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β-肾上腺素能刺激超灌流垂体细胞聚集体释放催乳素。

Beta-adrenergic stimulation of prolactin release from superfused pituitary cell aggregates.

作者信息

Denef C, Baes M

出版信息

Endocrinology. 1982 Jul;111(1):356-8. doi: 10.1210/endo-111-1-356.

Abstract

l-Isoproterenol (l-ISO), a specific agonist of beta-adrenergic receptors, evoked a prompt rise of prolactin (PRL) release from superfused anterior pituitary cell aggregates established in culture for 5 days. The effect was concentration-dependent between 1 and 100 nM. d-Isoproterenol was more than 2 orders of magnitude weaker than the l-isomer. When dopamine receptors were blocked with domperidone, PRL secretion was also stimulated by l-epinephrine (E) and l-norepinephrine (NE), the rank order of potency being l-ISO greater than E much greater than NE. Under the latter conditions dopamine and the alpha-adrenergic agonists, clonidine and phenylephrine, had no stimulatory effect at 1 microM. Stimulation of PRL release by l-ISO and E was blocked by the beta-receptor antagonist, propranolol, but not by the alpha-receptor blocker, prazosin.

摘要

左旋异丙肾上腺素(l-ISO)是β-肾上腺素能受体的特异性激动剂,可使培养5天的超融合垂体前叶细胞聚集体的催乳素(PRL)释放迅速增加。该效应在1至100 nM之间呈浓度依赖性。右旋异丙肾上腺素的作用比左旋异构体弱2个数量级以上。当用多潘立酮阻断多巴胺受体时,左旋肾上腺素(E)和左旋去甲肾上腺素(NE)也能刺激PRL分泌,效力顺序为l-ISO>E>>NE。在后一种情况下,多巴胺和α-肾上腺素能激动剂可乐定和去氧肾上腺素在1μM时无刺激作用。l-ISO和E对PRL释放的刺激被β受体拮抗剂普萘洛尔阻断,但不被α受体阻滞剂哌唑嗪阻断。

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