Suppr超能文献

关于大鼠逼尿肌神经源性收缩反应对阿托品耐药性的评论

Comments on the atropine resistance of the neurogenic contractile response of the rat detrusor muscle.

作者信息

Hammarström M, Sjöstrand N O

出版信息

Acta Physiol Scand. 1984 Dec;122(4):475-81. doi: 10.1111/j.1748-1716.1984.tb07536.x.

Abstract

The resistance to atropine or scopolamine of the neurogenic contractile response to field stimulation of intramural nerves of the rat detrusor was studied during the early phase of Wallerian degeneration in vitro and in vivo. The neurogenic contractile response to low frequency stimulation of control bladders was completely resistant to atropine or scopolamine in vitro. As a matter of fact the response was enchanced by the drugs. In vivo a transient shortening of the response could be seen. 26-34 h after bilateral extirpation of the pelvic ganglia there was prominent degeneration activity in the bladders in vitro as well as in vivo. Atropine or scopolamine inhibited this activity in vivo but enhanced it in vitro. The neurogenic contractile response to field stimulation of the bladder nerves was blocked in vivo but not in vitro by the antimuscarinic drugs 26-34 h after neurectomy. The results support the concept that the excitatory neurotransmission in the detrusor is essentially cholinergic. An explanation of the difference between the in vivo and the in vitro results based on differences in degree of blockade of pre- and post-junctional muscarinic receptors and diffusion of the antimuscarinics in the tissue is proposed.

摘要

在体外和体内沃勒变性早期,研究了大鼠逼尿肌壁内神经场刺激引起的神经源性收缩反应对阿托品或东莨菪碱的抗性。对照膀胱低频刺激引起的神经源性收缩反应在体外对阿托品或东莨菪碱完全具有抗性。事实上,该反应被药物增强。在体内,可观察到反应的短暂缩短。双侧切除盆腔神经节后26 - 34小时,膀胱在体外和体内均有明显的变性活动。阿托品或东莨菪碱在体内抑制这种活动,但在体外增强这种活动。神经切断术后26 - 34小时,抗毒蕈碱药物在体内阻断膀胱神经场刺激引起的神经源性收缩反应,但在体外未阻断。结果支持逼尿肌中兴奋性神经传递本质上是胆碱能的这一概念。基于节前和节后毒蕈碱受体阻断程度的差异以及抗毒蕈碱药物在组织中的扩散,提出了对体内和体外结果差异的解释。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验