Haberny S L, Berman Y, Meller E, Carr K D
Department of Pharmacology, New York University School of Medicine, New York, NY 10016, USA.
Neuroscience. 2004;125(1):289-98. doi: 10.1016/j.neuroscience.2004.01.037.
Results of behavioral and c-fos immunohistochemical studies have suggested that chronic food restriction and maintenance of animals at 75-80% of free-feeding body weight may increase d-1 dopamine (DA) receptor function. The purpose of the present study was to determine whether D-1 DA receptor binding and/or mitogen-activated protein kinase (MAPK) signaling in caudate-putamen (CPu) and nucleus accumbens (NAc) are increased in food-restricted subjects. In the first experiment, saturation binding of the D-1 DA receptor antagonist [3H]SCH-23390 indicated no difference between food-restricted and ad libitum fed rats with regard to density or affinity of d-1 binding sites in CPu or NAc. In the second experiment, activation of extracellular signal-regulated kinases (ERK1/2) and cyclic AMP response element-binding protein (CREB) by i.c.v. injection of the D-1 DA receptor agonist SKF-82958 (20 microg) were markedly greater in food-restricted than ad libitum fed rats. Given a prior finding that SKF-82958 does not differentially stimulate adenylyl cyclase in CPu or NAc of food-restricted versus ad libitum fed subjects, the present results suggest that increased D-1 DA receptor-mediated ERK1/2 MAP kinase signaling may mediate the enhanced downstream activation of CREB, c-fos, and behavioral responses in food-restricted subjects. It is of interest that food restriction also increased the activation of c-Jun N-terminal protein kinase/stress-activated protein kinase, but this effect was no greater in rats injected with SKF-82958 than in those injected with saline vehicle. This represents additional evidence of increased striatal cell signaling in food-restricted subjects, presumably in response to the i.c.v. injection procedure, although the underlying receptor mechanisms remain to be determined. There were no differences between feeding groups in protein levels of the major phosphatases, MKP-2 and PP1. The upregulation of striatal MAP kinase signaling in food-restricted animals may adaptively serve to facilitate associative learning but, at the same time, increase vulnerability to the rewarding and addictive properties of abused drugs.
行为学和c-fos免疫组化研究结果表明,长期食物限制并使动物维持在自由进食体重的75 - 80%,可能会增强D1多巴胺(DA)受体功能。本研究的目的是确定在食物限制的实验对象中,尾壳核(CPu)和伏隔核(NAc)中的D1 DA受体结合和/或丝裂原活化蛋白激酶(MAPK)信号传导是否增强。在第一个实验中,D1 DA受体拮抗剂[3H]SCH-23390的饱和结合表明,在CPu或NAc中,食物限制组和自由进食组大鼠在D1结合位点的密度或亲和力方面没有差异。在第二个实验中,通过脑室内注射D1 DA受体激动剂SKF-82958(20微克)对细胞外信号调节激酶(ERK1/2)和环磷酸腺苷反应元件结合蛋白(CREB)的激活,在食物限制组大鼠中明显大于自由进食组大鼠。鉴于先前的一项发现,即SKF-82958在食物限制组和自由进食组实验对象的CPu或NAc中对腺苷酸环化酶的刺激没有差异,目前的结果表明,D1 DA受体介导的ERK1/2 MAP激酶信号传导增强可能介导了食物限制组实验对象中CREB、c-fos的下游激活增强以及行为反应增强。有趣的是,食物限制也增加了c-Jun N端蛋白激酶/应激激活蛋白激酶的激活,但这种效应在注射SKF-82958的大鼠中并不比注射生理盐水的大鼠更大。这代表了食物限制组实验对象纹状体细胞信号传导增强的额外证据,推测是对脑室内注射程序的反应,尽管潜在的受体机制仍有待确定。喂食组之间主要磷酸酶MKP-2和PP1的蛋白质水平没有差异。食物限制动物纹状体MAP激酶信号传导的上调可能会适应性地促进联想学习,但同时也会增加对滥用药物的奖赏和成瘾特性的易感性。