, L; Wang, W; Wu, W, 2023) |
" However, the chemical profiles, metabolic transformation and pharmacokinetic behavior of XEC in vivo were unclear." | 1.91 | Metabolic profiling integrated with pharmacokinetics to reveal the material basis of Xiaokeyinshui extract combination in the treatment of type 2 diabetes in rats. ( Chen, JC; Fang, JB; Fu, XN; He, JX; Hu, ZF; Huang, R; Li, Q; Luo, D; Peng, HM; Tong, QL; Wan, LS; Wu, JL; Xia, RF; Xiang, ZN; Zhang, YL, 2023) |
"Berberine chloride is a dual topoisomerase I and II inhibitor, that exhibited potent antitumor activities against several malignancies." | 1.91 | Berberine chloride (dual topoisomerase I and II inhibitor) modulate mitochondrial uncoupling protein (UCP1) in molecular docking and dynamic with in-vitro cytotoxic and mitochondrial ATP production. ( Abdalla, M; Ferdous, MR; Song, Y; Xiaoling, L; Yang, M, 2023) |
"Berberine (BBR) is an isoquinoline alkaloid isolated from Coptis chinensis and possesses valuable pharmacological activities, including anti-inflammatory, anti-tumor, and alleviating several complications of type 2 diabetes mellitus (T2DM)." | 1.72 | Alleviation of Diabetic Tendon Injury via Activation of Tendon Fibroblasts Autophagy under Berberine Treatment. ( Li, Q; Liu, SH; Song, FC; Yuan, JQ; Zhang, L; Zhao, C; Zhu, MD, 2022) |
"Among adolescents, the incidence of type 2 diabetes mellitus (T2DM) has recently increased." | 1.62 | Remission of new-onset type 2 diabetes mellitus in an adolescent using an integrative medicine approach: A case report. ( Chan, Y; Hou, S; Lao, L; Shao, B; Shao, C, 2021) |
"Rat models of type 2 diabetes mellitus (T2DM) were established and were treated with berberine." | 1.62 | Macrovascular Protecting Effects of Berberine through Anti-inflammation and Intervention of BKCa in Type 2 Diabetes Mellitus Rats. ( Chen, M; Gu, L; Si, Y; Wu, Z; Yin, W; Zhang, T; Zhao, M, 2021) |
"Berberine is effective for type 2 diabetes mellitus (T2DM), but has limited use in clinic." | 1.62 | Berberine combined with stachyose improves glycometabolism and gut microbiota through regulating colonic microRNA and gene expression in diabetic rats. ( Cao, H; Fu, Y; Gao, X; Huan, Y; Ji, W; Lei, L; Li, C; Li, P; Liu, M; Liu, Q; Liu, S; Shen, Z; Sun, S, 2021) |
"Berberine (BBR) has therapeutic effect on diabetic nephropathy (DN), but its molecular mechanism is not completely clear." | 1.62 | Berberine Acts on C/EBPβ/lncRNA Gas5/miR-18a-5p Loop to Decrease the Mitochondrial ROS Generation in HK-2 Cells. ( Gan, L; Hu, Y; Liu, L; Xiang, P; Xing, Y; Xu, J; Ye, S; Zhu, J, 2021) |
" However, its oral bioavailability is poor." | 1.56 | Berberine alleviates type 2 diabetic symptoms by altering gut microbiota and reducing aromatic amino acids. ( Chen, H; Wang, D; Wang, W; Yan, L; Yao, Y, 2020) |
"Berberine (BBR) has been proved to possess the properties of improving metabolic disorders in patients with obesity or type 2 diabetes mellitus." | 1.56 | Berberine attenuates the abnormal ectopic lipid deposition in skeletal muscle. ( Jin, L; Meng, X; Ning, G; Wang, W; Yang, J; Yao, S; Yuan, Y; Zhang, H; Zhang, Y; Zhang, Z, 2020) |
" However, the low anti-diabetic activity and poor bioavailability of berberine (below 5%) by oral administration significantly limit its practical applications." | 1.56 | Synthesis of disaccharide modified berberine derivatives and their anti-diabetic investigation in zebrafish using a fluorescence-based technology. ( Jin, M; Kong, H; Li, X; Lin, H; Liu, K; Stoika, R; Wang, L, 2020) |
" However, the poor bioavailability of berberine limits its clinical applications." | 1.56 | Highly bioavailable berberine formulation ameliorates diabetic nephropathy through the inhibition of glomerular mesangial matrix expansion and the activation of autophagy. ( Chen, L; Guan, F; Wang, X; Xiao, D; Zhang, J; Zhang, M; Zhang, Y, 2020) |
"Berberine (BBR) is a widely used anti-diabetic agent, and liver glucokinase (GK) has been reported to be involved." | 1.51 | Berberine alleviates hyperglycemia by targeting hepatic glucokinase in diabetic db/db mice. ( Dang, Y; Ji, G; Li, M; Li, Q; Yao, Z; Zhang, L; Zhou, W; Zuo, J, 2019) |
"Berberine was administered p." | 1.48 | Berberine Alleviates Tau Hyperphosphorylation and Axonopathy-Associated with Diabetic Encephalopathy via Restoring PI3K/Akt/GSK3β Pathway. ( Chen, J; Chen, Q; Feng, Z; Hang, W; He, B; Wang, S; Wang, X; Wu, N; Xia, L; Zhang, Q; Zhou, X, 2018) |
"Pioglitazone treatment significantly increased urinary calcium, serum TRAP, mRNA expression of RANKL, PPAR-γ as well as significantly decreased Runx2, OPG, osteocalcin and AMPK levels in diabetic rats." | 1.46 | Pioglitazone-induced bone loss in diabetic rats and its amelioration by berberine: A portrait of molecular crosstalk. ( Adil, M; Kandhare, AD; Mansoori, MN; Sharma, M; Singh, D, 2017) |
"Treatment with berberine regulated BMP4 transcriptional pathways and brown adipose tissue transcriptional pathways and induced the gene mRNA expression of brown adipose tissue-specific genes in VWAT to develop browning gene phenotype of white adipose tissues, and then improved fat-induced insulin resistance." | 1.43 | [Regulations of berberine on gene expression of BMP4 transcriptional pathways to improve visceral white adipose tissues insulin resistance in type 2 diabetic hamsters]. ( Gao, ZN; Huang, L; Li, GS; Li, XY; Liu, XH; Liu, YL, 2016) |
"Berberine (BBR) has been shown to exhibit protective effects against diabetes and dyslipidemia." | 1.43 | Berberine Attenuates Development of the Hepatic Gluconeogenesis and Lipid Metabolism Disorder in Type 2 Diabetic Mice and in Palmitate-Incubated HepG2 Cells through Suppression of the HNF-4α miR122 Pathway. ( Chen, L; Hatch, GM; Lan, X; Wei, S; Yan, X; Yao, F; Yu, Y; Zhang, M, 2016) |
"Berberine (BBR) has been reported to have beneficial effects on diabetic nephropathy, but its action mechanism is still unclear." | 1.42 | Renoprotective effect of berberine on type 2 diabetic nephropathy in rats. ( Dong, X; Huang, XR; Lan, HY; Li, P; Pan, XP; Sun, SF; Wang, H; Wen, YM; Yan, MH; Zhang, HJ; Zhang, L; Zhang, WK; Zhao, TT, 2015) |
"Berberine treatment of palmitate-incubated H9c2 cells reduced hypertrophy, increased α-MHC expression and decreased β-MHC expression." | 1.42 | Berberine treatment prevents cardiac dysfunction and remodeling through activation of 5'-adenosine monophosphate-activated protein kinase in type 2 diabetic rats and in palmitate-induced hypertrophic H9c2 cells. ( Chang, W; Chen, L; Hatch, GM; Meng, Z; Yao, F; Yu, Y; Zhang, M, 2015) |
