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盐酸依福地平对应激所致心率及循环变化的影响。

Effects of efonidipine hydrochloride on heart rate and circulatory changes due to stress.

作者信息

Morimoto Satoshi, Jo Fusakazu, Maki Kei, Iwasaka Toshiji

机构信息

Department of Internal Medicine, Ohmihachiman Community Medical Center, Shiga, Japan.

出版信息

Clin Exp Hypertens. 2009 Feb;31(1):83-91. doi: 10.1080/10641960802627363.

Abstract

Efonidipine hydrochloride is a dual Ca channel blocker that inhibits T-type Ca channels, which are localized in the sinoatrial node and are involved in the pacemaker mechanism of the heart, as well as L-type Ca channels. In the present study, the effect of efonidipine hydrochloride in inhibiting an increase in heart rate along with changes in circulation during mental and physical stress was examined using normotensive volunteers. A mental arithmetic test caused significant increases in heart rate and blood pressure, which were significantly inhibited 3 hours after oral administration of 40 mg of efonidipine hydrochloride but not at 1 week after cessation of administration. In contrast, the plasma norepinephrine, epinephrine, renin activity, and aldosterone levels following the test were unchanged at both 3 hours and 1 week after administration of efonidipine hydrochloride. Physical stress in the form of cold by immersing one hand in ice water for 2 minutes induced similar increases in the heart rate and blood pressure, which were significantly reduced at 3 hours but not at 1 week after administration of efonidipine hydrochloride. The plasma levels of the humoral factors previously described following the physical stress were unchanged at either 3 hours or 1 week after administration of efonidipine hydrochloride. These results suggest that efonidipine hydrochloride inhibits increases in heart rate and blood pressure due to stress, presumably by blocking T-type Ca channels rather than by inhibiting the sympathetic nervous system. Therefore, efonidipine hydrochloride is expected to be a Ca antagonist that exhibits a strong cardioprotective effect.

摘要

盐酸埃福地平是一种双重钙通道阻滞剂,可抑制T型钙通道(位于窦房结,参与心脏的起搏机制)以及L型钙通道。在本研究中,使用血压正常的志愿者检测了盐酸埃福地平在精神和身体应激期间抑制心率增加以及循环变化的作用。心算测试导致心率和血压显著升高,口服40mg盐酸埃福地平3小时后这些升高受到显著抑制,但在停药1周后则未受到抑制。相比之下,盐酸埃福地平给药后3小时和1周时,测试后血浆去甲肾上腺素、肾上腺素、肾素活性和醛固酮水平均未改变。以将一只手浸入冰水中2分钟的形式施加的身体应激诱导了类似的心率和血压升高,盐酸埃福地平给药后3小时这些升高显著降低,但1周后未降低。盐酸埃福地平给药后3小时或1周时,上述身体应激后体液因子的血浆水平均未改变。这些结果表明,盐酸埃福地平抑制应激引起的心率和血压升高,可能是通过阻断T型钙通道而非抑制交感神经系统来实现的。因此,盐酸埃福地平有望成为一种具有强大心脏保护作用的钙拮抗剂。

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