Mitochondrial Toxicity of Tenofovir Dipivoxil Fumarate in HK-2 Cells
Qihui Luo, Junjun Zhao, Xinglei Feng, Zhengli Chen, Wen Zeng, Li Gong, Anchun Cheng, Yubo Shen, Chunmei Zhu
Available Online July 2016.
- https://doi.org/10.2991/bbe-16.2016.43How to use a DOI?
- Tenofovir Dipivoxil Fumarate, Hk-2 Cell, Mitochondrial Respiratory Chain Complex, Mitochondrial DNA, Mitochondrial Toxicity.
- Nucleoside analogs have been shown to have mitochondrial toxicity. In vitro tests can evaluate the mechanisms and severity of the toxicity. Tenofovir dipivoxil fumarate (TDF) is a novel drug for type B hepatitis. In this study, HK-2 cells were used to evaluate the effect of TDF on mitochondrial toxicity in the kidney. HK-2 cells were treated for 9 days in seven treatment groups. This study measured the inhibitory rate of cell proliferation, lactic acid levels, activities of mitochondrial respiratory chain complexes I–III, and mitochondrial DNA content as well as mitochondrial ultrastructure. Results exhibited that rates of cell proliferation, activities of complexes I, III and mitochondrial DNA content were reduced, but lactic acid levels increased in the 125 M TDF group. Mitochondrial ultrastructure was damaged in the 125 M TDF and 62.5 M TDF groups. Thus, the 125 M TDF group exhibited noticeable mitochondrial toxicity, whereas 62.5 M TDF presented weak mitochondrial toxicity, and 31.25 M TDF exhibited no obvious mitochondrial toxicity.
- Open Access
- This is an open access article distributed under the CC BY-NC license.
Cite this article
TY - CONF AU - Qihui Luo AU - Junjun Zhao AU - Xinglei Feng AU - Zhengli Chen AU - Wen Zeng AU - Li Gong AU - Anchun Cheng AU - Yubo Shen AU - Chunmei Zhu PY - 2016/07 DA - 2016/07 TI - Mitochondrial Toxicity of Tenofovir Dipivoxil Fumarate in HK-2 Cells BT - Proceedings of the 2016 International Conference on Biomedical and Biological Engineering PB - Atlantis Press SP - 266 EP - 277 SN - 2468-5747 UR - https://doi.org/10.2991/bbe-16.2016.43 DO - https://doi.org/10.2991/bbe-16.2016.43 ID - Luo2016/07 ER -