首页> 外文期刊>British Journal of Pharmacology >Involvement of K~+ channel permeability changes in the L-NAME and indomethacin resistant part of adenosine-5'-O- (2-thiodiphosphate)-induced relaxation of pancreatic vascular bed
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Involvement of K~+ channel permeability changes in the L-NAME and indomethacin resistant part of adenosine-5'-O- (2-thiodiphosphate)-induced relaxation of pancreatic vascular bed

机译:K〜+通道通透性变化参与腺苷5'-O-(2-硫代二磷酸)诱导的胰血管床松弛的L-NAME和吲哚美辛耐药部分

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摘要

We have previously demonstrated that adenosine-5'-O-(2-thiodiphosphate) (ADPβS), a potent P2Y- purinoceptor agonist, relaxed pancreatic vasculature not only through prostacyclin (PGI_2) and nitric oxide(NO) release from the endothelium but also through other mechanisms(s). in this study, we investigated the effects of an inhibitor of the Na~+/K~+ pump, of ATP-sensitive K~+(K_ATP) channels and of small (SK_Ca) or large (BK_Ca) conductance Ca~2+ -activated K~+ channels. Experiments were performed at basal tone and during the inhibition of NO synthase and cyclo-oxygenase.
机译:我们先前已经证明,强大的P2Y-嘌呤受体激动剂腺苷5'-O-(2-硫代二磷酸)(ADPβS)不仅通过前列腺素(PGI_2)和一氧化氮(NO)从内皮中释放,而且还松弛了胰腺血管通过其他机制。在这项研究中,我们研究了Na〜+ / K〜+泵抑制剂,ATP敏感性K〜+(K_ATP)通道以及小(SK_Ca)或大(BK_Ca)电导Ca〜2 +-的抑制剂的作用。激活的K〜+通道。实验是在基调和抑制NO合酶和环加氧酶的过程中进行的。

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