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三环化合物对内分泌系统的中枢作用——一项体外研究

Central effects of tricyclic compounds on the endocrine system--an in vitro study.

作者信息

Julesz J, Gálfi M, Molnár J, Vecsernyés M

机构信息

Endocrine Unit, A. Szent-Györgyi Medical University, Szeged, Hungary.

出版信息

Prog Brain Res. 1992;91:89-92. doi: 10.1016/s0079-6123(08)62322-5.

Abstract

The present study involves the effects on corticotropin (ACTH) release of neuro- and thymoleptic tricyclic antidepressant compounds (TrcACs: chlorpromazine, promethazine, haloperidol, imipramine, amitriptyline) and their interactions with lysine-8-vasopressin (LVP) and corticosterone (B). As an in vitro model, 14-day monolayer pituitary cell cultures of Wistar rats were employed. The ACTH concentrations of the supernatant media were measured by radioimmunoassay. TrcACs augmented ACTH release; their combination with LVP, however, did not result in further stimulation; moreover, when combined with TrcACs + LVP, B did not inhibit, but rather paradoxically increased their ACTH-releasing action. As none of these phenomena were followed by relevant changes in intracellular cyclic adenosine monophosphate content, the mechanism of action may be proposed to involve a protein kinase C route.

摘要

本研究涉及神经安定和抗精神病三环类抗抑郁化合物(TrcACs:氯丙嗪、异丙嗪、氟哌啶醇、丙咪嗪、阿米替林)对促肾上腺皮质激素(ACTH)释放的影响,以及它们与赖氨酸-8-加压素(LVP)和皮质酮(B)的相互作用。作为体外模型,采用了Wistar大鼠14天的单层垂体细胞培养物。通过放射免疫测定法测量上清培养基中的ACTH浓度。TrcACs增加了ACTH的释放;然而,它们与LVP联合使用并未导致进一步的刺激;此外,当与TrcACs + LVP联合使用时,B并未抑制,反而反常地增强了它们的ACTH释放作用。由于这些现象均未伴随细胞内环磷酸腺苷含量的相关变化,因此可以提出其作用机制可能涉及蛋白激酶C途径。

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