Caccia S, Anelli M, Ferrarese A, Fracasso C, Garattini S
Istituto di Ricerche Farmacologiche Mario Negri, Milan, Italy.
Eur J Pharmacol. 1993 Mar 16;233(1):71-7. doi: 10.1016/0014-2999(93)90350-q.
The importance of d-norfenfluramine in regard to the indole-depleting action of d-fenfluramine has not been well studied in sensitive animal species. The present study therefore examined the intensity and time course of the neurochemical effects of i.p. injected d-fenfluramine (2.5 and 5 mg/kg) and d-norfenfluramine (2.5 mg/kg) in vehicle- and SKF-525A-pretreated rats, relating the effects to the brain concentration-time profiles of the drug and its active metabolite. At the lower dose d-fenfluramine caused only a small, short-lasting decrease in brain serotonin (5-HT) without affecting the 5-hydroxyindoleacetic acid (5-HIAA). Higher doses affected both 5-HT and 5-HIAA (50-60 and 30-40% reductions, respectively), the effect being maximal for at least 8 h. d-Norfenfluramine reduced the brain content of 5-HT and 5-HIAA less (by about 30%) than 5 mg/kg d-fenfluramine did. Brain concentrations of d-norfenfluramine at the time of the maximal depletion of indoles were close to those of the metabolite after 5 mg/kg d-fenfluramine, indicating that the acute indole-depleting effects did not depend solely on the brain concentrations of its nor-metabolite. SKF-525A changed the metabolite-to-parent drug ratios in brain without appreciably influencing the action of d-fenfluramine. However, the maximum decrease in indole content caused by 2.5 mg/kg d-fenfluramine in SKF-525A-pretreated rats was only 12% of the control level, although the brain concentration of unchanged drug was comparable to that after 5 mg/kg d-fenfluramine in vehicle-pretreated rats.(ABSTRACT TRUNCATED AT 250 WORDS)
在敏感动物物种中,d-去甲氟苯丙胺在d-氟苯丙胺的吲哚消耗作用方面的重要性尚未得到充分研究。因此,本研究检测了腹腔注射d-氟苯丙胺(2.5和5mg/kg)和d-去甲氟苯丙胺(2.5mg/kg)对预先用溶媒和SKF-525A处理的大鼠的神经化学效应的强度和时程,并将这些效应与药物及其活性代谢物的脑浓度-时间曲线相关联。较低剂量的d-氟苯丙胺仅引起脑血清素(5-HT)小幅、短暂的降低,而不影响5-羟吲哚乙酸(5-HIAA)。较高剂量则同时影响5-HT和5-HIAA(分别降低50-60%和30-40%),该效应至少持续8小时达到最大值。d-去甲氟苯丙胺对5-HT和5-HIAA脑含量的降低程度(约30%)低于5mg/kg d-氟苯丙胺。吲哚最大耗竭时d-去甲氟苯丙胺的脑浓度接近5mg/kg d-氟苯丙胺给药后代谢物的浓度,表明急性吲哚消耗效应并非仅取决于其去甲代谢物的脑浓度。SKF-525A改变了脑中代谢物与母体药物的比例,但未明显影响d-氟苯丙胺的作用。然而,在SKF-525A预处理的大鼠中,2.5mg/kg d-氟苯丙胺引起的吲哚含量最大降低仅为对照水平的12%,尽管未改变药物的脑浓度与溶媒预处理大鼠中5mg/kg d-氟苯丙胺给药后的浓度相当。(摘要截短于250字)