Olszewski Pawel K, Cedernaes Jonathan, Olsson Fredrik, Levine Allen S, Schiöth Helgi B
Minnesota Obesity Center, Department of Food Science and Nutrition, University of Minnesota, Saint Paul, MN 55117, United States.
Neurosci Biobehav Rev. 2008 Jul;32(5):945-56. doi: 10.1016/j.neubiorev.2008.01.007. Epub 2008 Mar 29.
The Allen Brain Atlas, the most comprehensive in situ hybridization database, covers over 21,000 genes expressed in the mouse brain. Here we discuss the feasibility to utilize the ABA in research pertaining to the central regulation of feeding and we define advantages and vulnerabilities associated with the use of the atlas as a guidance tool. We searched for 57 feeding-related genes in the ABA, and of those 42 display distribution consistent with that described in previous reports. Detailed analyses of these 42 genes in the nucleus accumbens, ventral tegmental area, nucleus of the solitary tract, lateral hypothalamus, arcuate, paraventricular, ventromedial and dorsomedial nuclei suggests that molecules involved in feeding stimulation and termination are coexpressed in multiple consumption-related sites. Gene systems linked to energy needs, reward or satiation display a remarkably high level of overlap. This conclusion calls into question the classical concept of brain sites viewed as independent hunger or reward "centers" and favors the theory of a widespread feeding network comprising multiple neuroregulators affecting numerous aspects of consumption.
艾伦脑图谱是最全面的原位杂交数据库,涵盖了在小鼠大脑中表达的21000多个基因。在此,我们讨论利用该图谱进行与进食中枢调节相关研究的可行性,并确定将其用作指导工具的优势和弱点。我们在艾伦脑图谱中搜索了57个与进食相关的基因,其中42个基因的分布与先前报道一致。对伏隔核、腹侧被盖区、孤束核、下丘脑外侧区、弓状核、室旁核、腹内侧核和背内侧核中这42个基因的详细分析表明,参与进食刺激和终止的分子在多个与进食相关的位点共表达。与能量需求、奖赏或饱腹感相关的基因系统显示出非常高的重叠度。这一结论对将脑区视为独立的饥饿或奖赏“中心”的经典概念提出了质疑,并支持了一种广泛的进食网络理论,该网络由多个影响进食诸多方面的神经调节因子组成。