氯丙咪嗪治疗对犬血小板α 2-肾上腺素能接受性的影响。

Journal de pharmacologie Pub Date : 1986-10-01
A Villeneuve, M Berlan, H Paris, M A Tran, M Lafontan, J L Montastruc, P Montastruc
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引用次数: 0

摘要

研究氯丙咪嗪(5mg /kg s.c. / d,连续21 d)对家犬血小板α 2-肾上腺素受体的影响。血小板膜制剂的放射配体结合研究表明,抗抑郁治疗促进[3H]-育亨宾结合位点数量的减少。对pge1诱导的全血小板循环AMP积累的抑制测量表明,与α 2-肾上腺素能刺激立即相关的生物事件没有改变。氯米帕明处理的血小板对ADP或ADP +肾上腺素的聚集反应完全消失。氯丙咪嗪不影响氯氯醛麻醉犬对去甲肾上腺素或肾上腺素注射(在给予心得安和普唑嗪后)的舒张压反应。这项工作表明,α 2-肾上腺素能位点结合能力的变化并不总是与相关生理事件的改变有关。
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Effect of clomipramine treatment on dog platelet alpha 2-adrenergic receptivity.

The effects of clomipramine treatment (5 mg/kg s.c. a day during 21 days) on dog platelet alpha 2-adrenoreceptivity were investigated. The radioligand binding studies on platelet membrane preparations showed that the antidepressant treatment promotes a decrease in the number of [3H]-yohimbine binding sites. The measurement of the inhibition of PGE1-induced cyclic AMP accumulation in the whole platelet indicated that the biological event immediately associated with alpha 2-adrenergic stimulation was not modified. The aggregatory response to ADP or ADP plus adrenaline was totally abolished in clomipramine-treated platelets. The diastolic pressor responses to noradrenaline or adrenaline injections (after propranolol and prazosin administration) in chloralose anaesthetized dogs were not affected by clomipramine treatment. This work shows that variations in the binding capacities of alpha 2-adrenergic sites are not always linked to modifications of related physiological events.

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