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Abstract

Melanopsin, a photoactive pigment in cells of the inner retina, is one possible agent of sunlight's physiological effects on mood and its absorption spectrum peaks in blue wavelengths, which have been studied in light therapy for seasonal affective disorder.

Abstract

Research in the last century has demonstrated that light is a critical regulator of physiology in animals. More recent research has exposed the influence of light on human behavior, including the phenomenon of seasonal affective disorder (SAD). Repeated studies have shown that light treatment is effective in this disorder. The molecular mechanism by which the body absorbs the light that has energizing and antidepressant effects is still uncertain. This review presents evidence regarding the role of rod and cone photoreceptors, as well as the role of recently discovered nonvisual neuronal melanopsin-containing photoreceptors. The authors discuss an evolutionary-based theoretical model of humoral phototransduction. This model postulates that tetrapyrrole pigments, including hemoglobin and bilirubin, are blood-borne photoreceptors, regulating gasotransmitters such as carbon monoxide when exposed to light in the eye. Recent studies in an animal model for seasonality provide data consistent with this model. Understanding the molecular mechanisms by which light affects physiology may guide the development of therapies for SAD and other pathologies of circadian and circannual regulation.

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Published In

Go to American Journal of Psychiatry
Go to American Journal of Psychiatry
American Journal of Psychiatry
Pages: 1403 - 1412
PubMed: 23929223

History

Received: 25 January 2013
Revision received: 17 May 2013
Accepted: 28 May 2013
Published online: 1 December 2013
Published in print: December 2013

Authors

Details

Dan A. Oren, M.D.
From the Department of Psychiatry, School of Medicine, Yale University, New Haven, Conn.; and the Institute of Applied Biotechnology and Basic Sciences, University of Rzeszów, Rzeszów, Poland.
Marek Koziorowski, D.V.M., Ph.D.
From the Department of Psychiatry, School of Medicine, Yale University, New Haven, Conn.; and the Institute of Applied Biotechnology and Basic Sciences, University of Rzeszów, Rzeszów, Poland.
Paul H. Desan, M.D., Ph.D.
From the Department of Psychiatry, School of Medicine, Yale University, New Haven, Conn.; and the Institute of Applied Biotechnology and Basic Sciences, University of Rzeszów, Rzeszów, Poland.

Notes

Address correspondence to Dr. Oren ([email protected]).

Funding Information

Dr. Oren consulted for 2 hours in 2012 to a light therapy device manufacturer (Litebook Company); he received no financial support contributing to the time or work preparing this article. Dr. Desan has received research support for clinical trials of phototherapy devices for SAD from the Litebook Company in the last 36 months. Dr. Koziorowski has no financial relationship with commercial interests.

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