Correlations between neuronal nitric oxide synthase and muscarinic M3/M1 receptors in the rat retina

被引:16
作者
Borda, E
Berra, A
Saravia, M
Ganzinelli, S
Sterin-Borda, L
机构
[1] Univ Buenos Aires, Sch Dent, Pharmacol Unit, Buenos Aires, DF, Argentina
[2] Consejo Nacl Invest Cient & Tecn, Argentine Natl Res Council, RA-1033 Buenos Aires, DF, Argentina
[3] Univ Buenos Aires, Sch Med, Dept Pathol, Buenos Aires, DF, Argentina
[4] Univ Buenos Aires, Clin Hosp, Dept Ophthalmol, Buenos Aires, DF, Argentina
关键词
NOS; NO; mAChR; M-3; M-1; cGMP; nNOS mRNA;
D O I
10.1016/j.exer.2004.09.016
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
This study determined the different signal pathways involved in M-1/M-3 muscarinic acetylcholine receptor (mAChR) dependent stimulation of nitric oxide synthase (NOS) activity/cyclic GMP (cGMP) production and nNOS mRNA expression in rat retina. Exposure of the retina to different concentrations of carbachol caused an increase in NOS activity, cGMP production and phosphoinositol (PI) accumulation. The increase in NOS activity and cGMP content was blocked by L-NMMA and ODQ, respectively. Also, phospholipase C (PLC) and calcium/calmodulin (CaM) inhibition prevented the carbachol activation on NOS/cGMP pathways. Both, 4-DAMP and pirenzepine but not AF-DX 116 blocked the increase in NOS and cGMP induced by carbachol. Carbachol-stimulation of M-1/M-3 mAChR increased nNOS-mRNA levels associated with an increase of endogenous NO and cGMP production. The mechanism appears to occur secondarily to stimulation of PIs turnover via PLC. This triggers a cascade reaction involving CaM and soluble guanylate cyclase leading to NO and cGMP accumulation, that in turn, up regulates nNOS-mRNA gene expression. These results give novel insight into the mechanism involved in the regulation of nNOS-mRNA levels by mAChR activation of retina. (c) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:391 / 399
页数:9
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