Goldstein A
Stanford University, California.
J Psychoactive Drugs. 1991 Apr-Jun;23(2):123-33. doi: 10.1080/02791072.1991.10472231.
The neurobiology of drug addiction is being clarified. Research is revealing the anatomic pathways of primary drug reinforcement (reward) in the brain and the molecular architecture of the receptors on which addictive drugs act. All addictive drugs mimic (or occasionally block) the actions of some neurotransmitter; in the case of heroin or methadone an endogenous opioid, probably beta-endorphin. The groundwork is being laid for understanding Dole and Nyswander's "metabolic disease" concept as a concrete neurochemical abnormality of the endogenous opioid system. Thus, a stronger basis is developing for regarding methadone maintenance as a means of replacing a neurohormonal deficiency. Three practical conclusions that can be drawn from this model are: (1) methadone dosage must be adequate (never less than 50-80 mg); (2) it should be more widely accepted that some patients may require lifelong methadone maintenance; and (3) longer-acting, better stabilizing methadone congeners, such as LAAM and its metabolites, should be brought into general use.
药物成瘾的神经生物学正在逐步明晰。研究正在揭示大脑中主要药物强化(奖赏)的解剖学通路以及成瘾性药物作用的受体的分子结构。所有成瘾性药物都模仿(或偶尔阻断)某些神经递质的作用;就海洛因或美沙酮而言,它们模仿的是一种内源性阿片类物质,可能是β-内啡肽。正在为将多尔和尼斯万德的“代谢疾病”概念理解为内源性阿片系统具体的神经化学异常奠定基础。因此,将美沙酮维持治疗视为一种补充神经激素缺乏的手段的依据日益充分。从该模型可以得出三个实际结论:(1)美沙酮剂量必须足够(绝不能低于50 - 80毫克);(2)应该更广泛地接受一些患者可能需要终身美沙酮维持治疗这一观点;(3)作用时间更长、稳定性更好的美沙酮同系物,如左-α-乙酰美沙醇(LAAM)及其代谢产物,应得到广泛应用。