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运动训练增强了糖尿病Goto-Kakizaki(GK)大鼠的心肌内皮型一氧化氮合酶(eNOS)功能。

Exercise training enhanced myocardial endothelial nitric oxide synthase (eNOS) function in diabetic Goto-Kakizaki (GK) rats.

作者信息

Grijalva James, Hicks Steven, Zhao Xiangmin, Medikayala Sushma, Kaminski Pawel M, Wolin Michael S, Edwards John G

机构信息

Department of Physiology, New York Medical College, Valhalla NY, USA.

出版信息

Cardiovasc Diabetol. 2008 Nov 19;7:34. doi: 10.1186/1475-2840-7-34.

Abstract

BACKGROUND

Different mechanisms of diabetic-induced NO dysfunction have been proposed and central to most of them are significant changes in eNOS function as the rate-limiting step in NO bioavailability. eNOS exists in both monomeric and dimeric conformations, with the dimeric form catalyzing the synthesis of nitric oxide, while the monomeric form catalyzes the synthesis of superoxide (O2-). Diabetic-induced shifts to decrease the dimer:monomer ratio is thought to contribute to the degradation of nitric oxide (NO) bioavailability. Exercise has long been useful in the management of diabetes. Although exercise-induced increases expression of eNOS has been reported, it is unclear if exercise may alter the functional coupling of eNOS.

METHODS

To investigate this question, Goto-Kakizaki rats (a model of type II diabetes) were randomly assigned to a 9-week running program (train) or sedentary (sed) groups.

RESULTS

Exercise training significantly (p < .05) increased plantaris muscle cytochrome oxidase, significantly improved glycosylated hemoglobin (sed: 7.33 +/- 0.56%; train: 6.1 +/- 0.18%), ad improved insulin sensitivity. Exercise increased both total eNOS expression and the dimer:monomer ratio in the left ventricle LV (sed: 11.7 +/- 3.2%; train: 41.4 +/- 4.7%). Functional analysis of eNOS indicated that exercise induced significant increases in nitric oxide (+28%) production and concomitant decreases in eNOS-dependent superoxide (-12%) production. This effect was observed in the absence of tetrahydrobiopterin (BH4), but not in the presence of exogenous BH4. Exercise training also significantly decreased NADPH-dependent O2- activity.

CONCLUSION

Exercise-induced increased eNOS dimerization resulted in an increased coupling of the enzyme to facilitate production of NO at the expense of ROS generation. This shift that could serve to decrease diabetic-related oxidative stress, which should serve to lessen diabetic-related complications.

摘要

背景

已经提出了糖尿病诱导的一氧化氮(NO)功能障碍的不同机制,其中大多数机制的核心是内皮型一氧化氮合酶(eNOS)功能的显著变化,这是NO生物利用度的限速步骤。eNOS以单体和二聚体两种构象存在,二聚体形式催化一氧化氮的合成,而单体形式催化超氧化物(O2-)的合成。糖尿病诱导的二聚体与单体比例下降被认为会导致一氧化氮(NO)生物利用度的降低。长期以来,运动对糖尿病的管理一直很有帮助。尽管有报道称运动可诱导eNOS表达增加,但尚不清楚运动是否会改变eNOS的功能偶联。

方法

为了研究这个问题,将Goto-Kakizaki大鼠(II型糖尿病模型)随机分为9周跑步训练组(训练组)或久坐组(对照组)。

结果

运动训练显著(p <.05)增加了比目鱼肌细胞色素氧化酶,显著改善了糖化血红蛋白(对照组:7.33 +/- 0.56%;训练组:6.1 +/- 0.18%),并改善了胰岛素敏感性。运动增加了左心室(LV)中总eNOS表达以及二聚体与单体的比例(对照组:11.7 +/- 3.2%;训练组:41.4 +/- 4.7%)。eNOS的功能分析表明,运动诱导一氧化氮产生显著增加(+28%),同时eNOS依赖性超氧化物产生减少(-12%)。在没有四氢生物蝶呤(BH4)的情况下观察到了这种效应,但在存在外源性BH4的情况下未观察到。运动训练还显著降低了NADPH依赖性O2-活性。

结论

运动诱导的eNOS二聚化增加导致该酶的偶联增加,以促进NO的产生,同时减少活性氧的生成。这种转变有助于降低糖尿病相关的氧化应激,从而减轻糖尿病相关并发症。

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