Are We Getting Closer to Valid Translational Models for Major Depression?

被引:118
作者
Berton, Olivier [1 ]
Hahn, Chang-Gyu [1 ,2 ]
Thase, Michael E. [2 ]
机构
[1] Univ Penn, Dept Psychiat, Ctr Neurobiol & Behav, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Psychiat, Mood & Anxiety Disorders Treatment & Res Program, Philadelphia, PA 19104 USA
关键词
MEDIAL PREFRONTAL CORTEX; SOCIAL DEFEAT STRESS; ANTIDEPRESSANT RESPONSES; NUCLEUS-ACCUMBENS; COGNITIVE BIAS; ANIMAL-MODELS; BEHAVIOR; SEROTONIN; NEURONS; IDENTIFICATION;
D O I
10.1126/science.1222940
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Advances in characterizing the neuropathology and functional dysconnectivity of depression and promising trials with emerging circuit-targeted and fast-onset therapeutics are providing unprecedented opportunities to gain deeper insight into the neurobiology of this devastating and pervasive disorder. Because of practical and ethical limitations to dissecting these mechanisms in humans, continued progress will critically depend on our ability to emulate aspects of depressive symptomatology and treatment response in nonhuman organisms. Although various experimental models are currently available, they often draw skepticism from both clinicians and basic research scientists. We review recent progress and highlight some of the best leads to diversify and improve discovery end points for preclinical depression research.
引用
收藏
页码:75 / 79
页数:5
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