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酮色林。对其药效学和药代动力学特性以及在高血压和外周血管疾病中的治疗潜力的综述。

Ketanserin. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in hypertension and peripheral vascular disease.

作者信息

Brogden R N, Sorkin E M

机构信息

Adis Drug Information Services, Auckland, New Zealand.

出版信息

Drugs. 1990 Dec;40(6):903-49. doi: 10.2165/00003495-199040060-00010.

Abstract

Ketanserin is a 5-HT2 receptor antagonist without partial agonist properties which also possesses weak alpha 1-adrenoceptor antagonistic activity, which may explain its antihypertensive mechanism of action in patients with essential hypertension. It also inhibits the effects of serotonin on platelets in cardiovascular disease, inhibits vasoconstriction caused by the amine, and when administered intravenously improves some haemorheological indices in patients with ischaemic diseases. The antihypertensive effect of oral ketanserin 40 mg twice daily is comparable with that of total daily doses of metoprolol 200 mg, propranolol 160 mg, captopril 100 mg, enalapril 20 mg, hydrochlorothiazide 50 mg, or alpha-methyldopa 1000 mg and is achieved without adverse effect on plasma lipoproteins or carbohydrate metabolism in patients with concomitant diabetes mellitus. Evidence from prospective studies suggests a greater antihypertensive efficacy in the elderly than in younger patients. In patients with intermittent claudication, results have been inconsistent in small studies, while a large study showed no improvement in pain-free walking distance but fewer amputations compared to placebo. In Raynaud's phenomenon symptomatic improvement relative to placebo was achieved in larger trials. Its role in preventing atherosclerotic complications requires further investigation. Ketanserin is reasonably well tolerated, the frequency of adverse effects being comparable with that of other antihypertensive drugs in controlled trials. Dizziness, tiredness, oedema, dry mouth and weight gain are the most commonly reported effects. Ketanserin prolongs QT interval in a dose-related manner, and when given in certain predisposing circumstances ventricular arrhythmias and syncope may occur. Administered intravenously, ketanserin 10mg followed by an infusion of 2 to 4 mg/h controls moderate to severe pre- and postoperative hypertension in most patients, acting as a balanced vasodilator, lowering cardiac pre- and afterload. Although the arrhythmogenic potential of ketanserin in patients receiving potassium-depleting diuretics requires suitable precautions, it appears that its antihypertensive activity is suited to the elderly provided plasma potassium concentrations are normal at the start of treatment and are maintained within the normal range.

摘要

酮色林是一种无部分激动剂特性的5 - HT2受体拮抗剂,还具有较弱的α1 -肾上腺素能受体拮抗活性,这可能解释了其在原发性高血压患者中的降压作用机制。它还能抑制心血管疾病中血清素对血小板的作用,抑制该胺类引起的血管收缩,静脉给药时可改善缺血性疾病患者的一些血液流变学指标。每日口服两次40mg酮色林的降压效果与每日总剂量200mg美托洛尔、160mg普萘洛尔、100mg卡托普利、20mg依那普利、50mg氢氯噻嗪或1000mgα -甲基多巴相当,且对伴有糖尿病的患者的血浆脂蛋白或碳水化合物代谢无不良影响。前瞻性研究的证据表明,老年人的降压效果比年轻患者更好。在间歇性跛行患者中,小型研究的结果不一致,而一项大型研究表明,与安慰剂相比,无痛步行距离没有改善,但截肢次数减少。在雷诺现象中,大型试验显示相对于安慰剂有症状改善。其在预防动脉粥样硬化并发症中的作用需要进一步研究。酮色林耐受性较好,在对照试验中不良反应的发生率与其他抗高血压药物相当。头晕、疲劳、水肿、口干和体重增加是最常报告的不良反应。酮色林以剂量相关的方式延长QT间期,在某些易感情况下给药可能会发生室性心律失常和晕厥。静脉注射10mg酮色林,随后以2至4mg/h的速度输注,可控制大多数患者的中度至重度术前和术后高血压,作为一种平衡的血管扩张剂,降低心脏前负荷和后负荷。尽管在接受排钾利尿剂的患者中,酮色林的致心律失常潜力需要采取适当的预防措施,但似乎只要治疗开始时血浆钾浓度正常并维持在正常范围内,其降压活性就适用于老年人。

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