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藜芦碱诱导的大鼠离体左心房强直性收缩。哌唑嗪和WB4101新型直接保护作用的证据。

Veratrine-induced tetanic contracture of the rat isolated left atrium. Evidence for novel direct protective effects of prazosin and WB4101.

作者信息

Le Grand B, Marty A, Vieu S, Talmant J M, John G W

机构信息

Division of Cardiovascular Diseases, Centre de Recherche Pierre Fabre, Castres, France.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1993 Aug;348(2):184-90. doi: 10.1007/BF00164797.

Abstract

An investigation has been made of the putative direct myocardial protective effects of the alpha 1-adrenoceptor antagonists, prazosin and WB4101, against tetanic contractures of rat isolated left atria following modified Na+ channel function and consequent Ca2+ loading elicited by veratrine. Veratrine evoked concentration-dependent, reversible, tetanic contractures which were critically dependent upon the external Ca2+ concentration. Tetrodotoxin (TTX), prazosin, WB 4101 and R 56865 (0.1-10 microM) prevented tetanic contracture elicited by veratrine (100 micrograms/ml) at concentrations which were significantly lower than those which decreased active tension development. The apparent Hill coefficients (nH) obtained for TTX, prazosin, WB 4101 and R 56865 were comparable (range 0.79-0.93), and are consistent with a single site of action. In contrast, the class 1 antiarrhythmic agents, quinidine and lidocaine, elicited no significant inhibition of veratrine-induced contracture at 30 microM, but almost completely abolished the contractures at 100 microM. The nH values for quinidine and lidocaine were found to be significantly greater than unity (3.1 and 2.6, respectively). The L-type Ca2+ channel blockers, diltiazem, nicardipine, nifedipine and verapamil only weakly prevented tetanic contracture, whilst markedly, and concentration-dependently, decreasing active tension development. Neither atropine (10 microM) nor propranolol (1 microM) significantly modified either veratrine-induced contractures or active tension development. In conclusion, evidence is presented of novel, direct protective effects of prazosin and WB 4101 against tetanic contracture following modified Na+ channel function and Ca2+ loading provoked by veratrine. The precise mechanisms involved are unclear at present, but appear to be distinct from blockade of atrial alpha 1-adrenoceptors or L-type Ca2+ channels.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

已对α1肾上腺素能受体拮抗剂哌唑嗪和WB4101对藜芦碱改变钠通道功能并导致钙负荷增加后大鼠离体左心房强直性收缩的假定直接心肌保护作用进行了研究。藜芦碱引起浓度依赖性、可逆的强直性收缩,其严重依赖于细胞外钙浓度。河豚毒素(TTX)、哌唑嗪、WB4101和R56865(0.1 - 10微摩尔)在显著低于降低主动张力发展的浓度下,可预防藜芦碱(100微克/毫升)引起的强直性收缩。TTX、哌唑嗪、WB4101和R56865的表观希尔系数(nH)相当(范围为0.79 - 0.93),与单一作用位点一致。相比之下,1类抗心律失常药物奎尼丁和利多卡因在30微摩尔时对藜芦碱诱导的收缩无显著抑制作用,但在100微摩尔时几乎完全消除了收缩。发现奎尼丁和利多卡因的nH值显著大于1(分别为3.1和2.6)。L型钙通道阻滞剂地尔硫卓、尼卡地平、硝苯地平和维拉帕米仅微弱地预防强直性收缩,同时显著且浓度依赖性地降低主动张力发展。阿托品(10微摩尔)和普萘洛尔(1微摩尔)均未显著改变藜芦碱诱导的收缩或主动张力发展。总之,有证据表明哌唑嗪和WB4101对藜芦碱改变钠通道功能和钙负荷后引起的强直性收缩具有新的直接保护作用。目前涉及的精确机制尚不清楚,但似乎与心房α1肾上腺素能受体或L型钙通道的阻断不同。(摘要截短于250字)

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