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ABSTRACT: Background
Increased gene transcription of hypoxia-induced mediators of fibrosis in renal tissue has been identified in experimentally induced, ischemic chronic kidney disease (CKD).Objective
To characterize hypoxia-induced profibrotic pathways in naturally occurring CKD in cats.Animals
Twelve client-owned cats with CKD and 8 healthy control cats.Methods
In this prospective, cross-sectional study, bilateral renal tissue samples were assessed histologically for inflammation, tubular atrophy, and fibrosis, and by reverse transcription-quantitative PCR for characterization of transcript levels of hypoxia-inducible factor-1α (HIF1A), matrix metalloproteinases-2 (MMP2), -7 (MMP7), and -9 (MMP9), tissue inhibitor of metalloproteinase-1 (TIMP1), transforming growth
SUBMITTER: Lourenco BN
PROVIDER: S-EPMC7379026 | biostudies-literature | 2020 Jul
REPOSITORIES: biostudies-literature