Eating and Weight Disorders Program, Mount Sinai School of Medicine, One Gustave L. Levy Place, Box 1230, New York, NY 10029, USA.
Clin Psychol Rev. 2010 Aug;30(6):655-68. doi: 10.1016/j.cpr.2010.04.011. Epub 2010 May 31.
Serotonergic dysregulation is thought to underlie much of the pathology in bulimia nervosa (BN). The purpose of this review is to expand the serotonergic model by incorporating specific and nonspecific contributions of estrogens to the development and maintenance of bulimic pathology in order to guide research from molecular genetics to novel therapeutics for BN. Special emphasis is given to the organizing theory of general brain arousal which allows for integration of specific and nonspecific effects of these systems on behavioral endpoints such as binge eating or purging as well as arousal states such as fear, novelty seeking, or sex. Regulation of the serotonergic system by estrogens is explored, and genetic, epigenetic, and environmental estrogen effects on bulimic pathology and risk factors are discussed. Genetic and neuroscientific research support this two-system conceptualization of BN with both contributions to the developmental and maintenance of the disorder. Implications of an estrogenic-serotonergic model of BN are discussed as well as guidelines and suggestions for future research and novel therapeutic targets.
血清素能失调被认为是神经性贪食症(BN)发病机制的基础。本综述的目的是通过纳入雌激素对贪食症发病和维持的特定和非特定作用,扩展血清素能模型,以指导从分子遗传学到 BN 新疗法的研究。特别强调了一般大脑唤醒的组织理论,该理论允许这些系统对行为终点(如暴食或催吐)以及唤醒状态(如恐惧、新奇寻求或性)的特定和非特定作用进行整合。探讨了雌激素对 5-羟色胺能系统的调节,并讨论了遗传、表观遗传和环境雌激素对贪食症发病机制和危险因素的影响。遗传和神经科学研究支持 BN 的这种双系统概念化,这对疾病的发展和维持都有贡献。还讨论了 BN 的雌激素-5-羟色胺能模型的意义,以及对未来研究和新的治疗靶点的指导和建议。