Page last updated: 2024-10-27

fenofibrate and Body Weight

fenofibrate has been researched along with Body Weight in 81 studies

Pharmavit: a polyvitamin product, comprising vitamins A, D2, B1, B2, B6, C, E, nicotinamide, & calcium pantothene; may be a promising agent for application to human populations exposed to carcinogenic and genetic hazards of ionizing radiation; RN from CHEMLINE

Body Weight: The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms.

Research Excerpts

ExcerptRelevanceReference
" The aim of our study was to explore the changes in circulating Pref-1 concentrations in female subjects with obesity (OB) (n=19), females with obesity and type 2 diabetes mellitus (T2DM) (n=22), and sex- and age-matched healthy control subjects (C) (n=22), and to study its modulation by very low calorie diet (VLCD), acute hyperinsulinemia during isoglycemic-hyperinsulinemic clamp, and 3 months' treatment with PPAR-α agonist fenofibrate."9.17Serum preadipocyte factor-1 concentrations in females with obesity and type 2 diabetes mellitus: the influence of very low calorie diet, acute hyperinsulinemia, and fenofibrate treatment. ( Drapalova, J; Haluzik, M; Haluzikova, D; Kavalkova, P; Lacinova, Z; Matoulek, M; Mraz, M; Novak, D; Roubicek, T; Touskova, V; Trachta, P; Urbanova, M, 2013)
"To assess the effect of rimonabant, micronised fenofibrate and their combination on anthropometric and metabolic parameters in overweight/obese patients with dyslipidaemia."9.13Effect of rimonabant, micronised fenofibrate and their combination on cardiometabolic risk factors in overweight/obese patients: a pilot study. ( Elisaf, M; Filippatos, TD; Florentin, M; Kostara, C; Liberopoulos, EN; Mikhailidis, DP; Tselepis, A, 2008)
"Fenofibrate (FF) is commonly used clinically as a lipid-lowering drug, but whether it participates in endoplasmic reticulum (ER) stress and decreases inflammation in skeletal muscle is still unknown."7.83Fenofibrate improves high-fat diet-induced and palmitate-induced endoplasmic reticulum stress and inflammation in skeletal muscle. ( Bao, YY; Chen, GJ; Chen, L; Dai, F; Jiang, T; Lu, YX; Zhang, Q, 2016)
" Fructose administration resulted in significant increase in body weight, elevations of blood glucose, serum insulin, cholesterol, triglycerides, advanced glycation end products (AGEs), uric acid levels, insulin resistance index and blood pressure compared to control rats."7.80Ursodeoxycholic acid ameliorates fructose-induced metabolic syndrome in rats. ( Elshazly, SM; Mahmoud, AA, 2014)
" Fenofibrate, a lipid-modifying agent that acts as a PPARalpha agonist, may prevent adipocyte hypertrophy and insulin resistance by increasing intracellular lipolysis from adipose tissue."7.75Fenofibrate inhibits adipocyte hypertrophy and insulin resistance by activating adipose PPARalpha in high fat diet-induced obese mice. ( Jeong, S; Yoon, M, 2009)
" The aim of this study was to investigate the effect of two different treatment periods of fenofibrate (CAS 49562-28-9) on serum, heart and liver sialic acid levels in experimental hypercholesterolemia."7.74Effect of fenofibrate on serum and tissue sialic acid levels in short-term experimental hypercholesterolemia. ( Emekli, N; Oztürk, LK; Yarat, A, 2007)
"We investigated whether fenofibrate improves lipid metabolism and obesity in female ovariectomized (OVX) or sham-operated (SO) low density lipoprotein receptor-null (LDLR-null) mice."7.72Fenofibrate improves lipid metabolism and obesity in ovariectomized LDL receptor-null mice. ( Han, M; Jeong, S; Kang, JH; Kim, EY; Kim, M; Lee, H; Oh, GT; Yoon, M, 2003)
" To determine whether fenofibrate reduces body weight gain and adiposity in female sham-operated (Sham) and ovariectomized (OVX) C57BL/6J mice, the effects of fenofibrate on not only body weight, white adipose tissue (WAT) mass, and food intake, but also the expression of both leptin and PPARalpha target genes were measured."7.72Effects of fenofibrate on high-fat diet-induced body weight gain and adiposity in female C57BL/6J mice. ( Choi, JH; Han, M; Jeong, S; Kim, BH; Kim, J; Kim, M; Lee, H; Nam, KH; Nicol, CJ; Oh, GT; Yoon, M, 2004)
"Our previous study demonstrated that fenofibrate improves both lipid metabolism and obesity, in part through hepatic peroxisome proliferator-activated receptor alpha (PPARalpha) activation, in female ovariectomized, but not in sham-operated, low-density lipoprotein receptor-null (LDLR-null) mice."7.72Fenofibrate prevents obesity and hypertriglyceridemia in low-density lipoprotein receptor-null mice. ( Ahn, J; Han, M; Jeong, S; Kim, M; Kim, TW; Lee, H; Nam, KH; Oh, GT; Shin, C; Song, YH; Yoon, M, 2004)
"To determine whether the PPARalpha agonist fenofibrate regulates obesity and lipid metabolism with sexual dimorphism, we examined the effects of fenofibrate on body weight, white adipose tissue (WAT) mass, circulating lipids, and the expression of PPARalpha target genes in both sexes of high fat diet-fed C57BL/6J mice."7.71Fenofibrate regulates obesity and lipid metabolism with sexual dimorphism. ( Han, M; Jeong, S; Kim, JJ; Lee, H; Nicol, CJ; Oh, GT; Ryu, C; Seo, YJ; Yoon, M, 2002)
" We compared the pharmacological profile of a PPARalpha activator, fenofibrate, and a PPARgamma activator, rosiglitazone, on serum parameters, target gene expression, and body weight gain in (fa/fa) fatty Zucker rats and db/db mice as well as their association in db/db mice."7.70Fenofibrate and rosiglitazone lower serum triglycerides with opposing effects on body weight. ( Chaput, E; Edgar, AD; Saladin, R; Silvestre, M, 2000)
"The results indicate that, in experimental arthritis, fenofibrate decreases skeletal muscle atrophy through inhibition of the ubiquitin-proteasome system and myostatin."5.37Fenofibrate, a PPAR{alpha} agonist, decreases atrogenes and myostatin expression and improves arthritis-induced skeletal muscle atrophy. ( Castillero, E; Fernández-Galaz, C; Granado, M; López-Calderón, A; López-Menduiña, M; Martín, AI; Nieto-Bona, MP; Villanúa, MA, 2011)
" The aim of our study was to explore the changes in circulating Pref-1 concentrations in female subjects with obesity (OB) (n=19), females with obesity and type 2 diabetes mellitus (T2DM) (n=22), and sex- and age-matched healthy control subjects (C) (n=22), and to study its modulation by very low calorie diet (VLCD), acute hyperinsulinemia during isoglycemic-hyperinsulinemic clamp, and 3 months' treatment with PPAR-α agonist fenofibrate."5.17Serum preadipocyte factor-1 concentrations in females with obesity and type 2 diabetes mellitus: the influence of very low calorie diet, acute hyperinsulinemia, and fenofibrate treatment. ( Drapalova, J; Haluzik, M; Haluzikova, D; Kavalkova, P; Lacinova, Z; Matoulek, M; Mraz, M; Novak, D; Roubicek, T; Touskova, V; Trachta, P; Urbanova, M, 2013)
"During the 8-week double-blind phase in subjects receiving fenofibrate, the addition of P-OM3 (versus placebo) did not significantly change median (minimum, maximum) body weight (P-OM3 = 0 [-4."5.14The effect of prescription omega-3 fatty acids on body weight after 8 to 16 weeks of treatment for very high triglyceride levels. ( Bays, HE; Doyle, RT; Maki, KC; Stein, E, 2009)
"To assess the effect of rimonabant, micronised fenofibrate and their combination on anthropometric and metabolic parameters in overweight/obese patients with dyslipidaemia."5.13Effect of rimonabant, micronised fenofibrate and their combination on cardiometabolic risk factors in overweight/obese patients: a pilot study. ( Elisaf, M; Filippatos, TD; Florentin, M; Kostara, C; Liberopoulos, EN; Mikhailidis, DP; Tselepis, A, 2008)
