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重复给予抗抑郁药对大鼠脑内4A型磷酸二酯酶(PDE4A)的影响。

Effects of repeated antidepressant treatment of type 4A phosphodiesterase (PDE4A) in rat brain.

作者信息

Ye Y, Jackson K, O'Donnell J M

机构信息

Department of Pharmacology and Therapeutics, Louisiana State University Medical Center, Shreveport 71130-3932, USA.

出版信息

J Neurochem. 2000 Mar;74(3):1257-62. doi: 10.1046/j.1471-4159.2000.741257.x.

Abstract

In a previous study, an up-regulation of rolipram-sensitive, low-Km, cyclic AMP phosphodiesterase (PDE4) subtype PDE4A in rat cerebral cortex following repeated treatment of desipramine was observed. To determine whether this effect is shared by antidepressants from different pharmacological classes, PDE4A expression was examined using immunoblot analyses following repeated treatment with the norepinephrine re-uptake inhibitor desipramine, the monoamine oxidase inhibitor phenelzine, the atypical antidepressant trazodone, and the serotonin reuptake inhibitor fluoxetine. Desipramine, phenelzine, and fluoxetine all increased the intensities of the PDE4A bands in hippocampal preparations; trazodone did not. In preparations of cerebral cortex, the intensities of the PDE4A bands were increased following desipramine treatment, not changed following phenelzine or fluoxetine treatment, and decreased following trazodone treatment. It appears that repeated treatment with antidepressant drugs from different pharmacological classes produces similar effects on the expressions of PDE4A variants in hippocampus. This effect is not correlated with the changes in beta-adrenergic receptor densities, suggesting these antidepressants may at some point alter intracellular signal transduction pathways in a similar manner.

摘要

在先前的一项研究中,观察到在反复给予地昔帕明治疗后,大鼠大脑皮层中对咯利普兰敏感的低 Km 环磷酸腺苷磷酸二酯酶(PDE4)亚型 PDE4A 上调。为了确定这种效应是否为不同药理类别的抗抑郁药所共有,在用去甲肾上腺素再摄取抑制剂地昔帕明、单胺氧化酶抑制剂苯乙肼、非典型抗抑郁药曲唑酮和 5-羟色胺再摄取抑制剂氟西汀反复治疗后,使用免疫印迹分析检测了 PDE4A 的表达。地昔帕明、苯乙肼和氟西汀均增加了海马制剂中 PDE4A 条带的强度;曲唑酮则没有。在大脑皮层制剂中,地昔帕明治疗后 PDE4A 条带的强度增加,苯乙肼或氟西汀治疗后未改变,曲唑酮治疗后降低。看来,用不同药理类别的抗抑郁药反复治疗对海马中 PDE4A 变体的表达产生相似的影响。这种效应与β-肾上腺素能受体密度的变化无关,提示这些抗抑郁药可能在某些方面以相似的方式改变细胞内信号转导途径。

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