"This article focused on a comparative analysis on the pharmacokinetic and pharmacodynamic characteristics of berberine (BER) and jateorhizine(JAT) in Coptidis Rhizoma powder (HL-P) and their monomeric compounds (BER + JAT, BJ) in type 2 diabetic (T2D) rats to explore the beneficial." | 1.42 | [Pharmacokinetic and pharmacodynamic characteristics of berberine and jateorhizine in Coptidis Rhizoma powder and their monomeric compounds in type 2 diabetic rats]. ( Huang, R; Jiang, SJ; Li, JB; Lu, FE; Wei, SC; Xu, LJ; Xu, XH; Zou, X, 2015) |
"Low oral bioavailability of berberine due to poor solubility and membrane permeability limits its clinical use for treatment of diabetes." | 1.40 | Amorphous solid dispersion of berberine with absorption enhancer demonstrates a remarkable hypoglycemic effect via improving its bioavailability. ( Hatch, GM; Jingkai, G; Li, C; Ming, Z; Shengnan, W; Xiaojia, B; Zhaojie, M, 2014) |
"Berberine is known to improve glucose and lipid metabolism disorders, but it poorly absorbed into the blood stream from the gut." | 1.40 | Berberine moderates glucose metabolism through the GnRH-GLP-1 and MAPK pathways in the intestine. ( Li, M; Li, W; Ping, F; Wang, Z; Xiao, X; Yu, M; Zhang, H; Zhang, Q; Zheng, J, 2014) |
"Berberine (100 mg/kg) was administered by lavage to diabetic rats for 2 weeks and saline was given to controls." | 1.39 | Alteration of the intestinal barrier and GLP2 secretion in Berberine-treated type 2 diabetic rats. ( Chang, BC; Chen, LM; Kong, Y; Ren, HZ; Shan, CY; Wang, XY; Wang, Y; Xu, YG; Yang, JH; Zheng, MY, 2013) |
"Berberine has been widely used as an alternative medicine and proved to be effective for treatment of DM and dyslipidemia." | 1.38 | Alteration of hepatic glutathione peroxidase and superoxide dismutase expression in streptozotocin-induced diabetic mice by berberine. ( Chatuphonprasert, W; Jarukamjorn, K; Lao-ong, T; Nemoto, N, 2012) |
"Berberine (BBR) is a compound originally identified in a Chinese herbal medicine Huanglian (Coptis chinensis French)." | 1.37 | Berberine improves glucose metabolism in diabetic rats by inhibition of hepatic gluconeogenesis. ( Liang, H; Shen, Y; Tang, K; Weng, J; Xia, X; Yan, J; Yang, D; Ye, J; Yin, J; Zhang, Y, 2011) |
"Berberine has been reported to have antidiabetic properties." | 1.36 | Beneficial effect of berberine on hepatic insulin resistance in diabetic hamsters possibly involves in SREBPs, LXRα and PPARα transcriptional programs. ( Huang, L; Li, G; Liu, X; Liu, Y; Ma, C; Qin, C; Zhu, H, 2010) |
"Berberine has hypoglycemic and hypolipidemic effects on diabetic rats." | 1.36 | Berberine regulates peroxisome proliferator-activated receptors and positive transcription elongation factor b expression in diabetic adipocytes. ( Zhou, J; Zhou, S, 2010) |
"In animal models, treatment of type 2 diabetes mellitus rats with BBR lowered fasting blood glucose and fasting serum insulin, increased insulin sensitivity, and elevated InsR mRNA as well as PKC activity in the liver." | 1.35 | Berberine reduces insulin resistance through protein kinase C-dependent up-regulation of insulin receptor expression. ( Jiang, JD; Kong, WJ; Li, ZR; Pan, HN; Shan, N; Si, SY; Song, DQ; Wang, YM; Wei, J; Xue, R; Yang, P; You, XF; Zhang, H; Zhao, LX; Zhao, W; Zhou, ZX, 2009) |
" In conclusion, berberine restores diabetic endothelial dysfunction through enhanced NO bioavailability by up-regulating eNOS expression and down-regulating expression of NADPH oxidase." | 1.35 | Ameliorative effect of berberine on endothelial dysfunction in diabetic rats induced by high-fat diet and streptozotocin. ( Chen, L; Li, J; Liu, Y; Lv, X; Song, Y; Wang, C; Zhang, M, 2009) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (1.01) | 18.7374 |
1990's | 1 (1.01) | 18.2507 |
2000's | 8 (8.08) | 29.6817 |
2010's | 53 (53.54) | 24.3611 |
2020's | 36 (36.36) | 2.80 |
Authors | Studies |
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Zhang, S | 1 |
Wang, X | 7 |
Yin, W | 2 |
Liu, Z | 2 |
Zhou, M | 1 |
Xiao, D | 2 |
Liu, Y | 3 |
Peng, D | 1 |
Li, C | 4 |
Cao, H | 1 |
Huan, Y | 1 |
Ji, W | 1 |
Liu, S | 1 |
Sun, S | 1 |
Liu, Q | 1 |
Lei, L | 1 |
Liu, M | 1 |
Gao, X | 1 |
Fu, Y | 2 |
Li, P | 3 |
Shen, Z | 1 |
Shen, HR | 1 |
Xu, X | 4 |
Ye, D | 1 |
Li, XL | 1 |
Xu, J | 2 |
Liu, L | 2 |
Gan, L | 1 |
Hu, Y | 1 |
Xiang, P | 1 |
Xing, Y | 1 |
Zhu, J | 1 |
Ye, S | 1 |
Harrison, SA | 1 |
Gunn, N | 1 |
Neff, GW | 1 |
Kohli, A | 1 |
Flyer, A | 1 |
Goldkind, L | 1 |
Di Bisceglie, AM | 1 |
Guo, J | 1 |
Chen, H | 2 |
Zhang, X | 4 |
Lou, W | 1 |
Zhang, P | 2 |
Qiu, Y | 2 |
Zhang, C | 2 |
Wang, Y | 6 |
Liu, WJ | 1 |
Zhang, L | 4 |
Han, L | 3 |
Ma, J | 2 |
Wu, T | 1 |
Wei, Y | 1 |
Zhao, L | 5 |
Tong, X | 4 |
Zhu, MD | 1 |
Li, Q | 7 |
Yuan, JQ | 1 |
Song, FC | 1 |
Liu, SH | 1 |
Zhao, C | 1 |
Xia, QS | 1 |
Wu, F | 1 |
Wu, WB | 1 |
Dong, H | 4 |
Huang, ZY | 1 |
Xu, L | 1 |
Lu, FE | 2 |
Gong, J | 1 |
Zhang, JJ | 1 |
Zhou, R | 1 |
Deng, LJ | 1 |
Cao, GZ | 1 |
Zhang, Y | 8 |
Xu, H | 1 |
Hou, JY | 1 |
Ju, S | 1 |
Yang, HJ | 1 |
Lyu, Y | 1 |
Li, D | 1 |
Yuan, X | 1 |
Li, Z | 1 |
Zhang, J | 2 |
Ming, X | 1 |
Shaw, PC | 1 |
Kong, APS | 1 |
Zuo, Z | 1 |
Ferdous, MR | 1 |
Abdalla, M | 1 |
Yang, M | 1 |
Xiaoling, L | 1 |
Song, Y | 2 |
Behl, T | 2 |
Singh, S | 2 |
Sharma, N | 2 |
Zahoor, I | 1 |
Albarrati, A | 1 |
Albratty, M | 1 |
Meraya, AM | 1 |
Najmi, A | 1 |
Bungau, S | 2 |
Zheng, T | 1 |
Huo, Y | 1 |
Du, W | 1 |
Bi, XJ | 1 |
Lv, YQ | 1 |
Yang, XH | 1 |
Ge, Y | 1 |
Han, H | 1 |
Feng, JS | 1 |
Zhang, M | 9 |
Chen, L | 12 |
Xu, MZ | 1 |
Guan, FY | 1 |
Wang, H | 3 |
Zhang, H | 5 |
Gao, Z | 5 |
Zhang, Q | 4 |
Gu, C | 1 |
Bao, L | 1 |
Jin, Y | 1 |
Han, J | 3 |
Wang, W | 4 |
Qian, L | 1 |
Wu, W | 2 |
Li, H | 4 |
Luo, D | 4 |
Wei, R | 3 |
Sun, M | 3 |
Deng, H | 3 |
Bian, W | 3 |
Wei, H | 3 |
Huang, Y | 3 |
He, Q | 3 |
Guo, Y | 3 |
Gong, M | 3 |
Xia, Q | 3 |
Lu, F | 3 |
Wang, D | 4 |
Tong, QL | 1 |
Xiang, ZN | 1 |
Zhang, YL | 1 |
He, JX | 1 |
Hu, ZF | 1 |
Xia, RF | 1 |
Wu, JL | 1 |
Fu, XN | 1 |
Peng, HM | 1 |
Huang, R | 2 |
Wan, LS | 1 |
Chen, JC | 1 |
Fang, JB | 1 |
Bellavite, P | 1 |
Fazio, S | 1 |
Affuso, F | 1 |
Chen, Y | 1 |
Zhao, S | 1 |
Sun, L | 1 |
Yin, Z | 1 |
Li, X | 5 |
Iwakiri, Y | 1 |
Duan, Y | 1 |
Yan, A | 1 |
