Selleck Ryan A, Baldo Brian A
Department of Cellular and Molecular Pharmacology, Rosalind Franklin University of Medicine & Science, 3333 Green Bay Rd., North Chicago, IL, 60064, USA.
Department of Psychiatry, University of Wisconsin-Madison School of Medicine and Public Health, 6001 Research Park Blvd., Madison, WI, 53719, USA.
Psychopharmacology (Berl). 2017 May;234(9-10):1439-1449. doi: 10.1007/s00213-016-4522-4. Epub 2017 Jan 4.
Whereas reward-modulatory opioid actions have been intensively studied in subcortical sites such as the nucleus accumbens (Acb), the role of cortical opioid transmission has received comparatively little attention.
The objective of this study is to describe recent findings on the motivational actions of opioids in the prefrontal cortex (PFC), emphasizing studies of food motivation and ingestion. PFC-based opioid effects will be compared/contrasted to those elicited from the Acb, to glean possible common functional principles. Finally, the motivational effects of opioids will be placed within a network context involving the PFC, Acb, and hypothalamus.
Mu-opioid receptor (μ-OR) stimulation in both the Acb and PFC induces eating and enhances food-seeking instrumental behaviors; μ-OR signaling also enhances taste reactivity within a highly circumscribed zone of medial Acb shell. In both the Acb and PFC, opioid-sensitive zones are aligned topographically with the sectors that project to feeding-modulatory zones of the hypothalamus and intact glutamate transmission in the lateral/perifornical (LH-PeF) hypothalamic areas is required for both Acb- and PFC-driven feeding. Conversely, opioid-mediated feeding responses elicited from the PFC are negatively modulated by AMPA signaling in the Acb shell.
Opioid signaling in the PFC engages functionally opposed PFC➔hypothalamus and PFC➔Acb circuits, which, respectively, drive and limit non-homeostatic feeding, producing a disorganized and "fragmented" pattern of impulsive food-seeking behaviors and hyperactivity. In addition, opioids act directly in the Acb to facilitate food motivation and taste hedonics. Further study of this cortico-striato-hypothalamic circuit, and incorporation of additional opioid-responsive telencephalic structures, could yield insights with translational relevance for eating disorders and obesity.
尽管奖赏调节性阿片类药物的作用已在诸如伏隔核(Acb)等皮质下部位得到深入研究,但皮质阿片类药物传递的作用相对而言受到的关注较少。
本研究的目的是描述阿片类药物在前额叶皮质(PFC)中的动机作用的最新发现,重点是对食物动机和摄取的研究。将基于PFC的阿片类药物效应与从Acb引发的效应进行比较/对比,以收集可能的共同功能原理。最后,将阿片类药物的动机效应置于涉及PFC、Acb和下丘脑的网络背景中。
在Acb和PFC中,μ-阿片受体(μ-OR)的刺激均会诱发进食并增强寻求食物的工具性动作;μ-OR信号传导还会增强内侧Acb壳高度限定区域内的味觉反应。在Acb和PFC中,阿片类药物敏感区在拓扑结构上与投射到下丘脑进食调节区的区域对齐,并且Acb和PFC驱动的进食都需要外侧/穹窿周(LH-PeF)下丘脑区域完整的谷氨酸传递。相反,PFC引发的阿片类药物介导的进食反应受到Acb壳中AMPA信号的负调节。
PFC中的阿片类药物信号传导涉及功能相反的PFC→下丘脑和PFC→Acb回路,它们分别驱动和限制非稳态进食,产生冲动性觅食行为和多动的混乱且“碎片化”模式。此外,阿片类药物直接作用于Acb以促进食物动机和味觉享乐。对这种皮质-纹状体-下丘脑回路的进一步研究,以及纳入其他阿片类药物反应性端脑结构,可能会产生与饮食失调和肥胖症相关的具有转化意义的见解。