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去卵巢母羊子宫中缺乏催产素诱导的前列腺素F2α分泌反应及体外反应的激活

Absence of the oxytocin-induced prostaglandin F2 alpha secretory response in uterus from ovariectomized ewes and activation of the response in vitro.

作者信息

Sheldrick E L, Flick-Smith H C, Bendall D E, Flint A P

机构信息

Department of Cellular Physiology, Babraham Institute, Cambridge, UK.

出版信息

J Endocrinol. 1995 May;145(2):299-305. doi: 10.1677/joe.0.1450299.

Abstract

Oxytocin-induced prostaglandin F2 alpha (PGF2 alpha) responses were measured in explants of uterus from ovariectomized ewes on the day of tissue collection or after culture for 72 h in the presence or absence of oestradiol-17 beta (100 nmol/l). Oxytocin receptor binding activity was 210 +/- 47 fmol [3H]oxytocin bound per mg protein in fresh tissue and 89 +/- 24 and 90 +/- 17 fmol/mg in tissue cultured with control medium or with oestradiol respectively (means +/- S.E.M.). PGF2 alpha production during the hour following oxytocin administration to freshly collected tissue was 272 +/- 77 ng/g/h compared with 193 +/- 35 ng/g/h in the absence of oxytocin. These rates were 2789 +/- 1085 and 353 +/- 135 ng/g/h after culture for 72 h in control medium and 2022 +/- 496 and 342 +/- 134 ng/g/h after culture with oestradiol. Thus oestradiol had no effect on the culture-induced maturation of the PGF2 alpha response. Short-term exposure to arachidonic acid (66 mumol/l) did not increase PGF2 alpha production in fresh tissue but significantly increased basal but not oxytocin-induced PGF2 alpha production after 72 h in culture (P < 0.05). There was an absence of oxytocin-induced inositol phosphate turnover in fresh tissue but after culture concentrations of inositol mono-, bis- and trisphosphates were all significantly increased by oxytocin (P < 0.005). Antisera directed against G-protein alpha sub-units alpha i3, alpha o, alpha q, alpha 11 and the common beta subunit, and prostaglandin H-synthase-1 detected proteins that were present before and after culture.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在组织采集当天或在存在或不存在17β-雌二醇(100 nmol/l)的情况下培养72小时后,测量去卵巢母羊子宫外植体中催产素诱导的前列腺素F2α(PGF2α)反应。新鲜组织中催产素受体结合活性为每毫克蛋白质结合210±47 fmol [3H]催产素,在分别用对照培养基或雌二醇培养的组织中为89±24和90±17 fmol/mg(平均值±标准误)。向新鲜采集的组织中注射催产素后1小时内PGF2α的产生量为272±77 ng/g/h,而在未注射催产素时为193±35 ng/g/h。在对照培养基中培养72小时后,这些速率分别为2789±1085和353±135 ng/g/h,在与雌二醇一起培养后为2022±496和342±134 ng/g/h。因此,雌二醇对培养诱导的PGF2α反应成熟没有影响。短期暴露于花生四烯酸(66 μmol/l)不会增加新鲜组织中PGF2α的产生,但在培养72小时后显著增加基础状态下而非催产素诱导的PGF2α产生(P<0.05)。新鲜组织中不存在催产素诱导的肌醇磷酸周转,但培养后,肌醇单磷酸、双磷酸和三磷酸的浓度均因催产素而显著增加(P<0.005)。针对G蛋白α亚基αi3、αo、αq、α11和共同β亚基以及前列腺素H合酶-1的抗血清检测到培养前后均存在的蛋白质。(摘要截短至250字)

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