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Effect of agmatine on the development of morphine dependence in rats: potential role of cAMP system.

机译:胍丁胺对吗啡依赖大鼠发展的影响:cAMP系统的潜在作用。

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摘要

Agmatine is an endogenous amine derived from arginine that potentiates morphine analgesia and blocks symptoms of naloxone-precipitated morphine withdrawal in rats. In this study, we sought to determine whether treatment with agmatine during the development of morphine dependence inhibits the withdrawal symptoms and that the effect is mediated by cAMP system. Exposure of rats to morphine for 7 days resulted in marked naloxone-induced withdrawal symptoms and agmatine treatment along with morphine significantly decreasing the withdrawal symptoms. The levels of cAMP were markedly increased in morphine-treated rat brain slices when incubated with naloxone and this increase was significantly reduced in rats treated with morphine and agmatine. The induction of tyrosine hydroxylase after morphine exposure was also reduced in locus coeruleus when agmatine was administered along with morphine. We conclude that agmatine reduces the development of dependence to morphine and that this effect is probably mediated bythe inhibition of cAMP signaling pathway during chronic morphine exposure.
机译:胍丁胺是衍生自精氨酸的内源性胺,可增强吗啡镇痛作用,并阻止纳洛酮沉淀的吗啡戒断症状。在这项研究中,我们试图确定在吗啡依赖发展过程中使用胍丁胺治疗是否能抑制戒断症状,​​并且该作用是否由cAMP系统介导。将大鼠暴露于吗啡7天会导致明显的纳洛酮诱导的戒断症状,​​胍丁胺治疗与吗啡一起可显着降低戒断症状。与纳洛酮一起孵育时,吗啡处理的大鼠脑切片中的cAMP水平显着增加,而吗啡和胍丁胺处理的大鼠中cAMP的水平则明显降低。当与胍吗啡一起施用胍丁胺时,在吗啡暴露后酪氨酸羟化酪氨酸羟化酶的诱导也降低了。我们得出结论,胍丁胺减少了对吗啡的依赖性,这种作用可能是由慢性吗啡暴露期间对cAMP信号通路的抑制介导的。

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