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垂体前叶膜制剂中白三烯C4结合的特性分析。

Characterization of leukotriene C4 binding in anterior pituitary membrane preparations.

作者信息

Eberhardt I, Kiesel L, Rosenberg K, Klinga K, Runnebaum B

机构信息

Department of Gynecology and Obstetrics, University of Heidelberg, Federal Republic of Germany.

出版信息

Prostaglandins. 1991 Feb;41(2):185-99. doi: 10.1016/0090-6980(91)90030-j.

Abstract

Pituitary cells produce leukotrienes (LTs) and respond to exogenous administration of LTs by releasing gonadotropins. Specific high affinity leukotriene C4 (LTC4) binding has been found in membrane preparations of bovine anterior pituitaries. Unlabelled LTC4 displaced specific [3H]LTC4 binding. Other leukotrienes (LTB4, LTD4, LTE4, LTF4) did not compete with [3H]LTC4 for binding sites when administered at increasing concentrations together with a constant amount of radioligand indicating that the binding is highly specific for LTC4. Scatchard analysis of binding data obtained from saturation studies revealed a single binding site for [3H]LTC4 with a Kd of 8.95 +/- 5.53 nM and a B max of 15.44 +/- 6.93 pmol per mg of membrane protein. Glutathione S-transferase, a possible LTC4 binding site, did not display activity in the membrane fraction although the two glutathione derivates S-octylglutathione and S-decylglutathione competed with LTC4 in binding experiments. As leukotrienes are potent stimulators of gonadotropin secretion and modulators of gonadotropin-releasing hormone (GnRH)-induced gonadotropin release it is concluded that leukotrienes may be involved in the signal transduction pathway of GnRH and that they may act via a specific and high affinity receptor.

摘要

垂体细胞可产生白三烯(LTs),并且通过释放促性腺激素对外源性给予的LTs作出反应。在牛垂体前叶的膜制剂中发现了特异性高亲和力的白三烯C4(LTC4)结合。未标记的LTC4可取代特异性的[3H]LTC4结合。当与恒定剂量的放射性配体一起以递增浓度给予时,其他白三烯(LTB4、LTD4、LTE4、LTF4)并不与[3H]LTC4竞争结合位点,这表明该结合对LTC4具有高度特异性。对饱和研究获得的结合数据进行Scatchard分析,结果显示[3H]LTC4有一个单一结合位点,解离常数(Kd)为8.95±5.53 nM,最大结合容量(Bmax)为每毫克膜蛋白15.44±6.93 pmol。谷胱甘肽S-转移酶作为一个可能的LTC4结合位点,在膜部分未显示出活性,尽管两种谷胱甘肽衍生物S-辛基谷胱甘肽和S-癸基谷胱甘肽在结合实验中可与LTC4竞争。由于白三烯是促性腺激素分泌的强效刺激剂以及促性腺激素释放激素(GnRH)诱导的促性腺激素释放的调节剂,因此可以得出结论,白三烯可能参与GnRH的信号转导途径,并且它们可能通过一种特异性的高亲和力受体发挥作用。

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