首页> 外文期刊>Pfluegers Archiv: European Journal of Physiology >The role of angiotensin II in the feedback control of renin gene expression.
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The role of angiotensin II in the feedback control of renin gene expression.

机译:血管紧张素II在肾素基因表达的反馈控制中的作用。

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摘要

This study aimed to characterize the influence of endogenous angiotensin II on renal renin gene expression during different states of a stimulated and of a suppressed renin system. To this end the renin system in male Sprague Dawley rats was stimulated by unilateral renal artery clipping (0.2 mm clip), by furosemide (60 mg/kg per diem) or isoproterenol (160 microg/kg per diem), and by ingestion of a low-salt diet (0.02%), or was suppressed by setting a contralateral renal artery clip (0.2-mm clip) or by ingestion of a high-salt diet (4%). During the last 2 days of these different treatment regimens, the animals were treated with the angiotensin II AT1 receptor antagonist losartan (40 mg/kg per diem) and renal renin mRNA levels were assayed. Renin gene expression was stimulated four- to fivefold by renal artery clipping and isoproterenol infusion, two- to three-fold by furosemide and a low-salt diet, and about four-fold by losartan. Additional treatment with losartan potentiated the stimulatory effects of a low-salt diet, of furosemide and of isoproterenol infusion on renin gene expression, whilst there was no significant additional effect of losartan on renin gene expression in clipped kidneys. Both contralateral renal artery clipping and a high-salt diet decreased renin mRNA levels to about 50% of the control value. In rts with a unilateral clip, additional losartan treatment caused renin mRNA to increase to about 350% of the control value in the contralateral kidney but to only 100% of the control value in animals on a high-salt diet. These findings suggest that the enhanced formation of angiotensin II during a low-salt intake, during tubular inhibition of salt reabsorption or during beta-adrenoreceptor activation plays a relevant negative feedback role in the activation of the renin gene. Moreover, in rats with one hypoperfused kidney, angiotensin II could be involved in the inhibition of renin gene expression in the contralateral kidney. In hypoperfused kidneys, however, and in animals on a high-salt diet, angiotensin II appears to play a only a minor feedback role in the regulation of the renin gene.
机译:这项研究旨在表征内源性血管紧张素II对肾素系统受激和抑制的不同状态下肾素基因表达的影响。为此目的,雄性Sprague Dawley大鼠的肾素系统受到单侧肾动脉夹闭(0.2 mm夹),呋塞米(60 mg / kg /双受精)或异丙肾上腺素(160 microg / kg /双受精)的刺激。低盐饮食(0.02%),或通过设置对侧肾动脉夹(0.2 mm夹子)或摄入高盐饮食(4%)而被抑制。在这些不同的治疗方案的最后两天中,用血管紧张素II AT1受体拮抗剂氯沙坦(40 mg / kg /天)治疗动物,并测定肾素mRNA水平。肾动脉夹闭和异丙肾上腺素输注可刺激肾素基因表达四到五倍,速尿和低盐饮食可刺激肾素基因表达两到三倍,氯沙坦可刺激约四倍。氯沙坦的进一步治疗增强了低盐饮食,速尿和异丙肾上腺素输注对肾素基因表达的刺激作用,而氯沙坦对截短肾脏中的肾素基因表达没有明显的额外作用。对侧肾动脉截断和高盐饮食均可将肾素mRNA水平降低至对照值的约50%。在具有单侧夹的rts中,额外的氯沙坦治疗导致对侧肾脏中的肾素mRNA增加至对照值的约350%,但在高盐饮食的动物中仅增加至对照值的100%。这些发现表明,在低盐摄入期间,在盐分吸收的管状抑制过程中或在β-肾上腺素受体活化过程中,血管紧张素II的形成增强在肾素基因的活化中起相关的负反馈作用。而且,在具有一个低灌注肾脏的大鼠中,血管紧张素II可能参与了对侧肾脏中肾素基因表达的抑制。然而,在肾脏灌注不足的情况下以及在高盐饮食的动物中,血管紧张素II似乎在调节肾素基因中仅起次要的反馈作用。

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