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Review of the Pharmacological Properties and Clinical Usefulness of Muscarinic Agonists for Xerostomia in Patients with Sjögren's Syndrome.

Review of the Pharmacological Properties and Clinical Usefulness of Muscarinic Agonists for Xerostomia in Patients with Sjögren's Syndrome.

机构信息

Customer Satisfaction and Pharmaceutical Departments, Snow Brand Co. Ltd, Tokyo, Japan,

出版信息

Clin Drug Investig. 2002;22(2):67-73. doi: 10.2165/00044011-200222020-00001.

Abstract

The anti-xerostomia effects of muscarinic agonists (cholinomimetics) are reviewed. Cevimeline (cevimeline monohydrochloride hemihydrate) is a novel muscarinic agonist that stimulates salivary secretion in animals and humans both with normal salivary gland function and with impaired salivary secretion (xerostomia or oral dryness) as effectively as pilocarpine. Other classic and nonselective muscarinic agonists, such as arecoline, carbachol, muscarine and oxotremorine, as well as acetylcholine, failed to exhibit a sufficient salivation effect even at sublethal doses in animals.Oral administration of cevimeline 30mg to humans induces a moderate and lasting increase in salivary flow, and the effect is maintained for at least 4 to 6 hours, longer than with pilocarpine. Mean increases in salivary flow rates after cevimeline treatment were 2-fold higher than after placebo, and no evidence of tolerance of the pharmacological effect has been observed during prolonged administration for up to 12 months.The clinical efficacy of cevimeline in relieving symptoms of xerostomia, including oral dryness and difficulties in chewing, swallowing and speaking, has been demonstrated by placebo-controlled, double-blind, randomised clinical trials in the USA and Japan. In these studies, cevimeline 30mg three times daily increased salivary flow and improved the symptoms of xerostomia in a significantly higher percentage of patients compared with placebo. Some patients receiving cevimeline therapy for xerostomia experienced adverse events such as sweating, gastrointestinal symptoms (nausea, diarrhoea, abdominal pain and vomiting), dizziness and rigors; these effects were related to muscarinic activity and were generally mild and tolerable in comparison with those of pilocarpine.These findings suggest that muscarinic M3 agonists are suitable for the treatment of xerostomia. Cevimeline in particular has a long-lasting salivation effect with fewer adverse events than pilocarpine, and so is expected to be more useful for the treatment of xerostomia in patients with Sjögren's syndrome, reducing symptom severity and improving their quality of life.

摘要

本文综述了毒蕈碱激动剂(拟胆碱药)的抗口干作用。西维美林(盐酸西维美林一水合物)是一种新型的毒蕈碱受体激动剂,可刺激具有正常唾液腺功能和唾液分泌受损(口干或口腔干燥)的动物和人类的唾液分泌,其效果与毛果芸香碱一样有效。其他经典和非选择性毒蕈碱激动剂,如槟榔碱、卡巴胆碱、蕈毒碱和氧托溴铵以及乙酰胆碱,即使在亚致死剂量下,在动物中也没有表现出足够的唾液分泌作用。人体口服西维美林 30mg 可引起中等程度且持久的唾液流量增加,其作用可维持至少 4 至 6 小时,比毛果芸香碱长。西维美林治疗后的唾液流率平均增加了 2 倍,高于安慰剂,并且在长达 12 个月的延长给药期间没有观察到药物作用的耐受性。在美日进行的安慰剂对照、双盲、随机临床试验证实了西维美林缓解口干症状(包括口腔干燥和咀嚼、吞咽和说话困难)的临床疗效。在这些研究中,西维美林 30mg,每日 3 次,与安慰剂相比,可使更多的患者的唾液流量增加,并改善口干症状。一些接受西维美林治疗口干的患者出现了不良事件,如出汗、胃肠道症状(恶心、腹泻、腹痛和呕吐)、头晕和寒战;这些作用与毒蕈碱活性有关,与毛果芸香碱相比,通常较为轻微且可耐受。这些发现表明,毒蕈碱 M3 激动剂适用于口干的治疗。特别是西维美林与毛果芸香碱相比,具有持久的唾液分泌作用,不良事件更少,因此有望更有效地治疗干燥综合征患者的口干症,减轻症状严重程度,提高生活质量。

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