"Letrozole-treated rats showed successful induction of PCOS, confirmed by histopathology and significantly increased body weight, testosterone, insulin, AMH, and MDA, and decreased SOD."4.12Fenofibrate ameliorates letrozole-induced polycystic ovary in rats via modulation of PPARα and TNFα/CD95 pathway. ( El-Hussieny, M; Morsy, MA; Nair, AB; Refaie, MMM; Venugopala, KN; Zenhom, NM, 2022)
"Fenofibrate (FF) is commonly used clinically as a lipid-lowering drug, but whether it participates in endoplasmic reticulum (ER) stress and decreases inflammation in skeletal muscle is still unknown."3.83Fenofibrate improves high-fat diet-induced and palmitate-induced endoplasmic reticulum stress and inflammation in skeletal muscle. ( Bao, YY; Chen, GJ; Chen, L; Dai, F; Jiang, T; Lu, YX; Zhang, Q, 2016)
" Fenofibrate treated mice gained less body weight (BW) and had lower serum amyloid A (SAA) levels, but higher Interleukin (IL)-1α and MIP1α than other mice."3.80Statins and fibrates do not affect development of spontaneous cartilage damage in STR/Ort mice. ( Bastiaansen-Jenniskens, YM; Bierma-Zeinstra, SM; Botter, SM; Clockaerts, S; Gierman, LM; Kloppenburg, M; van Osch, GJ; Verhaar, JA; Wei, W; Weinans, H; Zuurmond, AM, 2014)
" Fructose administration resulted in significant increase in body weight, elevations of blood glucose, serum insulin, cholesterol, triglycerides, advanced glycation end products (AGEs), uric acid levels, insulin resistance index and blood pressure compared to control rats."3.80Ursodeoxycholic acid ameliorates fructose-induced metabolic syndrome in rats. ( Elshazly, SM; Mahmoud, AA, 2014)
" We followed the spontaneous evolution of liver steatosis and tested the therapeutic usefulness of metformin and fenofibrate in a model of steatosis, the Zucker diabetic fatty (ZDF) rat."3.75Nonalcoholic hepatic steatosis in Zucker diabetic rats: spontaneous evolution and effects of metformin and fenofibrate. ( Abdallah, P; Basset, A; Beylot, M; del Carmine, P; Forcheron, F; Haffar, G, 2009)
" Here, in an animal model of obesity and insulin resistance, the metabolic response to cevoglitazar, a dual PPARalpha/gamma, was characterized using a combination of in vivo and ex vivo magnetic resonance methodologies and compared to treatment effects of fenofibrate, a PPARalpha agonist, and pioglitazone, a PPARgamma agonist."3.75Effects of cevoglitazar, a dual PPARalpha/gamma agonist, on ectopic fat deposition in fatty Zucker rats. ( Boettcher, BR; Gao, J; Gounarides, JS; Laurent, D, 2009)
" Fenofibrate, a lipid-modifying agent that acts as a PPARalpha agonist, may prevent adipocyte hypertrophy and insulin resistance by increasing intracellular lipolysis from adipose tissue."3.75Fenofibrate inhibits adipocyte hypertrophy and insulin resistance by activating adipose PPARalpha in high fat diet-induced obese mice. ( Jeong, S; Yoon, M, 2009)
"The PPAR-alpha agonists fenofibrate and n-3 PUFA could efficiently activate AMPK-alpha1 mRNA expression in liver and skeletal muscle to exert body weight reduction and hypoglycaemic effect, respectively."3.75Comparative study between the effect of the peroxisome proliferator activated receptor-alpha ligands fenofibrate and n-3 polyunsaturated fatty acids on activation of 5'-AMP-activated protein kinase-alpha1 in high-fat fed rats. ( El-Razek, SM; Hashem, RM; Motawi, TM; Rashed, LA, 2009)
" After they were treated with combinations of high fat, fenofibrate (FF), or 17beta-estradiol (E) for 13 weeks, variables and determinants of obesity and lipid metabolism were measured using in vivo and in vitro approaches."3.74Inhibition of the actions of peroxisome proliferator-activated receptor alpha on obesity by estrogen. ( Jeong, S; Yoon, M, 2007)
" The aim of this study was to investigate the effect of two different treatment periods of fenofibrate (CAS 49562-28-9) on serum, heart and liver sialic acid levels in experimental hypercholesterolemia."3.74Effect of fenofibrate on serum and tissue sialic acid levels in short-term experimental hypercholesterolemia. ( Emekli, N; Oztürk, LK; Yarat, A, 2007)
" Despite similarities in total body weight in all groups, compared with control fed groups, chocolate-supplemented animals had significantly higher plasma triacylglyceride and non-esterified fatty acids and leptin (for all, P<0."3.73The effects of fenofibrate on metabolic and vascular changes induced by chocolate-supplemented diet in the rat. ( Fatani, S; Naderali, EK, 2005)
"We investigated whether fenofibrate improves lipid metabolism and obesity in female ovariectomized (OVX) or sham-operated (SO) low density lipoprotein receptor-null (LDLR-null) mice."3.72Fenofibrate improves lipid metabolism and obesity in ovariectomized LDL receptor-null mice. ( Han, M; Jeong, S; Kang, JH; Kim, EY; Kim, M; Lee, H; Oh, GT; Yoon, M, 2003)
"Peroxisome proliferator-activated receptor (PPAR) activation may prevent cardiac hypertrophy and inhibit production of endothelin-1 (ET-1), a hypertrophic agent."3.72Peroxisome proliferator-activated receptor-alpha and receptor-gamma activators prevent cardiac fibrosis in mineralocorticoid-dependent hypertension. ( Amiri, F; Diep, QN; Iglarz, M; Paradis, P; Schiffrin, EL; Touyz, RM; Viel, EC, 2003)
"The PPAR-gamma ligand rosiglitazone, but not the PPAR-alpha ligand fenofibrate, decreases intimal hyperplasia following balloon injury in both fatty and lean Zucker rats."3.72Differential effects of peroxisome proliferator activator receptor-alpha and gamma ligands on intimal hyperplasia after balloon catheter-induced vascular injury in Zucker rats. ( Desouza, CV; Diez, J; Dunne, B; Fonseca, VA; Matta, AS; McNamara, DB; Murthy, SN, 2003)
"Our previous study demonstrated that fenofibrate improves both lipid metabolism and obesity, in part through hepatic peroxisome proliferator-activated receptor alpha (PPARalpha) activation, in female ovariectomized, but not in sham-operated, low-density lipoprotein receptor-null (LDLR-null) mice."3.72Fenofibrate prevents obesity and hypertriglyceridemia in low-density lipoprotein receptor-null mice. ( Ahn, J; Han, M; Jeong, S; Kim, M; Kim, TW; Lee, H; Nam, KH; Oh, GT; Shin, C; Song, YH; Yoon, M, 2004)
" Fenofibrate treatment did not change serum lipid levels during the feeding period, but decreased high cholesterol diet-induced increases in body weight by 19% and serum TNF-alpha concentration by 44."3.72Fenofibrate reduces tumor necrosis factor-alpha serum concentration and adipocyte secretion of hypercholesterolemic rabbits. ( Wu, J; Zhao, SP, 2004)
" To determine whether fenofibrate reduces body weight gain and adiposity in female sham-operated (Sham) and ovariectomized (OVX) C57BL/6J mice, the effects of fenofibrate on not only body weight, white adipose tissue (WAT) mass, and food intake, but also the expression of both leptin and PPARalpha target genes were measured."3.72Effects of fenofibrate on high-fat diet-induced body weight gain and adiposity in female C57BL/6J mice. ( Choi, JH; Han, M; Jeong, S; Kim, BH; Kim, J; Kim, M; Lee, H; Nam, KH; Nicol, CJ; Oh, GT; Yoon, M, 2004)
"To determine whether the PPARalpha agonist fenofibrate regulates obesity and lipid metabolism with sexual dimorphism, we examined the effects of fenofibrate on body weight, white adipose tissue (WAT) mass, circulating lipids, and the expression of PPARalpha target genes in both sexes of high fat diet-fed C57BL/6J mice."3.71Fenofibrate regulates obesity and lipid metabolism with sexual dimorphism. ( Han, M; Jeong, S; Kim, JJ; Lee, H; Nicol, CJ; Oh, GT; Ryu, C; Seo, YJ; Yoon, M, 2002)
