期刊文献+

替米沙坦对自发性高血压大鼠肌肉组织中PPARγ和PPARδ表达的影响 被引量:2

Effect of Telmisartan on the Protein Expression of PPARγ and PPARδ in Skeletal Muscle Tissues from Spontaneous Hypertensive Rats
下载PDF
导出
摘要 目的观察替米沙坦对自发性高血压大鼠(SHR)肌肉组织和大鼠成肌细胞系L6细胞过氧化物酶体增殖激活受体(PPARγ、PPARδ)表达的影响,探讨替米沙坦影响糖代谢的可能机制。方法12只8周龄SHR分为对照组和替米沙坦干预组,经12周喂养后测鼠尾收缩压,取大腿肌肉组织用Westernblot检测PPARγ、PPARδ和血管紧张素Ⅱ1型受体(AT1R)表达;L6细胞分为对照组和替米沙坦组,干预24h后收集细胞用Westernblot检测PPARγ、PPARδ和AT1R表达。结果SHR替米沙坦组鼠尾收缩压较对照组明显下降(P<0.01),肌肉组织PPARγ、PPARδ表达增加(P<0.05);L6细胞替米沙坦组PPARγ、PPARδ的表达也增加(P<0.05和P<0.01)。结论替米沙坦除有降压作用外尚能促进肌肉组织中PPARγ和PPARδ的表达,这可能与替米沙坦改善糖代谢有关。 Objective To study the effect of telmisartan on the protein expression of peroxisome proliferator activated receptor γ and δ(PPARγ/PPARδ) in skeletal muscle tissues from spontaneous hypertensive rats (SHR) and in L6 skeletal myoblast. Methods Twelve 8-week-old male SHR were divided into normal diet group and normal diet plus telmisartan group. After 12-week admiru'stration,tail-cuff systolic blood pressures were measured and the protein expression of PPARγ/PPARδ and angiotensin Ⅱ type 1 receptor (AT1R) from skeletal muscle tissues were detected by Western blot. L6 cells were treated with telmisartan or blank for 24 hours, and then cells were collected for measurement of protein expression of PPARγ/PPARδ and AT1R by Westem blot. Results Tail-cuff systolic blood pressures were significantly decreased in telmisartan group (P 〈 0.05 ), while the expressions of PPARγ/and PPARδ in skeletal muscle tissues significantly increased (P 〈 0.05 ) compared with the control group. Telmisartan significantly increased the protein expressions of PPARγ/(P 〈 0.05 ) and PPARδ(P 〈 0.01 ) in L6 cells. Conclusion In addition to the role of blood pressure control, telmisartan can also increase the protein expressions of PPARγand PPARδ in the skeletal muscle of SHR, which would be implicated in the improvement of glycometabolism induced by telmisartan.
出处 《中国医科大学学报》 CAS CSCD 北大核心 2009年第3期172-174,共3页 Journal of China Medical University
基金 国家自然科学基金资助项目(30890042)
关键词 替米沙坦 肌肉组织 过氧化物酶体增殖激活受体 糖代谢 telmisartan skeletal muscle tissue peroxisome pmliferator activated receptor glycometabolism
  • 相关文献

参考文献9

  • 1Jandeleit-Dahm KA,Tikellis C, Reid CM,et al. Why blockade of the renin-angiotensin system reduces the incidence of new-onset diabetes [J]. J Hypertens, 2005,23(3 ) :463-473.
  • 2Yamana A,Arita M,Furuta M,et al. The angiotensin II receptor blocker telmisartan improves insulin resistance and has beneficial effects in hypertensive patients with type 2 diabetes and poor glycemic control [J]. Diabetes Res Clin Pract,2008,82( 1 ): 127-131.
  • 3Benndorf RA, Rudolph T,Appel D,et al Telmisartan improves insulin sensitivity in nondiabetic patients with essential hypertension [J]. Metabolism, 2006,55( 9 ) : 1159-1164.
  • 4Lee CH,Olson P,Hevener A,et al. PPARδ regulates glucose metabolism and insulin sensitivity[J]. PNAS, 2006,103(9) :3444- 3449.
  • 5Kramer DK,Khalili LA,Perrini S,et al. Direct activation of glucose transport in primary human myotubes after activation of peroxisome proliferator activated receptor δ [ J ]. Diabetes, 2005,54 ( 5 ), 1157- 1163.
  • 6Kubota N,Terauchi Y,Miki H,et al. PPARγ mediates high-fat dietinduced adipocyte hypertrophy and insulin resistance [J]. Mol Cell, 1999,4(4 ) : 597-609.
  • 7Benson SC, Pershadsingh HA, Ho Ci, et al. Identification of telmisartan as a uniqueangiotensin Ⅱ receptor antagonist with selective PPARγmodulating activity [ J ]. Hypertension, 2004,43 (5) : 993- 1002.
  • 8Mori Y, hob Y, Tajima N. Angiotensin Ⅱ receptor blockers downsize adipocytes in spontaneously Type 2 diabetic rats with visceral fat obesity [ J ]. Am J Hyperptens 2007,20(4 ) : 431--436.
  • 9Matsui T,Nakamura K,Ueno T,et al. Telmisartan,an angiotensin Ⅱ type 1 receptor blocker,inhibits advanced glycation end-product (AGE)-elicited hepatic insulin resistance via peroxisome proliferator-activated receptor-gamma activation [J ]. J Int Med Res, 2008,36 (2) : 237-243.

同被引文献19

引证文献2

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部