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Decreased steroid hormone synthesis from inorganic nitrite and nitrate: studies in vitro and in vivo.

机译:无机亚硝酸盐和硝酸盐类固醇激素合成的减少:体外和体内研究。

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Nitrites and nitrates are consumed nonchalantly in diet. Organic nitrates are also used as vasodilators in angina pectoris, but the therapy is associated with tolerance whose mechanism remains elusive. Previously, we found inorganic nitrate inhibited steroidogenesis in vitro. Because adrenocorticoids regulate water and electrolyte metabolism, tolerance may ensue from steroid deficiency. We have studied the effects of nitrite and nitrate on in vitro synthesis and in vivo blood levels of steroid hormones. In vitro, nitrite was more potent than nitrate in inhibiting human chorionic gonadotropin (hCG)-stimulated androgen synthesis by Mouse Leydig Tumor cells. At concentrations above 42 mM, nitrite completely inhibited androgen synthesis, and, unlike nitrate, the inhibition was irreversible by increasing hCG concentration. The cAMP production remained intact but reduced with both ions. The nitric oxide (NO) scavenger, 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxy-3-oxide (c-PTIO) significantly increased hCG- or cAMP-stimulated androgen synthesis in all buffers, suggesting that NO is a chemical species directly involved in the nitriteitrate-induced inhibition. This is further supported by c-PTIO countering the inhibitory action of methylene blue on androgen synthesis. Rats given distilled water containing 50 mg/L NaNO(2) or NaNO(3) for 4 weeks drank significantly less daily. At the end, their blood corticosterone and testosterone levels were significantly decreased. The adrenocortical histology showed bigger lipid droplets, which are pathogonomic of impaired steroidogenesis. Nitrite and nitrate are metabolized to NO, which binds heme in cytochrome P450 enzymes, thereby inhibiting steroidogenesis. Therapeutic nitrates likewise may decrease adrenal (and gonadal) steroidogenesis. Cortisol deficiency would impair water excretion causing volume expansion, and aldosterone deficiency would cause sodium loss and raised renin. Paradoxically, volume expansion without sodium retention and raised renin has all been reported in tolerance. Copyright 2000 Academic Press.
机译:饮食中的亚硝酸盐和硝酸盐是无消耗的。有机硝酸盐也可在心绞痛中用作血管扩张剂,但该疗法与耐受性相关,其机制尚不清楚。以前,我们发现无机硝酸盐在体外抑制类固醇生成。由于肾上腺皮质激素调节水和电解质的代谢,因此类固醇缺乏可能会引起耐受。我们已经研究了亚硝酸盐和硝酸盐对类固醇激素的体外合成和体内血液水平的影响。在体外,亚硝酸盐在抑制人绒毛膜促性腺激素(hCG)刺激的小鼠Leydig肿瘤细胞雄激素合成中比硝酸盐更有效。在高于42 mM的浓度下,亚硝酸盐会完全抑制雄激素的合成,并且与硝酸盐不同,该抑制作用通过增加hCG浓度是不可逆的。 cAMP产生保持不变,但两种离子均降低。一氧化氮(NO)清除剂2-(4-羧基苯基)-4,4,5,5-四甲基咪唑啉-1-氧-3-氧化物(c-PTIO)显着增加了hCG或cAMP刺激的雄激素合成缓冲液,表明NO是直接参与亚硝酸盐/硝酸盐诱导的抑制作用的化学物质。 c-PTIO抵消了亚甲基蓝对雄激素合成的抑制作用,进一步证明了这一点。给予含有50 mg / L NaNO(2)或NaNO(3)的蒸馏水的大鼠饮用4周的日摄入量明显减少。最后,他们的血液中皮质激素和睾丸激素水平显着下降。肾上腺皮质组织学显示较大的脂质滴,这是类固醇生成受损的病理学。亚硝酸盐和硝酸盐被代谢为NO,NO与细胞色素P450酶中的血红素结合,从而抑制类固醇生成。治疗性硝酸盐同样可以减少肾上腺(和性腺)类固醇生成。皮质醇缺乏会损害水的排泄,导致体积膨胀,醛固酮缺乏会导致钠流失和肾素升高。矛盾的是,据报道在没有钠保留和肾素升高的情况下体积膨胀都具有耐受性。版权所有2000学术出版社。

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