" We compared the pharmacological profile of a PPARalpha activator, fenofibrate, and a PPARgamma activator, rosiglitazone, on serum parameters, target gene expression, and body weight gain in (fa/fa) fatty Zucker rats and db/db mice as well as their association in db/db mice."3.70Fenofibrate and rosiglitazone lower serum triglycerides with opposing effects on body weight. ( Chaput, E; Edgar, AD; Saladin, R; Silvestre, M, 2000)
"In patients with type 2 diabetes and mixed hyperlipoproteinaemia, short-term atorvastatin as well as fenofibrate therapy had no significant effects on adiponectin, ghrelin or resistin levels."2.73Short-term therapy with atorvastatin or fenofibrate does not affect plasma ghrelin, resistin or adiponectin levels in type 2 diabetic patients with mixed hyperlipoproteinaemia. ( Frost, RJ; Otto, B; Otto, C; Parhofer, KG; Pfeiffer, AF; Spranger, J; Vogeser, M, 2007)
"When fenofibrate was administered to the fatty liver model created via GAN administration and liver steatosis was assessed, a reduction in liver fat deposition was observed, and this model was shown to be useful in drug evaluations involving fatty liver."1.62Establishment of an Adult Medaka Fatty Liver Model by Administration of a Gubra-Amylin-Nonalcoholic Steatohepatitis Diet Containing High Levels of Palmitic Acid and Fructose. ( Fujisawa, K; Kondo, K; Matsumoto, T; Nishimura, Y; Okubo, S; Sakaida, I; Takami, T; Yamada, Y; Yamamoto, N, 2021)
"In Ppara-null mice, MFD treatment increased body weight, adipose tissue, serum TG and impaired glucose tolerance."1.48PPARα-independent action against metabolic syndrome development by fibrates is mediated by inhibition of STAT3 signalling. ( Dai, M; Gonzalez, FJ; Hua, H; Huang, J; Lin, H; Liu, A; Liu, L; Wang, F; Xi, Y; Xu, G; Yang, J; Zhao, T, 2018)
"Moreover, this work implies the enhanced liver fibrosis (ELF) panel diagnostic performance in diagnosis of any and moderate degree of fibrosis in rats with NAFLD."1.46Potential involvement of PPAR α activation in diminishing the hepatoprotective effect of fenofibrate in NAFLD: Accuracy of non- invasive panel in determining the stage of liver fibrosis in rats. ( Abd-Elaziz, LF; Boctor, SS; El-Kharashi, OA; Hamed, AM, 2017)
"Fenofibrate was given to db/db mice in combination with anti-flt-1 hexamer and anti-flk-1 heptamer (VEGFR inhibition) for 12 weeks."1.40Therapeutic effects of fenofibrate on diabetic peripheral neuropathy by improving endothelial and neural survival in db/db mice. ( Chang, YS; Cho, YR; Hong, BY; Kim, HW; Kim, MY; Kim, TW; Kim, YS; Lim, JH; Park, CW, 2014)
"Treatment with fenofibrate exerted a better effect on clinical scoring."1.40Fenofibrate vs pioglitazone: Comparative study of the anti-arthritic potencies of PPAR-alpha and PPAR-gamma agonists in rat adjuvant-induced arthritis. ( Jouzeau, JY; Koufany, M; Moulin, D, 2014)
"Metformin has been reported to increase the expression of the glucagon-like peptide-1 (GLP-1) receptor in pancreatic beta cells in a peroxisome proliferator-activated receptor (PPAR)-α-dependent manner."1.39Effect of the combination of metformin and fenofibrate on glucose homeostasis in diabetic Goto-Kakizaki rats. ( Cho, YM; Kang, GH; Oh, TJ; Park, KS; Shin, JY, 2013)
" Oral dyskinesia was induced by chronic administration of haloperidol (1 mg/kg i."1.39Possible beneficial effect of peroxisome proliferator-activated receptor (PPAR)--α and γ agonist against a rat model of oral dyskinesia. ( Budhiraja, RD; Grover, S; Kumar, P; Singh, K; Vikram, V, 2013)
"The development of diabetic nephropathy was assessed biochemically and histologically."1.39Differential effects of low-dose fenofibrate treatment in diabetic rats with early onset nephropathy and established nephropathy. ( Balakumar, P; Kadian, S; Mahadevan, N, 2013)
"Fenofibrate treatment significantly attenuated oxidative damage, cytokines and improved mitochondrial complexes enzyme activity in brain."1.38Peroxisome proliferator-activated receptor-α activation attenuates 3-nitropropionic acid induced behavioral and biochemical alterations in rats: possible neuroprotective mechanisms. ( Bhateja, DK; Dhull, DK; Gill, A; Padi, SS; Reddy, BV; Sharma, S; Sidhu, A, 2012)
"Prevention of left ventricular hypertrophy remains a challenge in the prevention of hypertension-induced adverse cardiac remodeling."1.37Reactivation of peroxisome proliferator-activated receptor alpha in spontaneously hypertensive rat: age-associated paradoxical effect on the heart. ( Nair, RR; Purushothaman, S; Sathik, MM, 2011)
"The results indicate that, in experimental arthritis, fenofibrate decreases skeletal muscle atrophy through inhibition of the ubiquitin-proteasome system and myostatin."1.37Fenofibrate, a PPAR{alpha} agonist, decreases atrogenes and myostatin expression and improves arthritis-induced skeletal muscle atrophy. ( Castillero, E; Fernández-Galaz, C; Granado, M; López-Calderón, A; López-Menduiña, M; Martín, AI; Nieto-Bona, MP; Villanúa, MA, 2011)
"Fenofibrate (FF) has previously been shown to induce hepatocellular neoplasia in a conventional mouse bioassay (NDA 1993), but there has been no report to examine the carcinogenic susceptibility of rasH2 mice to this chemical."1.35Hepatocarcinogenic susceptibility of fenofibrate and its possible mechanism of carcinogenicity in a two-stage hepatocarcinogenesis model of rasH2 mice. ( Dewa, Y; Jin, M; Kawai, M; Matsumoto, S; Mitsumori, K; Nishimura, J; Saegusa, Y; Shibutani, M; Taniai, E, 2008)
"Fenofibrate treatment also prevented the diet-induced decrease in cardiac function and improved post-ischemic functional recovery."1.35Fenofibrate modulates cardiac and hepatic metabolism and increases ischemic tolerance in diet-induced obese mice. ( Aasum, E; Berge, RK; Gudbrandsen, OA; How, OJ; Khalid, AM; Larsen, TS, 2008)
"Fenofibrate is a drug that has been suggested to inhibit weight gain by increasing the catabolism of fatty acid in the hepatic mitochondria."1.34The increase in hepatic uncoupling by fenofibrate contributes to a decrease in adipose tissue in obese rats. ( Choi, SS; Hong, SH; Kim, DK; Lee, HJ; Lee, KI; Park, MK; Yoo, YH, 2007)
"Fenofibrate treatment dramatically reduced fasting blood glucose (P<0."1.33PPARalpha agonist fenofibrate improves diabetic nephropathy in db/db mice. ( Breyer, M; Cha, DR; Chen, L; Davis, L; Fan, X; Guan, Y; Hwang, MT; Park, CW; Striker, G; Su, D; Wu, J; Zhang, X; Zhang, Y; Zheng, F, 2006)
"Body weights were recorded weekly, and plasma lipid profiles were determined at 4-week intervals."1.33Paradoxical effects of fenofibrate and nicotinic acid in apo E-deficient mice. ( Bahadori, B; Declercq, V; Khademi, H; Moghadasian, MH; Moshtaghi-Kashanian, GR; Yeganeh, B, 2005)
"Fenofibrate increase mitochondrial fatty acid beta-oxidation in liver but not in skeletal muscle and lower the plasma levels of triglyceride and free fatty acid."1.31Fenofibrate lowers abdominal and skeletal adiposity and improves insulin sensitivity in OLETF rats. ( An, YJ; Choi, SS; Garber, AJ; Hong, SH; Hwang, TH; Kang, DY; Kim, DK; Kim, MC; Lee, HJ; Park, MK; Seo, SY, 2002)
"Fenofibrate is a member of the fibrate class of hypolipidemic agents used clinically to treat hypertriglyceridemia and mixed hyperlipidemia."1.31Effects of fenofibrate on lipid parameters in obese rhesus monkeys. ( Bodkin, NL; Brown, HR; Brown, PJ; Hansen, BC; Kliewer, SA; Lehmann, JM; Lewis, MC; Ott, RJ; Plunket, KD; Tong, WQ; Way, JM; Wilkison, WO; Winegar, DA, 2001)
"Eleven patients with hyperlipoproteinemia (HLP) type II A, were treated for 3 months with a new compound, a phenoxy-isobuturic acid derivative, procetofen, at a dosage of 100 mg t."1.26Treatment of hyperlipoproteinemia (HLP) type II A with a new phenoxy-isobuturic acid derivative, procetofen. ( Gustafson, A; Micheli, H; Pometta, D, 1979)

