Gustafsson B I, Delbro D S
Department of Physiology and Surgery, University of Göteborg, Sweden.
J Auton Nerv Syst. 1993 Aug-Sep;44(2-3):179-87. doi: 10.1016/0165-1838(93)90030-x.
The effects of blocking nitric oxide synthase with the arginine analog N omega-nitro-L-arginine (L-NNA) were investigated in anaesthetized cats, vagotomized and pretreated with guanethidine and atropine. Spontaneous NANC jejunal motility (recorded as the volume changes of an intraluminal balloon) was markedly increased in a dose-dependent and stereospecific manner. The effect of L-NNA was partly reversed by L-arginine, the substrate for nitric oxide (NO) synthesis. Thus, this study presents evidence for a tonic inhibitory influence, via the release of NO, on small intestinal motility in vivo. Furthermore, relaxations upon the L-NNA-induced hypermotility could be elicited by vagal nerve stimulation, which may suggest the existence of another NANC inhibitory transmitter. Hexamethonium abolished such relaxations but did not affect the tone or phasic activity after L-NNA.
在麻醉猫身上进行了研究,这些猫已切断迷走神经,并先用胍乙啶和阿托品预处理,以观察精氨酸类似物Nω-硝基-L-精氨酸(L-NNA)阻断一氧化氮合酶的作用。自发性非肾上腺素能非胆碱能(NANC)空肠蠕动(记录为腔内气囊的容积变化)以剂量依赖性和立体特异性方式显著增加。一氧化氮(NO)合成的底物L-精氨酸可部分逆转L-NNA的作用。因此,本研究提供了证据,表明在体内通过释放NO对小肠蠕动存在紧张性抑制作用。此外,迷走神经刺激可引起L-NNA诱导的运动亢进后的松弛,这可能提示存在另一种NANC抑制性递质。六甲铵消除了这种松弛,但不影响L-NNA后的张力或相性活动。