Mechanism of cytotoxicity of catechols and a naphthalenediol in PC12-AC cells: The connection between extracellular autoxidation and molecular electronic structure
ortho-Hydroxyphenols (catechols) form a common structural unit in naturally occurring antioxidants such as polyphenols. They also show pro-oxidant characteristics which depend on their particular structure. Here we examined the acetylated versions of three catechols and a naphthalenediol for cytotoxicity to adrenal PC12-AC cells. We found that the three catechols H1 (a p-methoxycatechol), H2 (a catechol analog of α-tocopherol), and H4 (a dioxymethylene-substituted catechol) strongly upregulate glutathione (GSH) in 24 h, whereas 1,4-dipropyl-2,3-naphthalenediol (DPND) does not. Upregulation of GSH is primarily caused by oxidative stress in the form of hydrogen peroxide generation, and both GSH upregulation and the rate of H 2O 2 generation correlate well with the cytotoxicity. The major source of H 2O 2 is autoxidation in the extracellular space, which results from transport of the (deacetylated) hydroquinone form outside the cell, rather than internal redox cycling. DPND is much less cytotoxic than any of the catechols. We show that this is because it cannot form a naphthoquinone due to the energy penalty associated with the loss of aromaticity in the benzene ring adjacent to the diol functional group. The relevance of these results to the design of antioxidants is discussed.
|Keywords||Autoxidation, Bond dissociation enthalpy, Catechol cytotoxicity, Free radicals, GSH upregulation, PC12 adrenal pheochromocytoma cells, Quinone redox cycling|
|Journal||Free Radical Biology and Medicine|
Chichirau, A. (Alexandru), Flueraru, M. (Mihaela), Chepelev, L.L. (Leonid L.), Wright, J.S, Willmore, W, Durst, T. (Tony), … Charron, M. (Martin). (2005). Mechanism of cytotoxicity of catechols and a naphthalenediol in PC12-AC cells: The connection between extracellular autoxidation and molecular electronic structure. Free Radical Biology and Medicine, 38(3), 344–355. doi:10.1016/j.freeradbiomed.2004.10.035