期刊文献+

芪参降脂饮对实验性动脉粥样硬化大鼠的血管内皮功能及胰岛素敏感性的影响 被引量:2

Effects of Qishenjiangzhiyin on insulin sensitivity and vascular endotheial function with experimental atherosclerosis rats
下载PDF
导出
摘要 目的探讨芪参降脂饮对实验性动脉粥样硬化(AS)大鼠的血管内皮功能及胰岛素敏感性(IS)的影响。方法24只大鼠随机分为正常对照组、高脂对照组、芪参降脂饮组,每组各8只,分别予以普通饲料和高脂饲料,芪参降脂饮组同时灌服芪参降脂饮。6 wk后分别测血脂谱、血FPG、FINS、ET、6-k-PGF1a、TXB2并计算ISI、TXB2/6-k-PGF1a。结果芪参降脂饮组大鼠TC、LDL-C、ET、TXB2、TXB2/6-k-PGF1a、FPG、FINS显著低于高脂对照组,而HDL-C、6-k-PGF1aI、SI明显升高(P<0.01)。结论芪参降脂饮可以改善血管内皮功能及增强IS进而起到抗AS的作用。 AIM To study the effects of Qishenjiangzhiyin(QSJZY) on vascular endotheial function and insulin sensitivity(IS) with experimental atherosclerosis(AS)rats induced by high fat diet. METHODS Twenty-four rats were randomized into 3 groups. One group served as normal control group, the second group was fed with high-fat diet and served as atherosclerosis model group. The third group was fed with high-fat diet in junction with QSJZY. Serum lipids, FPG, FINS, ET, 6-k-PGF1a, TXB2 were measured and ISI and TXB2/6-k-PGF1a were calculated after 6 wk after experiment. RESULTS In treatment group, TC, LDL-C, ET, TXB2, TXB2/6-k-PGF1a, FPG and FINS were significantly lower and HDL-C,6-k-PGF1a and ISI were significantly higher than those in high-fat group( P 〈 0.01 ). CONCLUSION QSJZY can improve vascular endotheial function and can enhance IS, which might be the mechanisms of QSJZY's antiatherosclerosis action.
出处 《中国临床药学杂志》 CAS 2006年第4期231-233,共3页 Chinese Journal of Clinical Pharmacy
基金 辽宁省教育厅科学研究计划资助(计划编号202203250)
关键词 芪参降脂饮 动脉粥样硬化 胰岛素抵抗 胰岛素敏感性 血管内皮功能 Qishenjiangzhiyin atherosclerosis insulin resistance insulin sensitivity vascular endotheial function
  • 相关文献

参考文献7

二级参考文献22

  • 1芮耀诚.抗动脉粥样硬化药物研究进展[J].国外医学(药学分册),1995,22(5):257-261. 被引量:15
  • 2吴开云,高摄渊,袁融,庄文华.维生素D诱发大鼠动脉粥样硬化的实验研究[J].解剖学报,1996,27(2):133-135. 被引量:31
  • 3[1]Kraegen EW, James DE, Bennett SP, et al. In vivo insulin sensitivity in the rat determined by euglycemic clamp[J]. Am J Physiol, 1983,245 (Endocrinol, Metab, 8):E1-E7.
  • 4[2]Storlien LH, Oakes ND, Pan DA, et al. Syndrome of insulin resistance in the rats: inducement by diet and amelioration with Benfluorex[J]. Diabetes, 1993,42:457-462.
  • 5[3]Defronzo RA, Tobin JD, Andres. Glucose clamp technique: a method for quantifying insulin secretion and resistance[J]. Am J Physiol,1979,237 (Endocri-nol,Metab,Gastrointest,Physiol,6):E214-E223.
  • 6[4]Coulston AM. The role of dietary fats in plant-based diets[J]. Am J Clin Nutr,1999,70(3 Suppl):512S-515S.
  • 7[5]Rattigan S, Filsell OH, Reppucci D, et al. Impaired basal and epinephrine-stimulated glucose uptake by hearts from rats fed high-fat diets[J]. Nutr Rep Int,1983,28:603-612.
  • 8[6]Hissin PJ, Karniele E, Simpson IA, et al. A possible mechanism of insulin resistance in the rat adipose cell with high-fat/low-carbohydrate feeding. Depletion of intracellular glucose transport systems[J]. Diabetes, 1982,31:589-592.
  • 9[7]Storlien LH, James DE, Burleigh KM, et al. Fat feeding causes widespread in vivo insulin resistance, decreased energy expenditure, and obesity in rats[J].Am J Physiol,1986,25(Endodrinol,Metab,14):E576-E583.
  • 10[8]Ye JM, Doyle PJ, Iglesias MA, et al. Peroxisome proliferator-activated receptor (PPAR)-alpha activation lowers muscle lipids and improves insulin sensitivity in high fat-fed rats: comparison with PPAR-gamma activation[J].Diabetes,2001,50(2):411-417.

共引文献326

同被引文献36

引证文献2

二级引证文献17

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