Sexually dimorphic prelimbic cortex mechanisms play a role in alcohol dependence: protection by endostatin

• Published in: Neuropsychopharmacology (New York, N.Y.) Vol. 46; no. 11; pp. 1937 - 1949
• Main Authors: Avchalumov, Yosef, Kreisler, Alison D, Xing, Nancy, Shayan, Amin A, Bharadwaj, Tejash, Watson, Jacob R, Sibley, Britta, Somkuwar, Sucharita S, Trenet, Wulfran, Olia, Sumaiya, Piña-Crespo, Juan C, Roberto, Marisa, Mandyam, Chitra D
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 01.10.2021; Springer International Publishing
• Subjects: Adaptation; Alcoholism - drug therapy; Angiogenesis; Angiogenesis inhibitors; Animal models; Animals; Ca2+/calmodulin-dependent protein kinase II; CD31 antigen; Cell adhesion molecules; Cell proliferation; Drinking behavior; Drug dependence; Endostatin; Endostatins; Endothelial Cells; Ethanol; Female; Females; Homeostasis; Male; Males; Microenvironments; NF-κB protein; Phosphorylation; Prefrontal Cortex; Rats; Sexual dimorphism; Sucrose; Synaptic plasticity; Synaptic transmission
• ISSN: 0893-133X; 1740-634X
• DOI: 10.1038/s41386-021-01075-6

Angiogenesis or proliferation of endothelial cells plays a role in brain microenvironment homeostasis. Previously we have shown enhanced expression of markers of angiogenesis in the medial prefrontal cortex during abstinence in an animal model of ethanol dependence induced by chronic intermittent ethanol vapor (CIE) and ethanol drinking (ED) procedure. Here we report that systemic injections of the angiogenesis inhibitor endostatin reduced relapse to drinking behavior in female CIE-ED rats without affecting relapse to drinking in male CIE-ED rats, and female and male nondependent ED rats. Endostatin did not alter relapse to sucrose drinking in both sexes. Endostatin reduced expression of platelet endothelial cell adhesion molecule-1 (PECAM-1) in all groups; however, rescued expression of tight junction protein claudin-5 in the prelimbic cortex (PLC) of female CIE-ED rats. In both sexes, CIE-ED enhanced microglial activation in the PLC and this was selectively prevented by endostatin in female CIE-ED rats. Endostatin prevented CIE-ED-induced enhanced NF-kB activity and expression and Fos expression in females and did not alter reduced Fos expression in males. Analysis of synaptic processes within the PLC revealed sexually dimorphic adaptations, with CIE-ED reducing synaptic transmission and altering synaptic plasticity in the PLC in females, and increasing synaptic transmission in males. Endostatin prevented the neuroadaptations in the PLC in females via enhancing phosphorylation of CaMKII, without affecting the neuroadaptations in males. Our multifaceted approach is the first to link PLC endothelial cell damage to the behavioral, neuroimmune, and synaptic changes associated with relapse to ethanol drinking in female subjects, and provides a new therapeutic strategy to reduce relapse in dependent subjects.