hydrogen sulfide has been researched along with Diabetic Cardiomyopathies in 18 studies
Hydrogen Sulfide: A flammable, poisonous gas with a characteristic odor of rotten eggs. It is used in the manufacture of chemicals, in metallurgy, and as an analytical reagent. (From Merck Index, 11th ed)
hydrogen sulfide : A sulfur hydride consisting of a single sulfur atom bonded to two hydrogen atoms. A highly poisonous, flammable gas with a characteristic odour of rotten eggs, it is often produced by bacterial decomposition of organic matter in the absence of oxygen.
thiol : An organosulfur compound in which a thiol group, -SH, is attached to a carbon atom of any aliphatic or aromatic moiety.
Diabetic Cardiomyopathies: Diabetes complications in which VENTRICULAR REMODELING in the absence of CORONARY ATHEROSCLEROSIS and hypertension results in cardiac dysfunctions, typically LEFT VENTRICULAR DYSFUNCTION. The changes also result in myocardial hypertrophy, myocardial necrosis and fibrosis, and collagen deposition due to impaired glucose tolerance.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The aim of the present study was to determine the role of hydrogen sulfide (H2S) in improving myocardial fibrosis and its effects on oxidative stress, endoplasmic reticulum (ER) stress and cell apoptosis in diabetic rats, by regulating the Janus kinase̸signal transducer and activator of transcription (JAK̸STAT) signaling pathway." | 7.88 | Hydrogen sulfide attenuates myocardial fibrosis in diabetic rats through the JAK/STAT signaling pathway. ( Chu, C; Jiang, Z; Li, Y; Li, Z; Liang, B; Liu, M; Yang, J, 2018) |
| "In order to explore the effects of hydrogen sulfide (H2S) on myocardial fibrosis in diabetic rats and its underlying mechanisms, intraperitoneal injections of streptozotocin were used to establish the diabetes models and sodium hydrosulfide (NaHS) was used as an exogenous donor of H2S." | 7.81 | Effects of hydrogen sulfide on myocardial fibrosis in diabetic rats: Changes in matrix metalloproteinases parameters. ( Li, F; Luo, J; Wu, Z; Xiao, T; Yang, J; Zeng, O, 2015) |
| "The aim of the present study was to determine the role of hydrogen sulfide (H2S) in improving myocardial fibrosis and its effects on oxidative stress, endoplasmic reticulum (ER) stress and cell apoptosis in diabetic rats, by regulating the Janus kinase̸signal transducer and activator of transcription (JAK̸STAT) signaling pathway." | 3.88 | Hydrogen sulfide attenuates myocardial fibrosis in diabetic rats through the JAK/STAT signaling pathway. ( Chu, C; Jiang, Z; Li, Y; Li, Z; Liang, B; Liu, M; Yang, J, 2018) |
| "Previous studies have suggested that exogenous hydrogen sulfide can alleviate the development of diabetic cardiomyopathy (DCM) by inhibiting oxidative stress, inflammation, and apoptosis." | 3.88 | Exogenous hydrogen sulfide attenuates the development of diabetic cardiomyopathy via the FoxO1 pathway. ( Chao, YL; Chen, SL; Gu, Y; Kong, XQ; Luo, J; Ren, XM; Ye, P; Zhang, DM; Zhu, YR; Zuo, GF, 2018) |
