TY - JOUR
T1 - Integrative physiology of depression and antidepressant drug action
T2 - Implications for serotonergic mechanisms of action and novel therapeutic strategies for treatment of depression
AU - Hale, Matthew W.
AU - Raison, Charles L.
AU - Lowry, Christopher A.
N1 - Funding Information:
We gratefully acknowledge Dr. Kenneth J. Wright for scholarly discussions related to the circadian physiology of thermoregulation and sleep. We also gratefully acknowledge the insightful comments and suggestions from three anonymous reviewers. This work was supported in part by grant no. 0845550 (CAL) from the National Science Foundation . Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the views of the National Science Foundation.
PY - 2013/1
Y1 - 2013/1
N2 - Major depressive disorder (MDD) is predicted to be the second leading cause of disability worldwide by the year 2020. Currently available treatments for MDD are suboptimal. Only 50% of MDD patients recover in less than 12 weeks with adequate treatment, and up to 20% of patients will fail to adequately respond to all currently available interventions. Moreover, current treatments come at the cost of significant central nervous system (CNS) side effects, further highlighting the need for more effective treatments with fewer side effects. A greater mechanistic understanding of MDD and the actions of antidepressant drugs would provide opportunities for development of novel therapeutic approaches to treatment. With this aim in mind, we explore the novel, but empirically supported, hypothesis that an evolutionarily ancient thermoafferent pathway, signaling via the spinoparabrachial pathway from serotonergic sensory cells in the skin and other epithelial linings to serotonergic neurons and depression-related circuits in the brain, is dysfunctional in MDD and that antidepressant therapies, including antidepressant drugs and exercise, act by restoring its function.
AB - Major depressive disorder (MDD) is predicted to be the second leading cause of disability worldwide by the year 2020. Currently available treatments for MDD are suboptimal. Only 50% of MDD patients recover in less than 12 weeks with adequate treatment, and up to 20% of patients will fail to adequately respond to all currently available interventions. Moreover, current treatments come at the cost of significant central nervous system (CNS) side effects, further highlighting the need for more effective treatments with fewer side effects. A greater mechanistic understanding of MDD and the actions of antidepressant drugs would provide opportunities for development of novel therapeutic approaches to treatment. With this aim in mind, we explore the novel, but empirically supported, hypothesis that an evolutionarily ancient thermoafferent pathway, signaling via the spinoparabrachial pathway from serotonergic sensory cells in the skin and other epithelial linings to serotonergic neurons and depression-related circuits in the brain, is dysfunctional in MDD and that antidepressant therapies, including antidepressant drugs and exercise, act by restoring its function.
KW - Antidepressant
KW - Major depression
KW - Selective serotonin reuptake inhibitor
KW - Thermoafferent
KW - Thermoregulation
KW - Thermoregulatory cooling
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U2 - 10.1016/j.pharmthera.2012.09.005
DO - 10.1016/j.pharmthera.2012.09.005
M3 - Review article
C2 - 23017938
AN - SCOPUS:84872360548
SN - 0163-7258
VL - 137
SP - 108
EP - 118
JO - Pharmacology and Therapeutics
JF - Pharmacology and Therapeutics
IS - 1
ER -