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Inhibition of Methylglyoxal-Induced AGEs/RAGE Expression Contributes to Dermal Protection by N-Acetyl-L-Cysteine
Author(s) -
Chuntao Yang,
Fuhui Meng,
Li Chen,
Xiang Li,
Laijian Cen,
Yuhua Wen,
Hui Zhang,
Caichen Li
Publication year - 2017
Publication title -
cellular physiology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.486
H-Index - 87
eISSN - 1421-9778
pISSN - 1015-8987
DOI - 10.1159/000458734
Subject(s) - methylglyoxal , glycation , hacat , rage (emotion) , chemistry , reactive oxygen species , glutathione , viability assay , inflammation , pharmacology , matrix metalloproteinase , biochemistry , immunology , medicine , cell , receptor , biology , in vitro , enzyme , neuroscience
Accumulation of advanced glycation end products (AGEs) is a major cause of diabetes mellitus (DM) skin complications. Methylglyoxal (MGO), a reactive dicarbonyl compound, is a crucial intermediate of AGEs generation. N-acetyl-L-cysteine (NAC), an active ingredient of some medicines, can induce endogenous GSH and hydrogen sulfide generation, and set off a condensation reaction with MGO. However, there is rare evidence to show NAC can alleviate DM-induced skin injury through inhibition of AGEs generation or toxicity. The present study aimed to observe the effects of NAC on MGO-induced inflammatory injury and investigate the roles of AGEs and its receptor (RAGE) in NAC's dermal protection in human HaCaT keratinocytes.

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