| Literature DB >> 33448693 |
Takeo Ishii1,2, Tomohiro Kumagae1,3, Hiromichi Wakui1, Shingo Urate1, Shohei Tanaka1, Eriko Abe1, Toru Suzuki1, Takahiro Yamaji1, Sho Kinguchi1, Ryu Kobayashi1, Kotaro Haruhara1, Takashi Nakamura4, Shuzo Kobayashi1,3, Kouichi Tamura1.
Abstract
Xanthine oxidoreductase (XOR) is a critical enzyme in purine metabolism and uric acid production, and its levels are reported to increase during stress, thereby promoting organ damage. Herein, we investigated the activity of XOR in a mouse model of aristolochic acid I (AA)-induced nephropathy, a type of nephrotoxic chronic kidney disease (CKD). A persistent decrease in renal function was observed in mice up to 4 weeks after 4 weeks of AA (2.5 mg kg-1 ) administration. Renal histology revealed an increase in tubular interstitial fibrosis over time. Although AA administration did not change XOR activity in the plasma, heart, liver, or muscle, XOR activity was persistently increased in renal tissue. Our results suggest that the renal tissue-specific increase in XOR activity is involved in the progression of tubulo-interstitial disorders, specifically fibrosis.Entities:
Keywords: aristolochic acid; mouse model; nephropathy; xanthine oxidoreductase
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Year: 2021 PMID: 33448693 PMCID: PMC7876505 DOI: 10.1002/2211-5463.13083
Source DB: PubMed Journal: FEBS Open Bio ISSN: 2211-5463 Impact factor: 2.792