Rettori V, Gimeno M, Lyson K, McCann S M
Department of Physiology, University of Texas Southwestern Medical Center, Dallas 75235-9040.
Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11543-6. doi: 10.1073/pnas.89.23.11543.
Nitric oxide (NO), formed by conversion of arginine to citrulline and NO by NO synthase, mediates relaxation of vascular smooth muscle. NO synthase has been demonstrated by immunocytochemical methods in neurons in various parts of the central nervous system including the hypothalamus. The latter finding suggested to us that NO might play a role in controlling the release of hypothalamic peptides. We have previously shown that norepinephrine mediates the release of luteinizing hormone-releasing hormone (LHRH) from LHRH terminals in the median eminence into the hypophyseal portal veins, which transport LHRH to the anterior pituitary gland to trigger release of luteinizing hormone from gonadotrophs. LHRH release from these terminals requires increased release of prostaglandin E2 (PGE2). PGE2 activates adenylate cyclase to produce cAMP, and then cAMP induces the exocytosis of LHRH secretory granules. In view of the evidence above and because of the developing evidence for the importance of NO in the central nervous system, it occurred to us that NO might be involved in this process. Consequently, we evaluated the role of NO in the release of PGE2 from medial basal hypothalamic fragments. As previously reported, norepinephrine (10 microM) increased PGE2 release from the hypothalamic fragments. The inhibitor of NO synthase NG-monomethyl-L-arginine (NMMA, 300 microM) blocked the stimulation of PGE2 release induced by norepinephrine but had no effect on the basal release of PGE2. Sodium nitroprusside (100 microM), which liberates NO, also elevated PGE2 release from the hypothalamic fragments. This elevation was not affected by NMMA, presumably because NMMA blocks enzymatic generation of NO but does not alter NO liberated by nitroprusside. When the NO liberated by nitroprusside was inactivated by hemoglobin (2 micrograms/ml), the effect of nitroprusside on PGE2 release was completely inhibited. Neither NMMA nor hemoglobin altered the basal release of PGE2, which indicates that NO is not responsible for basal PGE2 release. Addition of L-arginine (10 microM to 1 mM), the substrate for NO synthase, had no effect on basal PGE2 production. These results indicate that NO synthase is not activated in unstimulated hypothalamic fragments in vitro. The results suggest that norepinephrine activates NO synthase leading to the production of NO, which subsequently activates cyclooxygenase and results in the production of PGE2. PGE2 then activates adenylate cyclase leading to generation of increased cAMP, which induces exocytosis of secretory granules of LHRH and other neuropeptides released by PGE2. The indication that NO is essential to norepinephrine-induced release of PGE2 from hypothalamic fragments provides insight into the mechanism of LHRH release and the results open the possibility that the importance of NO to neuronal functions may be widespread in the nervous system.
一氧化氮(NO)由精氨酸经一氧化氮合酶转化为瓜氨酸和NO而形成,介导血管平滑肌舒张。通过免疫细胞化学方法已在包括下丘脑在内的中枢神经系统各部位的神经元中证实了一氧化氮合酶的存在。后一发现使我们推测NO可能在控制下丘脑肽的释放中起作用。我们先前已表明,去甲肾上腺素介导促黄体生成激素释放激素(LHRH)从中位隆起的LHRH终末释放到垂体门脉血管中,这些血管将LHRH转运至垂体前叶以触发促性腺激素细胞释放促黄体生成激素。这些终末释放LHRH需要增加前列腺素E2(PGE2)的释放。PGE2激活腺苷酸环化酶以产生cAMP,然后cAMP诱导LHRH分泌颗粒的胞吐作用。鉴于上述证据以及由于越来越多的证据表明NO在中枢神经系统中具有重要性,我们想到NO可能参与了这一过程。因此,我们评估了NO在从下丘脑内侧基底部片段释放PGE2中的作用。如先前报道,去甲肾上腺素(10微摩尔)增加了下丘脑片段中PGE2的释放。一氧化氮合酶抑制剂NG-甲基-L-精氨酸(NMMA,300微摩尔)阻断了去甲肾上腺素诱导的PGE2释放的刺激,但对PGE2的基础释放没有影响。释放NO的硝普钠(100微摩尔)也提高了下丘脑片段中PGE2的释放。这种升高不受NMMA的影响,推测是因为NMMA阻断了NO的酶促生成,但不会改变硝普钠释放的NO。当硝普钠释放的NO被血红蛋白(2微克/毫升)灭活时,硝普钠对PGE2释放的作用被完全抑制。NMMA和血红蛋白均未改变PGE2的基础释放,这表明NO不负责PGE2的基础释放。添加L-精氨酸(10微摩尔至1毫摩尔),即一氧化氮合酶的底物,对基础PGE2的产生没有影响。这些结果表明,在体外未受刺激的下丘脑片段中一氧化氮合酶未被激活。结果提示,去甲肾上腺素激活一氧化氮合酶导致NO的产生,随后NO激活环氧化酶并导致PGE2的产生。PGE2然后激活腺苷酸环化酶导致cAMP生成增加,进而诱导LHRH分泌颗粒以及由PGE2释放的其他神经肽的胞吐作用。NO对去甲肾上腺素诱导的下丘脑片段释放PGE2至关重要这一发现为LHRH释放机制提供了见解,并且这些结果开启了一种可能性,即NO对神经元功能的重要性在神经系统中可能很普遍。