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甘草的电药理学特征研究——应用人诱导多能干细胞衍生心肌细胞片层和慢性房室传导阻滞犬模型。

Electropharmacological Characterization of Licorice Using the Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Sheets and the Chronic Atrioventricular Block Dogs.

机构信息

Department of Pharmacology, Faculty of Medicine, Toho University, 5-21-16 Omori-nishi, Ota-ku, Tokyo, 143-8540, Japan.

Department of Traditional Medicine, Faculty of Medicine, Toho University, 6-11-1 Omori-nishi, Ota-ku, Tokyo, 143-8541, Japan.

出版信息

Cardiovasc Toxicol. 2023 Jun;23(5-6):207-217. doi: 10.1007/s12012-023-09795-5. Epub 2023 May 30.

Abstract

Licorice has been traditionally prescribed for palpitation, whereas its overdose has caused lethal arrhythmias including torsade de pointes. Licorice contains glycyrrhizic acid of ≥ 2% (w/w), which is hydrolyzed to glycyrrhetinic acid (GRA) in the intestine. Since their cardiac electropharmacological properties are not fully understood, we assessed them to ask mechanism of licorice-induced torsade de pointes. GRA at 0.1, 1 and 10 μg/mL was cumulatively applied to the human induced pluripotent stem cell-derived cardiomyocytes sheets (n = 6). GRA shortened spontaneous activation interval and repolarization period, and decreased maximum contraction velocity, indicating Ca channel blockade. It prolonged effective refractory period and post-repolarization refractoriness with a steep frequency-dependency, whereas it delayed conduction with a modest use-dependency, resembling lidocaine in the mode of Na channel-blocking action. Meanwhile, Kanzoto containing a decoction of licorice alone in a dose of 2 or 6 g/body/day was orally administered to the conscious chronic atrioventricular block dogs for 3 days (n = 4). Kanzoto prolonged QT interval with increasing its temporal dispersion, suggesting K channel suppression, and slightly decreased the plasma K concentration without inducing torsade de pointes. Moreover, it significantly suppressed atrial and idioventricular rates, leading to sinus arrest along with the onset of ventricular fibrillation in one animal, possibly due to Na channel blockade. These results indicate that electropharmacological profile of licorice can be explained by Na, Ca and K channels blockade, which may be associated with low torsadogenic risk, but might contribute to the onset of other types of lethal ventricular arrhythmias.

摘要

甘草历来被用于治疗心悸,但其过量使用可导致致命性心律失常,包括尖端扭转型室性心动过速。甘草含有甘草酸≥2%(w/w),在肠道中被水解为甘草次酸(GRA)。由于其心脏电药理学特性尚未完全阐明,我们评估了它们以了解甘草引起尖端扭转型室性心动过速的机制。将 GRA 以 0.1、1 和 10μg/mL 的浓度累积应用于人诱导多能干细胞衍生的心肌细胞片(n=6)。GRA 缩短自发激活间隔和复极化期,并降低最大收缩速度,表明钙通道阻断。它延长有效不应期和复极化后不应期,呈陡峭的频率依赖性,而在适度使用依赖性下延迟传导,类似于钠通道阻断作用的利多卡因。同时,Kanzoto 单独含有甘草汤,剂量为 2 或 6g/天,口服给予清醒的慢性房室传导阻滞犬 3 天(n=4)。Kanzoto 延长 QT 间期并增加其时间离散度,表明钾通道抑制,而血浆 K 浓度略有降低,不引起尖端扭转型室性心动过速。此外,它显著抑制心房和室性心率,导致窦性停搏,并在一只动物中出现心室颤动,可能是由于钠通道阻断。这些结果表明,甘草的电生理学特征可以用钠、钙和钾通道阻断来解释,这可能与低致扭转型风险有关,但可能导致其他类型的致命性室性心律失常的发生。

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