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脑脊液和血浆中去甲替林及其10-羟基代谢物的水平。

CSF and plasma levels of nortriptyline and its 10-hydroxy metabolite.

作者信息

Nordin C, Bertilsson L, Siwers B

出版信息

Br J Clin Pharmacol. 1985 Oct;20(4):411-3. doi: 10.1111/j.1365-2125.1985.tb05086.x.

Abstract

After 3 weeks' nortriptyline (NT) treatment the mean plasma concentration of its 10-hydroxy metabolite (10-OH-NT) (599 +/- 207 nmol l-1) was higher than that of the parent drug (433 +/- 199 nmol l-1) in 25 depressed patients. Also in the cerebrospinal fluid (CSF) the mean level of 10-OH-NT (67 +/- 20 nmol l-1) was higher than that of NT (39 +/- 23 nmol l-1). There was a strong correlation (P less than 0.001) between the CSF and plasma concentration of both NT (r = 0.92) and 10-OH-NT (r = 0.77). The interindividual variation in the CSF/plasma ratio of both compounds was small, compared to the variation in plasma levels. These results show that 10-OH-NT passes the blood-brain barrier as it is present in concentrations higher than those of NT in the CSF. 10-OH-NT has previously been shown to be a potent blocker of noradrenaline uptake and to have much less affinity for muscarinic receptors than NT itself. This active metabolite might therefore be a potential antidepressant with less disturbing anticholinergic side-effects.

摘要

在25名抑郁症患者接受3周去甲替林(NT)治疗后,其10-羟基代谢物(10-OH-NT)的平均血浆浓度(599±207 nmol/L)高于母体药物(433±199 nmol/L)。在脑脊液(CSF)中,10-OH-NT的平均水平(67±20 nmol/L)也高于NT(39±23 nmol/L)。脑脊液和血浆中NT(r = 0.92)及10-OH-NT(r = 0.77)的浓度之间存在强相关性(P<0.001)。与血浆水平的变化相比,两种化合物的脑脊液/血浆比值的个体间差异较小。这些结果表明,10-OH-NT能够通过血脑屏障,因为其在脑脊液中的浓度高于NT。先前已表明,10-OH-NT是去甲肾上腺素摄取的有效阻断剂,且与毒蕈碱受体的亲和力远低于NT本身。因此,这种活性代谢物可能是一种潜在的抗抑郁药,其抗胆碱能副作用较小。

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