| "In order to explore the effects of hydrogen sulfide (H2S) on myocardial fibrosis in diabetic rats and its underlying mechanisms, intraperitoneal injections of streptozotocin were used to establish the diabetes models and sodium hydrosulfide (NaHS) was used as an exogenous donor of H2S." | 3.81 | Effects of hydrogen sulfide on myocardial fibrosis in diabetic rats: Changes in matrix metalloproteinases parameters. ( Li, F; Luo, J; Wu, Z; Xiao, T; Yang, J; Zeng, O, 2015) |
| "Hydrogen sulfide (H2S) has been found to be the third gaseous signaling molecule with anti‑ER stress effects." | 1.43 | Hydrogen sulfide exhibits cardioprotective effects by decreasing endoplasmic reticulum stress in a diabetic cardiomyopathy rat model. ( Li, F; Li, L; Li, Y; Luo, J; Wu, Z; Xiao, T; Yang, J; Zeng, O, 2016) |
| "Hydrogen sulfide (H2S) is an endogenously produced signaling molecule that is critical for the regulation of cardiovascular homeostasis." | 1.42 | Hydrogen sulfide attenuates high fat diet-induced cardiac dysfunction via the suppression of endoplasmic reticulum stress. ( Barr, LA; Calvert, JW; Lambert, JP; Nicholson, CK; Shimizu, Y, 2015) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 12 (66.67) | 24.3611 |
| 2020's | 6 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Deng, NH | 1 |
| Luo, W | 1 |
| Gui, DD | 1 |
| Yan, BJ | 1 |
| Zhou, K | 1 |
| Tian, KJ | 1 |
| Ren, Z | 1 |
| Xiong, WH | 1 |
| Jiang, ZS | 1 |
| Carbone, F | 1 |
| Montecucco, F | 1 |
| Zhao, H | 1 |
| Liu, H | 2 |
| Yang, Y | 1 |
| Lan, T | 1 |
| Wang, H | 2 |
| Wu, D | 1 |
| Dugbartey, GJ | 1 |
| Wonje, QL | 1 |
| Alornyo, KK | 1 |
| Adams, I | 1 |
| Diaba, DE | 1 |
| Liu, X | 1 |
| Yang, R | 2 |
| Bai, W | 1 |
| Xu, X | 1 |
| Bi, F | 1 |
| Hao, Y | 1 |
| Yang, Q | 1 |
| Li, H | 1 |
| Lv, S | 1 |
| Liu, M | 1 |
| Li, Y | 2 |
| Liang, B | 1 |
| Li, Z | 1 |
| Jiang, Z | 1 |
| Chu, C | 1 |
| Yang, J | 3 |
| Ye, P | 1 |
| Gu, Y | 1 |
| Zhu, YR | 1 |
| Chao, YL | 1 |
| Kong, XQ | 1 |
| Luo, J | 3 |
| Ren, XM | 1 |
| Zuo, GF | 1 |
| Zhang, DM | 1 |
| Chen, SL | 1 |
| Kar, S | 1 |
| Kambis, TN | 1 |
| Mishra, PK | 1 |
| Patel, VB | 1 |
| McLean, BA | 1 |
| Chen, X | 1 |
| Oudit, GY | 1 |
| Zhou, X | 1 |
| An, G | 1 |
| Lu, X | 1 |
| Barr, LA | 1 |
| Shimizu, Y | 1 |
| Lambert, JP | 1 |
| Nicholson, CK | 1 |
| Calvert, JW | 1 |
| Yang, H | 1 |
| Mao, Y | 1 |
| Tan, B | 1 |
| Luo, S | 1 |
| Zhu, Y | 1 |
| Xiao, T | 2 |
| Zeng, O | 2 |
| Wu, Z | 2 |
| Li, F | 2 |
| Cheng, YS | 1 |
| Dai, DZ | 1 |
| Dai, Y | 1 |
| Zhu, DD | 1 |
| Liu, BC | 1 |
| Li, L | 1 |
| Jia, Q | 1 |
| Liu, XF | 1 |
| Gao, Q | 1 |
| Wang, L | 1 |
| Ma, SF | 1 |
| Yang, F | 1 |
| Yu, X | 1 |
| Li, T | 1 |
| Wu, J | 2 |
| Zhao, Y | 1 |
| Liu, J | 1 |
| Sun, A | 1 |
| Dong, S | 1 |
| Zhong, X | 1 |
| Xu, C | 1 |
| Lu, F | 1 |
| Zhang, W | 1 |
4 reviews available for hydrogen sulfide and Diabetic Cardiomyopathies
| Article | Year |
|---|---|
Hydrogen sulfide plays a potential alternative for the treatment of metabolic disorders of diabetic cardiomyopathy.
Topics: Animals; Diabetic Cardiomyopathies; Energy Metabolism; Humans; Hydrogen Sulfide; Insulin Resistance; | 2022 |
Hydrogen Sulfide Plays an Important Role by Regulating Endoplasmic Reticulum Stress in Diabetes-Related Diseases.
Topics: Diabetes Mellitus; Diabetic Cardiomyopathies; Endoplasmic Reticulum; Endoplasmic Reticulum Stress; H | 2022 |
Exogenous Hydrogen Sulfide Plays an Important Role by Regulating Autophagy in Diabetic-Related Diseases.
