补充l-精氨酸通过增强腹主动脉内皮型一氧化氮合酶基因表达,增加高盐饮食的Sprague-Dawley大鼠内皮依赖性松弛。

IF 2.3 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Clinical Medicine Insights. Cardiology Pub Date : 2020-01-29 eCollection Date: 2020-01-01 DOI:10.1177/1179546820902843
Abdullahi Adejare, Ahmed Oloyo, Chikodi Anigbogu, Smith Jaja
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引用次数: 6

摘要

背景:血管反应性异常和内皮型一氧化氮合酶(eNOS)基因表达降低是盐致高血压大鼠的标志。虽然l-精氨酸是一种公认的血管扩张剂,但它在盐诱导高血压中调节血管反应性的机制尚不清楚。目的:探讨口服l-精氨酸对高盐饮食后Sprague-Dawley大鼠血管反应性和eNOS基因表达的调节机制。方法:48只体重90 ~ 110 g的断奶雄性Sprague-Dawley大鼠随机分为6组,每组8只。ⅰ组随意饲喂正常大鼠饲料,为正常饮食组。第二组饲喂NaCl含量为8%的饲粮。III组和IV组分别采用正常和高盐饮食,然后口服补充l-精氨酸(100 mg/kg/d); V组和VI组分别采用正常和高盐饮食,然后同时给予l-精氨酸和l-硝基精氨酸甲酯(L-NAME);分别为100 mg/kg/天和40 mg/kg/天)。实验12周结束时,处死动物,观察血管反应性和基因表达水平。结果:高盐饮食显著降低大鼠腹主动脉(P eNOS)基因表达。然而,补充l-精氨酸改善了受损的内皮依赖性松弛和一氧化氮水平,同时改善了eNOS基因表达的减少。结论:本研究提示,口服补充l-精氨酸可通过改善大鼠腹主动脉eNOS基因表达,增强高盐饮食大鼠的内皮依赖性松弛。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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l-arginine Supplementation Increased Only Endothelium-Dependent Relaxation in Sprague-Dawley Rats Fed a High-Salt Diet by Enhancing Abdominal Aorta Endothelial Nitric Oxide Synthase Gene Expression.

Background: Abnormal vascular reactivity and reduced expression of endothelial nitric oxide synthase (eNOS) gene are hallmark of salt-induced hypertension in rats. Although l-arginine is an established vasodilator, the mechanism by which it modulates vascular reactivity in salt-induced hypertension is not clearly understood.

Objectives: This study was designed to investigate the mechanism by which oral l-arginine supplementation modulates vascular reactivity and eNOS gene expression in Sprague-Dawley rats fed a high-salt diet.

Methods: Forty-eight weaned male Sprague-Dawley rats of weight range 90 to 110 g were randomly divided into 6 groups of 8 rats per group. Group I was fed normal rat chow ad libitum and served as the Normal Diet group. Group II was fed a diet that contained 8% NaCl. Groups III and IV took normal and high-salt diet, respectively, and then received oral l-arginine supplementation (100 mg/kg/day), while groups V and VI took normal and high-salt diet, respectively, and then were co-administered with both l-arginine and l-nitro-arginine methyl ester (L-NAME; 100 mg/kg/day and 40 mg/kg/day, respectively) orally. At the end of 12-week experimental period, the animals were sacrificed to assess vascular reactivity and gene expression level.

Results: Our results show that high-salt diet significantly reduced (P < .05) endothelium-dependent relaxation response to acetylcholine and qualitatively reduced eNOS gene expression in the abdominal aorta of the rats. However, l-arginine supplementation improved the impaired endothelium-dependent relaxation and nitric oxide level while ameliorating the reduced eNOS gene expressions.

Conclusion: This study suggests that oral supplementation of l-arginine enhances endothelial-dependent relaxation in rats fed a high-salt diet by ameliorating eNOS gene expression in the abdominal aorta of the rats.

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来源期刊
Clinical Medicine Insights. Cardiology
Clinical Medicine Insights. Cardiology CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
5.20
自引率
3.30%
发文量
16
审稿时长
8 weeks
期刊最新文献
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