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Rosiglitazone restores nitric oxide synthase‐dependent reactivity of cerebral arterioles in rats exposed to prenatal alcohol

Authors :
Hong Zheng
Partha S. Saha
Kirsten R. Kim Sawtelle
Jamie L. Scholl
William G. Mayhan
Denise M. Arrick
Brittany N. Bamberg
Michael J. Watt
Source :
Alcoholism: Clinical and Experimental Research. 45:1359-1369
Publication Year :
2021
Publisher :
Wiley, 2021.

Abstract

BACKGROUND Prenatal exposure to alcohol leads to a greater incidence of many cardiovascular-related diseases, presumably via a mechanism that may involve increased oxidative stress. An agonist of peroxisome proliferator-activated receptor gamma (PPARγ; rosiglitazone) has been shown to suppress alcohol-induced neuroinflammation and oxidative stress. The goal of this study was to determine whether acute and chronic treatment with rosiglitazone could restore or prevent impaired nitric oxide synthase (NOS)-dependent responses of cerebral arterioles in male and female adult (14-16 weeks old) rats exposed to alcohol in utero. METHODS We fed Sprague-Dawley dams a liquid diet with or without 3% ethanol for the duration of their pregnancy (21-23 days). In the first series of studies, we examined the reactivity of cerebral arterioles to eNOS- (ADP), nNOS-dependent (NMDA), and NOS-independent agonists in male and female adult rats before and during acute (1 hour) topical application of rosiglitazone (1 µM). In a second series of studies, we examined the influence of chronic treatment with rosiglitazone (3 mg/kg/day in drinking water for 2-3 weeks) on the responses of cerebral arterioles in male and female adult rats exposed to alcohol in utero. RESULTS We found that in utero exposure to alcohol similarly reduced responses of cerebral arterioles to ADP and NMDA, but not to nitroglycerin in male and female adult rats. In addition, acute treatment of the male and female adult rats with rosiglitazone similarly restored this impairment in cerebral vascular function to that observed in controls. We also found that chronic treatment with rosiglitazone prevented impaired vascular function in male and female adult rats that were exposed to alcohol in utero. CONCLUSIONS PPARγ activation may be an effective and relevant treatment to reverse or prevent cerebral vascular abnormalities associated with prenatal exposure to alcohol.

Details

ISSN :
15300277 and 01456008
Volume :
45
Database :
OpenAIRE
Journal :
Alcoholism: Clinical and Experimental Research
Accession number :
edsair.doi.dedup.....1f60871ba5e8bbe5eb1ee746d4cf4ea8
Full Text :
https://doi.org/10.1111/acer.14634