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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Enhancement and inhibition of apomorphine-induced sensitization in rats exposed to immobilization stress: Relationship with adaptation to stress
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Enhancement and inhibition of apomorphine-induced sensitization in rats exposed to immobilization stress: Relationship with adaptation to stress

机译:增强和抑制阿扑吗啡诱导的固定应激大鼠致敏作用:与应激适应的关系

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Stress increases vulnerability to addiction while drugs of abuse impair coping responses and pre-dispose to depression. Pre-clinical research shows that stress exposure augments locomotor sensitization effects of drugs of abuse and impairs behavioral tolerance to repeated stress. The present study investigates relationship between behavioral tolerance to repeated immobilization stress and apomorphine-induced sensitization. Apomorphine was injected either before exposure or after the termination of immobilization, daily for 5 days, to monitor drug-induced behavioral sensitization and tolerance in immobilization stress-induced anorexia. We find that apomorphine-induced sensitization is enhanced and tolerance to repeated immobilization is impaired if the drug is administered before exposure to stress episode. Conversely, apomorphine-induced sensitization is inhibited and adaptation to stress is facilitated if the drug is administered after the termination of stress episode. It shows that apomorphine, if experienced during stress, produces greater sensitization and impairs stress tolerance. Conversely, sensitization effects of apomorphine are blocked and tolerance to stress is facilitated in animals receiving drug after the termination of stress episode. It is suggested that additive effects of stress and apomorphine on mesocorticolimbic dopamine neurotransmission and 5-HT-1A influences on dopamine neurotransmission may have a role in the modulation of apomorphine sensitization and tolerance to repeated immobilization stress. The results may help develop potential pharmacotherapies when substance abuse/dependence disorder and depression occur together.
机译:压力增加了成瘾的脆弱性,而滥用药物会削弱应对反应并易患抑郁症。临床前研究表明,压力暴露会增强滥用药物的运动敏化作用,并削弱行为对反复压力的耐受性。本研究调查了行为耐受性对反复固定压力与阿扑吗啡诱导的致敏之间的关系。在暴露前或固定终止后每天注射阿扑吗啡5天,以监测药物诱导的行为敏化和固定应激诱导的厌食症的耐受性。我们发现,如果药物在暴露于应激事件之前给药,则阿扑吗啡诱导的致敏作用增强,并且对反复固定的耐受性受损。相反,如果在应激发作终止后给予该药物,则阿扑吗啡诱导的致敏作用被抑制并且促进了对应激的适应。它表明,阿扑吗啡,如果在压力期间经历,会产生更高的敏化度并损害压力耐受性。相反,在应激发作终止后,在接受药物治疗的动物中,阿扑吗啡的致敏作用被阻断,并增强了对压力的耐受性。提示应激和阿扑吗啡对中皮质皮质多巴胺神经传递的累加效应和5-HT-1A对多巴胺神经传递的影响可能在阿扑吗啡敏化的调节和对反复固定压力的耐受性中起作用。当药物滥用/依赖性障碍和抑郁症同时发生时,这些结果可能有助于开发潜在的药物治疗方法。

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