Topics: Animals; Autophagy; Depressive Disorder; Diabetes Mellitus; Diabetic Angiopathies; Diabetic Cardiomy | 2021 |
Hydrogen sulfide-mediated regulation of cell death signaling ameliorates adverse cardiac remodeling and diabetic cardiomyopathy.
Topics: Animals; Apoptosis; Autophagy; Cardiovascular Agents; Diabetic Cardiomyopathies; Humans; Hydrogen Su | 2019 |
14 other studies available for hydrogen sulfide and Diabetic Cardiomyopathies
| Article | Year |
|---|---|
Hydrogen sulphide: Diabetic cardiomyopathy as the paradigm of its pleiotropic function.
Topics: Diabetes Mellitus; Diabetic Cardiomyopathies; Humans; Hydrogen Sulfide | 2022 |
Alpha-lipoic acid treatment improves adverse cardiac remodelling in the diabetic heart - The role of cardiac hydrogen sulfide-synthesizing enzymes.
Topics: Animals; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Diabetic Cardiomyopathies; Hydr | 2022 |
Involvement of amylin B-H2S-connexin 43 signaling pathway in vascular dysfunction and enhanced ischemia-reperfusion-induced myocardial injury in diabetic rats.
Topics: Amylin Receptor Agonists; Animals; Carbenoxolone; Connexin 43; Diabetic Angiopathies; Diabetic Cardi | 2020 |
Hydrogen sulfide attenuates myocardial fibrosis in diabetic rats through the JAK/STAT signaling pathway.
Topics: Animals; Apoptosis; Diabetes Mellitus, Experimental; Diabetic Cardiomyopathies; Endoplasmic Reticulu | 2018 |
Exogenous hydrogen sulfide attenuates the development of diabetic cardiomyopathy via the FoxO1 pathway.
Topics: Animals; Apoptosis; Diabetic Cardiomyopathies; Disease Models, Animal; Forkhead Box Protein O1; Hear | 2018 |
Hydrogen sulfide: an old gas with new cardioprotective effects.
Topics: Animals; Diabetic Cardiomyopathies; Hydrogen Sulfide; Male | 2015 |
Hydrogen sulfide attenuates the development of diabetic cardiomyopathy.
Topics: Animals; Cytokines; Diabetic Cardiomyopathies; Hydrogen Sulfide; Inflammation Mediators; Male; Oxida | 2015 |
Hydrogen sulfide attenuates high fat diet-induced cardiac dysfunction via the suppression of endoplasmic reticulum stress.
Topics: Adiponectin; Administration, Oral; AMP-Activated Protein Kinases; Animals; Diabetic Cardiomyopathies | 2015 |
The protective effects of endogenous hydrogen sulfide modulator, S-propargyl-cysteine, on high glucose-induced apoptosis in cardiomyocytes: A novel mechanism mediated by the activation of Nrf2.
Topics: Animals; Antioxidants; Apoptosis; Blood Glucose; Cell Line; Cystathionine gamma-Lyase; Cysteine; Cyt | 2015 |
Effects of hydrogen sulfide on myocardial fibrosis in diabetic rats: Changes in matrix metalloproteinases parameters.
Topics: Animals; Diabetes Mellitus, Experimental; Diabetic Cardiomyopathies; Fibrosis; Heart; Hydrogen Sulfi | 2015 |
Exogenous hydrogen sulphide ameliorates diabetic cardiomyopathy in rats by reversing disordered calcium-handling system in sarcoplasmic reticulum.
Topics: Animals; Calcium; Diabetes Mellitus, Experimental; Diabetic Cardiomyopathies; Disease Models, Animal | 2016 |
Hydrogen sulfide exhibits cardioprotective effects by decreasing endoplasmic reticulum stress in a diabetic cardiomyopathy rat model.
Topics: Animals; Blood Glucose; Body Weight; Cardiotonic Agents; Diabetic Cardiomyopathies; Disease Models, | 2016 |
[Effect of hydrogen sulfide on oxidative stress and endoplasmic reticulum stress in diabetic cardiomyopathy].
Topics: Animals; Apoptosis; Caspase 12; Diabetes Mellitus, Experimental; Diabetic Cardiomyopathies; Endoplas | 2016 |
Exogenous H
Topics: Animals; Apoptosis; Blood Glucose; Blotting, Western; Cytochromes c; Diabetes Mellitus, Experimental | 2017 |