Singh Malini E, McGregor Iain S, Mallet Paul E
School of Psychology, University of New England, Armidale, NSW, Australia.
Neuropsychopharmacology. 2006 Jan;31(1):58-69. doi: 10.1038/sj.npp.1300770.
In the present study, the effects of perinatal exposure to Delta(9)-tetrahydrocannabinol (THC) on heroin-induced place conditioning and Fos-immunoreactivity (Fos-IR) were examined. Male albino Wistar rats (N=104) were pretreated with vehicle (n=52) or 5 mg/kg THC (n=52) from postnatal days 4 through 14. At approximately 8 weeks of age, 72 rats were divided into six equal groups (n=12 per group) and injected subcutaneously (s.c.) with vehicle, 0.5, or 2.0 mg/kg heroin and tested in an unbiased two-compartment place conditioning task. In vehicle-pretreated rats, 2.0 mg/kg but not 0.5 mg/kg heroin produced a significant place preference. Perinatal THC exposure significantly enhanced the rewarding properties of both doses of heroin. In the second experiment, 32 rats were divided into four equal groups (n=8 per group) and injected with vehicle or 0.5 mg/kg heroin s.c. and perfused 2-h later. Fos-IR was examined in several brain regions directly or indirectly involved in reward. Acute administration of heroin in vehicle pretreated rats increased Fos-IR in the central, medial, and dorsomedial caudate putamen (CPu), nucleus accumbens (NAC, core and shell regions), lateral septum, islands of Calleja-major (ICjM), bed nucleus of the stria terminalis (BNST), central nucleus of the amygdala (CEA), dorsolateral and dorsomedial periaqueductal gray (PAG), ventral tegmental area (VTA), Edinger-Westphal nucleus (EW). Perinatal THC exposure significantly increased heroin-induced Fos-IR in the dorsomedial CPu. Conversely, perinatal THC exposure reduced heroin-induced Fos-IR in the NAC (shell), BNST, CEA, dorsolateral and lateral PAG, VTA, and EW. The present study demonstrates an increase in the rewarding properties of heroin following exposure to THC at an early age and provides new evidence regarding possible neural correlates underlying this behavioral alteration. Neuropsychopharmacology (2006) 31, 58-69. doi:10.1038/sj.npp.1300770; published online 25 May 2005.
在本研究中,检测了围产期暴露于Δ⁹-四氢大麻酚(THC)对海洛因诱导的位置偏爱及Fos免疫反应性(Fos-IR)的影响。雄性白化Wistar大鼠(N = 104)在出生后第4天至第14天用赋形剂(n = 52)或5 mg/kg THC(n = 52)进行预处理。在大约8周龄时,将72只大鼠分成六个相等的组(每组n = 12),并皮下注射(s.c.)赋形剂、0.5或2.0 mg/kg海洛因,然后在无偏倚的双室位置偏爱任务中进行测试。在经赋形剂预处理的大鼠中,2.0 mg/kg而非0.5 mg/kg海洛因产生了显著的位置偏爱。围产期THC暴露显著增强了两种剂量海洛因的奖赏特性。在第二个实验中,将32只大鼠分成四个相等的组(每组n = 8),皮下注射赋形剂或0.5 mg/kg海洛因,并在2小时后进行灌注。在直接或间接参与奖赏的几个脑区检测Fos-IR。在经赋形剂预处理的大鼠中急性给予海洛因增加了尾壳核(CPu)中央、内侧和背内侧、伏隔核(NAC,核心和壳区)、外侧隔区、大卡耶哈岛(ICjM)、终纹床核(BNST)、杏仁核中央核(CEA)、背外侧和背内侧导水管周围灰质(PAG)、腹侧被盖区(VTA)、动眼神经副核(EW)中的Fos-IR。围产期THC暴露显著增加了海洛因诱导的背内侧CPu中的Fos-IR。相反,围产期THC暴露降低了海洛因诱导的NAC(壳区)、BNST、CEA、背外侧和外侧PAG、VTA及EW中的Fos-IR。本研究证明了幼年暴露于THC后海洛因奖赏特性的增加,并提供了关于这种行为改变潜在神经相关性的新证据。《神经精神药理学》(2006年)31卷,58 - 69页。doi:10.1038/sj.npp.1300770;2005年5月25日在线发表。