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自主神经药物对锦龟(Pseudemys scripta)肾素释放的影响。

Effect of autonomic agents on renin release in the turtle, Pseudemys scripta.

作者信息

Cipolle M D, Zehr J E, Reinhart G A

出版信息

Am J Physiol. 1986 Dec;251(6 Pt 2):R1103-8. doi: 10.1152/ajpregu.1986.251.6.R1103.

Abstract

Experiments were conducted in the freshwater turtle, Pseudemys scripta, to study the effect of autonomic agents on the control of renin in this primitive species. The unique finding in these studies was that, unlike mammals, isoproterenol infusion fails to increase renin activity even though heart rate and arterial pressure patterns indicated that systemic responses were similar to that in mammals. On the other hand, acetylcholine (ACh) infusion resulted in a prompt threefold elevation (P less than 0.01) of renin activity. This response was blocked by propranolol but not atropine. Other experiments demonstrated that ACh elicited a prompt elevation of circulating norepinephrine and epinephrine in these turtles and led to the hypothesis that the renin response to ACh was secondary to the release of endogenous catecholamines. This hypothesis was supported by the fact that, in reserpinized turtles, ACh failed to elicit the usual renin response. Further evidence stemmed from the fact that epinephrine administration led to a prompt fourfold increase (P less than 0.01) in renin, which could be blocked by propranolol. On the other hand, phenoxybenzamine failed to block the response under identical conditions. Taken as a whole, these data suggest that in this primitive species renin activity is elevated by endogenous catecholamines even though isoproterenol, a classical beta-adrenergic agonist, is without effect. These data illustrate again the need for caution when assuming analogy when comparing responses in primitive species with that of mammals.

摘要

实验以淡水龟(伪彩龟)为对象,研究自主神经药物对这种原始物种肾素调控的影响。这些研究中的独特发现是,与哺乳动物不同,即便心率和动脉血压模式显示全身反应与哺乳动物相似,但输注异丙肾上腺素仍无法增加肾素活性。另一方面,输注乙酰胆碱(ACh)导致肾素活性迅速升高三倍(P<0.01)。此反应被普萘洛尔阻断,但未被阿托品阻断。其他实验表明,ACh使这些乌龟体内循环的去甲肾上腺素和肾上腺素迅速升高,并由此提出假设,即肾素对ACh的反应继发于内源性儿茶酚胺的释放。这一假设得到以下事实的支持:在接受利血平处理的乌龟中,ACh未能引发通常的肾素反应。进一步的证据源于以下事实:给予肾上腺素导致肾素迅速升高四倍(P<0.01),这可被普萘洛尔阻断。另一方面,在相同条件下,酚苄明未能阻断该反应。总体而言,这些数据表明,在这种原始物种中,即便经典的β-肾上腺素能激动剂异丙肾上腺素无效,但内源性儿茶酚胺仍可提高肾素活性。这些数据再次说明,在将原始物种的反应与哺乳动物的反应进行类比时,需要谨慎。

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