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. 2016 Jun 8;311(2):F450–F458. doi: 10.1152/ajprenal.00187.2016

Table 1.

Gene expression of Nox1, Cybb (Nox2), Nox3, Nox4, and Ncf2 (p67phox) in isolated components of the nephron from rats with SS genomic background fed 0.4% and 4% NaCl for 7 days

Nephron Segments
Gene Name mTAL Glo PT OMCD
0.4 % NaCl
Nox4 3.6 ± 0.6 3.0 ± 1.7 210.4 ± 75.5 1.1 ± 0.3
Ncf2 (p67phox) 0.2 ± 0.0 0.8 ± 0.1 0.2 ± 0.1 0.3 ± 0.1
Cybb (Nox2) 3.5 ± 0.3 9.9 ± 0.9 2.6 ± 0.3 3.3 ± 0.4
Nox1 0.7 ± 0.1 0.5 ± 0.0 0.6 ± 0.1 1.1 ± 0.1
Nox3 0.0 ± 0.0 0.0 ± 0.0 0.0 ± 0.0 0.0 ± 0.0
4 % NaCl for 7 days
Nox4 3.0 ± 0.1 3.1 ± 1.2 155.9 ± 52.6 2.0 ± 0.4
Ncf2 (p67phox) 0.5 ± 0.1 0.8 ± 0.1 0.4 ± 0.1 0.3 ± 0.1
Cybb (Nox2) 5.6 ± 0.6 11.1 ± 0.2 6.1 ± 1.0 4.4 ± 0.8
Nox1 0.6 ± 0.0 0.4 ± 0.1 0.7 ± 0.1 1.2 ± 0.1
Nox3 0.0 ± 0.0 0.0 ± 0.0 0.0 ± 0.0 0.0 ± 0.0

Values (means ± SE) are expressed as FPKM (fragments per kilobase of transcript per million mapped reads). Gene expression was determined by RNA-seq in isolated components of the nephron from rats with salt-sensitive (SS) genomic background. Glo, glomerulus; mTAL, medullary thick ascending limb of Henle; OMCD, outer medullary collecting duct; PT, proximal tubule.