MacCarthy E P, Bloomfield S S
Pharmacotherapy. 1983 Jul-Aug;3(4):193-219. doi: 10.1002/j.1875-9114.1983.tb03252.x.
Labetalol is a combined alpha- and beta-adrenoceptor blocking agent for oral and intravenous use in the treatment of hypertension. It is a nonselective antagonist at beta-adrenoceptors and a competitive antagonist of postsynaptic alpha 1-adrenoceptors. Labetalol is more potent at beta that at alpha 1 adrenoceptors in man; the ratio of beta-alpha antagonism is 3:1 after oral and 6.9:1 after intravenous administration. Labetalol is readily absorbed in man after oral administration, but the drug, which is lipid soluble, undergoes considerable hepatic first-pass metabolism and has an absolute bioavailability of approximately 25%. There are no active metabolites, and the elimination half-life of the drug is approximately 6 hours. Unlike conventional beta-adrenoceptor blocking drugs without intrinsic sympathomimetic activity, labetalol, when given acutely, produces a decrease in peripheral vascular resistance and blood pressure with little alteration in heart rate or cardiac output. However, like conventional beta-blockers, labetalol may influence the renin-angiotensin-aldosterone system and respiratory function. Clinical studies have shown that the antihypertensive efficacy of labetalol is superior to placebo and to diuretic therapy and is at least comparable to that of conventional beta-blockers, methyldopa, clonidine and various adrenergic neuronal blockers. Labetalol administered alone or with a diuretic is often effective when other antihypertensive regimens have failed. Studies have shown that labetalol is effective in the treatment of essential hypertension, renal hypertension, pheochromocytoma, pregnancy hypertension and hypertensive emergencies. In addition, preliminary studies indicate that labetalol may be of value in the management of ischemic heart disease. The most troublesome side effect of labetalol therapy is posture-related dizziness. Other reported side effects of the drug include gastrointestinal disturbances, tiredness, headache, scalp tingling, skin rashes, urinary retention and impotence. Side effects related to the beta-adrenoceptor blocking effect of labetalol, including asthma, heart failure and Raynaud's phenomenon, have been reported in rare instances.
拉贝洛尔是一种α和β肾上腺素能受体阻断剂,可口服和静脉注射用于治疗高血压。它是β肾上腺素能受体的非选择性拮抗剂,也是突触后α1肾上腺素能受体的竞争性拮抗剂。在人体中,拉贝洛尔对β肾上腺素能受体的作用强于对α1肾上腺素能受体的作用;口服后β-α拮抗作用的比值为3:1,静脉给药后为6.9:1。拉贝洛尔口服后在人体中易于吸收,但该药物脂溶性高,会经历相当程度的肝脏首过代谢,绝对生物利用度约为25%。没有活性代谢产物,药物的消除半衰期约为6小时。与没有内在拟交感活性的传统β肾上腺素能受体阻断药物不同,拉贝洛尔急性给药时会使外周血管阻力和血压降低,而心率或心输出量变化不大。然而,与传统β受体阻滞剂一样,拉贝洛尔可能会影响肾素-血管紧张素-醛固酮系统和呼吸功能。临床研究表明,拉贝洛尔的降压疗效优于安慰剂和利尿剂治疗,至少与传统β受体阻滞剂、甲基多巴、可乐定及各种肾上腺素能神经阻滞剂相当。当其他降压方案无效时,单独使用拉贝洛尔或与利尿剂合用通常有效。研究表明,拉贝洛尔对原发性高血压、肾性高血压、嗜铬细胞瘤、妊娠高血压和高血压急症有效。此外,初步研究表明拉贝洛尔在缺血性心脏病的治疗中可能有价值。拉贝洛尔治疗最麻烦的副作用是体位性头晕。该药物其他报告的副作用包括胃肠道不适、疲劳、头痛、头皮刺痛、皮疹、尿潴留和阳痿。罕见情况下报告了与拉贝洛尔β肾上腺素能受体阻断作用相关的副作用,包括哮喘、心力衰竭和雷诺现象。