ANIMAL MODELS OF BIPOLAR MANIA: THE PAST, PRESENT AND FUTURE

被引:89
|
作者
Logan, R. W. [1 ]
McClung, C. A. [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Psychiat, 450 Technol Dr,Suite 223, Pittsburgh, PA 15219 USA
关键词
bipolar disorder; animal models; mania; circadian rhythms; genetics; mood stabilizers; GLYCOGEN-SYNTHASE KINASE-3; SOCIAL RHYTHM THERAPY; GLUTATHIONE-DEFICIENT MICE; GENETIC MOUSE MODEL; IOWA GAMBLING TASK; PREFRONTAL CORTEX; SLEEP-DEPRIVATION; BETA-CATENIN; DECISION-MAKING; DOUBLE-BLIND;
D O I
10.1016/j.neuroscience.2015.08.041
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Bipolar disorder (BD) is the sixth leading cause of disability in the world according to the World Health Organization and affects nearly six million (similar to 2.5% of the population) adults in the United State alone each year. BD is primarily characterized by mood cycling of depressive (e.g., helplessness, reduced energy and activity, and anhedonia) and manic (e.g., increased energy and hyperactivity, reduced need for sleep, impulsivity, reduced anxiety and depression), episodes. The following review describes several animal models of bipolar mania with a focus on more recent findings using genetically modified mice, including several with the potential of investigating the mechanisms underlying 'mood' cycling (or behavioral switching in rodents). We discuss whether each of these models satisfy criteria of validity (i.e., face, predictive, and construct), while highlighting their strengths and limitations. Animal models are helping to address critical questions related to pathophysiology of bipolar mania, in an effort to more clearly define necessary targets of first-line medications, lithium and valproic acid, and to discover novel mechanisms with the hope of developing more effective therapeutics. Future studies will leverage new technologies and strategies for integrating animal and human data to reveal important insights into the etiology, pathophysiology, and treatment of BD. This article is part of a Special Issue entitled: Neuropsychiatric Disease. (C) 2015 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:163 / 188
页数:26
相关论文
共 50 条
  • [1] Animal models of tendon calcification: Past, present, and future
    Li, Ruichen
    Lai, Canhao
    Luo, Hong
    Lan, Yujian
    Duan, Xinfang
    Bao, Dingsu
    Hou, Zhipeng
    Liu, Huan
    Fu, Shijie
    [J]. ANIMAL MODELS AND EXPERIMENTAL MEDICINE, 2024, 7 (04) : 471 - 483
  • [2] Animal models of tendon calcification:Past, present, and future
    Ruichen Li
    Canhao Lai
    Hong Luo
    Yujian Lan
    Xinfang Duan
    Dingsu Bao
    Zhipeng Hou
    Huan Liu
    Shijie Fu
    [J]. Animal Models and Experimental Medicine., 2024, 7 (04) - 483
  • [3] Animal models of lupus nephritis: the past, present and a future outlook
    Katikaneni, Divya
    Morel, Laurence
    Scindia, Yogesh
    [J]. AUTOIMMUNITY, 2024, 57 (01)
  • [4] Animal models of narcolepsy and the hypocretin/orexin system: Past, present, and future
    Tisdale, Ryan K.
    Yamanaka, Akihiro
    Kilduff, Thomas S.
    [J]. SLEEP, 2021, 44 (06) : 1 - 15
  • [5] Animal Models of Vestibular Evoked Myogenic Potentials: The Past, Present, and Future
    Corneil, Brian D.
    Camp, Aaron J.
    [J]. FRONTIERS IN NEUROLOGY, 2018, 9
  • [6] Animal foraging: past, present and future
    Perry, G
    Pianka, ER
    [J]. TRENDS IN ECOLOGY & EVOLUTION, 1997, 12 (09) : 360 - 364
  • [7] Animal behavior: past, present and future
    Ruebnstein, Dustin R.
    [J]. INTEGRATIVE AND COMPARATIVE BIOLOGY, 2016, 56 : E191 - E191
  • [8] ANIMAL MEMORY - PAST, PRESENT AND FUTURE
    MACPHAIL, EM
    [J]. QUARTERLY JOURNAL OF EXPERIMENTAL PSYCHOLOGY SECTION B-COMPARATIVE AND PHYSIOLOGICAL PSYCHOLOGY, 1986, 38 (04): : 349 - 364
  • [9] Inflammatory bowel disease, past, present and future: lessons from animal models
    Atsushi Mizoguchi
    Emiko Mizoguchi
    [J]. Journal of Gastroenterology, 2008, 43 : 1 - 17
  • [10] Inflammatory bowel disease, past, present and future: lessons from animal models
    Mizoguchi, Atsushi
    Mizoguch, Emiko
    [J]. JOURNAL OF GASTROENTEROLOGY, 2008, 43 (01) : 1 - 17