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一种评估去甲肾上腺素诱导兔耳动脉细胞内和细胞外钙离子动员的简单方法。

A simple procedure for assessing norepinephrine-induced cellular and extracellular Ca++ mobilization in rabbit ear artery.

作者信息

Manzini S, Maggi C A, Meli A

出版信息

J Pharmacol Methods. 1982 Aug;8(1):47-57. doi: 10.1016/0160-5402(82)90007-9.

Abstract

Although the response of vascular smooth muscle to norepinephrine (NE) is biphasic in nature, there is no simple procedure for the separate quantitative analysis of intracellular and extracellular Ca++ dependent NE-induced contractions. Intraluminal NE in high-K+Ca++-free medium produces a dose-dependent contraction which is selectively antagonized by procaine (1 X 10(-3) M--5 X 10(-3) M). Subsequent reperfusion with normal Krebs of NE-pretreated arterial segments results in a dose-dependent contraction which is strictly related to extracellular Ca++ concentration and is selectively inhibited by verapamil (5 X 10(-6) M--5 X 10(-5) M). These results can be interpreted as an indication that this procedure is suitable for the separate analysis of the capability of vasoactive drugs to differentially mobilize cellular and extracellular Ca++ pools in perfused rabbit ear artery preparations.

摘要

尽管血管平滑肌对去甲肾上腺素(NE)的反应本质上是双相的,但对于细胞内和细胞外Ca++依赖性NE诱导的收缩进行单独定量分析,尚无简单的方法。在高钾无钙培养基中的腔内NE产生剂量依赖性收缩,可被普鲁卡因(1×10(-3)M - 5×10(-3)M)选择性拮抗。随后用正常的Krebs液对NE预处理的动脉段进行再灌注,会产生剂量依赖性收缩,这与细胞外Ca++浓度密切相关,并被维拉帕米(5×10(-6)M - 5×10(-5)M)选择性抑制。这些结果可以解释为,该方法适用于在灌注兔耳动脉制剂中,对血管活性药物差异性动员细胞内和细胞外Ca++池的能力进行单独分析。

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