Nitroglycerin induces DNA damage and vascular cell death in the setting of nitrate tolerance.

Abstract:

:Nitroglycerin (GTN) and other organic nitrates are widely used vasodilators. Their side effects are development of nitrate tolerance and endothelial dysfunction. Given the potential of GTN to induce nitro-oxidative stress, we investigated the interaction between nitro-oxidative DNA damage and vascular dysfunction in experimental nitrate tolerance. Cultured endothelial hybridoma cells (EA.hy 926) and Wistar rats were treated with GTN (ex vivo: 10-1000 µM; in vivo: 10, 20 and 50 mg/kg/day for 3 days, s.c.). The level of DNA strand breaks, 8-oxoguanine and O (6)-methylguanine DNA adducts was determined by Comet assay, dot blot and immunohistochemistry. Vascular function was determined by isometric tension recording. DNA adducts and strand breaks were induced by GTN in cells in vitro in a concentration-dependent manner. GTN in vivo administration leads to endothelial dysfunction, nitrate tolerance, aortic and cardiac oxidative stress, formation of DNA adducts, stabilization of p53 and apoptotic death of vascular cells in a dose-dependent fashion. Mice lacking O (6)-methylguanine-DNA methyltransferase displayed more vascular O (6)-methylguanine adducts and oxidative stress under GTN therapy than wild-type mice. Although we were not able to prove a causal role of DNA damage in the etiology of nitrate tolerance, the finding of GTN-induced DNA damage such as the mutagenic and toxic adduct O (6)-methylguanine, and cell death supports the notion that GTN based therapy may provoke adverse side effects, including endothelial function. Further studies are warranted to clarify whether GTN pro-apoptotic effects are related to an impaired recovery of patients upon myocardial infarction.

journal_name

Basic Res Cardiol

authors

Mikhed Y,Fahrer J,Oelze M,Kröller-Schön S,Steven S,Welschof P,Zinßius E,Stamm P,Kashani F,Roohani S,Kress JM,Ullmann E,Tran LP,Schulz E,Epe B,Kaina B,Münzel T,Daiber A

doi

10.1007/s00395-016-0571-4

subject

Has Abstract

pub_date

2016-07-01 00:00:00

pages

52

issue

4

eissn

0300-8428

issn

1435-1803

pii

10.1007/s00395-016-0571-4

journal_volume

111

pub_type

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