Li, S | 1 |
Liu, B | 1 |
Yan, Y | 1 |
Zhang, W | 2 |
Xu, JH | 1 |
Yu, T | 1 |
Chen, QK | 1 |
Guan, F | 2 |
Wang, L | 2 |
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Khodayar, MJ | 1 |
Javadipour, M | 1 |
Liang, Y | 1 |
Yin, M | 1 |
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Ni, J | 1 |
Jia, D | 1 |
Li, ZW | 1 |
Gao, Y | 1 |
Feng, Y | 2 |
Ma, M | 1 |
Li, W | 3 |
Li, M | 2 |
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Li, R | 1 |
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He, Y | 1 |
Hai, L | 1 |
Wu, Y | 1 |
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Yu, M | 1 |
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Li, Y | 2 |
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Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
A Proof-of-Concept and Dose-Ranging Study Investigating the Efficacy and Safety of HTD1801 in Adults With NASH and T2DM[NCT03656744] | Phase 2 | 101 participants (Actual) | Interventional | 2018-11-26 | Completed | ||
Assess the Effects of Berberine in Reducing Abdominal Visceral Adipose Tissue Among Individuals With Obesity and Non-alcoholic Fatty Liver Disease[NCT05647915] | Phase 4 | 326 participants (Anticipated) | Interventional | 2022-12-15 | Not yet recruiting | ||
Effects of Berberine Plus Inulin on Diabetes Care in Patients With Latent Autoimmune Diabetes in Adults: A Randomized Controlled Trial[NCT04698330] | Phase 4 | 240 participants (Anticipated) | Interventional | 2022-05-31 | Not yet recruiting | ||
Probiotics and BeRberine on the Efficacy and Change of Gut MicrObiota in paTients With Newly Diagnosed Type 2 diabEtes(PREMOTE Study)[NCT02861261] | Phase 3 | 400 participants (Anticipated) | Interventional | 2016-08-18 | Active, not recruiting | ||
Role of Pioglitazone and Berberine in Treatment of Non-alcoholic Fatty Liver Disease(NAFLD) Patients With Impaired Glucose Regulation or Type 2 Diabetes Mellitus[NCT00633282] | Phase 2 | 184 participants (Actual) | Interventional | 2008-03-31 | Completed | ||
Effectiveness and Safety of Berberine Hydrochloride and Bifidobacterium in People With Abnormal Glucose Level: an Multicenter, Randomized, Double-blinded, Placebo-controlled Study.[NCT03330184] | 300 participants (Actual) | Interventional | 2015-10-31 | Completed | |||
Effect of Berberine on Cardiovascular Disease Risk Factors: a Mechanistic Randomized Controlled Trial[NCT03770325] | Phase 2/Phase 3 | 84 participants (Actual) | Interventional | 2019-04-01 | Completed | ||
A Single-center, Randomized, Open-label, Controlled, Dose-escalating, Parallel-group Study to Assess the Anti-platelet Effect of Berberine in Patients Receiving Aspirin and Clopidogrel After Percutaneous Coronary Intervention[NCT03378934] | Phase 4 | 64 participants (Anticipated) | Interventional | 2018-09-26 | Recruiting | ||
A Double-blind, Randomized, Placebo-controlled Trial of Berberine as an Adjuvant to Treat Antipsychotic-induced Metabolic Syndrome in Patients With Schizophrenia Spectrum Disorders[NCT02983188] | Phase 2/Phase 3 | 113 participants (Actual) | Interventional | 2018-04-25 | Completed | ||
The Effect of Berberine on the Secretion of Incretin in Normal Man[NCT05947370] | Early Phase 1 | 16 participants (Actual) | Interventional | 2022-10-12 | Completed | ||
Efficacy and Safety of Berberine on Primary Prevention of Cardiovascular Diseases and Diabetes in Metabolic Syndrome: a Randomized, Controlled Trial[NCT05105321] | Phase 4 | 5,200 participants (Anticipated) | Interventional | 2021-12-31 | Not yet recruiting | ||
Efficacy and Safety of Berberine in Non-alcoholic Steatohepatitis: a Multicentre, Randomised, Placebo-controlled Trial[NCT03198572] | Phase 4 | 120 participants (Anticipated) | Interventional | 2017-08-16 | Recruiting | ||
The Effects of Daily Anti-inflammatory Supplementation on Foundation Pain Index Scores in Chronic Opiate Patients[NCT05896878] | 20 participants (Anticipated) | Interventional | 2023-07-10 | Enrolling by invitation | |||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
The primary endpoint was the absolute change in liver fat content (LFC) as measured by magnetic resonance imaging derived proton density fat fraction (MRI-PDFF) from Baseline to Week 18. (NCT03656744)
Timeframe: Baseline through study Week 18
Intervention | Change in percentage of liver fat (Mean) |
---|---|
500mg HTD1801, Bid | -2.918 |
1000mg HTD1801, Bid | -4.829 |
Placebo, Bid | -1.962 |
Absolute change in alanine aminotransferase (ALT) from Baseline to Week 18. (NCT03656744)
Timeframe: Baseline through study week 18
Intervention | U/L (Mean) |
---|---|
500mg HTD1801, Bid | -4 |
1000mg HTD1801, Bid | -19 |
Placebo, Bid | -3 |
Absolute change in aspartate aminotransferase (AST) from Baseline to Week 18. (NCT03656744)
Timeframe: Baseline through study week 18
Intervention | U/L (Mean) |
---|---|
500mg HTD1801, Bid | 0 |
1000mg HTD1801, Bid | -13 |
Placebo, Bid | -3 |
Change in the enhanced liver fibrosis (ELF) score. The ELF score is calculated using a published algorithm combining the values of a set of extracellular matrix markers, including TIMP-1, PIIINP, and HA. The ELF score has been reported to show good correlations with fibrosis stages in chronic liver disease, with higher ELF scores associated with higher fibrosis stages. The ELF score is hence used as a prognostic marker for disease progression: ELF score < 9.8 : Low risk of progression, ELF score 9.8 to < 11.3 : Moderate risk of progression and ELF score > = 11.3 : High risk of progression. (NCT03656744)
Timeframe: Baseline through study week 18
Intervention | score on a scale (Mean) |
---|---|
500mg HTD1801, Bid | 0.05 |
1000mg HTD1801, Bid | -0.10 |
Placebo, Bid | -0.05 |
Change in fasting glucose from Baseline to Week 18 . (NCT03656744)
Timeframe: Baseline through study Week 18
Intervention | mg/dL (Mean) |
---|---|
500mg HTD1801, Bid | 120 |
1000mg HTD1801, Bid | 129 |
Placebo, Bid | 131 |
Change in fibroblast growth factor 19 (FGF19) from Baseline to Week 18 (NCT03656744)
Timeframe: Baseline through study week 18
Intervention | μmol/L (Mean) |
---|---|
500mg HTD1801, Bid | -11 |
1000mg HTD1801, Bid | -9 |
Placebo, Bid | -40 |
Change in hyaluronic acid (HA) from Baseline to Week 18. (NCT03656744)
Timeframe: Baseline through study week 18
Intervention | µg/L (Mean) |
---|---|
500mg HTD1801, Bid | -0.64 |
1000mg HTD1801, Bid | -5.25 |
Placebo, Bid | -3.83 |
