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. 2015 Feb;352(2):346–357. doi: 10.1124/jpet.114.221085

Fig. 3.

Fig. 3.

Disruption of mitochondrial homeostasis in endotoxic AKI. Total RNA and DNA were harvested from renal cortical tissue of mice treated with saline vehicle or LPS (10 mg/kg i.p.) at 1, 3, 18, and 42 hours. (A) Expression of key regulators of mitochondrial biogenesis (NRF-1, TFAM), nuclear-encoded components of the electron transport chain (NDUFS1, NDUFB8, ATPSβ), and mitochondrial-encoded respiratory proteins (COX1, ND1) were measured at the mRNA level (n = 6/group). (B) Relative mitochondrial DNA content in the renal cortex was determined by qRT-PCR analysis (n = 5–6 animals/group). Data are shown as expression relative to vehicle-treated animals (mean ± S.E.M.). *P < 0.05 versus time point controls.