Abdullahi Adejare, Ahmed Oloyo, Chikodi Anigbogu, Smith Jaja
{"title":"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。","authors":"Abdullahi Adejare, Ahmed Oloyo, Chikodi Anigbogu, Smith Jaja","doi":"10.1177/1179546820902843","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Abnormal vascular reactivity and reduced expression of endothelial nitric oxide synthase (<i>eNOS</i>) 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.</p><p><strong>Objectives: </strong>This study was designed to investigate the mechanism by which oral l-arginine supplementation modulates vascular reactivity and <i>eNOS</i> gene expression in Sprague-Dawley rats fed a high-salt diet.</p><p><strong>Methods: </strong>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 <i>ad libitum</i> 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.</p><p><strong>Results: </strong>Our results show that high-salt diet significantly reduced (<i>P</i> < .05) endothelium-dependent relaxation response to acetylcholine and qualitatively reduced <i>eNOS</i> 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 <i>eNOS</i> gene expressions.</p><p><strong>Conclusion: </strong>This study suggests that oral supplementation of l-arginine enhances endothelial-dependent relaxation in rats fed a high-salt diet by ameliorating <i>eNOS</i> gene expression in the abdominal aorta of the rats.</p>","PeriodicalId":10419,"journal":{"name":"Clinical Medicine Insights. Cardiology","volume":"14 ","pages":"1179546820902843"},"PeriodicalIF":2.3000,"publicationDate":"2020-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/1179546820902843","citationCount":"6","resultStr":"{\"title\":\"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.\",\"authors\":\"Abdullahi Adejare, Ahmed Oloyo, Chikodi Anigbogu, Smith Jaja\",\"doi\":\"10.1177/1179546820902843\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Abnormal vascular reactivity and reduced expression of endothelial nitric oxide synthase (<i>eNOS</i>) 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.</p><p><strong>Objectives: </strong>This study was designed to investigate the mechanism by which oral l-arginine supplementation modulates vascular reactivity and <i>eNOS</i> gene expression in Sprague-Dawley rats fed a high-salt diet.</p><p><strong>Methods: </strong>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 <i>ad libitum</i> 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.</p><p><strong>Results: </strong>Our results show that high-salt diet significantly reduced (<i>P</i> < .05) endothelium-dependent relaxation response to acetylcholine and qualitatively reduced <i>eNOS</i> 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 <i>eNOS</i> gene expressions.</p><p><strong>Conclusion: </strong>This study suggests that oral supplementation of l-arginine enhances endothelial-dependent relaxation in rats fed a high-salt diet by ameliorating <i>eNOS</i> gene expression in the abdominal aorta of the rats.</p>\",\"PeriodicalId\":10419,\"journal\":{\"name\":\"Clinical Medicine Insights. Cardiology\",\"volume\":\"14 \",\"pages\":\"1179546820902843\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2020-01-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1177/1179546820902843\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical Medicine Insights. 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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.