Change in high-density lipoprotein cholesterol (HDL-c) from Baseline to Week 18. (NCT03656744)
Timeframe: Baseline through study week 18
Intervention | mg/dL (Mean) |
---|---|
500mg HTD1801, Bid | 1 |
1000mg HTD1801, Bid | 0 |
Placebo, Bid | 0 |
Change in homeostasis model assessment-estimated insulin resistance (HOMA-IR) from Baseline to Week 18. The higher the HOMA-IR score, the more insulin resistant a person is. Values of <1 are considered optimal while values >2.9 indicate significant insulin resistance. (NCT03656744)
Timeframe: Baseline through study week 18
Intervention | score on a scale (Mean) |
---|---|
500mg HTD1801, Bid | -3.38 |
1000mg HTD1801, Bid | -4.21 |
Placebo, Bid | -6.66 |
Change in low-density lipoprotein cholesterol (LDL-c) from Baseline to Week 18. (NCT03656744)
Timeframe: Baseline visit through study week 18
Intervention | mg/dL (Mean) |
---|---|
500mg HTD1801, Bid | 5 |
1000mg HTD1801, Bid | -16 |
Placebo, Bid | 0 |
Change in N-terminal pro-peptide of type III collagen (PIIINP) from Baseline to Week 18. (NCT03656744)
Timeframe: Baseline through study week 18
Intervention | µg/L (Mean) |
---|---|
500mg HTD1801, Bid | 0.68 |
1000mg HTD1801, Bid | 0.03 |
Placebo, Bid | -0.31 |
Change in Pro-C3 from Baseline to Week 18 for subjects with elevated Pro-C3 at Baseline. (NCT03656744)
Timeframe: Baseline through study week 18
Intervention | ng/mL (Mean) |
---|---|
500mg HTD1801, Bid | 0.5 |
1000mg HTD1801, Bid | -2.3 |
Placebo, Bid | -0.8 |
Change in serum triglycerides from Baseline to Week 18. (NCT03656744)
Timeframe: Baseline through study week 18
Intervention | mg/dL (Mean) |
---|---|
500mg HTD1801, Bid | -41 |
1000mg HTD1801, Bid | -24 |
Placebo, Bid | 18 |
Change in tissue inhibitor of metalloproteinases 1 (TIMP-1) from Baseline to Week 18. (NCT03656744)
Timeframe: Baseline through study week 18
Intervention | µg/L (Mean) |
---|---|
500mg HTD1801, Bid | 1.8 |
1000mg HTD1801, Bid | -8.9 |
Placebo, Bid | -6.0 |
Changes in total bile acids from Baseline to Week 18. (NCT03656744)
Timeframe: Baseline through study week 18
Intervention | μmol/L (Mean) |
---|---|
500mg HTD1801, Bid | 1307 |
1000mg HTD1801, Bid | 1625 |
Placebo, Bid | -581 |
Changes in HbA1c from Baseline to Week 18. (NCT03656744)
Timeframe: Baseline through study week 18
Intervention | Percentage (Mean) |
---|---|
500mg HTD1801, Bid | -0.3 |
1000mg HTD1801, Bid | -0.6 |
Placebo, Bid | 0.1 |
AEs were mapped to MedDRA version 20.1 preferred term (PT) and system organ class (SOC). If the subject experienced multiple events that mapped to a single preferred term, the greatest severity grade according to CTCAE Version 4.0, and strongest investigator assessment of relation to study medication was assigned to the preferred term. If an event had a missing severity or relationship, it was classified as having the highest severity and/or strongest relationship to study medication. The occurrence of TEAEs was summarized by treatment group by SOC, PT, and severity. Separate summaries of treatment-emergent serious adverse events (SAEs), TEAEs related to study drug, severe or life threatening TEAEs, and TEAEs leading to the discontinuation of study treatment were generated. Additionally, the occurrence of liver-specific AEs was summarized by treatment group. All reported adverse events were listed for individual subjects showing verbatim term, PT and SOC. (NCT03656744)
Timeframe: Adverse events were collected from the time the subject signed the informed consent form through the date of the last visit for a specific subject, that is, approximately 24 weeks in total for a completed subject.
Intervention | Participants (Count of Participants) |
---|---|
500mg HTD1801, Bid | 21 |
1000mg HTD1801, Bid | 26 |
Placebo, Bid | 20 |
Number of subjects who achieved ≥5% absolute reduction in liver fat content (LFC) as measured by magnetic resonance imaging derived proton density fat fraction (MRI-PDFF) from Baseline to Week 18. (NCT03656744)
Timeframe: Baseline through study Week 18
Intervention | Participants (Count of Participants) |
---|---|
500mg HTD1801, Bid | 10 |
1000mg HTD1801, Bid | 12 |
Placebo, Bid | 8 |
Number of subjects who normalized liver fat content (LFC) to <5% as measured by magnetic resonance imaging derived proton density fat fraction (MRI-PDFF) at Week 18. (NCT03656744)
Timeframe: Baseline through study Week 18
Intervention | Participants (Count of Participants) |
---|---|
500mg HTD1801, Bid | 1 |
1000mg HTD1801, Bid | 0 |
Placebo, Bid | 0 |
Proportion of subjects who achieved ≥ 30% relative reduction in liver fat content (LFC) as measured by magnetic resonance imaging derived proton density fat fraction (MRI-PDFF) from Baseline to Week 18. (NCT03656744)
Timeframe: Baseline through study week 18
Intervention | Participants (Count of Participants) |
---|---|
500mg HTD1801, Bid | 6 |
1000mg HTD1801, Bid | 10 |
Placebo, Bid | 7 |
Proportion of subjects with elevated alanine aminotransferase (ALT) at Baseline who normalized ALT at Week 18. (NCT03656744)
Timeframe: Baseline through study week 18
Intervention | Participants (Count of Participants) |
---|---|
500mg HTD1801, Bid | 3 |
1000mg HTD1801, Bid | 9 |
Placebo, Bid | 5 |
Relative change in liver fat content (LFC) as measured by magnetic resonance imaging derived proton density fat fraction (MRI-PDFF) from Baseline to Week 18. (NCT03656744)
Timeframe: Baseline through study week 18
Intervention | Percentage change (Mean) |
---|---|
500mg HTD1801, Bid | -15.097 |
1000mg HTD1801, Bid | -24.140 |
Placebo, Bid | -8.322 |
22 reviews available for berberine and Diabetes Mellitus, Type 2
Article | Year |
---|---|
The Effect of Berberine on Metabolic Profiles in Type 2 Diabetic Patients: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.
Topics: Berberine; Diabetes Mellitus, Type 2; Humans; Randomized Controlled Trials as Topic | 2021 |
Expatiating the Pharmacological and Nanotechnological Aspects of the Alkaloidal Drug Berberine: Current and Future Trends.
Topics: Alkaloids; Anti-Inflammatory Agents; Berberine; Diabetes Mellitus, Type 2; Female; Humans; Nanotechn | 2022 |
The mechanism of berberine alleviating metabolic disorder based on gut microbiome.
Topics: Bacteria; Berberine; Diabetes Mellitus, Type 2; Gastrointestinal Microbiome; Humans; Non-alcoholic F | 2022 |
Multi-target regulation of intestinal microbiota by berberine to improve type 2 diabetes mellitus.
