Suppr超能文献

[从硝苯地平、普鲁卡因和吲哚美辛的抑制作用分析氧合血红蛋白对脑动脉致痉作用的机制]

[On the mechanism underlying spasmogenic actions of oxy-hemoglobin on the cerebral artery, analyzed from the inhibitory effects of nicardipine, procaine and indomethacin].

作者信息

Doi M

机构信息

Department of Neurosurgery, Iwate Medical University, School of Medicine, Morioka, Japan.

出版信息

No Shinkei Geka. 1988 Feb;16(2):123-30.

PMID:3368031
Abstract

The present study was to analyze the basic mechanism underlying spasmogenic actions of Oxy-hemoglobin (Oxy-Hb) on the bovine cerebral arteries. Using helical strips of the middle cerebral arteries (M2), the changes in muscular tension during an isometric contraction induced by either Oxy-Hb, hydrogen peroxide (H2O2), high potassium-ion-Tyrode (30 mM K+), prostaglandin F2 alpha (PGF2 alpha), or carbocyclic thromboxane A2 (cTXA2) were recorded on the polygraph. Blocking effects of nicardipine, procaine indomethacin were compared on the contractions produced by each reagent described above. The results obtained are summarized as follows. 1) H2O2 dissolved in different concentrations produced arterial contractions similar to those by equimolar Oxy-Hb, showing similar dose-response curves. In contrast, equimolar met-hemoglobin (Met-Hb) always produced much weaker contractions. When the equimolar H2O2 was applied during an Oxy-Hb-induced contraction, the response to H2O2 was completely occluded. When H2O2 was applied during a Met-Hb-induced contraction, the response to H2O2 was not occluded and always additive to the response to Met-Hb. Indomethacin blocked both responses to Oxy-Hb and H2O2, showing similar dose dependence. 2) The above results suggested that Oxy-Hb induced contraction consisted of two components; a strong contraction by active oxygen within Hb molecule, and a weak contraction by Hb molecule itself. The former may be mediated by some PG's which are produced inside the muscle cells as the results of arachidonic acid release and subsequent cyclooxygenase activation.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究旨在分析氧合血红蛋白(Oxy-Hb)对牛脑动脉产生致痉作用的基本机制。使用大脑中动脉(M2)的螺旋条带,在等长收缩过程中,通过多导记录仪记录由Oxy-Hb、过氧化氢(H2O2)、高钾离子-台氏液(30 mM K+)、前列腺素F2α(PGF2α)或碳环血栓素A2(cTXA2)诱导的肌肉张力变化。比较尼卡地平、普鲁卡因、吲哚美辛对上述每种试剂产生的收缩的阻断作用。所得结果总结如下。1)溶解于不同浓度的H2O2产生的动脉收缩与等摩尔Oxy-Hb产生的收缩相似,显示出相似的剂量反应曲线。相比之下,等摩尔的高铁血红蛋白(Met-Hb)总是产生弱得多的收缩。当在Oxy-Hb诱导的收缩过程中应用等摩尔H2O2时,对H2O2的反应完全被阻断。当在Met-Hb诱导的收缩过程中应用H2O2时,对H2O2的反应未被阻断,并且总是与对Met-Hb的反应相加。吲哚美辛阻断对Oxy-Hb和H2O2的反应,显示出相似的剂量依赖性。2)上述结果表明,Oxy-Hb诱导的收缩由两个成分组成;Hb分子内活性氧引起的强烈收缩和Hb分子本身引起的微弱收缩。前者可能由一些前列腺素介导,这些前列腺素是花生四烯酸释放和随后环氧化酶激活后在肌肉细胞内产生的。(摘要截断于250字)

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