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The molecular mechanisms demonstrated that HKC notably downregulated the protein expression of NADPH oxidase (NOX)-1, NOX-2, NOX-4, -smooth muscle actin (SMA), and the p-extracellular signal-regulated kinase (ERK)1/2 by inhibiting the NADPH oxidase/reactive oxygen species (ROS)/ERK signaling pathways in renal tissue in rats with chronic renal failure induced by adenine in vivo [40]