Research

Studies (81)

TimeframeStudies, this research(%)All Research%
pre-19907 (8.64)18.7374
1990's3 (3.70)18.2507
2000's44 (54.32)29.6817
2010's25 (30.86)24.3611
2020's2 (2.47)2.80

Authors

AuthorsStudies
Ashton, MJ1
Ashford, A1
Loveless, AH1
Riddell, D1
Salmon, J1
Stevenson, GV1
Papi Reddy, K1
Singh, AB1
Puri, A1
Srivastava, AK1
Narender, T1
Mokale, SN1
Sanap, PT1
Shinde, DB1
Porcelli, L1
Gilardi, F1
Laghezza, A1
Piemontese, L1
Mitro, N1
Azzariti, A1
Altieri, F1
Cervoni, L1
Fracchiolla, G1
Giudici, M1
Guerrini, U1
Lavecchia, A1
Montanari, R1
Di Giovanni, C1
Paradiso, A1
Pochetti, G1
Simone, GM1
Tortorella, P1
Crestani, M1
Loiodice, F1
Fujisawa, K1
Takami, T1
Okubo, S1
Nishimura, Y1
Yamada, Y1
Kondo, K1
Matsumoto, T1
Yamamoto, N1
Sakaida, I1
Morsy, MA1
El-Hussieny, M1
Zenhom, NM1
Nair, AB1
Venugopala, KN1
Refaie, MMM1
Hua, H1
Yang, J1
Lin, H1
Xi, Y1
Dai, M1
Xu, G1
Wang, F1
Liu, L1
Zhao, T1
Huang, J1
Gonzalez, FJ1
Liu, A1
Oh, TJ1
Shin, JY1
Kang, GH1
Park, KS1
Cho, YM1
Grover, S1
Kumar, P1
Singh, K1
Vikram, V1
Budhiraja, RD1
Kavalkova, P1
Touskova, V1
Roubicek, T1
Trachta, P1
Urbanova, M1
Drapalova, J1
Haluzikova, D1
Mraz, M1
Novak, D1
Matoulek, M1
Lacinova, Z1
Haluzik, M1
Wei, W1
Clockaerts, S1
Bastiaansen-Jenniskens, YM1
Gierman, LM1
Botter, SM1
Bierma-Zeinstra, SM1
Weinans, H1
Verhaar, JA1
Kloppenburg, M1
Zuurmond, AM1
van Osch, GJ1
Cho, YR1
Lim, JH1
Kim, MY1
Kim, TW2
Hong, BY1
Kim, YS1
Chang, YS1
Kim, HW1
Park, CW2
Greene-Schloesser, D1
Payne, V1
Peiffer, AM1
Hsu, FC1
Riddle, DR1
Zhao, W1
Chan, MD1
Metheny-Barlow, L1
Robbins, ME1
Koufany, M1
Jouzeau, JY1
Moulin, D1
Mahmoud, AA1
Elshazly, SM1
Zhou, C1
Zhou, J1
Han, N1
Liu, Z1
Xiao, B1
Yin, J1
Chu, ZS1
Yu, ZL1
Pan, SY1
Jia, ZH1
Wang, XY1
Zhang, Y2
Zhu, PL1
Wang, XJ1
Ko, KM1
Shih, CC1
Wu, JB1
Jian, JY1
Lin, CH1
Ho, HY1
Abd El-Haleim, EA1
Bahgat, AK1
Saleh, S1
Dai, F1
Jiang, T1
Bao, YY1
Chen, GJ1
Chen, L2
Zhang, Q1
Lu, YX1
Hamed, AM1
El-Kharashi, OA1
Boctor, SS1
Abd-Elaziz, LF1
Metais, C1
Forcheron, F3
Abdallah, P2
Basset, A3
Del Carmine, P3
Bricca, G1
Beylot, M3
Nishimura, J3
Dewa, Y3
Okamura, T2
Jin, M3
Saegusa, Y3
Kawai, M2
Umemura, T2
Shibutani, M2
Mitsumori, K3
Florentin, M1
Liberopoulos, EN1
Filippatos, TD1
Kostara, C1
Tselepis, A1
Mikhailidis, DP1
Elisaf, M1
Matsumoto, S1
Taniai, E1
Porta, N1
Vallée, L1
Lecointe, C1
Bouchaert, E1
Staels, B1
Bordet, R1
Auvin, S1
Laurent, D1
Gounarides, JS1
Gao, J1
Boettcher, BR1
Zhao, Z1
Lee, YJ1
Kim, SK1
Kim, HJ1
Shim, WS1
Ahn, CW1
Lee, HC1
Cha, BS1
Ma, ZA1
Jeong, S6
Yoon, M6
Haffar, G1
Motawi, TM1
Hashem, RM1
Rashed, LA1
El-Razek, SM1
Knapik-Czajka, M1
Gozdzialska, A1
Jaskiewicz, J1
Bays, HE1
Maki, KC1
Doyle, RT1
Stein, E1
Castillero, E1
Nieto-Bona, MP1
Fernández-Galaz, C1
Martín, AI1
López-Menduiña, M1
Granado, M1
Villanúa, MA1
López-Calderón, A1
Chen, W1
Zhang, LH1
Liu, HY1
Zhou, XB1
Wang, LL1
del Campo, L1
Blanco-Rivero, J1
Balfagon, G1
Purushothaman, S1
Sathik, MM1
Nair, RR1
Bhateja, DK1
Dhull, DK1
Gill, A1
Sidhu, A1
Sharma, S1
Reddy, BV1
Padi, SS1
Pettersen, JC1
Pruimboom-Brees, I1
Francone, OL1
Amacher, DE1
Boldt, SE1
Kerlin, RL1
Ballinger, WE1
Sisková, K1
Bilka, F1
Adameová, A1
Balazová, A1
Mydla, M1
Pauliková, I1
Kadian, S1
Mahadevan, N1
Balakumar, P1
Lee, HJ2
Choi, SS2
Park, MK2
An, YJ1
Seo, SY1
Kim, MC1
Hong, SH2
Hwang, TH1
Kang, DY1
Garber, AJ1
Kim, DK2
Iglarz, M2
Touyz, RM2
Amiri, F2
Lavoie, MF1
Diep, QN2
Schiffrin, EL2
Nicol, CJ2
Lee, H4
Han, M4
Kim, JJ1
Seo, YJ1
Ryu, C1
Oh, GT4
Guillou, H1
Martin, P1
Jan, S1
D'Andrea, S1
Roulet, A1
Catheline, D1
Rioux, V1
Pineau, T1
Legrand, P1
Kang, JH1
Kim, EY1
Kim, M4
Viel, EC1
Paradis, P1
Warren, JM1
Simon, VA1
Bartolini, G1
Erickson, KL1
Mackey, BE1
Kelley, DS1
Tuomilehto, J1
Desouza, CV1
Murthy, SN1
Diez, J1
Dunne, B1
Matta, AS1
Fonseca, VA1
McNamara, DB1
Cornwell, PD1
De Souza, AT1
Ulrich, RG1
Ahn, J1
Song, YH1
Shin, C1
Nam, KH2
Zhao, SP1
Wu, J2
Kim, J1
Kim, BH1
Choi, JH1
Sebestjen, M1
Keber, I1
Zegura, B1
Simcic, S1
Bozic, M1
Fressart, MM1
Stegnar, M1
Yeganeh, B2
Moshtaghi-Kashanian, GR2
Declercq, V2
Moghadasian, MH2
Reifel-Miller, A1
Otto, K1
Hawkins, E1
Barr, R1
Bensch, WR1
Bull, C1
Dana, S1
Klausing, K1
Martin, JA1
Rafaeloff-Phail, R1
Rafizadeh-Montrose, C1
Rhodes, G1
Robey, R1
Rojo, I1
Rungta, D1
Snyder, D1
Wilbur, K1
Zhang, T1
Zink, R1
Warshawsky, A1
Brozinick, JT1
Khademi, H1
Bahadori, B1
Choi, KC1
Ryu, OH1
Lee, KW1
Kim, HY1
Seo, JA1
Kim, SG1
Kim, NH1
Choi, DS1
Baik, SH1
Choi, KM1
Naderali, EK1
Fatani, S1
Zhang, X1
Cha, DR1
Su, D1
Hwang, MT1
Fan, X1
Davis, L1
Striker, G1
Zheng, F1
Breyer, M1
Guan, Y1
Serisier, S1
Briand, F1
Ouguerram, K1
Siliart, B1
Magot, T1
Nguyen, P1
Pierno, S1
Didonna, MP1
Cippone, V1
De Luca, A1
Pisoni, M1
Frigeri, A1
Nicchia, GP1
Svelto, M1
Chiesa, G1
Sirtori, C1
Scanziani, E1
Rizzo, C1
De Vito, D1
Conte Camerino, D1
Yoo, YH1
Lee, KI1
Otto, C1
Otto, B1
Frost, RJ1
Vogeser, M1
Pfeiffer, AF1
Spranger, J1
Parhofer, KG1
Aasum, E1
Khalid, AM1
Gudbrandsen, OA1
How, OJ1
Berge, RK1
Larsen, TS1
Muguruma, M1
Oztürk, LK1
Yarat, A1
Emekli, N1
Barnard, SD1
Molello, JA1
Caldwell, WJ1
Lebeau, JE1
Bélichard, P1
Pruneau, D1
Zhiri, A1
Arnaiz, SL1
Travacio, M1
Llesuy, S1
Boveris, A1
Yamamoto, K1
Fukuda, N1
Zhang, L1
Sakai, T1
Chaput, E1
Saladin, R1
Silvestre, M1
Edgar, AD1
Winegar, DA1
Brown, PJ1
Wilkison, WO1
Lewis, MC1
Ott, RJ1
Tong, WQ1
Brown, HR1
Lehmann, JM1
Kliewer, SA1
Plunket, KD1
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Hansen, BC1
Micheli, H1
Pometta, D1
Gustafson, A1
Ujházy, E1
Onderová, E1
Horáková, M1
Bencová, E1
Durisová, M1
Nosál, R1
Balonová, T1
Zeljenková, D1
Fournel, S1
Magdalou, J1
Pinon, P1
Siest, G1
Mounié, J1
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Goudonnet, H1
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Clinical Trials (2)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase IV Study to Assess the Efficacy and Safety of Adjunctive Omacor Therapy in Hypertriglyceridemic Subjects Treated With Antara, Followed by an 8-week Extension[NCT00246636]Phase 4167 participants (Actual)Interventional2005-10-31Completed
Effects of Fenofibrate on Metabolic and Reproductive Parameters in Polycystic Ovary Syndrome. A Randomized, Double-Blind, Placebo-Controlled Trial[NCT00884819]4 participants (Actual)Interventional2008-12-31Terminated (stopped due to Poor recruitment)
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Reviews