Topics: Berberine; Blood Glucose; Diabetes Mellitus, Type 2; Gastrointestinal Microbiome; Humans; Insulin Re | 2022 |
Multi-target regulation of intestinal microbiota by berberine to improve type 2 diabetes mellitus.
Topics: Berberine; Blood Glucose; Diabetes Mellitus, Type 2; Gastrointestinal Microbiome; Humans; Insulin Re | 2022 |
Multi-target regulation of intestinal microbiota by berberine to improve type 2 diabetes mellitus.
Topics: Berberine; Blood Glucose; Diabetes Mellitus, Type 2; Gastrointestinal Microbiome; Humans; Insulin Re | 2022 |
Multi-target regulation of intestinal microbiota by berberine to improve type 2 diabetes mellitus.
Topics: Berberine; Blood Glucose; Diabetes Mellitus, Type 2; Gastrointestinal Microbiome; Humans; Insulin Re | 2022 |
A Descriptive Review of the Action Mechanisms of Berberine, Quercetin and Silymarin on Insulin Resistance/Hyperinsulinemia and Cardiovascular Prevention.
Topics: Animals; Berberine; Cardiovascular Diseases; Diabetes Mellitus, Type 2; Humans; Insulin Resistance; | 2023 |
Efficacy and safety of berberine in the treatment of type 2 diabetes with insulin resistance: Protocol for a systematic review.
Topics: Berberine; Blood Glucose; China; Diabetes Mellitus, Type 2; Humans; Insulin Resistance; Randomized C | 2019 |
Nano-based delivery systems for berberine: A modern anti-cancer herbal medicine.
Topics: Antineoplastic Agents; Apoptosis; Berberine; Diabetes Mellitus, Type 2; Herbal Medicine; Humans | 2020 |
Mechanism of Natural Drugs on Nonalcoholic Fatty Liver Disease.
Topics: Berberine; Diabetes Mellitus, Type 2; Humans; Insulin Resistance; Liver; Non-alcoholic Fatty Liver D | 2021 |
A spotlight on underlying the mechanism of AMPK in diabetes complications.
Topics: AMP-Activated Protein Kinases; Animals; Berberine; Diabetes Complications; Diabetes Mellitus, Type 2 | 2021 |
Mode of action of berberine on lipid metabolism: a new-old phytochemical with clinical applications?
Topics: Animals; Berberine; Diabetes Mellitus, Type 2; Dyslipidemias; Humans; Lipid Metabolism; Lipids; Non- | 2017 |
[Berberine regulates type 2 diabetes mellitus related with insulin resistance].
Topics: Berberine; Diabetes Mellitus, Type 2; Drugs, Chinese Herbal; Humans; Hypoglycemic Agents; Insulin Re | 2017 |
New Insights into the Mechanisms of Chinese Herbal Products on Diabetes: A Focus on the "Bacteria-Mucosal Immunity-Inflammation-Diabetes" Axis.
Topics: Animals; Berberine; Curcumin; Diabetes Mellitus, Type 2; Drugs, Chinese Herbal; Gastrointestinal Mic | 2017 |
Effects of berberine on blood glucose in patients with type 2 diabetes mellitus: a systematic literature review and a meta-analysis.
Topics: Berberine; Blood Glucose; Diabetes Mellitus, Type 2; Drug Therapy, Combination; Fasting; Glycated He | 2019 |
Learning from berberine: Treating chronic diseases through multiple targets.
Topics: Berberine; China; Chronic Disease; Diabetes Mellitus, Type 2; Heart Diseases; Humans; Hyperlipidemia | 2015 |
[Progress of berberine for treatment of type 2 diabetes].
Topics: Animals; Berberine; Diabetes Mellitus, Type 2; Glucose; Humans; Hypoglycemic Agents; Insulin; Lipid | 2014 |
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension.
Topics: Antihypertensive Agents; Berberine; Diabetes Mellitus, Type 2; Humans; Hyperlipidemias; Hypertension | 2015 |
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension.
Topics: Antihypertensive Agents; Berberine; Diabetes Mellitus, Type 2; Humans; Hyperlipidemias; Hypertension | 2015 |
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension.
Topics: Antihypertensive Agents; Berberine; Diabetes Mellitus, Type 2; Humans; Hyperlipidemias; Hypertension | 2015 |
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension.
Topics: Antihypertensive Agents; Berberine; Diabetes Mellitus, Type 2; Humans; Hyperlipidemias; Hypertension | 2015 |
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension.
Topics: Antihypertensive Agents; Berberine; Diabetes Mellitus, Type 2; Humans; Hyperlipidemias; Hypertension | 2015 |
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension.
Topics: Antihypertensive Agents; Berberine; Diabetes Mellitus, Type 2; Humans; Hyperlipidemias; Hypertension | 2015 |
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension.
Topics: Antihypertensive Agents; Berberine; Diabetes Mellitus, Type 2; Humans; Hyperlipidemias; Hypertension | 2015 |
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension.
Topics: Antihypertensive Agents; Berberine; Diabetes Mellitus, Type 2; Humans; Hyperlipidemias; Hypertension | 2015 |
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension.
Topics: Antihypertensive Agents; Berberine; Diabetes Mellitus, Type 2; Humans; Hyperlipidemias; Hypertension | 2015 |
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension.
Topics: Antihypertensive Agents; Berberine; Diabetes Mellitus, Type 2; Humans; Hyperlipidemias; Hypertension | 2015 |
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension.
Topics: Antihypertensive Agents; Berberine; Diabetes Mellitus, Type 2; Humans; Hyperlipidemias; Hypertension | 2015 |
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension.
Topics: Antihypertensive Agents; Berberine; Diabetes Mellitus, Type 2; Humans; Hyperlipidemias; Hypertension | 2015 |
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension.
Topics: Antihypertensive Agents; Berberine; Diabetes Mellitus, Type 2; Humans; Hyperlipidemias; Hypertension | 2015 |
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension.
Topics: Antihypertensive Agents; Berberine; Diabetes Mellitus, Type 2; Humans; Hyperlipidemias; Hypertension | 2015 |
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension.
Topics: Antihypertensive Agents; Berberine; Diabetes Mellitus, Type 2; Humans; Hyperlipidemias; Hypertension | 2015 |
Meta-analysis of the effect and safety of berberine in the treatment of type 2 diabetes mellitus, hyperlipemia and hypertension.
Topics: Antihypertensive Agents; Berberine; Diabetes Mellitus, Type 2; Humans; Hyperlipidemias; Hypertension | 2015 |
Berberine as a therapy for type 2 diabetes and its complications: From mechanism of action to clinical studies.
Topics: Animals; Berberine; Diabetes Mellitus, Type 2; Humans; Hypoglycemic Agents | 2015 |
Potential benefits of berberine in the management of perimenopausal syndrome.
Topics: Berberine; Cardiovascular Diseases; Diabetes Mellitus, Type 2; Female; Humans; Insulin Resistance; L | 2015 |
[Effect of berberine in treating type 2 diabetes mellitus and complications and its relevant mechanisms].
Topics: Animals; Berberine; Blood Glucose; Diabetes Complications; Diabetes Mellitus, Type 2; Drugs, Chinese | 2015 |
Modulating gut microbiota as an anti-diabetic mechanism of berberine.
Topics: Animals; Berberine; Blood Glucose; Diabetes Mellitus, Type 2; Gastrointestinal Tract; Gene Expressio | 2011 |
Antidiabetic properties of berberine: from cellular pharmacology to clinical effects.
Topics: Animals; Berberine; Cardiovascular Diseases; Diabetes Mellitus, Type 2; Humans; Hypoglycemic Agents; | 2012 |
GPR40: a therapeutic target for mediating insulin secretion (review).
