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肾上腺素合成选择性抑制剂SK&F 64139对大鼠催乳素分泌的影响。

Effect of a selective inhibitor of epinephrine synthesis, SK&F 64 139, on prolactin secretion in the rat.

作者信息

Castro-e-Silva E, Nonaka K O, Antunes-Rodrigues J

出版信息

Braz J Med Biol Res. 1986;19(3):389-94.

PMID:3594004
Abstract

The participation of central epinephrine in prolactin secretion was investigated in rats by testing the effects of SK&F 64 139, a selective inhibitor of phenylethanolamine-N-methyltransferase. The drug is reported to dramatically reduce brain epinephrine concentration without affecting norepinephrine or dopamine levels. When SK&F 64 139 was administered (40 mg/kg, ip) to male rats or to female rats during diestrus or proestrus, plasma prolactin levels were not different from those of control groups. Lactating and ovariectomized rats, however, responded to the same SK&F 64 139 dose with an increase in plasma prolactin levels: 210.02 +/- 22.72 vs 378.66 +/- 42.57 (mean +/- SEM) for control of lactating rats, and 4.35 +/- 0.52 vs 6.21 +/- 0.60 ng/ml for control ovariectomized rat. These results suggest that epinephrine may play a functional inhibitory role in prolactin secretion in the lactating and ovariectomized rat.

摘要

通过测试苯乙醇胺 -N-甲基转移酶的选择性抑制剂SK&F 64139的作用,研究了大鼠中枢肾上腺素在催乳素分泌中的参与情况。据报道,该药物可显著降低脑内肾上腺素浓度,而不影响去甲肾上腺素或多巴胺水平。当对雄性大鼠或处于动情间期或动情前期的雌性大鼠腹腔注射SK&F 64139(40mg/kg)时,血浆催乳素水平与对照组无差异。然而,泌乳大鼠和去卵巢大鼠对相同剂量的SK&F 64139有反应,血浆催乳素水平升高:泌乳大鼠对照组为210.02±22.72,给药组为378.66±42.57(平均值±标准误);去卵巢大鼠对照组为4.35±0.52,给药组为6.21±0.60ng/ml。这些结果表明,肾上腺素可能在泌乳大鼠和去卵巢大鼠的催乳素分泌中发挥功能性抑制作用。

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