作者
Pin-I Chen, Aiqin Cao, Kazuya Miyagawa, Nancy F Tojais, Jan K Hennigs, Caiyun G Li, Nathaly M Sweeney, Audrey S Inglis, Lingli Wang, Dan Li, Matthew Ye, Brian J Feldman, Marlene Rabinovitch
发表日期
2017/1/26
期刊
JCI insight
卷号
2
期号
2
出版商
American Society for Clinical Investigation
简介
Amphetamine (AMPH) or methamphetamine (METH) abuse can cause oxidative damage and is a risk factor for diseases including pulmonary arterial hypertension (PAH). Pulmonary artery endothelial cells (PAECs) from AMPH-associated-PAH patients show DNA damage as judged by γH2AX foci and DNA comet tails. We therefore hypothesized that AMPH induces DNA damage and vascular pathology by interfering with normal adaptation to an environmental perturbation causing oxidative stress. Consistent with this, we found that AMPH alone does not cause DNA damage in normoxic PAECs, but greatly amplifies DNA damage in hypoxic PAECs. The mechanism involves AMPH activation of protein phosphatase 2A, which potentiates inhibition of Akt. This increases sirtuin 1, causing deacetylation and degradation of HIF1α, thereby impairing its transcriptional activity, resulting in a reduction in pyruvate …
引用总数
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