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Amlodipine

氨氯地平

Mechanism of action:

Amlodipine 是一種二氫吡啶類鈣離子通道阻斷劑(dihydropyridine calcium channel blocker)。Amlodipine 選擇性抑制血管平滑肌細胞膜上的 L 型鈣離子通道(L-type Ca²⁺ channel),減少鈣離子進入細胞內。因為細胞內 Ca²⁺ 濃度下降,肌動蛋白與肌球蛋白的交互作用減弱,導致血管平滑肌放鬆,使外週血管阻力降低與冠狀動脈擴張。

​Reference(s):

1. Katoh M et al. (2000). Inhibitory potencies of 1,4-dihydropyridine calcium antagonists to P-glycoprotein-mediated transport: comparison with the effects on CYP3A4. Pharm Res. 


2. Darvari R et al. (2004). Concentration dependency of modulatory effect of amlodipine on P-glycoprotein efflux activity of doxorubicin—a comparison with tamoxifen. J Pharm Pharmacol. 


3. Kuzuya T et al. (2003). Amlodipine, but not MDR1 polymorphisms, alters the pharmacokinetics of cyclosporine A in Japanese kidney transplant recipients. Transplantation.

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