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α-2肾上腺素能受体敏感性与抗抑郁治疗的作用机制。长期阿米替林治疗的效果。

Alpha-2 adrenergic receptor sensitivity and the mechanism of action of antidepressant therapy. The effect of long-term amitriptyline treatment.

作者信息

Charney D S, Heninger G R, Sternberg D E

出版信息

Br J Psychiatry. 1983 Mar;142:265-75. doi: 10.1192/bjp.142.3.265.

Abstract

It has been hypothesized that the mechanism of action of antidepressant treatments is related to their ability to decrease the sensitivity of the alpha-2 adrenergic autoreceptor. In order to assess alpha-adrenergic autoreceptor sensitivity, the effects of clonidine, the alpha-2 adrenergic receptor agonist, on plasma levels of the norepinephrine metabolite 3-methoxy-4-hydroxyphenethyleneglycol (MHPG), blood pressure (BP) and patient-rated sedation were measured in nine depressed patients before and during amitripytline treatment. Postsynaptic alpha-2 adrenergic receptor sensitivity was assessed by determining the growth hormone (GH) response to clonidine before and during treatment. Amitriptyline significantly attenuated the effects of clonidine on plasma MHPG, standing systolic BP, and sedation, indicating that alpha-2 adrenergic autoreceptors had become subsensitive. In addition, baseline plasma MHPG levels were significantly reduced. Amitriptyline had no effect on the GH response to clonidine.

摘要

有假说认为,抗抑郁治疗的作用机制与其降低α-2肾上腺素能自身受体敏感性的能力有关。为了评估α-肾上腺素能自身受体的敏感性,在9名抑郁症患者接受阿米替林治疗前及治疗期间,测定了α-2肾上腺素能受体激动剂可乐定对去甲肾上腺素代谢产物3-甲氧基-4-羟基苯乙二醇(MHPG)的血浆水平、血压(BP)及患者自评镇静作用的影响。通过测定治疗前及治疗期间可乐定对生长激素(GH)的反应来评估突触后α-2肾上腺素能受体的敏感性。阿米替林显著减弱了可乐定对血浆MHPG、站立位收缩压及镇静作用的影响,表明α-2肾上腺素能自身受体已变得不敏感。此外,基线血浆MHPG水平显著降低。阿米替林对可乐定引起的GH反应无影响。

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