Nakagami Y, Suda T, Yajima F, Ushiyama T, Tomori N, Sumitomo T, Demura H, Shizume K
Brain Res. 1986 Oct 29;386(1-2):232-6. doi: 10.1016/0006-8993(86)90159-9.
We investigated the effects of serotonin, cyproheptadine and reserpine on corticotropin-releasing factor (CRF) release from the rat hypothalamus, and the effect of cyproheptadine on CRF-induced adrenocorticotropic hormone (ACTH) secretion from the anterior pituitary (AP) in vitro using a perifusion system for rat hypothalami and AP, and a rat CRF radioimmunoassay. Cyproheptadine, 10(-8) M, had a direct inhibitory effect on both basal and 10(-9) M CRF-induced ACTH secretion from the rat AP in vitro. In addition, 10(-9)-10(-7) M cyproheptadine inhibited basal CRF release in a dose-dependent fashion, and also suppressed serotonin- and KCl-induced CRF release. Conversely, 10(-9)-10(-7) M reserpine failed to influence CRF release from the rat hypothalamus. These results indicate that a serotonergic mechanism may be involved in the CRF-releasing mechanism, and inhibition of depolarization-dependent calcium entry into cells and/or nerve endings. In addition an anti-serotonergic mechanism is involved in the inhibitory action of cyproheptadine.
我们使用大鼠下丘脑和垂体前叶的灌流系统以及大鼠促肾上腺皮质激素释放因子(CRF)放射免疫分析法,研究了血清素、赛庚啶和利血平对大鼠下丘脑CRF释放的影响,以及赛庚啶对体外培养的垂体前叶(AP)中CRF诱导的促肾上腺皮质激素(ACTH)分泌的影响。10(-8) M的赛庚啶对体外培养的大鼠垂体前叶基础状态下以及10(-9) M CRF诱导的ACTH分泌均有直接抑制作用。此外,10(-9)-10(-7) M的赛庚啶以剂量依赖方式抑制基础CRF释放,并且还抑制血清素和氯化钾诱导的CRF释放。相反,10(-9)-10(-7) M的利血平未能影响大鼠下丘脑CRF的释放。这些结果表明,一种血清素能机制可能参与了CRF释放机制,并且抑制了依赖去极化的钙进入细胞和/或神经末梢。此外,抗血清素能机制参与了赛庚啶的抑制作用。