Mann K, Widmann U
Psychiatrische Klinik, Eberhard-Karls-Universität Tübingen.
Fortschr Neurol Psychiatr. 1995 Jun;63(6):238-47. doi: 10.1055/s-2007-996622.
The authors deal with the heuristic value of the "neurobiological model of alcohol dependence". It allows the study of the influence of a defined noxe on different brain structures. Additionally, it enables the quantification of regeneration and restitution processes in abstinence. Because of this, the alcoholism model goes beyond dementia, the model which has dominated brain research so far. Neuropathological studies in humans and animals found a reduction in the volume of white matter and a partial degeneration, or even loss of specific neurons. According to animal data, this could to a certain extent be genetically determined. Alcohol exerts a distinct influence on different neurotransmitter systems. This research will deepen our understanding of the neurotoxic and psychotropic properties of alcohol, and of the development of dependence. Little is known about the role of astrocytes in the reaction of the brain to alcohol. Here again, the neurobiological model of alcohol dependence could be of value in learning more about their interactions with neurons. Using Magnetic Resonance Imaging and CAT-scans, the decrease in volume of white and grey matter was demonstrated in vivo. The degree and the time course of brain damage seems to be influenced less by drinking history than by age and gender. There is evidence that female alcoholics develop brain damage more readily than men. When abstinent, an increase in the volume of white and grey matter can be observed. This is not due to the rehydration of brain tissue alone. Future research will need to deal with the question of whether the central nervous system is capable of partial regeneration. For the study of neuroplasticity, the neurobiological model of alcohol dependence seems to be particularly well suited.
作者探讨了“酒精依赖的神经生物学模型”的启发价值。它有助于研究特定损伤因素对不同脑结构的影响。此外,它能够对戒酒过程中的再生和恢复过程进行量化。正因如此,酒精中毒模型超越了迄今为止主导脑研究的痴呆症模型。对人类和动物的神经病理学研究发现白质体积减小,特定神经元部分退化甚至丧失。根据动物数据,这在一定程度上可能由基因决定。酒精对不同神经递质系统有显著影响。这项研究将加深我们对酒精的神经毒性和精神活性特性以及依赖发展的理解。关于星形胶质细胞在大脑对酒精反应中的作用知之甚少。在此,酒精依赖的神经生物学模型在更多了解它们与神经元的相互作用方面可能具有价值。使用磁共振成像和计算机断层扫描,在活体中证实了白质和灰质体积的减小。脑损伤的程度和时间进程似乎受饮酒史的影响小于受年龄和性别的影响。有证据表明女性酗酒者比男性更容易发生脑损伤。戒酒时,可以观察到白质和灰质体积增加。这不仅仅是由于脑组织的再水化。未来的研究需要探讨中枢神经系统是否能够部分再生的问题。对于神经可塑性的研究,酒精依赖的神经生物学模型似乎特别合适。