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催乳素对人醛固酮分泌性腺瘤的体外作用。

The effect of prolactin on human aldosterone-producing adenomas in vitro.

作者信息

Carroll J E, Campanile C P, Goodfriend T L

出版信息

J Clin Endocrinol Metab. 1982 Apr;54(4):689-92. doi: 10.1210/jcem-54-4-689.

Abstract

There is evidence for an unidentified aldosterone-stimulating factor of pituitary origin. We measured the effect of ovine PRL (oPRL) on aldosterone secretion by isolated cell suspensions of human aldosterone-producing adenomas (APAs) and compared it to the effects of angiotensins, ACTH, and potassium (K+). In the first APA, the aldosteronotropic action of large doses of oPRL was double that of angiotensin II (AII); the response to ACTH was triple that to AII, while K+ had a small stimulatory effect. Results with the second APA showed that physiological concentrations of oPRL caused a response nearly double that to AII, but, once again, less than the response to ACTH; K+ was inert. ACTH contamination of the oPRL preparation was too minute to account for these findings. We conclude that oPRL possesses aldosterone-stimulating activity in APAs greater than that of angiotensins and potassium, but less that that of ACTH. These data suggest a role for PRL in aldosterone secretion by aldosterone-producing adenomas.

摘要

有证据表明存在一种来源不明的垂体醛固酮刺激因子。我们测定了羊催乳素(oPRL)对人醛固酮分泌性腺瘤(APA)分离细胞悬液醛固酮分泌的影响,并将其与血管紧张素、促肾上腺皮质激素(ACTH)和钾(K+)的影响进行比较。在第一个APA中,大剂量oPRL的醛固酮促分泌作用是血管紧张素II(AII)的两倍;对ACTH的反应是对AII反应的三倍,而K+的刺激作用较小。第二个APA的结果表明,生理浓度的oPRL引起的反应几乎是对AII反应的两倍,但同样小于对ACTH的反应;K+无活性。oPRL制剂中ACTH的污染程度极小,无法解释这些发现。我们得出结论,oPRL在APA中具有的醛固酮刺激活性大于血管紧张素和钾,但小于ACTH。这些数据表明PRL在醛固酮分泌性腺瘤的醛固酮分泌中起作用。

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