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Volume 82, Issue 2, Pages 111-119 (February 2010)


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Age-related changes of n-3 and n-6 polyunsaturated fatty acids in the anterior cingulate cortex of individuals with major depressive disorder

Sarah M. Conklinab, Caroline A. Runyanc, Sherry Leonardd, Ravinder D. Reddyae, Matthew F. Muldoonaf, Jeffrey K. YaoaegCorresponding Author Informationemail address

Received 9 September 2009; accepted 4 December 2009. published online 08 January 2010.

Abstract 

Accumulating evidence finds a relative deficiency of peripheral membrane fatty acids in persons with affective disorders such as unipolar and bipolar depression. Here we sought to investigate whether postmortem brain fatty acids within the anterior cingulate cortex (BA-24) varied according to the presence of major depression at the time of death. Using capillary gas chromatography we measured fatty acids in a depressed group (n=12), and in a control group without lifetime history of psychiatric diagnosis (n=14). Compared to the control group, the depressed group showed significantly lower concentrations of numerous saturated and polyunsaturated fatty acids including both the n-3 and n-6 fatty acids. Additionally, significant correlations between age at death and precursor (or metabolites) in the n-3 fatty acid pathway were demonstrated in the depressed group but not in control subjects. In the n-6 fatty acid family, the ratio of 20:3(n-6)/18:2(n-6) was higher in patients than in control groups, whereas the ratio of 20:4(n-6)/20:3(n-6) was relatively decreased in patients. Lastly, a significant negative correlation between age and the ratio of 20:4(n-6) to 22:6(n-3) was found in patients, but not in controls. Taken together, decreases in 22:6(n-3) may be caused, at least in part, by the diminished formation of 20:5(n-3), which is derived from 20:4(n-3) through a Δ5 desaturase reaction. The present findings from postmortem brain tissue raise the possibility that an increased ratio of 20:4(n-6) to 22:6(n-3) may provide us with a biomarker for depression. Future research should further investigate these relationships.

a Medical Research Service, VA Pittsburgh Healthcare System, Pittsburgh, PA, USA

b Neuroscience Program and Department of Psychology, Allegheny College, Meadville, PA, USA

c Picower Institute for Learning and Memory, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, USA

d Denver VA Medical Center, and Departments of Psychiatry and Pharmacology, University of Colorado Health Sciences Center, Denver, CO, USA

e Department of Psychiatry, University of Pittsburgh Medical Center, Pittsburgh, PA, USA

f Center for Clinical Pharmacology, University of Pittsburgh, School of Medicine, Pittsburgh, PA, USA

g Department of Pharmaceutical Sciences, University of Pittsburgh School of Pharmacy, Pittsburgh, PA, USA

Corresponding Author InformationCorresponding author: Tel.: +14129545787; fax: +14129545786

PII: S0952-3278(09)00205-1

doi:10.1016/j.plefa.2009.12.002


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