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孕酮和17α-羟孕酮。人类精子中钙内流的新型刺激物。

Progesterone and 17 alpha-hydroxyprogesterone. Novel stimulators of calcium influx in human sperm.

作者信息

Blackmore P F, Beebe S J, Danforth D R, Alexander N

机构信息

Department of Pharmacology, Eastern Virginia Medical School, Norfolk 23501.

出版信息

J Biol Chem. 1990 Jan 25;265(3):1376-80.

PMID:2104840
Abstract

Progesterone and 17 alpha-hydroxyprogesterone (but not other steroids such as testosterone, corticosterone, beta-estradiol, estrone, dehydroepiandrosterone, 20 alpha-hydroxypregnen-3-one, androstenedione, and pregnenolone) were shown to cause an immediate increase, in free cytosolic calcium ([Ca2+]i) in both capacitated and noncapacitated human sperm, using the fluorescent indicator fura 2. Significant increases in [Ca2+]i were observed with 10 ng/ml progesterone, while maximum effects were seen with 1 microgram/ml progesterone. Two other steroids 11 beta-hydroxyprogesterone and 5 alpha-pregnane-3,20-dione exhibited significant activity to increase [Ca2+]i. This increase in [Ca2+]i elicited by progesterone was entirely due to Ca2+ influx from the extracellular medium since the increase in [Ca2+]i was blocked by the Ca2+ chelator EGTA (2.5 mM) and the Ca2+ channel antagonist La3+ (0.25 mM) when added to the medium containing 2.5 mM Ca2+. Progesterone also stimulated the uptake of Mn2+ into sperm as measured by the quenching of fura 2 fluorescence. Progesterone has been found in human follicular fluid at levels capable of stimulating increases in [Ca2+]i. The similarities in responses induced by human follicular fluid and progesterone an increase in [Ca2+]i, and hence the acrosome reaction, is progesterone and/or 17 alpha-hydroxyprogesterone. Progesterone (1 microgram/ml) did not increase [Ca2+]i in somatic cells such as adipocytes, hepatocytes, Balb/c 3T3 cells, normal rat kidney, or DDT1 MF-2 cells. The effects of these progestins to increase [Ca2+]i, by activating a receptor-operated calcium channel, is the first report of such an activity in sperm. This phenomena possibly opens up a new field of steroid action in the area of sterility, fertility, and contraception at the level of the sperm.

摘要

使用荧光指示剂fura 2发现,孕酮和17α-羟孕酮(但不是其他类固醇,如睾酮、皮质酮、β-雌二醇、雌酮、脱氢表雄酮、20α-羟基孕烯-3-酮、雄烯二酮和孕烯醇酮)可使获能和未获能的人类精子胞质游离钙([Ca2+]i)立即增加。观察到10 ng/ml孕酮可使[Ca2+]i显著增加,而1 μg/ml孕酮可产生最大效应。另外两种类固醇11β-羟孕酮和5α-孕烷-3,20-二酮也表现出显著增加[Ca2+]i的活性。孕酮引起的[Ca2+]i增加完全是由于Ca2+从细胞外介质流入,因为当加入含有2.5 mM Ca2+的培养基中时,[Ca2+]i的增加被Ca2+螯合剂EGTA(2.5 mM)和Ca2+通道拮抗剂La3+(0.25 mM)阻断。通过fura 2荧光淬灭测量,孕酮还刺激精子摄取Mn2+。已发现人卵泡液中孕酮的水平能够刺激[Ca2+]i增加。人卵泡液和孕酮诱导的反应相似——[Ca2+]i增加,进而引发顶体反应,是孕酮和/或17α-羟孕酮所致。1 μg/ml孕酮不会使脂肪细胞、肝细胞、Balb/c 3T3细胞、正常大鼠肾细胞或DDT1 MF-2细胞等体细胞中的[Ca2+]i增加。这些孕激素通过激活受体操纵的钙通道增加[Ca2+]i的作用,是精子中此类活性的首次报道。这一现象可能在不育、生育和避孕领域精子水平上开辟类固醇作用的新领域。

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