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酒精对泌乳大鼠促甲状腺激素释放激素诱导的催乳素反应的影响:体内和体外研究

Alcohol effects on TRH-induced prolactin response in lactating rats: in vivo and in vitro studies.

作者信息

Subramanian M G, Savoy-Moore R T

机构信息

Department of Obstetrics and Gynecology, Wayne State University, Detroit, MI 48201.

出版信息

Alcohol. 1993 Jan-Feb;10(1):11-5. doi: 10.1016/0741-8329(93)90047-r.

Abstract

The site of action of alcohol in inhibiting suckling-induced prolactin release in lactating rats was examined by in vivo and in vitro studies. In vivo, sulpiride- and thyrotropin-releasing hormone (TRH)-induced prolactin release was studied in lactating rats separated from their litter. On day 7, dams were implanted with an atrial catheter. On day 10, pups were removed from dams at 0800 h and, after 5 h, an extension was attached to the catheter. An hour later, a baseline blood sample was removed and was followed by sulpiride (40 micrograms/kg) administration. Additional blood samples were withdrawn over 1 h. After the 60-min sample, sulpiride-administered rats were infused with 0.0, 1.0, or 2.0 g/kg b.wt. alcohol. Following alcohol, a postinfusion blood sample was removed, TRH (4.0 micrograms/kg) was administered, and subsequent blood samples were obtained 5, 10, 20, and 30 min after TRH. For in vitro studies, cells from lactating rats in midlactation were enzymatically dissociated, plated, and on culture day 5 were exposed to 0 or 10 nM TRH. Each set of cells were additionally exposed to 0, 100, or 300 mg% alcohol and media harvested after 4 h. In a subsequent study, plated cells were exposed to increasing doses of TRH in the presence of 0, 100, or 300 mg% alcohol and media harvested as above. Prolactin in plasma (in vivo studies) and medium (in vitro studies) was measured by RIA.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过体内和体外研究,检测了酒精抑制泌乳大鼠吮乳诱导的催乳素释放的作用位点。在体内,研究了在与幼崽分开的泌乳大鼠中,舒必利和促甲状腺激素释放激素(TRH)诱导的催乳素释放。在第7天,给母鼠植入心房导管。在第10天,于08:00将幼崽从母鼠处移走,5小时后,在导管上连接延长管。1小时后,采集基线血样,随后给予舒必利(40微克/千克)。在1小时内抽取额外的血样。在60分钟的样本采集后,给接受舒必利治疗的大鼠输注0.0、1.0或2.0克/千克体重的酒精。酒精输注后,采集输注后血样,给予TRH(4.0微克/千克),并在给予TRH后5、10、20和30分钟采集后续血样。对于体外研究,将泌乳中期的泌乳大鼠的细胞进行酶解、铺板,并在培养第5天暴露于0或10 nM的TRH。每组细胞还额外暴露于0、100或300 mg%的酒精中,并在4小时后收集培养基。在随后的研究中,将铺板的细胞在存在0、100或300 mg%酒精的情况下暴露于递增剂量的TRH,并如上所述收集培养基。通过放射免疫分析法(RIA)测定血浆(体内研究)和培养基(体外研究)中的催乳素。(摘要截断于250字)

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