Suppr超能文献

UD-CG 115——一种强心哒嗪酮,可提高环磷酸腺苷水平并延长豚鼠乳头肌的动作电位。

UD-CG 115--a cardiotonic pyridazinone which elevates cyclic AMP and prolongs the action potential in guinea-pig papillary muscle.

作者信息

Honerjäger P, Heiss A, Schäfer-Korting M, Schönsteiner G, Reiter M

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1984 Mar;325(3):259-69. doi: 10.1007/BF00495953.

Abstract

The mechanism of the positive inotropic effect of a benzimidazole-pyridazinone, UD-CG 115, was analysed in the isolated guinea-pig papillary muscle contracting isometrically at a frequency of 0.2 Hz. UD-CG 115 produced a slowly developing and poorly reversible positive inotropic effect increasing with concentration (3-300 mumol/l). The effect amounted to 30 and 74% of the maximum inotropic effect of a standard, dihydroouabain, at 34 and 300 mumol/l, respectively. Low concentrations shortened and 300 mumol/l UD-CG 115 significantly prolonged the duration of contraction. The enhancement of the maximum rate of relaxation, S2, was intermediate between those produced by isoprenaline and dihydroouabain, respectively. UD-CG 115 prolonged the duration of the transmembrane action potential (90% repol .) by up to 22% at 300 mumol/l, whereas an equieffective concentration of isoprenaline did not consistently alter action potential duration. UD-CG 115 increased Vmax and overshoot, and prolonged the duration, of slow action potentials elicited at 24 mmol/l [K]0. The inotropic potency of UD-CG 115 was not significantly changed by reserpine pretreatment of the guinea pig or by the presence of 1 mumol/l(-)-propranolol, 3 mumol/l phentolamine or 10 mumol/l cimetidine. Neither was it reduced by 10 mumol/l TTX. The inotropic effect of 100 mumol/l UD-CG 115 remained unchanged when [K]0 was elevated from 3.2 to 12.0 mmol/l. A sarcolemmal preparation of guinea- pig ventricular Na,K-ATPase was only slightly inhibited by the highest concentration of UD-CG 115.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在离体豚鼠乳头肌以0.2Hz频率进行等长收缩的实验中,分析了苯并咪唑哒嗪酮UD-CG 115的正性肌力作用机制。UD-CG 115产生缓慢发展且可逆性较差的正性肌力作用,该作用随浓度(3 - 300μmol/L)增加。在34和300μmol/L时,该作用分别达到标准品双氢哇巴因最大肌力作用的30%和74%。低浓度时缩短收缩持续时间,而300μmol/L的UD-CG 115显著延长收缩持续时间。最大舒张速率S2的增强分别介于异丙肾上腺素和双氢哇巴因所产生的增强之间。在300μmol/L时,UD-CG 115使跨膜动作电位(90%复极化)持续时间延长高达22%,而异丙肾上腺素的等效应浓度并未持续改变动作电位持续时间。UD-CG 115增加了在24mmol/L[K]0时诱发的慢动作电位的Vmax和超射,并延长了其持续时间。豚鼠经利血平预处理或存在1μmol/L(-)-普萘洛尔、3μmol/L酚妥拉明或10μmol/L西咪替丁时,UD-CG 115的肌力作用无显著变化。10μmol/L的河豚毒素也未使其降低。当[K]0从3.2mmol/L升高至12.0mmol/L时,100μmol/L UD-CG115的肌力作用保持不变。豚鼠心室肌Na,K - ATP酶的肌膜制剂仅在UD-CG 115的最高浓度时受到轻微抑制。(摘要截短于250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验