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地昔帕明与米安色林的慢性联合治疗:增强大鼠5-HT1A受体功能并改变5-HT1A/5-HT2受体相互作用

Chronic, combined treatment with desipramine and mianserin: enhanced 5-HT1A receptor function and altered 5-HT1A/5-HT2 receptor interaction in rats.

作者信息

Lund A, Mjellem N

机构信息

Department of Physiology, University of Bergen, Norway.

出版信息

Pharmacol Biochem Behav. 1993 Aug;45(4):777-83. doi: 10.1016/0091-3057(93)90120-i.

Abstract

A greater percentage of depressed patients respond to combined treatment with a tricyclic antidepressant and the tetracyclic antidepressant mianserin than to treatment with these drugs given alone. The functional sensitivity of the 5-hydroxytryptamine (5-HT)1A receptor, and the functional interaction between the 5-HT1A and the 5-HT2 receptors were investigated after treatment with desipramine and mianserin either alone or combined for 21-28 days. Pretreatment with desipramine and mianserin in combination induced the most intense 5-HT syndrome and the greatest fall in colonic temperature after injection of the 5-HT1A agonist 8-hydroxy-2-(di-n-propylamino)-tetralin (8-OH-DPAT). The rats pretreated with desipramine alone had the largest elevation of the response temperature in the increasing temperature hot-plate test after injection of 8-OH-DPAT. After the combined pretreatment with desipramine and mianserin, no enhanced functional response in these tests was found when the 5-HT1A and the 5-HT2 receptors were stimulated simultaneously using 8-OH-DPAT and the 5-HT2 agonist, (+/-)-1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane HCl (DOI), contrasting the findings for desipramine or mianserin treatments given alone, where an increased functional response was found for the colonic temperature and the response temperature in the increasing temperature hot-plate test. In vitro receptor binding using [3H]-8-OH-DPAT as ligand revealed an increase in Kd and Bmax in the spinal cord after chronic treatment with the combination of desipramine and mianserin. In the hippocampus and the frontal cortex the changes were small.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

与单独使用这些药物治疗相比,更多比例的抑郁症患者对三环类抗抑郁药与四环类抗抑郁药米安色林联合治疗有反应。在用去甲丙咪嗪和米安色林单独或联合治疗21 - 28天后,研究了5 - 羟色胺(5 - HT)1A受体的功能敏感性以及5 - HT1A与5 - HT2受体之间的功能相互作用。联合使用去甲丙咪嗪和米安色林预处理后,注射5 - HT1A激动剂8 - 羟基 - 2 -(二正丙基氨基)四氢萘(8 - OH - DPAT)后诱发了最强烈的5 - HT综合征和结肠温度最大幅度下降。单独用去甲丙咪嗪预处理的大鼠在注射8 - OH - DPAT后,在升温热板试验中反应温度升高幅度最大。在用去甲丙咪嗪和米安色林联合预处理后,当同时使用8 - OH - DPAT和5 - HT2激动剂(±)-1 -(2,5 - 二甲氧基 - 4 - 碘苯基)-2 - 氨基丙烷盐酸盐(DOI)刺激5 - HT1A和5 - HT2受体时,在这些试验中未发现功能反应增强,这与单独给予去甲丙咪嗪或米安色林治疗的结果形成对比,在单独治疗中,结肠温度和升温热板试验中的反应温度出现了功能反应增强。使用[3H] - 8 - OH - DPAT作为配体的体外受体结合研究显示,长期联合使用去甲丙咪嗪和米安色林后脊髓中的解离常数(Kd)和最大结合容量(Bmax)增加。在海马体和额叶皮质中,变化较小。(摘要截短于250字)

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