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静脉注射硝苯地平或阿折地平对大鼠开环压力感受性反射静态特性的急性影响。

Acute effects of intravenous nifedipine or azelnidipine on open-loop baroreflex static characteristics in rats.

作者信息

Yamamoto Hiromi, Kawada Toru, Shimizu Shuji, Kamiya Atsunori, Turner Michael J, Miyazaki Shunichi, Sugimachi Masaru

机构信息

Division of Cardiology, Department of Medicine, Faculty of Medicine, Kinki University, Osaka 589-8511, Japan.

Department of Cardiovascular Dynamics, National Cerebral and Cardiovascular Center, Osaka 565-8565, Japan.

出版信息

Life Sci. 2015 Apr 1;126:37-41. doi: 10.1016/j.lfs.2015.01.024. Epub 2015 Feb 21.

DOI:10.1016/j.lfs.2015.01.024
PMID:25707754
Abstract

AIMS

To assess the acute effects of intravenous azelnidipine, a third-generation L-type calcium channel blocker, on sympathetic outflow from the central nervous system and to compare the effects of intravenous azelnidipine with those of intravenous nifedipine.

MAIN METHODS

In anesthetized Wistar Kyoto rats, carotid sinus baroreceptor regions were isolated. Changes in sympathetic nerve activity (SNA) and arterial pressure (AP) in response to a stepwise baroreceptor pressure input were examined before and during intravenous nifedipine or azelnidipine (for each: 100 μg/kg bolus followed by 300 μg/kg/h infusion, n = 6).

KEY FINDINGS

Nifedipine significantly reduced the range of the AP response from 76.8 ± 7.4 to 45.4 ± 7.0 mmHg (P < 0.01) but did not affect the range of the SNA response (from 84.4 ± 5.1 to 85.9 ± 10.2%) or the SNA maximum gain (from 2.26 ± 0.28 to 2.35 ± 0.55%/mmHg). Similarly, azelnidipine significantly reduced the range of the AP response from 62.4 ± 3.9 to 31.4 ± 4.1 mmHg (P<0.01) but did not affect the range of the SNA response (from 71.2 ± 5.5 to 74.9 ± 7.2%) or the SNA maximum gain (from 1.64 ± 0.17 to 2.08 ± 0.26%/mmHg).

SIGNIFICANCE

A depressor dose of nifedipine or azelnidipine does not have an acute sympathoinhibitory effect in normotensive Wistar Kyoto rats even when the level of SNA was varied over the entire operating range of the carotid sinus baroreflex.

摘要

目的

评估第三代L型钙通道阻滞剂阿折地平静脉注射对中枢神经系统交感神经输出的急性影响,并比较阿折地平静脉注射与硝苯地平静脉注射的效果。

主要方法

在麻醉的Wistar Kyoto大鼠中,分离颈动脉窦压力感受器区域。在静脉注射硝苯地平或阿折地平之前和期间(每种药物:100μg/kg推注,随后以300μg/kg/h输注,n = 6),检查对逐步压力感受器压力输入的交感神经活动(SNA)和动脉压(AP)的变化。

主要发现

硝苯地平显著降低了AP反应范围,从76.8±7.4降至45.4±7.0 mmHg(P<0.01),但不影响SNA反应范围(从84.4±5.1至85.9±10.2%)或SNA最大增益(从2.26±0.28至2.35±0.55%/mmHg)。同样,阿折地平显著降低了AP反应范围,从62.4±3.9降至31.4±4.1 mmHg(P<0.01),但不影响SNA反应范围(从71.2±5.5至74.9±7.2%)或SNA最大增益(从1.64±0.17至2.08±0.26%/mmHg)。

意义

即使在颈动脉窦压力反射的整个工作范围内SNA水平发生变化,硝苯地平和阿折地平的降压剂量在正常血压的Wistar Kyoto大鼠中也没有急性交感神经抑制作用。

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