Literature DB >> 12733699

Bezafibrate improves hypertension and insulin sensitivity in humans.

Jong Il Kim1, Takeshi Tsujino, Yoshio Fujioka, Komei Saito, Mitsuhiro Yokoyama.   

Abstract

We examined cellular membrane fatty acid composition and insulin sensitivity in patients with mild essential hypertension and hyperlipidemia, and investigated whether bezafibrate, a lipid-lowering drug, could improve elevated blood pressure and insulin sensitivity in these subjects by ameliorating cellular membrane fatty acid composition. Twenty-seven subjects were recruited. Twelve men with mild essential hypertension [systolic blood pressure (SBP) between 140 mmHg and 160 mmHg] and hypertriglyceridemia (plasma triglyceride concentration over 150 mg/dl) were designated the HL group. Fifteen men with mild essential hypertension and normotriglyceridemia (plasma triglyceride concentration below 150 mg/dl) were designated the NL group. Subjects in the HL group were given bezafibrate 400 mg/dl and those in the NL group were given placebo for 3 months. Bezafibrate significantly reduced SBP (140 +/- 2.6 to 131.8 +/- 2.6 mmHg, mean +/- SEM), diastolic blood pressure (DBP) (87.8 +/- 2.0 to 82.8 +/- 2.6 mmHg), fasting plasma triglyceride concentration (225.5 +/- 23.5 to 102.9 +/- 10.9 mg/dl), fasting plasma insulin concentration (9.6 +/- 0.8 to 7.1 +/- 0.8 microU/ml), and homeostasis model assessment scores (HOMA-R, 2.4 +/- 0.2 to 1.7 +/- 0.2), and significantly improved the insulin sensitivity index (56.0 +/- 3.0 to 70.7 +/- 4.8 mg x l2/mmol x mU x min) in the HL group. Regarding erythrocyte membrane fatty acid composition, bezafibrate reduced the percentages of saturated fatty acids (SFA) and increased the percentage of polyunsaturated fatty acids (PUFA). Plasma triglyceride concentrations were positively correlated with HOMA-R (r = 0.50, p < 0.01) and SFA (r = 0.39, p < 0.05), and negatively correlated with PUFA (r = -0.45, p < 0.05) before administration of placebo or bezafibrate. In conclusion, an improvement of hyperlipidemia by bezafibrate may be attributed to reduction of blood pressure and amelioration of insulin sensitivity. Abnormalities in membrane lipid composition may play an important role in these metabolic disorders.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12733699     DOI: 10.1291/hypres.26.307

Source DB:  PubMed          Journal:  Hypertens Res        ISSN: 0916-9636            Impact factor:   3.872


  7 in total

Review 1.  Lipid therapy for cardiovascular disease with insulin resistance, diabetes, or the metabolic syndrome.

Authors:  Sander J Robins
Journal:  Curr Cardiol Rep       Date:  2005-11       Impact factor: 2.931

2.  Increases in mitochondrial biogenesis impair carcinogenesis at multiple levels.

Authors:  Xiao Wang; Carlos T Moraes
Journal:  Mol Oncol       Date:  2011-08-05       Impact factor: 6.603

3.  Inhibitory effect of insulin on vasopressin-induced intracellular calcium response is blunted in hyperinsulinemic hypertensive patients: role of membrane fatty acid composition.

Authors:  Koichi Maekawa; Takeshi Tsujino; Komei Saito; Jong Il Kim; Yoshihiro Ikeda; Noriaki Emoto; Mitsuhiro Yokoyama
Journal:  Heart Vessels       Date:  2006-07       Impact factor: 1.814

Review 4.  Dual and pan-peroxisome proliferator-activated receptors (PPAR) co-agonism: the bezafibrate lessons.

Authors:  Alexander Tenenbaum; Michael Motro; Enrique Z Fisman
Journal:  Cardiovasc Diabetol       Date:  2005-09-16       Impact factor: 9.951

5.  Dyslipidemia Increases the Risk of Incident Hypertension in a Large Taiwanese Population Follow-Up Study.

Authors:  Yu-Hsuan Lin; Yi-Hsueh Liu; Da-Wei Wu; Ho-Ming Su; Szu-Chia Chen
Journal:  Nutrients       Date:  2022-08-10       Impact factor: 6.706

Review 6.  Balanced pan-PPAR activator bezafibrate in combination with statin: comprehensive lipids control and diabetes prevention?

Authors:  Alexander Tenenbaum; Enrique Z Fisman
Journal:  Cardiovasc Diabetol       Date:  2012-11-14       Impact factor: 9.951

7.  Elevation of C-reactive protein in people with prehypertension.

Authors:  Dana E King; Brent M Egan; Arch G Mainous; Mark E Geesey
Journal:  J Clin Hypertens (Greenwich)       Date:  2004-10       Impact factor: 3.738

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.