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口服避孕药对大鼠脑和垂体阿片肽的影响。

Effect of oral contraceptives on the rat brain and pituitary opioid peptides.

作者信息

Tejwani G A, Vaswani K K, Barbacci J C

出版信息

Peptides. 1985 May-Jun;6(3):555-61. doi: 10.1016/0196-9781(85)90120-2.

Abstract

This study was designed to explore the hormonal regulation of CNS opioid peptide levels in female Sprague Dawley rats. Forty-eight animals were divided into 2 equal groups for acute and chronic studies. Each group was further divided into 4 subgroups, each containing 6 animals. Each rat in the control group received an inert pill (in 0.25 ml corn oil daily by gavage); the second group, 15 micrograms norethindrone (NE, a potent progestin present in the oral contraceptive Micronor); the third group, 15 micrograms NE and 1 microgram ethinyl estradiol, EE2 (present in the oral contraceptive Modicon) and the fourth group, 10 times the dose of the third group. Rats were treated either acutely for 5 days or chronically for 7 weeks. Opioid peptides were estimated by radioimmunoassay. Acute administration of 150 micrograms NE + 10 micrograms EE2 decreased the levels of methionine-enkephalin (ME), leucine-enkephalin (LE), dynorphin (DYN) and beta-endorphin like immunoreactivity (beta-EI) by about 50% in the pituitary. The same dose on chronic administration also decreased DYN, but increased the levels of ME and LE in the pituitary by 331 and 69%, respectively. In the hypothalamus, chronic administration of NE + EE2 increased the level of ME (155%) and LE (87%) as well as of DYN (97%). In the striatum, the levels of LE (33%) and DYN (115%) were elevated during chronic administration. It is concluded that the acute administration of NE + EE2, in general, reduces the levels of ME, LE, DYN and beta-EI.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究旨在探讨雌性斯普拉格-道利大鼠中枢神经系统阿片肽水平的激素调节。48只动物分为两组,分别进行急性和慢性研究。每组再分为4个亚组,每组6只动物。对照组的每只大鼠每天经口灌胃给予一粒惰性药丸(溶于0.25 ml玉米油中);第二组给予15微克炔诺酮(NE,口服避孕药Micronor中的一种强效孕激素);第三组给予15微克NE和1微克乙炔雌二醇(EE2,口服避孕药Modicon中的成分),第四组给予第三组剂量的10倍。大鼠分别接受5天的急性治疗或7周的慢性治疗。通过放射免疫测定法评估阿片肽。急性给予150微克NE + 10微克EE2可使垂体中甲硫氨酸脑啡肽(ME)、亮氨酸脑啡肽(LE)、强啡肽(DYN)和β-内啡肽样免疫反应性(β-EI)水平降低约50%。慢性给予相同剂量也可降低DYN,但垂体中ME和LE水平分别升高331%和69%。在下丘脑,慢性给予NE + EE2可使ME(155%)、LE(87%)以及DYN(97%)水平升高。在纹状体中,慢性给药期间LE(33%)和DYN(115%)水平升高。结论是,一般而言,急性给予NE + EE2会降低ME、LE、DYN和β-EI的水平。(摘要截选至250词)

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