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Changing Mechanisms of Opiate Tolerance and Withdrawal during Early Development: Animal Models of the Human Experience

机译:早期发育中阿片耐受和戒断的变化机制:人类经验的动物模型

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Human infants may be exposed to opiates through placental transfer from an opiate-using mother or through the direct administration of such drugs to relieve pain (e.g., due to illness or neonatal surgery). Infants of many species show physical dependence and tolerance to Opiates. The magnitude of tolerance and the nature of withdrawal differ from those of the adult. Moreover, the mechanisms that contribute to the chronic effects of opiates are not well understood in the infant but include biologicalprocesses that are both common to and distinct from those of the adult. We review the animal research literature on the effects of chronic and acute opiate exposure in infants and identify mechanisms of withdrawal and tolerance that are similar to and different from those understood in adults. These mechanisms include opioid pharmacology, underlying neural substrates, and the involvement of other neurotransmitter systems. It appears that brain circuitry and opioid receptor types are similar but that NMDA receptor function is immature in the infant. Intracellular signaling cascades may differ but data are complicated by differences between the effects of chronic versus acute morphine treatment. Given the limited treatment options for the dependent infant patient, further study of the biological functions that are al-tered by chronic opiate treatment is necessary to guide evidenced-based treatment modalities.
机译:人类婴儿可能​​会通过使用鸦片的母亲从胎盘转移或通过直接使用此类药物缓解疼痛(例如,由于疾病或新生儿手术)而暴露于鸦片。许多物种的婴儿对阿片类药物表现出身体依赖性和耐受性。宽容的程度和退缩的性质与成年人不同。此外,在婴儿中对引起阿片类药物的慢性作用的机制尚不十分了解,但包括成年人所共有和不同的生物过程。我们回顾了动物研究文献对婴儿慢性和急性阿片类药物暴露的影响,并确定了与成年人了解和相似的戒断和耐受机制。这些机制包括阿片类药物的药理作用,潜在的神经基质以及其他神经递质系统的参与。看来婴儿的脑回路和阿片样物质受体类型相似,但NMDA受体功能尚不成熟。细胞内信号传导级联可能会有所不同,但慢性吗啡和急性吗啡治疗的效果之间的差异使数据变得复杂。鉴于对依赖的婴儿患者的治疗选择有限,因此有必要进一步研究慢性阿片类药物治疗所改变的生物学功能,以指导循证治疗方法。

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