Topics: Animals; Benzofurans; Berberine; Clinical Trials, Phase II as Topic; Diabetes Mellitus, Type 2; Fatt | 2012 |
10 trials available for berberine and Diabetes Mellitus, Type 2
Article | Year |
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A phase 2, proof of concept, randomised controlled trial of berberine ursodeoxycholate in patients with presumed non-alcoholic steatohepatitis and type 2 diabetes.
Topics: Adiposity; Adult; Aged; Berberine; Diabetes Mellitus, Type 2; Female; Glycated Hemoglobin; Humans; L | 2021 |
A phase 2, proof of concept, randomised controlled trial of berberine ursodeoxycholate in patients with presumed non-alcoholic steatohepatitis and type 2 diabetes.
Topics: Adiposity; Adult; Aged; Berberine; Diabetes Mellitus, Type 2; Female; Glycated Hemoglobin; Humans; L | 2021 |
A phase 2, proof of concept, randomised controlled trial of berberine ursodeoxycholate in patients with presumed non-alcoholic steatohepatitis and type 2 diabetes.
Topics: Adiposity; Adult; Aged; Berberine; Diabetes Mellitus, Type 2; Female; Glycated Hemoglobin; Humans; L | 2021 |
A phase 2, proof of concept, randomised controlled trial of berberine ursodeoxycholate in patients with presumed non-alcoholic steatohepatitis and type 2 diabetes.
Topics: Adiposity; Adult; Aged; Berberine; Diabetes Mellitus, Type 2; Female; Glycated Hemoglobin; Humans; L | 2021 |
Gut microbiome-related effects of berberine and probiotics on type 2 diabetes (the PREMOTE study).
Topics: Berberine; Diabetes Mellitus, Type 2; Female; Gastrointestinal Microbiome; Glycated Hemoglobin; Huma | 2020 |
Gut microbiome-related effects of berberine and probiotics on type 2 diabetes (the PREMOTE study).
Topics: Berberine; Diabetes Mellitus, Type 2; Female; Gastrointestinal Microbiome; Glycated Hemoglobin; Huma | 2020 |
Gut microbiome-related effects of berberine and probiotics on type 2 diabetes (the PREMOTE study).
Topics: Berberine; Diabetes Mellitus, Type 2; Female; Gastrointestinal Microbiome; Glycated Hemoglobin; Huma | 2020 |
Gut microbiome-related effects of berberine and probiotics on type 2 diabetes (the PREMOTE study).
Topics: Berberine; Diabetes Mellitus, Type 2; Female; Gastrointestinal Microbiome; Glycated Hemoglobin; Huma | 2020 |
Gender differences in the efficacy of pioglitazone treatment in nonalcoholic fatty liver disease patients with abnormal glucose metabolism.
Topics: Berberine; Diabetes Mellitus, Type 2; Female; Glucose; Humans; Male; Non-alcoholic Fatty Liver Disea | 2021 |
Effectiveness and safety of bifidobacteria and berberine in people with hyperglycemia: study protocol for a randomized controlled trial.
Topics: Adolescent; Adult; Aged; Berberine; Bifidobacterium; Biomarkers; Blood Glucose; Child; China; Combin | 2018 |
Berberine lowers blood glucose in type 2 diabetes mellitus patients through increasing insulin receptor expression.
Topics: Aged; Berberine; Blood Glucose; Cell Line; Diabetes Mellitus, Type 2; Female; Gene Expression; Human | 2010 |
Effect of traditional Chinese medicine berberine on type 2 diabetes based on comprehensive metabonomics.
Topics: Aged; Berberine; Chromatography, Liquid; Diabetes Mellitus, Type 2; Double-Blind Method; Dyslipidemi | 2010 |
[Research on therapeutic effect and hemorrheology change of berberine in new diagnosed patients with type 2 diabetes combining nonalcoholic fatty liver disease].
Topics: Adult; Alanine Transaminase; Berberine; Diabetes Mellitus, Type 2; Drugs, Chinese Herbal; Fatty Live | 2011 |
Treatment of type 2 diabetes and dyslipidemia with the natural plant alkaloid berberine.
Topics: Adult; Aged; Berberine; Cholesterol, LDL; Diabetes Mellitus, Type 2; Double-Blind Method; Dyslipidem | 2008 |
Efficacy of berberine in patients with type 2 diabetes mellitus.
Topics: Adult; Aged; Berberine; Cholesterol, HDL; Diabetes Mellitus, Type 2; Drug Therapy, Combination; Fema | 2008 |
[Clinical study on jiang tang san in treating non-insulin dependent diabetes mellitus patients].
Topics: Adult; Aged; Berberine; Blood Glucose; Blood Pressure; Diabetes Mellitus, Type 2; Drugs, Chinese Her | 1994 |
67 other studies available for berberine and Diabetes Mellitus, Type 2
Article | Year |
---|---|
Synthesis and hypoglycemic activity of 9-O-(lipophilic group substituted) berberine derivatives.
Topics: Berberine; Diabetes Mellitus, Type 2; Hep G2 Cells; Humans; Hypoglycemic Agents; Spectrum Analysis | 2016 |
Berberine combined with stachyose improves glycometabolism and gut microbiota through regulating colonic microRNA and gene expression in diabetic rats.
Topics: Animals; Berberine; Colon; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Gastrointesti | 2021 |
Berberine Improves the Symptoms of DHEA-Induced PCOS Rats by Regulating Gut Microbiotas and Metabolites.
Topics: Animals; Berberine; Dehydroepiandrosterone; Diabetes Mellitus, Type 2; Female; Gastrointestinal Micr | 2021 |
Berberine Acts on C/EBPβ/lncRNA Gas5/miR-18a-5p Loop to Decrease the Mitochondrial ROS Generation in HK-2 Cells.
Topics: Animals; Apoptosis; Berberine; CCAAT-Enhancer-Binding Protein-beta; Diabetes Mellitus, Experimental; | 2021 |
Exploring the synergistic and complementary effects of berberine and paeoniflorin in the treatment of type 2 diabetes mellitus by network pharmacology.
Topics: Animals; Berberine; Blood Glucose; Diabetes Mellitus, Type 2; Disease Models, Animal; Drugs, Chinese | 2022 |
Alleviation of Diabetic Tendon Injury via Activation of Tendon Fibroblasts Autophagy under Berberine Treatment.
Topics: Animals; Apoptosis; Autophagy; Berberine; Diabetes Mellitus, Type 2; Fibroblasts; Rats; Tendon Injur | 2022 |
Berberine reduces hepatic ceramide levels to improve insulin resistance in HFD-fed mice by inhibiting HIF-2α.
Topics: Animals; Basic Helix-Loop-Helix Transcription Factors; Berberine; Ceramides; Diabetes Mellitus, Type | 2022 |
Huangbai liniment and berberine promoted wound healing in high-fat diet/Streptozotocin-induced diabetic rats.
Topics: Animals; Berberine; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Diet, High-Fat; Drug | 2022 |
Effects of combination treatment with metformin and berberine on hypoglycemic activity and gut microbiota modulation in db/db mice.
Topics: Animals; Berberine; Chromatography, Liquid; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type | 2022 |
Berberine chloride (dual topoisomerase I and II inhibitor) modulate mitochondrial uncoupling protein (UCP1) in molecular docking and dynamic with in-vitro cytotoxic and mitochondrial ATP production.
Topics: Adenosine Triphosphate; Adipocytes, Brown; Adipose Tissue, Brown; Berberine; Chlorides; Diabetes Mel | 2023 |
Exploration of Isoquinoline Alkaloids as Potential Inhibitors against Human Islet Amyloid Polypeptide.
Topics: Amyloid; Berberine; Diabetes Mellitus, Type 2; Humans; Islet Amyloid Polypeptide; Isoquinolines; Pro | 2022 |
A New Berberine Preparation Protects Pancreatic Islet Cells from Apoptosis Mediated by Inhibition of Phospholipase A
Topics: Animals; Apoptosis; Berberine; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Insulin-S | 2022 |
Berberine Regulates GPX4 to Inhibit Ferroptosis of Islet β Cells.
