Elevated DNA Oxidation and DNA Repair Enzyme Expression in Brain White Matter in Major Depressive Disorder

Autor: Katherine C. Burgess, Attila Szebeni, Russell W. Brown, Craig A. Stockmeier, Katalin Szebeni, Michelle J. Chandley, T. DiPeri, Luke A. Johnson, Jessica D. Crawford, Gregory A. Ordway, Liza J. Hernandez
Rok vydání: 2016
Předmět:
Male
Poly (ADP-Ribose) Polymerase-1
medicine.disease_cause
DNA Glycosylases
Rats
Sprague-Dawley

0302 clinical medicine
PARP1
oxidative stress
Pharmacology (medical)
Aged
80 and over

messenger RNA
Base excision repair
Middle Aged
White Matter
3. Good health
Oligodendroglia
anhedonia
Psychiatry and Mental health
medicine.anatomical_structure
8-Hydroxy-2'-Deoxyguanosine
Female
medicine.symptom
Adult
medicine.medical_specialty
Adolescent
DNA repair
Uncinate fasciculus
Biology
behavioral disciplines and activities
Gene Expression Regulation
Enzymologic

White matter
Young Adult
03 medical and health sciences
Internal medicine
medicine
Animals
Humans
Interpersonal Relations
Regular Research Article
Aged
Pharmacology
Depressive Disorder
Major

Deoxyguanosine
Anhedonia
DNA
DNA oxidation
Molecular biology
Rats
030227 psychiatry
Disease Models
Animal

Endocrinology
Astrocytes
Schizophrenia
oligodendrocyte
030217 neurology & neurosurgery
Oxidative stress
Zdroj: International Journal of Neuropsychopharmacology
ISSN: 1469-5111
1461-1457
DOI: 10.1093/ijnp/pyw114
Popis: Background: Pathology of white matter in brains of patients with major depressive disorder (MDD) is well-documented, but the cellular and molecular basis of this pathology are poorly understood. Methods: Levels of DNA oxidation and gene expression of DNA damage repair enzymes were measured in Brodmann area 10 (BA10) and/or amygdala (uncinate fasciculus) white matter tissue from brains of MDD (n=10) and psychiatrically normal control donors (n=13). DNA oxidation was also measured in BA10 white matter of schizophrenia donors (n=10) and in prefrontal cortical white matter from control rats (n=8) and rats with repeated stress-induced anhedonia (n=8). Results: DNA oxidation in BA10 white matter was robustly elevated in MDD as compared to control donors, with a smaller elevation occurring in schizophrenia donors. DNA oxidation levels in psychiatrically affected donors that died by suicide did not significantly differ from DNA oxidation levels in psychiatrically affected donors dying by other causes (non-suicide). Gene expression levels of two base excision repair enzymes, PARP1 and OGG1, were robustly elevated in oligodendrocytes laser captured from BA10 and amygdala white matter of MDD donors, with smaller but significant elevations of these gene expressions in astrocytes. In rats, repeated stress-induced anhedonia, as measured by a reduction in sucrose preference, was associated with increased DNA oxidation in white, but not gray, matter. Conclusions: Cellular residents of brain white matter demonstrate markers of oxidative damage in MDD. Medications that interfere with oxidative damage or pathways activated by oxidative damage have potential to improve treatment for MDD.
Databáze: OpenAIRE