1 review available for fenofibrate and Body Weight

ArticleYear
Reducing coronary heart disease associated with type 2 diabetes: lifestyle intervention and treatment of dyslipidaemia.
    Diabetes research and clinical practice, 2003, Volume: 61 Suppl 1

    Topics: Body Weight; Clinical Trials as Topic; Coronary Disease; Diabetes Mellitus, Type 2; Drug Therapy, Co

2003

Trials

5 trials available for fenofibrate and Body Weight

ArticleYear
Serum preadipocyte factor-1 concentrations in females with obesity and type 2 diabetes mellitus: the influence of very low calorie diet, acute hyperinsulinemia, and fenofibrate treatment.
    Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme, 2013, Volume: 45, Issue:11

    Topics: Anthropometry; Body Weight; Calcium-Binding Proteins; Caloric Restriction; Diabetes Mellitus, Type 2

2013
Effect of rimonabant, micronised fenofibrate and their combination on cardiometabolic risk factors in overweight/obese patients: a pilot study.
    Expert opinion on pharmacotherapy, 2008, Volume: 9, Issue:16

    Topics: Blood Pressure; Body Mass Index; Body Weight; Cardiovascular System; Female; Fenofibrate; Heart; Hum

2008
The effect of prescription omega-3 fatty acids on body weight after 8 to 16 weeks of treatment for very high triglyceride levels.
    Postgraduate medicine, 2009, Volume: 121, Issue:5

    Topics: Adult; Aged; Body Weight; Double-Blind Method; Drug Administration Schedule; Drug Therapy, Combinati

2009
Statin and fibrate treatment of combined hyperlipidemia: the effects on some novel risk factors.
    Thrombosis and haemostasis, 2004, Volume: 92, Issue:5

    Topics: Adult; Arteriosclerosis; Blood Coagulation; Blood Coagulation Factors; Body Weight; C-Reactive Prote

2004
Short-term therapy with atorvastatin or fenofibrate does not affect plasma ghrelin, resistin or adiponectin levels in type 2 diabetic patients with mixed hyperlipoproteinaemia.
    Acta diabetologica, 2007, Volume: 44, Issue:2

    Topics: Adiponectin; Aged; Atorvastatin; Body Mass Index; Body Weight; Cross-Over Studies; Diabetes Mellitus

2007

Other Studies

75 other studies available for fenofibrate and Body Weight

ArticleYear
Heterocyclic analogues of chlorcyclizine with potent hypolipidemic activity.
    Journal of medicinal chemistry, 1984, Volume: 27, Issue:10

    Topics: Animals; Body Weight; Chemical Phenomena; Chemistry; Cholesterol, Dietary; Eating; Hypolipidemic Age

1984
Synthesis of novel triterpenoid (lupeol) derivatives and their in vivo antihyperglycemic and antidyslipidemic activity.
    Bioorganic & medicinal chemistry letters, 2009, Aug-01, Volume: 19, Issue:15

    Topics: Animals; Anti-Inflammatory Agents; Body Weight; Chemistry, Pharmaceutical; Cricetinae; Diabetes Mell

2009
Synthesis and hypolipidemic activity of novel 2-(4-(2-substituted aminothiazole-4-yl) phenoxy) acetic acid derivatives.
    European journal of medicinal chemistry, 2010, Volume: 45, Issue:7

    Topics: Acetates; Animals; Body Weight; Female; Hypolipidemic Agents; Lipid Metabolism; Male; Motor Activity

2010
Synthesis, characterization and biological evaluation of ureidofibrate-like derivatives endowed with peroxisome proliferator-activated receptor activity.
    Journal of medicinal chemistry, 2012, Jan-12, Volume: 55, Issue:1

    Topics: Adipocytes; Animals; Antineoplastic Agents; Benzoxazoles; Body Weight; Calorimetry; Cell Differentia

2012
Establishment of an Adult Medaka Fatty Liver Model by Administration of a Gubra-Amylin-Nonalcoholic Steatohepatitis Diet Containing High Levels of Palmitic Acid and Fructose.
    International journal of molecular sciences, 2021, Sep-14, Volume: 22, Issue:18

    Topics: Animals; Body Weight; Diet, High-Fat; Disease Models, Animal; Female; Fenofibrate; Fructose; Gene Ex

2021
Fenofibrate ameliorates letrozole-induced polycystic ovary in rats via modulation of PPARα and TNFα/CD95 pathway.
    European review for medical and pharmacological sciences, 2022, Volume: 26, Issue:20

