The double edged sword of neural plasticity: Increasing serotonin levels leads to both greater vulnerability to depression and improved capacity to recover

被引:120
作者
Branchi, Igor [1 ]
机构
[1] Ist Super Sanita, Dept Cell Biol & Neurosci, Sect Behav Neurosci, I-00161 Rome, Italy
关键词
Biological sensitivity to context; Antidepressant; Adaptive phenotypic plasticity; SSRI; SSRE; Mood disorder; Environment; 5-HTTLPR; Serotonin transporter; Major depression; SUBGENUAL PREFRONTAL CORTEX; GENE POLYMORPHISM 5-HTTLPR; NEUROTROPHIC FACTOR BDNF; STRESSFUL LIFE EVENTS; BIOLOGICAL SENSITIVITY; REUPTAKE INHIBITORS; HIPPOCAMPAL VOLUME; ENVIRONMENT INTERACTIONS; ANTIDEPRESSANT TREATMENT; NEURONAL PLASTICITY;
D O I
10.1016/j.psyneuen.2010.08.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Major depression is a chronic, recurring and potentially life-threatening illness that affects up to 10% of the population worldwide. Pharmacological and genetic studies highlight the serotonergic system as being a key player in the disorder. However, despite drugs designed to boost serotonin transmission represent the first line of therapy for depression, the role of this system still remains elusive. Here, I propose a new theoretical framework, the undirected susceptibility to change model, potentially accounting for the experimental and clinical results concerning the role of this neurotransmitter in depression. Since the capacity of the individual to change its physiology and behavior according to the environment is dependent on neural plasticity which, in turn, is controlled by serotonin, I assume that changes in the levels of serotonin affect the sensitivity to the environment. Consequently, the undirected susceptibility to change model predicts that an increase of serotonin levels, for instance induced through selective serotonin reuptake inhibitor (SSRI) administration, does not affect mood per se, but - acting as a catalyzer - enhances neural plasticity and, thus, the effects of the environment on mood. However, since the environment can be either supportive or adverse, its effects can be beneficial or detrimental. Therefore enhancing the serotonin system can increase the likelihood both of developing the psychopathology and recovering from it. This model, on the one hand, suggests an explanation for the limited SSRI efficacy described in clinical studies and allows apparently contradictory data to be reconciled; on the other, it describes neural plasticity as a double edged sword that, according to the quality of the environment, may have either positive or negative consequences. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:339 / 351
页数:13
相关论文
共 133 条
[1]   Regulation of hippocampal gene expression is conserved in two species subjected to different stressors and antidepressant treatments [J].
Alfonso, J ;
Frick, LR ;
Silberman, DM ;
Palumbo, ML ;
Genaro, AM ;
Frasch, AC .
BIOLOGICAL PSYCHIATRY, 2006, 59 (03) :244-251
[2]  
[Anonymous], ANIMAL PERSONALITIES
[3]   Serotonin Mediates Behavioral Gregarization Underlying Swarm Formation in Desert Locusts [J].
Anstey, Michael L. ;
Rogers, Stephen M. ;
Ott, Swidbert R. ;
Burrows, Malcolm ;
Simpson, Stephen J. .
SCIENCE, 2009, 323 (5914) :627-630
[4]  
Azmitia EC, 1999, NEUROPSYCHOPHARMACOL, V21, pS33
[5]   Costs of disorders of the brain in Europe [J].
Balak, N. ;
Elmaci, I. .
EUROPEAN JOURNAL OF NEUROLOGY, 2007, 14 (02) :E9-E9
[6]   Selective serotonin reuptake inhibitors and risk of suicide: a systematic review of observational studies [J].
Barbui, Corrado ;
Esposito, Eleonora ;
Cipriani, Andrea .
CANADIAN MEDICAL ASSOCIATION JOURNAL, 2009, 180 (03) :291-297
[7]   The utility of the non-human primate model for studying gene by environment interactions in behavioral research [J].
Barr, CS ;
Newman, TK ;
Becker, ML ;
Parker, CC ;
Champoux, M ;
Lesch, KP ;
Goldman, D ;
Suomi, SJ ;
Higley, JD .
GENES BRAIN AND BEHAVIOR, 2003, 2 (06) :336-340
[8]  
Belmaker RH, 2008, NEW ENGL J MED, V358, P55, DOI [10.1056/NEJMra073096, 10.1038/nrdp.2016.65]
[9]   Vulnerability genes or plasticity genes? [J].
Belsky, J. ;
Jonassaint, C. ;
Pluess, M. ;
Stanton, M. ;
Brummett, B. ;
Williams, R. .
MOLECULAR PSYCHIATRY, 2009, 14 (08) :746-754
[10]  
Belsky J., 2005, ORIGINS SOCIAL MIND, P139