Topics: Berberine; Diabetes Mellitus, Type 1; Diabetes Mellitus, Type 2; Ferroptosis; Reactive Oxygen Specie | 2023 |
Investigating the Mechanism of Rhizoma Coptidis-Eupatorium fortunei Medicine in the Treatment of Type 2 Diabetes Based on Network Pharmacology and Molecular Docking.
Topics: Antineoplastic Agents; Berberine; Diabetes Mellitus, Type 2; Drugs, Chinese Herbal; Eupatorium; Inte | 2022 |
Investigating the Mechanism of Rhizoma Coptidis-Eupatorium fortunei Medicine in the Treatment of Type 2 Diabetes Based on Network Pharmacology and Molecular Docking.
Topics: Antineoplastic Agents; Berberine; Diabetes Mellitus, Type 2; Drugs, Chinese Herbal; Eupatorium; Inte | 2022 |
Investigating the Mechanism of Rhizoma Coptidis-Eupatorium fortunei Medicine in the Treatment of Type 2 Diabetes Based on Network Pharmacology and Molecular Docking.
Topics: Antineoplastic Agents; Berberine; Diabetes Mellitus, Type 2; Drugs, Chinese Herbal; Eupatorium; Inte | 2022 |
Investigating the Mechanism of Rhizoma Coptidis-Eupatorium fortunei Medicine in the Treatment of Type 2 Diabetes Based on Network Pharmacology and Molecular Docking.
Topics: Antineoplastic Agents; Berberine; Diabetes Mellitus, Type 2; Drugs, Chinese Herbal; Eupatorium; Inte | 2022 |
Metabolic profiling integrated with pharmacokinetics to reveal the material basis of Xiaokeyinshui extract combination in the treatment of type 2 diabetes in rats.
Topics: Alkaloids; Animals; Berberine; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Drugs, Ch | 2023 |
Berberine protects mice against type 2 diabetes by promoting PPARγ-FGF21-GLUT2-regulated insulin sensitivity and glucose/lipid homeostasis.
Topics: Animals; Berberine; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Glucose; Homeostasis | 2023 |
Effects of berberine and metformin on intestinal inflammation and gut microbiome composition in db/db mice.
Topics: Animals; Berberine; Blood Glucose; Body Weight; Diabetes Mellitus, Experimental; Diabetes Mellitus, | 2019 |
Highly bioavailable berberine formulation ameliorates diabetic nephropathy through the inhibition of glomerular mesangial matrix expansion and the activation of autophagy.
Topics: AMP-Activated Protein Kinases; Animals; Autophagy; Berberine; Diabetes Mellitus, Experimental; Diabe | 2020 |
Synthesis of disaccharide modified berberine derivatives and their anti-diabetic investigation in zebrafish using a fluorescence-based technology.
Topics: Animals; Berberine; Blood Glucose; Diabetes Mellitus, Type 2; Disaccharides; Disease Models, Animal; | 2020 |
Berberine attenuates the abnormal ectopic lipid deposition in skeletal muscle.
Topics: Animals; Berberine; Diabetes Mellitus, Type 2; Humans; Lipids; Mice; Mitochondria, Muscle; Muscle, S | 2020 |
Macrovascular Protecting Effects of Berberine through Anti-inflammation and Intervention of BKCa in Type 2 Diabetes Mellitus Rats.
Topics: Animals; Anti-Inflammatory Agents; Aorta, Thoracic; Berberine; Cell Movement; Cell Proliferation; Ce | 2021 |
Berberine alleviates type 2 diabetic symptoms by altering gut microbiota and reducing aromatic amino acids.
Topics: Amino Acids, Aromatic; Animals; Berberine; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type | 2020 |
Remission of new-onset type 2 diabetes mellitus in an adolescent using an integrative medicine approach: A case report.
Topics: Berberine; Blood Glucose; Child; Diabetes Mellitus, Type 2; Diet; Drugs, Chinese Herbal; Exercise; G | 2021 |
Antidiabetic Effects of Gegen Qinlian Decoction via the Gut Microbiota Are Attributable to Its Key Ingredient Berberine.
Topics: Animals; Berberine; Diabetes Mellitus, Type 2; Drugs, Chinese Herbal; Gastrointestinal Microbiome; H | 2020 |
[Effect of berberine on insulin resistance in diabetic rats].
Topics: Animals; Berberine; Blood Glucose; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Insul | 2020 |
In silico network pharmacology and in vivo analysis of berberine-related mechanisms against type 2 diabetes mellitus and its complications.
Topics: Animals; Berberine; Blood Glucose; Body Weight; Computational Biology; Computer Simulation; Diabetes | 2021 |
Berberine Slows the Progression of Prediabetes to Diabetes in Zucker Diabetic Fatty Rats by Enhancing Intestinal Secretion of Glucagon-Like Peptide-2 and Improving the Gut Microbiota.
Topics: Animals; Berberine; Cells, Cultured; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Dis | 2021 |
Pioglitazone-induced bone loss in diabetic rats and its amelioration by berberine: A portrait of molecular crosstalk.
Topics: Animals; Berberine; Biomarkers; Blood Glucose; Bone and Bones; Bone Density; Diabetes Mellitus, Expe | 2017 |
[Regulations of berberine on gene expression of BMP4 transcriptional pathways to improve visceral white adipose tissues insulin resistance in type 2 diabetic hamsters].
Topics: Activating Transcription Factor 2; Adipose Tissue, Brown; Adipose Tissue, White; Animals; Berberine; | 2016 |
Protective role of berberine and Coptischinensis extract on T2MD rats and associated islet Rin‑5f cells.
Topics: Animals; Berberine; Blood Glucose; Cell Cycle Checkpoints; Cell Line; Cell Proliferation; Cell Survi | 2017 |
Berberine Inhibits Oxygen Consumption Rate Independent of Alteration in Cardiolipin Levels in H9c2 Cells.
Topics: Animals; Berberine; Cardiolipins; Cell Line; Cyclophilins; Diabetes Mellitus, Type 2; DNA Replicatio | 2017 |
Berberine Alleviates Tau Hyperphosphorylation and Axonopathy-Associated with Diabetic Encephalopathy via Restoring PI3K/Akt/GSK3β Pathway.
Topics: Animals; Axons; Berberine; Cells, Cultured; Chromones; Diabetes Mellitus, Type 2; Diabetic Nephropat | 2018 |
SirT3 regulates diabetogenic effects caused by arsenic: An implication for mitochondrial complex II modification.
Topics: Animals; Arsenic; Berberine; Blood Glucose; Diabetes Mellitus, Type 2; Electron Transport Complex II | 2019 |
A novel berberine-metformin hybrid compound exerts therapeutic effects on obese type 2 diabetic rats.
Topics: 3T3 Cells; Adipogenesis; Adipose Tissue, White; Animals; Berberine; Diabetes Mellitus, Type 2; Femal | 2019 |
Berberine alleviates hyperglycemia by targeting hepatic glucokinase in diabetic db/db mice.
Topics: Animals; Berberine; Blood Glucose; Diabetes Mellitus, Type 2; Glucokinase; Glucose; Hepatocytes; Hum | 2019 |
Alteration of the intestinal barrier and GLP2 secretion in Berberine-treated type 2 diabetic rats.
Topics: Animals; Berberine; Diabetes Mellitus, Type 2; Drugs, Chinese Herbal; Glucagon-Like Peptide 2; Gluco | 2013 |
Amorphous solid dispersion of berberine with absorption enhancer demonstrates a remarkable hypoglycemic effect via improving its bioavailability.
Topics: Administration, Oral; Animals; Berberine; Biological Availability; Blood Glucose; Caco-2 Cells; Calo | 2014 |
Synthesis and in vitro evaluation of 12-(substituted aminomethyl) berberrubine derivatives as anti-diabetics.
