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首页> 外文期刊>Clinical and experimental pharmacology & physiology >Factors, fiction and endothelium-derived hyperpolarizing factor.
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Factors, fiction and endothelium-derived hyperpolarizing factor.

机译:因素,小说和内皮源性超极化因子。

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Summary 1. The principal mediators of vascular tone are neural, endothelial and physical stimuli that result in the initiation of dilator and constrictor responses to facilitate the control of blood pressure. Two primary vasodilatory stimuli produced by the endothelium are nitric oxide (NO) and prostaglandins. An additional endothelium-dependent vasodilatory mechanism is characterized as the hyperpolarization-mediated relaxation that remains after the inhibition of the synthesis of NO and prostaglandins. This mechanism is due to the action of a so-called endothelium-derived hyperpolarizing factor (EDHF) and is dependent on either the release of diffusible factor(s) and/or to a direct contact-mediated mechanism. 2. Most evidence supports the concept that 'EDHF' activity is dependent on contact-mediated mechanisms. This involves the transfer of an endothelium-derived electrical current, as an endothelium-derived hyperpolarization (EDH), through direct heterocellular coupling of endothelial cells and smooth muscle cells via myoendothelial gap junctions (MEGJ). However, there is a lack of consensus with regard to the nature and mechanism of action of EDHF/EDH (EDH(F)), which has been shown to vary within and between vascular beds, as well as among species, strains, sex and during development, ageing and disease. 3. In addition to actual heterogeneity in EDH(F), further heterogeneity has resulted from the less-than-optimal design, analysis and interpretation of data in some key papers in the EDHF literature; with such views being perpetuated in the subsequent literature. 4. The focus of the present brief review is to examine what factors are proposed as EDH(F) and highlight the correlative structural and functional studies from our laboratory that demonstrate an integral role for MEGJ in the conduction of EDH, which account for the heterogeneity in EDH(F), while incorporating the reported diffusible mechanisms in the regulation of this activity. Furthermore, in addition to the reported heterogeneity in the nature and mechanism of action of EDH(F), the contribution of experimental design and technique to this heterogeneity will be examined.
机译:总结1.血管紧张程度的主要介质是神经,内皮和物理刺激,可引起扩张器和收缩器反应的启动,从而有助于控制血压。内皮产生的两个主要血管舒张刺激是一氧化氮(NO)和前列腺素。附加的内皮依赖性血管舒张机制的特征在于超极化介导的松弛,其在抑制NO和前列腺素的合成后仍然存在。该机制是由于所谓的内皮衍生的超极化因子(EDHF)的作用,并且取决于可扩散因子的释放和/或直接接触介导的机制。 2.大多数证据支持“ EDHF”活性取决于接触介导机制的概念。这涉及通过内皮细胞和平滑肌细胞通过肌内皮间隙连接(MEGJ)的直接异源偶联,转移内皮源电流,作为内皮源超极化(EDH)。但是,关于EDHF / EDH(EDH(F))的性质和作用机理尚缺乏共识,事实表明,EDHF / EDH(EDH(F))在血管床内和血管床之间以及物种,品系,性别和性别之间存在差异。在发育,衰老和疾病中。 3.除了EDH(F)中的实际异质性外,EDHF文献中某些关键论文的数据设计,分析和解释还不够理想,导致了更多的异质性;这种观点在随后的文献中得以保留。 4.本简要综述的重点是研究提出了哪些因素被认为是EDH(F),并强调了我们实验室的相关结构和功能研究,这些研究证明了MEGJ在EDH的传导中起着不可或缺的作用,这解释了异质性在EDH(F)中,同时将报道的扩散机制纳入该活性的调节中。此外,除了已报道的EDH(F)的性质和作用机理的异质性外,还将检验实验设计和技术对该异质性的贡献。

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