Planeta C S, Lepsch L B, Alves R, Scavone C
Universidade Estadual Paulista, Laboratório de Neuropsicofarmacologia, Faculdade de Ciências Farmacêuticas, AraraquaraSP, Brasil.
Braz J Med Biol Res. 2013 Nov;46(11):909-915. doi: 10.1590/1414-431X20133379. Epub 2013 Oct 15.
Cocaine is a widely used drug and its abuse is associated with physical, psychiatric and social problems. Abnormalities in newborns have been demonstrated to be due to the toxic effects of cocaine during fetal development. The mechanism by which cocaine causes neurological damage is complex and involves interactions of the drug with several neurotransmitter systems, such as the increase of extracellular levels of dopamine and free radicals, and modulation of transcription factors. The aim of this review was to evaluate the importance of the dopaminergic system and the participation of inflammatory signaling in cocaine neurotoxicity. Our study showed that cocaine activates the transcription factors NF-κB and CREB, which regulate genes involved in cellular death. GBR 12909 (an inhibitor of dopamine reuptake), lidocaine (a local anesthetic), and dopamine did not activate NF-κB in the same way as cocaine. However, the attenuation of NF-κB activity after the pretreatment of the cells with SCH 23390, a D1 receptor antagonist, suggests that the activation of NF-κB by cocaine is, at least partially, due to activation of D1 receptors. NF-κB seems to have a protective role in these cells because its inhibition increased cellular death caused by cocaine. The increase in BDNF (brain-derived neurotrophic factor) mRNA can also be related to the protective role of both CREB and NF-κB transcription factors. An understanding of the mechanisms by which cocaine induces cell death in the brain will contribute to the development of new therapies for drug abusers, which can help to slow down the progress of degenerative processes.
可卡因是一种广泛使用的毒品,其滥用与身体、精神和社会问题相关。已证实新生儿的异常是由于胎儿发育期间可卡因的毒性作用所致。可卡因导致神经损伤的机制很复杂,涉及该药物与多种神经递质系统的相互作用,如细胞外多巴胺水平和自由基的增加,以及转录因子的调节。本综述的目的是评估多巴胺能系统的重要性以及炎症信号在可卡因神经毒性中的作用。我们的研究表明,可卡因激活转录因子NF-κB和CREB,它们调节参与细胞死亡的基因。GBR 12909(一种多巴胺再摄取抑制剂)、利多卡因(一种局部麻醉剂)和多巴胺不会以与可卡因相同的方式激活NF-κB。然而,用D1受体拮抗剂SCH 23390对细胞进行预处理后,NF-κB活性的减弱表明,可卡因对NF-κB的激活至少部分是由于D1受体的激活。NF-κB似乎在这些细胞中具有保护作用,因为其抑制会增加可卡因导致的细胞死亡。脑源性神经营养因子(BDNF)mRNA的增加也可能与CREB和NF-κB转录因子的保护作用有关。了解可卡因在大脑中诱导细胞死亡的机制将有助于开发针对药物滥用者的新疗法,这有助于减缓退行性过程的进展。