Pulvirenti L
Mondino-Tor Vergata Center for Experimental Neurobiology, Department of Biology, University of Rome Tor Vergata, Italy.
Funct Neurol. 1993 Nov-Dec;8(6):433-40.
The epidemic growth of the use of controlled substances has brought their toxic effects to clinical attention. Several drugs of abuse are known to induce nerve cell toxicity after acute and chronic administration. In addition, it has been suggested that the three main classes of abused substances, namely psychostimulants, ethanol and opiates, also induce changes in the function of discrete neural pathways. These alterations may eventually be responsible for the loss of behavioral control often observed during the natural history of the addiction process. Therefore, biochemical and behavioral toxicity deserve equal attention. A complex neural network within the forebrain limbic system which has been characterized over the past few years seems to mediate drug-seeking behavior and maintain drug self-administration in rodents. A striking similarity has been observed between this circuit and the neural substrates of motivated behavior. This review focuses on the possibility that drugs of abuse may acquire significance as reinforcers by usurping the physiological role of this circuit which normally operates to ensure survival of the individual. This may represent a subtle mechanism through which drugs of abuse may induce behavioral toxicity even in the absence of nerve cell loss.
受控物质使用的迅速增长已使其毒性作用引起临床关注。已知几种滥用药物在急性和慢性给药后会诱发神经细胞毒性。此外,有人提出,三类主要的滥用物质,即精神兴奋剂、乙醇和阿片类药物,也会引起离散神经通路功能的变化。这些改变最终可能是成瘾过程自然史中经常观察到的行为控制丧失的原因。因此,生化毒性和行为毒性值得同等关注。在过去几年中已被明确的前脑边缘系统内的复杂神经网络似乎介导了啮齿动物的觅药行为并维持药物自我给药。在这个回路与动机行为的神经基质之间观察到了惊人的相似性。本综述关注的可能性是,滥用药物可能通过篡夺该回路的生理作用而作为强化物获得重要性,该回路通常运作以确保个体的生存。这可能代表了一种微妙的机制,通过这种机制,滥用药物即使在没有神经细胞损失的情况下也可能诱发行为毒性。