Yanik Medaim, Vural Huseyin, Kocyigit Abdurrahim, Tutkun Hamdi, Zoroglu Süleyman Salih, Herken Hasan, Savaş Haluk Asuman, Köylü Alpay, Akyol Omer
Department of Psychiatry, Faculty of Medicine, University of Harran, Sanliurfa, Turkey.
Neuropsychobiology. 2003;47(2):61-5. doi: 10.1159/000070010.
The reciprocal regulation of arginase and nitric oxide synthase (NOS) in L-arginine-metabolizing pathways has been demonstrated. There are various evidences of the role of the nitric oxide (NO) in several neuropsychiatric disorders including schizophrenia. However, there is no study which has investigated the role of arginase as an important part of the arginine regulatory system affecting NOS activity in schizophrenia. This study aims to investigate arginase, manganese (Mn) and total nitrite levels (a metabolite of NO) and their relationship to the arginine-NO pathway in patients with schizophrenia. Arginase activities, Mn and total nitrite levels were measured in plasma from 46 patients with schizophrenia and 32 healthy control subjects. Plasma arginase activities and Mn were found to be significantly lower and total nitrite level higher in patients with schizophrenia compared with controls. Our results suggest that the arginine-NO pathway is involved in the pathogenesis of schizophrenia.
已证实精氨酸酶与一氧化氮合酶(NOS)在L-精氨酸代谢途径中存在相互调节作用。有多种证据表明一氧化氮(NO)在包括精神分裂症在内的多种神经精神疾病中发挥作用。然而,尚无研究探讨精氨酸酶作为影响精神分裂症中NOS活性的精氨酸调节系统重要组成部分的作用。本研究旨在调查精神分裂症患者体内的精氨酸酶、锰(Mn)和总亚硝酸盐水平(NO的一种代谢产物)及其与精氨酸-NO途径的关系。对46例精神分裂症患者和32名健康对照者的血浆进行了精氨酸酶活性、Mn和总亚硝酸盐水平的检测。结果发现,与对照组相比,精神分裂症患者的血浆精氨酸酶活性和Mn显著降低,总亚硝酸盐水平升高。我们的结果表明,精氨酸-NO途径参与了精神分裂症的发病机制。