首页> 美国卫生研究院文献>The Journal of Physiology >Relaxation mechanisms induced by stimulation of nerves and by nitric oxide in sheep urethral muscle.
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Relaxation mechanisms induced by stimulation of nerves and by nitric oxide in sheep urethral muscle.

机译:绵羊尿道肌肉中神经刺激和一氧化氮诱导的放松机制。

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摘要

Isolated transverse and longitudinally oriented preparations of sheep urethra precontracted with noradrenaline responded to electrical field stimulation (EFS) with stimulus-dependent non-adrenergic, non-cholinergic (NANC) relaxations. Exogenous nitric oxide (NO) (acidified NaNO2), S-nitroso-L-cysteine (NC), sodium nitroprusside (SNP), 8-Br-cGMP, dibutyryl-cAMP, forskolin and isoprenaline each relaxed precontracted transverse urethral preparations in a concentration-dependent manner in order of protency: NC > forskolin > isoprenaline = SNP > NO > 8-Br-cGMP = dibutyryl-cAMP. Longitudinally oriented preparations responded to NO and NC with concentration-dependent relaxation, no different from that observed in transverse strips. Methylene blue (MB) and oxyhaemoglobin (HbO2) each shifted the concentration-response curve for NO to the right without affecting EFS-induced relaxation. Similarly, concentration-dependent responses to NC were not affected by MB. The inhibition of relaxation to NO by MB was prevented by superoxide dismutase, suggesting the inhibition was caused by extracellular generation of superoxide anions. EFS-induced relaxation was accompanied by elevation of cGMP. However, for the same level of relaxation, exogenous NO and NC induced 15- and 23-times higher increases in cGMP values, respectively, than EFS. cAMP levels were not affected by EFS- or NO-induced relaxation, although a large increase accompanied relaxation induced by forskolin. Forskolin also increased cGMP content. Pretreatment with MB reduced basal levels of cGMP and inhibited both relaxation and rise in cGMP levels induced by NO. SNP-elicited relaxant responses, in the presence of MB, were accompanied by an accumulation of cGMP; cAMP levels were unaffected. MB reduced cGMP levels induced by NC, while the relaxant response was unchanged. In urethral preparations prelabelled with [3H]myoinositol, exposure to NA caused an accumulation of [3H]inositol phosphates, which was unaffected by pretreatment with 8-Br-cGMP or dibutyryl-cAMP. EFS failed to induce a relaxant response in excess [K+]o-contracted preparations, while relaxation with exogenous NO was unaffected. Ouabain abolished EFS-induced relaxation and reduced responses to NO. Neither TEA nor glibenclamide affected relaxation to either EFS or NO. Relaxation elicited by SNP was not accompanied by any change in cGMP or cAMP levels, and was unaffected by MB, HbO2, K+ channel blockers (TEA and glibenclamide), ouabain or high [K+]o solution. This suggested that relaxation was caused by a mechanism independent of NO generation. A dense network of NADPH diaphorase-positive fibres associated with both the circular and longitudinal smooth muscle layers of sheep urethra was found.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:用去甲肾上腺素预收缩的绵羊尿道的横向和纵向分离制剂对电场刺激(EFS)产生了依赖于刺激的非肾上腺素能,非胆碱能(NANC)松弛作用。外源性一氧化氮(NO)(酸化的NaNO2),S-亚硝基-L-半胱氨酸(NC),硝普钠(SNP),8-Br-cGMP,二丁酰-cAMP,福斯高林和异丙肾上腺素各自在一定浓度下放松了预收缩的横向尿道制剂依赖性的依依依依顺序:NC>福司可林>异丙肾上腺素= SNP> NO> 8-Br-cGMP =二丁酰基-cAMP。纵向定向制剂对NO和NC的响应与浓度有关,与横向试纸条中观察到的弛豫无差别。亚甲基蓝(MB)和氧合血红蛋白(HbO2)各自将NO的浓度-响应曲线向右移动,而不影响EFS诱导的松弛。同样,对NC的浓度依赖性反应不受MB影响。超氧化物歧化酶阻止了MB对NO松弛的抑制作用,表明该抑制作用是由细胞外产生超氧化物阴离子引起的。 EFS引起的放松伴随cGMP升高。但是,对于相同的放松水平,外源NO和NC诱导的cGMP值分别比EFS高15倍和23倍。 cAMP水平不受EFS或NO诱导的弛豫的影响,尽管伴随毛喉素诱导的弛豫大大增加。佛司可林还增加了cGMP含量。 MB预处理可降低cGMP的基础水平,并抑制NO诱导的cGMP水平的松弛和升高。在存在MB的情况下,SNP引起的松弛反应伴随着cGMP的积累。 cAMP水平不受影响。 MB降低了NC诱导的cGMP水平,而松弛反应没有变化。在预先标记有[3H]肌醇的尿道制剂中,暴露于NA会引起[3H]肌醇磷酸酯的积累,这不受8-Br-cGMP或二丁酰-cAMP预处理的影响。 EFS未能在过量的[K +] o收缩制剂中引起松弛反应,而外源NO的松弛并未受到影响。瓦巴因废除了EFS引起的松弛并减少了对NO的反应。 TEA和格列本脲均不影响EFS或NO的松弛。 SNP引起的放松并不伴随cGMP或cAMP水平的任何变化,并且不受MB,HbO2,K +通道阻滞剂(TEA和格列本脲),哇巴因或高[K +] o溶液的影响。这表明弛豫是由与NO生成无关的机制引起的。发现了与绵羊尿道的圆形和纵向平滑肌层相关的NADPH心肌黄递酶阳性纤维的密集网络。(摘要截短了400个单词)

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