Telmisartan is effective to ameliorate metabolic syndrome in rat model - a preclinical report

被引:10
作者
Chen, Kai-Chun [1 ]
Li, Yingxiao [1 ,2 ]
Chang, Wei-Ting [2 ,3 ]
Kuo, Feng Yu [4 ]
Chen, Zhih-Cherng [3 ,5 ]
Cheng, Juei-Tang [2 ,6 ]
机构
[1] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Psychosomat Internal Med, Kagoshima 8908544, Japan
[2] Chi Mei Med Ctr, Dept Med Res, Tainan 71003, Taiwan
[3] Chi Mei Med Ctr, Dept Cardiol, Tainan 71003, Taiwan
[4] Kaohsiung Vet Gen Hosp, Cardiovasc Ctr, Kaohsiung 81362, Taiwan
[5] Chia Nan Univ Pharm & Sci, Dept Pharm, Tainan 71701, Taiwan
[6] Chang Jung Christian Univ, Inst Med Sci, 1 Changda Rd, Tainan 71101, Taiwan
来源
DIABETES METABOLIC SYNDROME AND OBESITY-TARGETS AND THERAPY | 2018年 / 11卷
关键词
metabolic syndrome; telmisartan; PPAR delta; GSK0660; diet; PROLIFERATOR-ACTIVATED-RECEPTOR; IMPROVES INSULIN-RESISTANCE; RENIN-ANGIOTENSIN SYSTEM; DIET-INDUCED OBESITY; BLOOD-PRESSURE; SKELETAL-MUSCLE; HYPERTENSIVE PATIENTS; WEIGHT-GAIN; SENSITIVITY; BLOCKADE;
D O I
10.2147/DMSO.S187092
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Metabolic syndrome (MS) is known to be associated with hypertension, insulin resistance, and dyslipidemia, and it raises the risk for cardiovascular diseases and diabetes mellitus. Telmisartan is used in clinic as an angiotensin II receptor blocker and it is also identified as activating peroxisome proliferator-activated receptors delta (PPAR delta). Activation of PPAR delta produced beneficial effects on fatty acid metabolism and glucose metabolism. This study aims to investigate the effects of telmisartan on the modulation of MS in rats fed a high-fat/high-sodium diet. Methods: Rats were fed with a high-fat/high-sodium diet and received injections of streptozotocin at low dose to induce MS. Then, rats with MS were treated with telmisartan. The weight, glucose tolerance, and insulin sensitivity were measured. The lipid profiles were also obtained. The weights of retroperitoneal and epididymal fat pads were determined. The role of PPR delta in telmisartan treatment was identified in rats pretreated with the specific antagonist GSK0660. Results: The results showed that telmisartan, but not losartan, significantly reduced plasma glucose and plasma insulin, and improved insulin resistance in rats with MS. Telmisartan also decreased blood pressure and lipids more significantly than losartan. Moreover, GSK0660 effectively reversed the effects of telmisartan in the MS rats. In the MS group, telmisartan activated PPAR delta to enhance the levels of phosphorylated GLUT4 in muscle or the expression of phosphoenolpyruvate carboxykinase (PIRPCK) in the liver, which was also abolished by GSK0660. Telmisartan is useful to ameliorate hypertension and insulin resistance in rats with MS. Telmisartan improves the insulin resistance through increased expression of GLUT4 and down-regulation of PEPCK via PPAR delta-dependent mechanisms. Conclusion: Telmisartan has been proven to ameliorate MS, particularly in the prediabetes state. Therefore, telmisartan is suitable to develop for the management of MS in clinics.
