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Effects of Nitric Oxide on Slow Waves and Spontaneous Contraction of Guinea Pig Gastric Antral Circular Muscle

机译:一氧化氮对豚鼠胃窦胃环形肌的慢波和自发收缩的影响

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References(30) Cited-By(5) 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 Nω-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 Ca2+-activated or ATP-sensitive K+ channels.
机译:参考文献(30)被引用者(5)我们研究了一氧化氮(NO)供体,S-亚硝基-L-半胱氨酸(Cys-NO)和3-吗啉代亚砜亚胺盐酸盐(SIN-1)对慢波和收缩的影响豚鼠胃窦环形肌中的活性。在存在阿托品和胍乙啶的情况下,电场刺激(EFS)降低了相收缩的幅度。 NO合酶抑制剂Nω-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] oxadiazolo [4,3-a] quinoxalin-1-one均显着抑制EFS的作用(ODQ)。 Cys-NO和SIN-1模仿了EFS对阶段性收缩的作用,并以浓度依赖的方式降低了慢波的振幅,而对频率和静止膜电位没有影响。相较于慢波,相收缩对NO供体更敏感。 ODQ拮抗NO供体的抑制作用,而膜可渗透的cGMP类似物8-溴-cGMP模仿了NO供体的抑制作用。几种K +通道阻滞剂,如木瓜蛋白酶,纤维毒素和格列本脲对SIN-1的抑制作用没有影响。这些结果表明,NO通过豚鼠胃窦中的cGMP依赖性机制抑制了相收缩和慢波。 NO的作用不太可能通过激活Ca2 +激活或ATP敏感的K +通道来介导。

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