    Topics: Animals; Anti-Mullerian Hormone; Body Weight; Disease Models, Animal; Female; Fenofibrate; Humans; I

2022
PPARα-independent action against metabolic syndrome development by fibrates is mediated by inhibition of STAT3 signalling.
    The Journal of pharmacy and pharmacology, 2018, Volume: 70, Issue:12

    Topics: 3T3-L1 Cells; Adipose Tissue; Animals; Body Weight; Fenofibrate; Fibric Acids; Gemfibrozil; Glucose

2018
Effect of the combination of metformin and fenofibrate on glucose homeostasis in diabetic Goto-Kakizaki rats.
    Experimental & molecular medicine, 2013, Jul-05, Volume: 45

    Topics: Animals; Blood Glucose; Body Weight; Diabetes Mellitus, Experimental; Drug Therapy, Combination; Exe

2013
Possible beneficial effect of peroxisome proliferator-activated receptor (PPAR)--α and γ agonist against a rat model of oral dyskinesia.
    Pharmacology, biochemistry, and behavior, 2013, Volume: 111

    Topics: Animals; Antipsychotic Agents; Behavior, Animal; Body Weight; Disease Models, Animal; Fenofibrate; H

2013
Statins and fibrates do not affect development of spontaneous cartilage damage in STR/Ort mice.
    Osteoarthritis and cartilage, 2014, Volume: 22, Issue:2

    Topics: Animals; Arthritis, Experimental; Biomarkers; Body Weight; Cartilage, Articular; Diet; Drug Evaluati

2014
Therapeutic effects of fenofibrate on diabetic peripheral neuropathy by improving endothelial and neural survival in db/db mice.
    PloS one, 2014, Volume: 9, Issue:1

    Topics: 8-Hydroxy-2'-Deoxyguanosine; Adenosine Monophosphate; AMP-Activated Protein Kinases; Animals; Blood

2014
The peroxisomal proliferator-activated receptor (PPAR) α agonist, fenofibrate, prevents fractionated whole-brain irradiation-induced cognitive impairment.
    Radiation research, 2014, Volume: 181, Issue:1

    Topics: Animals; Behavior, Animal; Body Weight; Cognition; Doublecortin Protein; Fenofibrate; Male; Motor Ac

2014
Fenofibrate vs pioglitazone: Comparative study of the anti-arthritic potencies of PPAR-alpha and PPAR-gamma agonists in rat adjuvant-induced arthritis.
    Bio-medical materials and engineering, 2014, Volume: 24, Issue:1 Suppl

    Topics: Animals; Anti-Inflammatory Agents; Arthritis, Experimental; Body Weight; Bone and Bones; Bone Densit

2014
Ursodeoxycholic acid ameliorates fructose-induced metabolic syndrome in rats.
    PloS one, 2014, Volume: 9, Issue:9

    Topics: Animals; Blood Glucose; Blood Pressure; Body Weight; Cholesterol; Fenofibrate; Fructose; Glutathione

2014
Beneficial effects of neomangiferin on high fat diet-induced nonalcoholic fatty liver disease in rats.
    International immunopharmacology, 2015, Volume: 25, Issue:1

    Topics: Amino Acid Transport System ASC; Animals; Body Weight; Carnitine O-Palmitoyltransferase; Cholesterol

2015
A comparative study between Wuweizi seed and its post-ethanol extraction residue in normal and hypercholesterolemic mice.
    Lipids in health and disease, 2015, Aug-25, Volume: 14

    Topics: Adipose Tissue; Animals; Anticholesteremic Agents; Blood Glucose; Body Weight; Cholesterol, Dietary;

2015
(-)-Epicatechin-3-O-β-D-allopyranoside from Davallia formosana, Prevents Diabetes and Hyperlipidemia by Regulation of Glucose Transporter 4 and AMP-Activated Protein Kinase Phosphorylation in High-Fat-Fed Mice.
    International journal of molecular sciences, 2015, Oct-20, Volume: 16, Issue:10

    Topics: AMP-Activated Protein Kinases; Animals; Blood Glucose; Body Weight; Diabetes Mellitus, Type 2; Fenof

2015
Effects of combined PPAR-γ and PPAR-α agonist therapy on fructose induced NASH in rats: Modulation of gene expression.
    European journal of pharmacology, 2016, Feb-15, Volume: 773

    Topics: Adiponectin; Adipose Tissue; Animals; Blood Glucose; Body Weight; Dose-Response Relationship, Drug;

2016
Fenofibrate improves high-fat diet-induced and palmitate-induced endoplasmic reticulum stress and inflammation in skeletal muscle.
    Life sciences, 2016, Jul-15, Volume: 157

    Topics: Animals; Body Weight; Cell Line; Diet, High-Fat; Endoplasmic Reticulum Stress; Female; Fenofibrate;

2016
Potential involvement of PPAR α activation in diminishing the hepatoprotective effect of fenofibrate in NAFLD: Accuracy of non- invasive panel in determining the stage of liver fibrosis in rats.
    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 2017, Volume: 85

    Topics: Animals; Body Weight; Fenofibrate; Gene Expression Regulation; Glomerular Filtration Rate; Hypolipid

2017
Adiponectin receptors: expression in Zucker diabetic rats and effects of fenofibrate and metformin.
    Metabolism: clinical and experimental, 2008, Volume: 57, Issue:7

    Topics: Animals; Blood Glucose; Body Weight; Diabetes Mellitus, Experimental; Eating; Fatty Acids, Nonesteri

2008
Role of Nrf2 and oxidative stress on fenofibrate-induced hepatocarcinogenesis in rats.
    Toxicological sciences : an official journal of the Society of Toxicology, 2008, Volume: 106, Issue:2

    Topics: Animals; Body Weight; Feeding Behavior; Fenofibrate; Gene Expression Profiling; Glutathione Peroxida

2008
Hepatocarcinogenic susceptibility of fenofibrate and its possible mechanism of carcinogenicity in a two-stage hepatocarcinogenesis model of rasH2 mice.
    Toxicologic pathology, 2008, Volume: 36, Issue:7

    Topics: Animals; Body Weight; Carcinogenicity Tests; Diethylnitrosamine; Disease Models, Animal; Fenofibrate

2008
Fenofibrate, a peroxisome proliferator-activated receptor-alpha agonist, exerts anticonvulsive properties.
    Epilepsia, 2009, Volume: 50, Issue:4

    Topics: 3-Hydroxybutyric Acid; Analysis of Variance; Animals; Body Weight; Diet, Ketogenic; Disease Models,

2009
Effects of cevoglitazar, a dual PPARalpha/gamma agonist, on ectopic fat deposition in fatty Zucker rats.
    Diabetes, obesity & metabolism, 2009, Volume: 11, Issue:6

    Topics: Abdominal Fat; Adiposity; Animals; Body Weight; Dietary Fats; Disease Models, Animal; Fenofibrate; H

2009
Rosiglitazone and fenofibrate improve insulin sensitivity of pre-diabetic OLETF rats by reducing malonyl-CoA levels in the liver and skeletal muscle.
    Life sciences, 2009, May-08, Volume: 84, Issue:19-20

    Topics: AMP-Activated Protein Kinases; Animals; Body Weight; Diabetes Mellitus, Experimental; Diet; Fenofibr

2009
Fenofibrate inhibits adipocyte hypertrophy and insulin resistance by activating adipose PPARalpha in high fat diet-induced obese mice.
    Experimental & molecular medicine, 2009, Jun-30, Volume: 41, Issue:6

    Topics: 3T3 Cells; Adipocytes; Animals; Blood Glucose; Body Weight; Cell Enlargement; Dietary Fats; Fenofibr

2009
Nonalcoholic hepatic steatosis in Zucker diabetic rats: spontaneous evolution and effects of metformin and fenofibrate.
    Obesity (Silver Spring, Md.), 2009, Volume: 17, Issue:7

    Topics: Animals; Blood Glucose; Body Weight; Diabetes Mellitus, Experimental; Disease Models, Animal; Eating

2009
Comparative study between the effect of the peroxisome proliferator activated receptor-alpha ligands fenofibrate and n-3 polyunsaturated fatty acids on activation of 5'-AMP-activated protein kinase-alpha1 in high-fat fed rats.
    The Journal of pharmacy and pharmacology, 2009, Volume: 61, Issue:10

