Necessity of Hippocampal Neurogenesis for the Therapeutic Action of Antidepressants in Adult Nonhuman Primates

被引:186
作者
Perera, Tarique D. [1 ,2 ]
Dwork, Andrew J. [1 ,2 ,6 ]
Keegan, Kathryn A. [1 ,2 ]
Thirumangalakudi, Lakshmi [1 ,2 ]
Lipira, Cecilia M. [1 ,2 ]
Joyce, Niamh [1 ,2 ]
Lange, Christopher [3 ]
Higley, J. Dee [5 ]
Rosoklija, Gorazd [1 ,2 ,6 ,7 ]
Hen, Rene [1 ,2 ]
Sackeim, Harold A. [1 ,2 ]
Coplan, Jeremy D. [4 ]
机构
[1] Columbia Univ, Dept Psychiat, Coll Phys & Surg, Med Ctr, New York, NY 10027 USA
[2] New York State Psychiat Inst & Hosp, New York, NY 10032 USA
[3] SUNY Brooklyn, Dept Radiol, Brooklyn, NY USA
[4] SUNY Brooklyn, Dept Psychiat, Brooklyn, NY USA
[5] Brigham Young Univ, Provo, UT 84602 USA
[6] Columbia Univ, Dept Pathol & Cell Biol, Coll Phys & Surg, Med Ctr, New York, NY USA
[7] Macedonian Acad Sci & Arts, Skopje, Macedonia
来源
PLOS ONE | 2011年 / 6卷 / 04期
关键词
NEWLY GENERATED NEURONS; CHRONIC MILD STRESS; RAT DENTATE GYRUS; CHRONIC FLUOXETINE; RHESUS-MONKEYS; SYNAPTIC PLASTICITY; CELL-PROLIFERATION; DECLARATIVE MEMORY; MACAQUE MONKEYS; GRANULE CELLS;
D O I
10.1371/journal.pone.0017600
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
Background: Rodent studies show that neurogenesis is necessary for mediating the salutary effects of antidepressants. Nonhuman primate (NHP) studies may bridge important rodent findings to the clinical realm since NHP-depression shares significant homology with human depression and kinetics of primate neurogenesis differ from those in rodents. After demonstrating that antidepressants can stimulate neurogenesis in NHPs, our present study examines whether neurogenesis is required for antidepressant efficacy in NHPs. Materials/Methodology: Adult female bonnets were randomized to three social pens (N = 6 each). Pen-1 subjects were exposed to control-conditions for 15 weeks with half receiving the antidepressant fluoxetine and the rest receiving saline-placebo. Pen-2 subjects were exposed to 15 weeks of separation-stress with half receiving fluoxetine and half receiving placebo. Pen-3 subjects 2 weeks of irradiation (N = 4) or sham-irradiation (N = 2) and then exposed to 15 weeks of stress and fluoxetine. Dependent measures were weekly behavioral observations and postmortem neurogenesis levels. Results: Exposing NHPs to repeated separation stress resulted in depression-like behaviors (anhedonia and subordinance) accompanied by reduced hippocampal neurogenesis. Treatment with fluoxetine stimulated neurogenesis and prevented the emergence of depression-like behaviors. Ablation of neurogenesis with irradiation abolished the therapeutic effects of fluoxetine. Non-stressed controls had normative behaviors although the fluoxetine-treated controls had higher neurogenesis rates. Across all groups, depression-like behaviors were associated with decreased rates of neurogenesis but this inverse correlation was only significant for new neurons in the anterior dentate gyrus that were at the threshold of completing maturation. Conclusion: We provide evidence that induction of neurogenesis is integral to the therapeutic effects of fluoxetine in NHPs. Given the similarity between monkeys and humans, hippocampal neurogenesis likely plays a similar role in the treatment of clinical depression. Future studies will examine several outstanding questions such as whether neuro-suppression is sufficient for producing depression and whether therapeutic neuroplastic effects of fluoxetine are specific to antidepressants.
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页数:13
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