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Merck

Ritonavir-induced hepatotoxicity and ultrastructural changes of hepatocytes.

Ultrastructural pathology (2014-08-01)
Chang-Chun Kuang, Ying Wang, Peng-Chao Hu, Fang-Fang Gao, Lang Bu, Xian-Mei Wen, Qing-Ming Xiang, Hui Song, Qun Li, Lei Wei, Ke Li
RESUMEN

To investigate the effect of ritonavir on hepatocyte proliferation, we detected the change of cleaved caspase-3 expression level in the hepatocytes. Furthermore, the morphological and ultrastructural changes of hepatocytes derived from RTV-treated mice have been observed. The results showed that ritonavir can evidently inhibit hepatocyte proliferation and increase cleaved caspase-3 expression level. Under the electron microscope, chromatin margination, mitochondrial cristae disappearance, karyopyknosis and cytoplasmic vacuolization can be observed in the hepatocytes of mice treated with ritonavir. In conclusion, the mechanism of ritonavir's hepatotoxicity is that it induces apoptosis of hepatocytes via the caspase-cascade system.

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Sigma-Aldrich
Azul de tiazolil Bromuro de tetrazolio, 98%
Sigma-Aldrich
Azul de tiazolil Bromuro de tetrazolio, powder, BioReagent, suitable for cell culture, suitable for insect cell culture, ≥97.5% (HPLC)
Sigma-Aldrich
Bicinchoninic acid disodium salt hydrate, ≥98% (HPLC)
Ritonavir, European Pharmacopoeia (EP) Reference Standard