    Topics: AMP-Activated Protein Kinases; Animals; Blood Glucose; Body Weight; Carnitine O-Palmitoyltransferase

2009
Adverse effect of fenofibrate on branched-chain alpha-ketoacid dehydrogenase complex in rat's liver.
    Toxicology, 2009, Dec-21, Volume: 266, Issue:1-3

    Topics: 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide); Amino Acids, Branched-Chain; Animals; Blotting, W

2009
Lipase maturation factor 1: its expression in Zucker diabetic rats, and effects of metformin and fenofibrate.
    Diabetes & metabolism, 2009, Volume: 35, Issue:6

    Topics: Adipose Tissue; Analysis of Variance; Animals; Blood Glucose; Body Weight; Diabetes Mellitus; Enzyme

2009
Fenofibrate, a PPAR{alpha} agonist, decreases atrogenes and myostatin expression and improves arthritis-induced skeletal muscle atrophy.
    American journal of physiology. Endocrinology and metabolism, 2011, Volume: 300, Issue:5

    Topics: Animals; Arthritis, Experimental; Atrophy; Body Weight; Eating; Fenofibrate; Gene Expression; Hypoli

2011
Combination of fenofibrate and rosiglitazone synergistically ameliorate dyslipidemia and insulin resistance in mice with MSG metabolic syndrome.
    Yao xue xue bao = Acta pharmaceutica Sinica, 2010, Volume: 45, Issue:11

    Topics: 11-beta-Hydroxysteroid Dehydrogenase Type 1; Adipose Tissue, White; Animals; Animals, Newborn; Blood

2010
Fenofibrate increases neuronal vasoconstrictor response in mesenteric arteries from diabetic rats: role of noradrenaline, neuronal nitric oxide and calcitonin gene-related peptide.
    European journal of pharmacology, 2011, Volume: 666, Issue:1-3

    Topics: Animals; Body Weight; Calcitonin Gene-Related Peptide; Diabetes Mellitus; Electric Stimulation; Feno

2011
Reactivation of peroxisome proliferator-activated receptor alpha in spontaneously hypertensive rat: age-associated paradoxical effect on the heart.
    Journal of cardiovascular pharmacology, 2011, Volume: 58, Issue:3

    Topics: Aging; Animals; Azo Compounds; Blood Pressure; Body Weight; Cholesterol; Disease Models, Animal; Ene

2011
Peroxisome proliferator-activated receptor-α activation attenuates 3-nitropropionic acid induced behavioral and biochemical alterations in rats: possible neuroprotective mechanisms.
    European journal of pharmacology, 2012, Jan-05, Volume: 674, Issue:1

    Topics: Animals; Behavior, Animal; Body Weight; Brain; Catalase; Cytokines; Extremities; Fenofibrate; Glutat

2012
The PPARα agonists fenofibrate and CP-778875 cause increased β-oxidation, leading to oxidative injury in skeletal and cardiac muscle in the rat.
    Toxicologic pathology, 2012, Volume: 40, Issue:3

    Topics: Animals; Blood Chemical Analysis; Body Weight; Dose-Response Relationship, Drug; Female; Fenofibrate

2012
Influence of lipid imbalance on butyrylcholinesterase activity and biotransformation efficiency.
    Die Pharmazie, 2012, Volume: 67, Issue:4

    Topics: Adipose Tissue, White; Animals; Benzoylcholine; Biotransformation; Body Weight; Butyrylcholinesteras

2012
Differential effects of low-dose fenofibrate treatment in diabetic rats with early onset nephropathy and established nephropathy.
    European journal of pharmacology, 2013, Jan-05, Volume: 698, Issue:1-3

    Topics: Animals; Blood Glucose; Blood Urea Nitrogen; Body Weight; Creatinine; Diabetic Nephropathies; Dose-R

2013
Fenofibrate lowers abdominal and skeletal adiposity and improves insulin sensitivity in OLETF rats.
    Biochemical and biophysical research communications, 2002, Aug-16, Volume: 296, Issue:2

    Topics: Abdomen; Adipose Tissue; Animals; Body Weight; Carnitine O-Palmitoyltransferase; CD36 Antigens; Diab

2002
Effect of peroxisome proliferator-activated receptor-alpha and -gamma activators on vascular remodeling in endothelin-dependent hypertension.
    Arteriosclerosis, thrombosis, and vascular biology, 2003, Jan-01, Volume: 23, Issue:1

    Topics: Animals; Blood Pressure; Body Weight; Endothelin-1; Endothelins; Extracellular Matrix; Fenofibrate;

2003
Fenofibrate regulates obesity and lipid metabolism with sexual dimorphism.
    Experimental & molecular medicine, 2002, Dec-31, Volume: 34, Issue:6

    Topics: Adipose Tissue; Animals; Body Composition; Body Weight; Diet; Dietary Fats; Female; Fenofibrate; Gen

2002
Comparative effect of fenofibrate on hepatic desaturases in wild-type and peroxisome proliferator-activated receptor alpha-deficient mice.
    Lipids, 2002, Volume: 37, Issue:10

    Topics: Animals; Body Weight; Fatty Acid Desaturases; Fatty Acids; Fenofibrate; Liver; Male; Mice; Mice, Kno

2002
Fenofibrate improves lipid metabolism and obesity in ovariectomized LDL receptor-null mice.
    Biochemical and biophysical research communications, 2003, Feb-28, Volume: 302, Issue:1

    Topics: Adipose Tissue; Animals; Body Weight; Fenofibrate; Lipid Metabolism; Mice; Mice, Knockout; Obesity;

2003
Peroxisome proliferator-activated receptor-alpha and receptor-gamma activators prevent cardiac fibrosis in mineralocorticoid-dependent hypertension.
    Hypertension (Dallas, Tex. : 1979), 2003, Volume: 42, Issue:4

    Topics: Animals; Blood Pressure; Body Weight; Cardiomegaly; Collagen; Desoxycorticosterone; Endothelin-1; En

2003
Trans-10,cis-12 CLA increases liver and decreases adipose tissue lipids in mice: possible roles of specific lipid metabolism genes.
    Lipids, 2003, Volume: 38, Issue:5

    Topics: Acyl-CoA Oxidase; Adiponectin; Adipose Tissue; Animals; Apolipoprotein A-I; Apolipoprotein C-III; Ap

2003
Differential effects of peroxisome proliferator activator receptor-alpha and gamma ligands on intimal hyperplasia after balloon catheter-induced vascular injury in Zucker rats.
    Journal of cardiovascular pharmacology and therapeutics, 2003, Volume: 8, Issue:4

    Topics: Animals; Biomarkers; Blood Glucose; Body Weight; Catheterization; Cholesterol; Diabetes Mellitus, Ty

2003
Profiling of hepatic gene expression in rats treated with fibric acid analogs.
    Mutation research, 2004, May-18, Volume: 549, Issue:1-2

    Topics: Animals; Body Weight; Fenofibrate; Gene Expression Profiling; Liver; Male; Organ Size; Rats

2004
Fenofibrate prevents obesity and hypertriglyceridemia in low-density lipoprotein receptor-null mice.
    Metabolism: clinical and experimental, 2004, Volume: 53, Issue:5

    Topics: Acyl-CoA Oxidase; Adipose Tissue; Animals; Apolipoproteins C; Body Weight; Cholesterol; Dietary Fats

2004
Fenofibrate reduces tumor necrosis factor-alpha serum concentration and adipocyte secretion of hypercholesterolemic rabbits.
    Clinica chimica acta; international journal of clinical chemistry, 2004, Volume: 347, Issue:1-2

    Topics: Adipocytes; Animals; Body Weight; Cells, Cultured; Depression, Chemical; Dose-Response Relationship,

2004
Effects of fenofibrate on high-fat diet-induced body weight gain and adiposity in female C57BL/6J mice.
    Metabolism: clinical and experimental, 2004, Volume: 53, Issue:10

    Topics: Adipose Tissue; Animals; Body Composition; Body Weight; Dietary Fats; Eating; Fatty Acids; Female; F

