099 Aspirin protects against UVB-induced DNA damage through activation of AMP kinase
نویسندگان
چکیده
The anti-inflammatory and chemopreventive activities of aspirin (ASA) may be mediated through its cyclooxygenase (COX) inhibitor function. We have previously shown that ASA can protect against ultraviolet (UV) radiation-induced skin inflammation DNA damage, but the role in UV-induced damage mechanism underlying protection are poorly characterized. Using immunodeficient NSG mice immunocompetent C57BL/6 treated with immune cell-depleting antibodies, we found was not required for UVB-induced 8-oxoguanine (8-OG) cyclobutane pyrimidine dimers (CPD) vivo. Unlike ASA, neither immediate metabolite salicylate nor COX indomethacin reduced 8-OG or CPD melanocyte Melan-a keratinocyte HaCat cells vitro. Moreover, addition prostaglandin-E2 (PGE2) did reverse protective effect on UVB-treated cells. Phosphorylation 5' AMP-activated protein kinase (AMPK), observed ASA-treated cells, could blocked by AMPK Compound C (Comp C). Cells Comp C, however, were protected damage. Finally, injection partially reversed mouse These studies suggest confers activation rather than inhibition.
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ژورنال
عنوان ژورنال: Journal of Investigative Dermatology
سال: 2022
ISSN: ['1523-1747', '0022-202X']
DOI: https://doi.org/10.1016/j.jid.2022.05.034