引用
收藏
页码:901 / 911
页数:11
相关论文
共 61 条
  • [51] High-salt in addition to high-fat diet may enhance inflammation and fibrosis in liver steatosis induced by oxidative stress and dyslipidemia in mice
    Uetake, Yuzaburo
    Ikeda, Hitoshi
    Irie, Rie
    Tejima, Kazuaki
    Matsui, Hiromitsu
    Ogura, Sayoko
    Wang, Hong
    Mu, ShengYu
    Hirohama, Daigoro
    Ando, Katsuyuki
    Sawamura, Tatsuya
    Yatomi, Yutaka
    Fujita, Toshiro
    Shimosawa, Tatsuo
    [J]. LIPIDS IN HEALTH AND DISEASE, 2015, 14
  • [52] Dyslipidaemia in type II diabetic mice does not aggravate contractile impairment but increases ventricular stiffness
    Van den Bergh, An
    Vanderper, Annelies
    Vangheluwe, Peter
    Desjardins, Fanny
    Nevelsteen, Ines
    Verreth, Wim
    Wuytack, Frank
    Holvoet, Paul
    Flameng, Willem
    Balligand, Jean-Luc
    Herijgers, Paul
    [J]. CARDIOVASCULAR RESEARCH, 2008, 77 (02) : 371 - 379
  • [53] Metabolic effect of telmisartan and losartan in hypertensive patients with metabolic syndrome
    Vitale, Cristiana
    Mercuro, Giuseppe
    Castiglioni, Carlotta
    Cornoldi, Alessandra
    Tulli, Arianna
    Fini, Massimo
    Volterrani, Maurizio
    Rosano, Giuseppe M. C.
    [J]. CARDIOVASCULAR DIABETOLOGY, 2005, 4 (1)
  • [54] Regulation of muscle fiber type and running endurance by PPARδ
    Wang, YX
    Zhang, CL
    Yu, RT
    Cho, HK
    Nelson, MC
    Bayuga-Ocampo, CR
    Ham, J
    Kang, H
    Evans, RM
    [J]. PLOS BIOLOGY, 2004, 2 (10) : 1532 - 1539
  • [55] Angiotensin II-induced NADPH oxidase activation impairs insulin signaling in skeletal muscle cells
    Wei, Yongzhong
    Sowers, James R.
    Nistala, Ravi
    Gong, Heping
    Uptergrove, Grace M. -E.
    Clark, Suzanne E.
    Morris, E. Matthew
    Szary, Nicholas
    Manrique, Camila
    Stump, Craig S.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (46) : 35137 - 35146
  • [56] DEFINITIONS AND CHARACTERISTICS OF SODIUM SENSITIVITY AND BLOOD-PRESSURE RESISTANCE
    WEINBERGER, MH
    MILLER, JZ
    LUFT, FC
    GRIM, CE
    FINEBERG, NS
    [J]. HYPERTENSION, 1986, 8 (06) : 127 - 134
  • [57] Animal models of metabolic syndrome: a review
    Wong, Sok Kuan
    Chin, Kok-Yong
    Suhaimi, Farihah Hj
    Fairus, Ahmad
    Ima-Nirwana, Soelaiman
    [J]. NUTRITION & METABOLISM, 2016, 13 : 1 - 12
  • [58] Telmisartan inhibits vasoconstriction via PPARγ-dependent expression and activation of endothelial nitric oxide synthase
    Yuen, Chi Yung
    Wong, Wing Tak
    Tian, Xiao Yu
    Wong, Siu Ling
    Lau, Chi Wai
    Yu, Jun
    Tomlinson, Brian
    Yao, Xiaoqiang
    Huang, Yu
    [J]. CARDIOVASCULAR RESEARCH, 2011, 90 (01) : 122 - 129
  • [59] A novel mice model of metabolic syndrome: the high-fat-high-fructose diet-fed ICR mice
    Zhang Zhuhua
    Wang Zhiquan
    Yang Zhen
    Niu Yixin
    Zhang Weiwei
    Li Xiaoyong
    Liu Yueming
    Zhang Hongmei
    Qin Li
    Su Qing
    [J]. EXPERIMENTAL ANIMALS, 2015, 64 (04) : 435 - 442
  • [60] Link between the renin-angiotensin system and insulin resistance: Implications for cardiovascular disease
    Zhou, Ming-Sheng
    Schulman, Ivonne H.
    Zeng, Qiang
    [J]. VASCULAR MEDICINE, 2012, 17 (05) : 330 - 341