首页> 外文期刊>The Journal of Physiology >Manganese stimulates luteinizing hormone releasing hormone secretion in prepubertal female rats: hypothalamic site and mechanism of action.
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Manganese stimulates luteinizing hormone releasing hormone secretion in prepubertal female rats: hypothalamic site and mechanism of action.

机译:锰刺激青春期前雌性大鼠的黄体生成激素释放激素分泌:下丘脑部位和作用机理。

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We have shown recently that Mn2+ stimulates gonadotropin secretion via an action at the hypothalamic level, and a diet supplemented with a low dose of the element is capable of advancing the time of female puberty. In this study, we used an in vitro approach to investigate the mechanism by which Mn2+ induces luteinizing hormone-releasing hormone (LHRH) secretion from prepubertal female rats. The medial basal hypothalamus from 30-day-old rats was incubated in Locke solution for 30 min to assess basal LHRH secretion, then incubated with buffer alone or buffer plus either a nitric oxide synthase (NOS) inhibitor (N-monomethyl-L-arginine (NMMA); 300 or 500 microM) or a soluble guanylyl cyclase (sGC) inhibitor (1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ); 100 or 250 microM) for another 30 min. Finally, the incubation continued for a further 30 min, but in the presence of MnCl2 (50 or 250 microM) to assess the effect of the blockers on stimulated LHRH secretion. Both 50 and 250 microM MnCl2 stimulated LHRH release (P < 0.05 and P < 0.01, respectively). The addition of 300-500 microM NMMA to the medium did not block Mn2+-stimulated release of LHRH, even with the higher dose of MnCl2. Furthermore, while 50, 100 and 250 microM MnCl2 all significantly induced LHRH release, the two lowest doses did not stimulate total nitrite released from the same tissue, an effect only observed with the highest dose. Taken together, these data suggest that Mn2+ is not an effective stimulator of NO. Conversely, inhibiting sGC with ODQ blocked the Mn2+-stimulated secretion of LHRH in a dose-dependent manner, indicating that GC is the site of action of Mn2+. Additionally, we showed that Mn2+ stimulated cGMP and LHRH from the same tissues, and that downstream blocking of protein kinase G formation with KT5823 (10 microM) inhibited Mn2+-induced LHRH release. These data demonstrate that the principal action of Mn2+ within the hypothalamus is to activate sGC directly and/or as a cofactor with available NO, hence generating cGMP and resulting in prepubertal LHRH release.
机译:最近我们发现,Mn2 +通过下丘脑水平的刺激刺激促性腺激素的分泌,补充低剂量元素的饮食能够延长女性青春期的时间。在这项研究中,我们使用一种体外方法来研究Mn2 +诱导青春期前雌性大鼠促黄体生成激素释放激素(LHRH)分泌的机制。将30日龄大鼠的内侧基底下丘脑在Locke溶液中孵育30分钟以评估基底LHRH分泌,然后与单独的缓冲液或缓冲液加一氧化氮合酶(NOS)抑制剂(N-单甲基-L-精氨酸)一起孵育(NMMA); 300或500 microM)或可溶性鸟苷基环化酶(sGC)抑制剂(1H- [1,2,4]恶二唑并[4,3-a]喹喔啉-1-酮(ODQ); 100或250 microM)再过30分钟最后,继续温育另外30分钟,但在MnCl2(50或250 microM)存在下评估阻滞剂对刺激的LHRH分泌的影响。 50和250 microM MnCl2均可刺激LHRH释放(分别为P <0.05和P <0.01)。向培养基中添加300-500 microM NMMA不会阻止Mn2 +刺激的LHRH释放,即使使用更高剂量的MnCl2也是如此。此外,尽管50、100和250 microM MnCl2均能显着诱导LHRH释放,但两次最低剂量并不能刺激从同一组织释放的总亚硝酸盐,只有在最高剂量下才能观察到这种效果。综上所述,这些数据表明Mn 2+不是有效的NO刺激剂。相反,用ODQ抑制sGC可以剂量依赖的方式阻断Mn2 +刺激的LHRH分泌,这表明GC是Mn2 +的作用部位。此外,我们表明Mn2 +刺激了来自相同组织的cGMP和LHRH,并且下游用KT5823(10 microM)阻止蛋白激酶G的形成抑制了Mn2 +诱导的LHRH释放。这些数据表明,下丘脑中Mn2 +的主要作用是直接激活sGC和/或与可用NO一起作为辅因子,从而产生cGMP并导致青春期前LHRH释放。

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