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去甲替林在小鼠血浆和脑内高浓度时抗不动效应的自我抑制作用。

Self-inhibiting action of nortriptyline's anti-immobility effect at high plasma and brain levels in mice.

作者信息

Reis de Oliveria I, Diquet B, Van der Meersch V, Dardennes R, Gonidec J, do Prado-Lima P A

机构信息

Clinique des Maladies Mentales et de l'Encéphale, Paris, France.

出版信息

Psychopharmacology (Berl). 1990;102(4):553-6. doi: 10.1007/BF02247141.

DOI:10.1007/BF02247141
PMID:2096414
Abstract

Animals were treated acutely with 0, 2.5, 5, 10, 20 and 40 mg/kg nortriptyline (NT) 30 min before the tail suspension test (TST). They were sacrificed after test for evaluation of plasma and brain levels of NT. The anti-immobility effect increased with increasing doses and concentrations of the drug, reaching statistical significance (P less than 0.01, Dunnett test) at a dose of 20 mg/kg, 865 ng/ml in plasma and 11 micrograms/g in brain tissue. The anti-immobility effect was, however, blocked with the highest, non-toxic, concentrations. Results seem to indicate a biphasic curvilinear relationship between plasma and brain levels of NT and behaviour in mice.

摘要

在进行悬尾实验(TST)前30分钟,给动物急性注射0、2.5、5、10、20和40毫克/千克的去甲替林(NT)。实验结束后将它们处死,以评估血浆和脑组织中NT的水平。随着药物剂量和浓度的增加,抗不动效应增强,在剂量为20毫克/千克时达到统计学显著性(P小于0.01,Dunnett检验),此时血浆中浓度为865纳克/毫升,脑组织中浓度为11微克/克。然而,最高的无毒浓度会阻断抗不动效应。结果似乎表明小鼠血浆和脑组织中NT水平与行为之间存在双相曲线关系。

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