Generation and characterization of mouse knockout for glyoxalase 1

被引:26
|
作者
Jang, Sumi [1 ]
Kwon, David Min [1 ,2 ]
Kwon, Kyu [1 ,3 ]
Park, Chankyu [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Biol Sci, 291 Daehak Ro, Daejeon 34141, South Korea
[2] City Hope Natl Med Ctr, High Throughput Screening Core, 1500 East Duarte Rd, Duarte, CA 91010 USA
[3] Univ Illinois, Dept Biochem & Mol Genet, MBRB 2318,900 S Ashland Ave, Chicago, IL 60607 USA
基金
新加坡国家研究基金会;
关键词
Methylglyoxal; Glyoxalase; 1; Advanced glycation end products; Anxiety; REGULATE ANXIETY; CARBONYL STRESS; METHYLGLYOXAL; EXPRESSION; GLYCATION; PROTEINS; GLO1;
D O I
10.1016/j.bbrc.2017.06.063
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glyoxalase 1 (Glo1) is the first enzyme involved in glutathione-dependent detoxification of methylglyoxal, eventually generating D-lactate by the second enzyme glyoxalase 2 (Glo2). An accumulation of intracellular glyoxal and methylglyoxal leads to protein malfunction and mutation via formation of the advanced glycation end products (AGEs). Studies on mouse behavior suggest that methylglyoxal has anxiolytic properties. In this report, we generated and characterized a mouse knockout for Glo1. The knockout mice were viable without a pronounced phenotypic defect. Increased level of AGEs in Glo1 knockout mice was detected by immunoblotting with anti-MGH1 in liver homogenate, but not in brain. Alterations in behavior were observed in open field, light-dark transition, and tail suspension test. Open field data indicate increased exploration for novel environment and entry/stay in center zone in Glo1 knockout mice. In addition, increased light-dark transition and immobility was observed in the knockout mice. These data indicate that Glo1 knockout reduces anxiety-like behavior, but increases depression like behavior. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:460 / 465
页数:6
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