Topics: 3T3-L1 Cells; Adipocytes; Animals; Berberine; Diabetes Mellitus, Type 2; Dose-Response Relationship, | 2014 |
Berberine moderates glucose metabolism through the GnRH-GLP-1 and MAPK pathways in the intestine.
Topics: Animals; Berberine; Blood Glucose; Body Weight; Carbohydrate Metabolism; Diabetes Mellitus, Experime | 2014 |
Renoprotective effect of berberine on type 2 diabetic nephropathy in rats.
Topics: Animals; Berberine; Diabetes Mellitus, Type 2; Diabetic Nephropathies; Inflammation Mediators; Male; | 2015 |
The marketing of unproven drugs for diabetes and dyslipidaemia in India.
Topics: Berberine; Diabetes Mellitus, Type 2; Drug Approval; Drug Industry; Dyslipidemias; Humans; Hydroxych | 2015 |
Indian endocrinologists start debate on diabetes drug.
Topics: Berberine; Diabetes Mellitus, Type 2; Drug Approval; Drug Industry; Dyslipidemias; Humans; Hydroxych | 2015 |
Berberine treatment prevents cardiac dysfunction and remodeling through activation of 5'-adenosine monophosphate-activated protein kinase in type 2 diabetic rats and in palmitate-induced hypertrophic H9c2 cells.
Topics: AMP-Activated Protein Kinases; Animals; Berberine; Cardiomegaly; Cell Line; Diabetes Mellitus, Type | 2015 |
Effects of berberine and pomegranate seed oil on plasma phospholipid metabolites associated with risks of type 2 diabetes mellitus by U-HPLC/Q-TOF-MS.
Topics: Animals; Berberine; Biomarkers; Chromatography, High Pressure Liquid; Diabetes Mellitus, Type 2; Lyt | 2015 |
Drug approvals in India.
Topics: Berberine; Diabetes Mellitus, Type 2; Drug Approval; Drug Industry; Dyslipidemias; Humans; Hydroxych | 2016 |
Drug approvals in India.
Topics: Berberine; Diabetes Mellitus, Type 2; Drug Approval; Drug Industry; Dyslipidemias; Humans; Hydroxych | 2016 |
Drug approvals in India - Authors' reply.
Topics: Berberine; Diabetes Mellitus, Type 2; Drug Approval; Drug Industry; Dyslipidemias; Humans; Hydroxych | 2016 |
Berberine Pretreatment Confers Cardioprotection Against Ischemia-Reperfusion Injury in a Rat Model of Type 2 Diabetes.
Topics: AMP-Activated Protein Kinases; Animals; Arrhythmias, Cardiac; Berberine; Biomarkers; Blood Glucose; | 2016 |
Metabolomics Study of Type 2 Diabetes Mellitus and the AntiDiabetic Effect of Berberine in Zucker Diabetic Fatty Rats Using Uplc-ESI-Hdms.
Topics: Animals; Berberine; Chromatography, High Pressure Liquid; Diabetes Mellitus, Type 2; Drugs, Chinese | 2016 |
Berberine Attenuates Development of the Hepatic Gluconeogenesis and Lipid Metabolism Disorder in Type 2 Diabetic Mice and in Palmitate-Incubated HepG2 Cells through Suppression of the HNF-4α miR122 Pathway.
Topics: Acetyl-CoA Carboxylase; Animals; Berberine; Blood Glucose; Carnitine O-Palmitoyltransferase; Cell Su | 2016 |
[Pharmacokinetic and pharmacodynamic characteristics of berberine and jateorhizine in Coptidis Rhizoma powder and their monomeric compounds in type 2 diabetic rats].
Topics: Animals; Berberine; Blood Glucose; Coptis; Diabetes Mellitus, Type 2; Drugs, Chinese Herbal; Humans; | 2015 |
Berberine reduces insulin resistance through protein kinase C-dependent up-regulation of insulin receptor expression.
Topics: Animals; Berberine; Cell Line, Tumor; Diabetes Mellitus, Type 1; Diabetes Mellitus, Type 2; Female; | 2009 |
Anti-diabetic effects of cinnamaldehyde and berberine and their impacts on retinol-binding protein 4 expression in rats with type 2 diabetes mellitus.
Topics: Acrolein; Animals; Berberine; Blotting, Western; Body Weight; Diabetes Mellitus, Type 2; Glucose Tra | 2008 |
The characterization of high-fat diet and multiple low-dose streptozotocin induced type 2 diabetes rat model.
Topics: Alkaloids; Animals; Berberine; Blood Glucose; Diabetes Mellitus, Type 2; Dietary Fats; Disease Model | 2008 |
Ameliorative effect of berberine on endothelial dysfunction in diabetic rats induced by high-fat diet and streptozotocin.
Topics: Animals; Berberine; Body Weight; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Dietary | 2009 |
Hypoglycemic and insulin-sensitizing effects of berberine in high-fat diet- and streptozotocin-induced diabetic rats.
Topics: Adiponectin; Animals; Berberine; Blood Glucose; C-Reactive Protein; Cholesterol; Diabetes Mellitus, | 2011 |
Berberine elicits anti-arrhythmic effects via IK1/Kir2.1 in the rat type 2 diabetic myocardial infarction model.
Topics: Animals; Anti-Arrhythmia Agents; Berberine; Diabetes Mellitus, Type 2; Disease Models, Animal; Male; | 2011 |
Beneficial effect of berberine on hepatic insulin resistance in diabetic hamsters possibly involves in SREBPs, LXRα and PPARα transcriptional programs.
Topics: Animals; Berberine; Cricetinae; Diabetes Mellitus, Type 2; Female; Gene Expression Profiling; Gene E | 2010 |
Berberine regulates peroxisome proliferator-activated receptors and positive transcription elongation factor b expression in diabetic adipocytes.
Topics: 3T3-L1 Cells; Adipocytes; Adipogenesis; Adiposity; Animals; Berberine; Diabetes Mellitus, Type 2; Do | 2010 |
Berberine improves glucose metabolism in diabetic rats by inhibition of hepatic gluconeogenesis.
Topics: Animals; Berberine; Blood Glucose; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Down- | 2011 |
Berberine-improved visceral white adipose tissue insulin resistance associated with altered sterol regulatory element-binding proteins, liver x receptors, and peroxisome proliferator-activated receptors transcriptional programs in diabetic hamsters.
Topics: Adipose Tissue; Animals; Base Sequence; Berberine; Cricetinae; Diabetes Mellitus, Type 2; DNA Primer | 2011 |
Anti-diabetic effects of TongGuanWan, a Chinese traditional herbal formula, in C57BL/KsJ-db/db mice.
Topics: Acrolein; Administration, Oral; Animals; Berberine; Blood Glucose; Body Weight; Cholesterol, HDL; Ch | 2012 |
Alteration of hepatic glutathione peroxidase and superoxide dismutase expression in streptozotocin-induced diabetic mice by berberine.
Topics: Animals; Antioxidants; Berberine; Blood Glucose; Diabetes Mellitus, Type 2; Down-Regulation; Glutath | 2012 |
Antihyperglycemic activity with DPP-IV inhibition of alkaloids from seed extract of Castanospermum australe: Investigation by experimental validation and molecular docking.
Topics: Alkaloids; Animals; Berberine; Blood Glucose; Castanospermum; Diabetes Mellitus, Experimental; Diabe | 2012 |
Berberine improves glucose metabolism through induction of glycolysis.
Topics: 3T3-L1 Cells; Adenosine Monophosphate; Adenosine Triphosphate; Adipocytes; AMP-Activated Protein Kin | 2008 |
Effect of berberine on PPARalpha/delta/gamma expression in type 2 diabetic rat retinae.
Topics: Animals; Berberine; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Diabetic Retinopathy | 2007 |
[Therapeutic effect of berberine on 60 patients with type II diabetes mellitus and experimental research].
Topics: Adult; Aged; Alloxan; Animals; Berberine; Berberine Alkaloids; Blood Glucose; Diabetes Mellitus, Exp | 1988 |