Chronic inhibition of nitric oxide synthase activity by N^G-nitro-l-arginine induces nitric oxide synthase expression in the developing rat cerebellum

详细信息	查看全文 | 推荐本文 |

• 作者：Zoltá ; n Serf艖z艖^a ; ^{serfozo@tres.blki.hu} ; Beá ; ta Lontay^b ; Zoltá ; n Kukor^c ; Ferenc Erd艖di^b
• 关键词：l-ARG ; l-arginine ; BSA ; bovine serum albumin ; DAB ; 3.3-diamino-benzidin ; HRP ; horseradish peroxidase ; l-NAME ; NG-nitro-l-arginine methylester ; NBT ; nitrotetrazole blue ; NGS ; normal goat serum ; NO ; nitric oxide ; l-NNA ; NG-nitro-l-arginine ; e ; i ; nNOS ; endoth
• 刊名：Neurochemistry International
• 出版年：2012
• 期刊代码：120_01970186
• 类别：bio
• 出版时间：May, 2012
• 卷：60
• 期：6
• 页码：605-615
• 文件大小：1101 K

摘要

Studies on chronic inhibition of nitric oxide synthase (NOS) in the CNS suggest a plastic change in nitric oxide (NO) synthesis in areas related to motor control, which might protect the animal from the functional and behavioral consequences of NO deficiency. In the present study, the acute and chronic effect of the substrate analogue inhibitor N^G-nitro-l-arginine (l-NNA) was examined on NO production, NO-sensitive cyclic guanosine monophosphate (cGMP) levels and the expression of NOS isoforms in the developing rat cerebellum. Acute intraperitoneal administration of the inhibitor (5-200 mg/kg) to 21-day-old rats reduced NOS activity and NO concentration dose dependently by 70-90%and the tissue cGMP level by 60-80%. By contrast, chronic application of l-NNA between postnatal days 4-21 diminished the total NOS activity and NO concentration only by 30%, and the tissue cGMP level by 10-50%. Chronic treatment of 10 mg/kg l-NNA induced neuronal (n)NOS expression in granule cells, as revealed by in situ hybridization, NADPH-diaphorase histochemistry and Western-blot, but it had no significant influence on tissue cGMP level or on layer formation of the cerebellum. However, a higher concentration (50 mg/kg) of l-NNA decreased the intensity of the NADPH-diaphorase reaction in granule cells, significantly reduced cGMP production, and retarded layer formation and induced inducible (i)NOS expression & activity in glial cells. Treatments did not affect endothelial (e)NOS expression. The administration of the biologically inactive isomer D-NNA (50 mg/kg) or saline was ineffective. The present findings suggest the existence of a concentration-dependent compensatory mechanism against experimentally-induced cronich inhibition of NOS, including nNOS or iNOS up-regulation, which might maintain a steady-state NO level in the developing cerebellum.