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Effects of repeated phencyclidine treatment on serotonin transporter in rat brain.

机译:苯环利定反复治疗对大鼠脑中5-羟色胺转运蛋白的影响。

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摘要

Phencyclidine (PCP) is known to be an inhibitor of serotonin (5-HT) uptake and to increase serotonergic activity. The development of tolerance to serotonergic stereotyped behaviors induced by repeated PCP treatment and changes of 5-HT transporters were examined. Backpedalling was significantly reduced in frequency following 14 days PCP treatment (7.5 mg/kg per day). Furthermore, repeated PCP treatment decreased the equilibrium dissociation constant (Kd) of [3H]paroxetine binding to 5-HT transporters in whole brain excluding the cerebellum without any change of maximum number of binding sites (Bmax). Single treatment with PCP failed to change binding parameters. These results indicate that repeated PCP treatment causes tolerance in serotonergic stereotyped behavior and increases affinity of 5-HT transporters for [3H]paroxetine binding. The increased affinity of 5-HT transporters could represent compensatory responses to chronic inhibition of 5-HT uptake by PCP.
机译:已知苯环利定(PCP)是5-羟色胺(5-HT)吸收的抑制剂,并能增加血清素能活性。研究了对反复PCP处理和5-HT转运蛋白变化引起的血清素定型行为耐受性的发展。 PCP治疗14天(每天7.5 mg / kg)后,返足的频率显着降低。此外,重复的PCP处理降低了[3H] paroxetine与除小脑外的全脑中与5-HT转运蛋白结合的平衡解离常数(Kd),而没有改变最大结合位点(Bmax)。 PCP的单次治疗未能改变结合参数。这些结果表明,重复的PCP处理可导致对血清素能定型行为的耐受,并增加5-HT转运蛋白对[3H] paroxetine结合的亲和力。 5-HT转运蛋白亲和力的增加可能代表对PCP慢性抑制5-HT摄取的补偿性反应。

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