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接受阿米替林或多塞平维持治疗的患者血清中的抗胆碱能活性。

Anticholinergic activity in the serum of patients receiving maintenance amitriptyline or doxepin therapy.

作者信息

Aaltonen L, Syvälahti E, Iisalo E, Peltomäki T

出版信息

Acta Pharmacol Toxicol (Copenh). 1985 Jan;56(1):75-80. doi: 10.1111/j.1600-0773.1985.tb01256.x.

DOI:10.1111/j.1600-0773.1985.tb01256.x
PMID:3976405
Abstract

The anticholinergic activity in serum of depressive patients receiving amitriptyline (50-300 mg/day) or doxepin (50-225 mg/day) was measured using a radioreceptor assay. In this method the membrane suspension prepared from rat brain was able to bind the potent muscarinic antagonist, quinuclidinyl benzilate. Using atropine as a standard, the antimuscarinic activity of several compounds can be measured in the serum of patients receiving drugs with anticholinergic effects or side-effects. The steady state serum levels of amitriptyline and doxepin and their desmethylated metabolites, nortriptyline and desmethyldoxepin were measured by radioimmunoassay in the same serum samples. The antimuscarinic activity in serum measured as atropine equivalents was 2.7 +/- 0.4 (S.E.M.) ng/ml in amitriptyline patients and 1.1 +/- 0.2 ng/ml in doxepin patients. There was a highly significant correlation (P less than 0.001) between amitriptyline (r = 0.92) and nortriptyline (r = 0.79) concentrations and serum antimuscarinic activity. The correlation was less clear, although statistically significant for doxepin (r = 0.42, P less than 0.05) and desmethyldoxepin (r = 0.58, P less than 0.01). The better correlation between serum drug levels and antimuscarinic activity in amitriptyline than in doxepin patients is probably due to the higher affinity of amitriptyline and its desmethylated metabolite to muscarinic receptors with the doses used in the present study. The method may have clinical applications e.g. in evaluation of excessive anticholinergic activity in patients.

摘要

采用放射受体分析法测定接受阿米替林(50 - 300毫克/天)或多塞平(50 - 225毫克/天)治疗的抑郁症患者血清中的抗胆碱能活性。在该方法中,由大鼠脑制备的膜悬浮液能够结合强效毒蕈碱拮抗剂苄基喹宁环酯。以阿托品为标准品,可在接受具有抗胆碱能作用或副作用药物治疗的患者血清中测定几种化合物的抗毒蕈碱活性。在同一血清样本中,通过放射免疫分析法测定阿米替林和多塞平及其去甲基化代谢产物去甲替林和去甲多塞平的稳态血清水平。以阿托品当量衡量,阿米替林治疗患者血清中的抗毒蕈碱活性为2.7±0.4(标准误)纳克/毫升,多塞平治疗患者为1.1±0.2纳克/毫升。阿米替林(r = 0.92)和去甲替林(r = 0.79)浓度与血清抗毒蕈碱活性之间存在高度显著相关性(P<0.001)。多塞平(r = 0.42,P<0.05)和去甲多塞平(r = 0.58,P<0.01)的相关性虽不太明显,但具有统计学意义。与多塞平治疗患者相比,阿米替林治疗患者血清药物水平与抗毒蕈碱活性之间的相关性更好,这可能是由于在本研究中使用的剂量下,阿米替林及其去甲基化代谢产物对毒蕈碱受体具有更高的亲和力。该方法可能具有临床应用价值,例如用于评估患者体内抗胆碱能活性过高的情况。

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Acta Pharmacol Toxicol (Copenh). 1985 Jan;56(1):75-80. doi: 10.1111/j.1600-0773.1985.tb01256.x.
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