Kim Taewan, La Junho, Lee Janghern, Yang Ilsuk
Department of Veterinary Physiology, College of Veterinary Medicine, Seoul National University, Republic of Korea.
J Pharmacol Sci. 2003 Aug;92(4):337-47. doi: 10.1254/jphs.92.337.
We examined the effects of nitric oxide (NO) donors, S-nitroso-L-cysteine (Cys-NO) and 3-morpholinosydnonimine hydrochloride (SIN-1), on slow waves and contractile activity in the circular muscle of guinea pig gastric antrum. In the presence of atropine and guanethidine, electrical field stimulation (EFS) reduced the amplitude of phasic contraction. The effect of EFS was significantly inhibited by both the NO synthase inhibitor N(omega)-nitro-L-arginine methyl ester and a soluble guanylate cyclase inhibitor 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ). Cys-NO and SIN-1 mimicked the effect of EFS on phasic contraction and reduced the amplitude of slow waves in a concentration-dependent manner, with no effect on frequency and resting membrane potential. Phasic contraction was more sensitive to NO donors than slow waves. The inhibitory effects of NO donors were antagonized by ODQ and mimicked by a membrane permeable cGMP analogue 8-bromo-cGMP. Several K(+) channel blockers such as apamin, iberiotoxin, and glibenclamide had no effect on the inhibitory action of SIN-1. These results suggest that NO inhibits the phasic contraction and slow waves through cGMP-dependent mechanisms in guinea pig gastric antrum. The effect of NO is unlikely to be mediated by the activation of Ca(2+)-activated or ATP-sensitive K(+) channels.
我们研究了一氧化氮(NO)供体S-亚硝基-L-半胱氨酸(Cys-NO)和盐酸3-吗啉代 sydnonimine(SIN-1)对豚鼠胃窦环行肌慢波和收缩活动的影响。在阿托品和胍乙啶存在的情况下,电场刺激(EFS)降低了相性收缩的幅度。EFS的作用被一氧化氮合酶抑制剂N(ω)-硝基-L-精氨酸甲酯和可溶性鸟苷酸环化酶抑制剂1H-[1,2,4]恶二唑并[4,3-a]喹喔啉-1-酮(ODQ)显著抑制。Cys-NO和SIN-1模拟了EFS对相性收缩的作用,并以浓度依赖的方式降低了慢波的幅度,对频率和静息膜电位没有影响。相性收缩对NO供体比慢波更敏感。NO供体的抑制作用被ODQ拮抗,并被膜通透性cGMP类似物8-溴-cGMP模拟。几种钾(K+)通道阻滞剂,如蜂毒明肽、iberiotoxin和格列本脲对SIN-1的抑制作用没有影响。这些结果表明,NO通过cGMP依赖机制抑制豚鼠胃窦的相性收缩和慢波。NO的作用不太可能通过钙(Ca2+)激活的或ATP敏感的钾(K+)通道的激活来介导。