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一氧化氮:在神经毒性中的作用。

Nitric oxide: role in neurotoxicity.

作者信息

Dawson V L

机构信息

Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287, USA.

出版信息

Clin Exp Pharmacol Physiol. 1995 Apr;22(4):305-8. doi: 10.1111/j.1440-1681.1995.tb02005.x.

Abstract
  1. Nitric oxide (NO) is a novel neuronal messenger molecule which interacts with surrounding neurones, not by synaptic transmission but by diffusion between cells. 2. NO is produced following stimulation of the enzyme, NO synthase (NOS). After synthesis, NO exerts its biological actions by diffusion to the site of action. Therefore, the way to regulate the physiological actions of NO is to regulate NOS. 3. NOS is activated by the influx of calcium from glutamate-activated N-methyl-D-aspartate receptors. Overactivation of these receptors leads to overproduction of NO and neuronal cell death. 4. NOS can be regulated at the catalytic site, at the flavo-proteins, at the calmodulin site and by phosphorylation. 5. In excess, NO is toxic to neurones. This toxicity is mediated largely by an interaction with the superoxide anion, presumably through the generation of the oxidant, peroxynitrite. 6. NO or peroxynitrite-mediated neuronal injury involves the activation of the nuclear protein, poly(ADP-ribose)synthetase.
摘要
  1. 一氧化氮(NO)是一种新型的神经信使分子,它与周围神经元相互作用,不是通过突触传递,而是通过细胞间扩散。2. NO在酶一氧化氮合酶(NOS)受到刺激后产生。合成后,NO通过扩散到作用部位发挥其生物学作用。因此,调节NO生理作用的方法是调节NOS。3. NOS通过谷氨酸激活的N-甲基-D-天冬氨酸受体使钙内流而被激活。这些受体的过度激活会导致NO过度产生和神经元细胞死亡。4. NOS可在催化位点、黄素蛋白、钙调蛋白位点以及通过磷酸化进行调节。5. 过量时,NO对神经元有毒性。这种毒性很大程度上是通过与超氧阴离子相互作用介导的,可能是通过生成氧化剂过氧亚硝酸盐。6. NO或过氧亚硝酸盐介导的神经元损伤涉及核蛋白聚(ADP-核糖)合成酶的激活。

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