2004
Combination of dietary phytosterols plus niacin or fenofibrate: effects on lipid profile and atherosclerosis in apo E-KO mice.
    The Journal of nutritional biochemistry, 2005, Volume: 16, Issue:4

    Topics: Animals; Apolipoproteins E; Arteriosclerosis; Body Weight; Cholesterol; Cholesterol, HDL; Diet; Feno

2005
A peroxisome proliferator-activated receptor alpha/gamma dual agonist with a unique in vitro profile and potent glucose and lipid effects in rodent models of type 2 diabetes and dyslipidemia.
    Molecular endocrinology (Baltimore, Md.), 2005, Volume: 19, Issue:6

    Topics: Adiponectin; Alkynes; Animals; Binding, Competitive; Body Weight; Cholesterol; Cholesterol, HDL; Cho

2005
Paradoxical effects of fenofibrate and nicotinic acid in apo E-deficient mice.
    Journal of cardiovascular pharmacology, 2005, Volume: 46, Issue:1

    Topics: Animals; Aorta; Apolipoproteins E; Arteriosclerosis; Body Weight; Cholesterol, Dietary; Cholesterol,

2005
Effect of PPAR-alpha and -gamma agonist on the expression of visfatin, adiponectin, and TNF-alpha in visceral fat of OLETF rats.
    Biochemical and biophysical research communications, 2005, Oct-28, Volume: 336, Issue:3

    Topics: Adiponectin; Adipose Tissue; Animals; Blood Glucose; Body Weight; Cytokines; Diabetes Mellitus, Type

2005
The effects of fenofibrate on metabolic and vascular changes induced by chocolate-supplemented diet in the rat.
    European journal of pharmacology, 2005, Oct-03, Volume: 521, Issue:1-3

    Topics: Animals; Body Weight; Cacao; Carbachol; Dietary Supplements; Dose-Response Relationship, Drug; Endot

2005
PPARalpha agonist fenofibrate improves diabetic nephropathy in db/db mice.
    Kidney international, 2006, Volume: 69, Issue:9

    Topics: Albuminuria; Animals; Blood Glucose; Body Weight; Cells, Cultured; Collagen Type I; Diabetes Mellitu

2006
Fenofibrate lowers lipid parameters in obese dogs.
    The Journal of nutrition, 2006, Volume: 136, Issue:7 Suppl

    Topics: Animals; Body Weight; Dog Diseases; Dogs; Dyslipidemias; Female; Fenofibrate; Hypolipidemic Agents;

2006
Effects of chronic treatment with statins and fenofibrate on rat skeletal muscle: a biochemical, histological and electrophysiological study.
    British journal of pharmacology, 2006, Volume: 149, Issue:7

    Topics: Action Potentials; Animals; Aquaporin 4; Atorvastatin; Body Weight; Chloride Channels; Dose-Response

2006
The increase in hepatic uncoupling by fenofibrate contributes to a decrease in adipose tissue in obese rats.
    Journal of Korean medical science, 2007, Volume: 22, Issue:2

    Topics: Adipose Tissue; Animals; Body Temperature; Body Weight; Energy Metabolism; Fenofibrate; Hypolipidemi

2007
Inhibition of the actions of peroxisome proliferator-activated receptor alpha on obesity by estrogen.
    Obesity (Silver Spring, Md.), 2007, Volume: 15, Issue:6

    Topics: Adiposity; Animals; Body Weight; Cells, Cultured; DNA-Binding Proteins; Estradiol; Female; Fenofibra

2007
Fenofibrate modulates cardiac and hepatic metabolism and increases ischemic tolerance in diet-induced obese mice.
    Journal of molecular and cellular cardiology, 2008, Volume: 44, Issue:1

    Topics: Acyl-CoA Oxidase; Animals; Body Weight; Carnitine O-Palmitoyltransferase; Diet; Fenofibrate; Gene Ex

2008
Possible involvement of oxidative stress in fenofibrate-induced hepatocarcinogenesis in rats.
    Archives of toxicology, 2008, Volume: 82, Issue:9

    Topics: 8-Hydroxy-2'-Deoxyguanosine; Alkylating Agents; Animals; Body Weight; Carcinogens; Deoxyguanosine; D

2008
Effect of fenofibrate on serum and tissue sialic acid levels in short-term experimental hypercholesterolemia.
    Arzneimittel-Forschung, 2007, Volume: 57, Issue:12

    Topics: Animals; Body Weight; Cholesterol; Cholesterol, LDL; Eating; Fenofibrate; Hypercholesterolemia; Hypo

2007
[Comparative study of the effects of probucol, fenofibrate and clofibrate on liver ultrastructure in rats (author's transl)].
    La Nouvelle presse medicale, 1980, Oct-30, Volume: 9, Issue:40

    Topics: Animals; Body Weight; Clofibrate; Fenofibrate; Hypolipidemic Agents; Lipids; Liver; Microbodies; Mic

1980
Effect of a long-term treatment with lovastatin or fenofibrate on hepatic and cardiac ubiquinone levels in cardiomyopathic hamster.
    Biochimica et biophysica acta, 1993, Jul-21, Volume: 1169, Issue:1

    Topics: Animals; Body Weight; Cardiomyopathies; Cricetinae; Female; Fenofibrate; Heart; Hydroxymethylglutary

1993
Hydrogen peroxide metabolism during peroxisome proliferation by fenofibrate.
    Biochimica et biophysica acta, 1995, Dec-12, Volume: 1272, Issue:3

    Topics: Acyl-CoA Oxidase; Animals; Antioxidants; Body Weight; Catalase; Diet; Female; Fenofibrate; Glutathio

1995
Altered hepatic metabolism of fatty acids in rats fed a hypolipidaemic drug, fenofibrate.
    Pharmacological research, 1996, Volume: 33, Issue:6

    Topics: Acetoacetates; Animals; Body Weight; Cholesterol; Diet; Fatty Acids; Fenofibrate; Hypolipidemic Agen

1996
Fenofibrate and rosiglitazone lower serum triglycerides with opposing effects on body weight.
    Biochemical and biophysical research communications, 2000, May-10, Volume: 271, Issue:2

    Topics: Acyl-CoA Oxidase; Animals; Apolipoprotein A-I; Apolipoprotein C-III; Apolipoproteins C; Body Weight;

2000
Effects of fenofibrate on lipid parameters in obese rhesus monkeys.
    Journal of lipid research, 2001, Volume: 42, Issue:10

    Topics: Amino Acid Sequence; Animals; Apolipoproteins; Base Sequence; Blood Glucose; Blotting, Western; Body

2001
Treatment of hyperlipoproteinemia (HLP) type II A with a new phenoxy-isobuturic acid derivative, procetofen.
    International journal of clinical pharmacology and biopharmacy, 1979, Volume: 17, Issue:12

    Topics: Adult; Aged; Apolipoproteins; Body Weight; Cholesterol; Female; Fenofibrate; Humans; Hyperlipoprotei

1979
Teratological study of the hypolipidaemic drugs etofylline clofibrate (VULM) and fenofibrate in Swiss mice.
    Pharmacology & toxicology, 1989, Volume: 64, Issue:3

    Topics: Animals; Body Weight; Clofibrate; Female; Fenofibrate; Fetus; Gestational Age; Hypolipidemic Agents;

1989
Differential induction profile of drug-metabolizing enzymes after treatment with hypolipidaemic agents.
    Xenobiotica; the fate of foreign compounds in biological systems, 1987, Volume: 17, Issue:4

    Topics: Animals; Biphenyl Compounds; Body Weight; Butyrophenones; Clofibrate; Clofibric Acid; Cytochrome P-4

1987
Inductive effects of fenofibrate and metabolism of phenobarbital.
    Fundamental & clinical pharmacology, 1988, Volume: 2, Issue:4

    Topics: Animals; Body Weight; Cytochrome P-450 Enzyme System; Fenofibrate; In Vitro Techniques; Liver; Male;

1988
Fenofibrate and colestipol: effects on serum and lipoprotein lipids and apolipoproteins in familial hypercholesterolaemia.
    European journal of clinical pharmacology, 1986, Volume: 30, Issue:2

    Topics: Adult; Apolipoproteins; Body Weight; Cholesterol; Cholesterol, HDL; Colestipol; Female; Fenofibrate;

1986