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首页> 外文期刊>Psychoneuroendocrinology: An International Journal >Serotonin 2 receptor modulation of hyperthermia, corticosterone, and hippocampal serotonin depletions following serial exposure to chronic stress and methamphetamine.
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Serotonin 2 receptor modulation of hyperthermia, corticosterone, and hippocampal serotonin depletions following serial exposure to chronic stress and methamphetamine.

机译:连续暴露于慢性应激和甲基苯丙胺后,热疗,皮质酮和海马5-羟色胺消耗的5-羟色胺2受体调节。

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Chronic stress precipitates drug seeking behavior and alters the effects of drugs of abuse. Although it is known that chronic stress potentiates acute neurochemical and hyperthermic responses to the drug of abuse methamphetamine, no studies have investigated if and how chronic stress alters other physiological responses to methamphetamine. Therefore the objective of these studies was to determine if 10 days of chronic unpredictable stress modulates corticosterone (CORT) responses to methamphetamine and furthermore how chronic stress may modulate methamphetamine-induced increases in hyperthermia and CORT. As chronic stress potentiates hyperthermic responses to serotonin 2 (5-HT2) stimulation and 5-HT2 receptors are important in mediating both hyperthermic and CORT responses, we also investigated if 5-HT2 antagonism would block hyperthermia and CORT secretion by the serial exposure to stress and methamphetamine (stress/methamphetamine). The results of these studies illustrate that stress potentiates methamphetamine-induced increases in body temperature and CORT secretion and that these increases are blocked by the 5-HT2 antagonist ketanserin. Furthermore, the combination of stress and methamphetamine depletes 5-HT content in the hippocampus 7 days after methamphetamine administration which is blocked by the 5-HT2 antagonist ketanserin. Overall, these results indicate a pharmacological mechanism for the depletion of hippocampal 5-HT by the serial exposure to stress and methamphetamine and further illustrate the deleterious interactions between chronic stress and methamphetamine use.
机译:慢性应激会激发寻求药物的行为,并改变滥用药物的影响。尽管已知慢性应激会增强对滥用甲基苯丙胺药物的急性神经化学和高温反应,但尚无研究调查慢性应激是否以及如何改变对甲基苯丙胺的其他生理反应。因此,这些研究的目的是确定10天的慢性不可预知的压力是否能调节皮质酮(CORT)对甲基苯丙胺的反应,以及慢性压力如何调节甲基苯丙胺引起的高热和CORT升高。由于慢性应激会增强对5-羟色胺2(5-HT2)刺激的高温反应,而5-HT2受体在介导高温和CORT反应中均很重要,因此我们还研究了5-HT2拮抗作用是否会因连续暴露于压力而阻止高温和CORT分泌和甲基苯丙胺(应力/甲基苯丙胺)。这些研究的结果表明,压力增强了甲基苯丙胺诱导的体温和CORT分泌的增加,而这些增加被5-HT2拮抗剂酮色林所阻止。此外,应激和甲基苯丙胺的组合在甲基苯丙胺给药后7天消耗了海马中的5-HT含量,其被5-HT 2拮抗剂酮色林阻断。总体而言,这些结果表明了通过连续暴露于应激和甲基苯丙胺来消耗海马5-HT的药理机制,并进一步说明了慢性应激与甲基苯丙胺之间的有害相互作用。

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