Vazquez Vincent, Penit-Soria Jacqueline, Durand Claudette, Besson Marie Jo, Giros Bruno, Daugé Valérie
Institut National de la Santé et de la Recherche Médicale, U513, Laboratoire de Neurobiologie et Psychiatrie, Université Paris XII, Faculté de Médecine, 94010 Créteil, France.
J Neurosci. 2005 May 4;25(18):4453-62. doi: 10.1523/JNEUROSCI.4807-04.2005.
Maternal deprivation can trigger long-lasting molecular and cellular modifications in brain functions and might facilitate the appearance of pathogenic behaviors. This study focuses on the vulnerability to develop morphine dependence in adult rats that were separated from their mother and littermates for 3 h per day for 14 d after birth and examines the adaptive changes in the enkephalinergic pathways. Place-preference conditioning was observed with 2 mg/kg morphine in deprived rats, whereas 5 mg/kg morphine was necessary to induce conditioning in nondeprived animals. A prolonged morphine conditioning was shown in deprived rats. A strong increase in oral morphine self-administration behavior and preference was observed in deprived rats. Only a very slight increase in preference for sucrose solution, a more ethological reinforcer known to interact with the opioid system, was shown in deprived rats. These results indicate that this postnatal environment change leads to a hypersensitivity to the reinforcing properties of morphine and to the development of morphine dependence. A significant decrease in preproenkephalin mRNA expression was observed in the nucleus accumbens and the caudate-putamen nucleus of deprived rats. The basal extracellular levels of the Met-enkephalin-like immunoreactivity in the nucleus accumbens were significantly lower in deprived rats when compared with nondeprived animals, whereas no change in mu-opioid receptor binding occurred. These results strongly support that maternal deprivation leads to a basal hypoactivity of the enkephalinergic system and hypersensitivity to morphine effects. Together, our results suggest that maternal deprivation in pups likely represents a risk factor for morphine dependence in adult rats.
母婴分离可引发大脑功能中持久的分子和细胞改变,并可能促使致病行为的出现。本研究聚焦于出生后每天与母亲和同窝幼崽分离3小时,持续14天的成年大鼠对吗啡依赖的易感性,并研究脑啡肽能通路的适应性变化。在剥夺组大鼠中,给予2mg/kg吗啡可观察到位置偏爱条件反射,而在未剥夺组动物中则需要5mg/kg吗啡才能诱导出条件反射。剥夺组大鼠表现出延长的吗啡条件反射。剥夺组大鼠口服吗啡的自我给药行为和偏爱显著增加。剥夺组大鼠对蔗糖溶液(一种已知与阿片系统相互作用的更具行为学强化作用的物质)的偏爱仅略有增加。这些结果表明,这种出生后环境变化导致对吗啡强化特性的超敏反应以及吗啡依赖的发展。在剥夺组大鼠的伏隔核和尾状-壳核中,前脑啡肽原mRNA表达显著降低。与未剥夺组动物相比,剥夺组大鼠伏隔核中蛋氨酸脑啡肽样免疫反应性的基础细胞外水平显著降低,而μ-阿片受体结合无变化。这些结果有力地支持了母婴分离导致脑啡肽能系统基础活性降低以及对吗啡作用超敏的观点。总之,我们的结果表明幼崽期的母婴分离可能是成年大鼠吗啡依赖的一个危险因素。