(a) Representative images of KIM-1 (n = 5 mice for YO+Veh; n = 7 mice for YO+DQ / 6–10 images per mice) and LTL (n = 5 mice for YO+Veh; n = 7 mice for YO+DQ / 6–8 images per mice) and (b) quantification of KIM-1 positive area (%) and LTL + tubular number as a marker of healthy renal tubules. (c) Measurements of KIM-1 levels and (d) blood urea nitrogen and creatine in serum of YO+Veh (n = 5) and YO+DQ mice (n = 8). (e) Scores of ATN, interstitial inflammation, interstitial fibrosis and tubular atrophy of renal cortex (n = 5 for YO+Veh; n = 6 for YO+DQ). (f) Representative images of Oil red O (n = 5 mice for YO+Veh; n = 7 mice for YO+DQ / 8–15 images per mice), Sirius red (n = 5 mice for YO+Veh; n = 7 mice for YO+DQ; 10–15 images per mice) and Masson’s Trichrom (n = 4 for YO+Veh; n = 5 for YO+DQ; 15–20 images per mice) staining and (g-h) quantification of Oil Red O-positive and fibrotic areas. (i) Quantification of fibrosis-related mRNAs encoding Col1a1, Col3a1, Col4a1, and Col4a2 in the liver (n = 4 for YO+Veh; n = 5 for YO+DQ). Data are means ± s.e.m. of biologically independent samples and each data point represents an individual mouse. A two-tailed t test with a Welch’s correction (b-d), Student’s t test (g-h) with *, P < 0.05; **, P < 0.01, multiple Mann-Whitney tests (e) and multiple t-tests (i) with a two-stage linear step-up procedure of Benjamini, Krieger and Yekutieli, with Q = 5%, *q < 0.05 was used for statistical analysis. Scale bars are shown in each image. Rel, relative.