Direct exposure of non-equilibrium atmospheric pressure plasma confers simultaneous oxidative and ultraviolet modifications in biomolecules

• Published in: Journal of Clinical Biochemistry and Nutrition 2014, Vol.55(3), pp.207-215
• Main Authors: Okazaki, Yasumasa, Wang, Yue, Tanaka, Hiromasa, Mizuno, Masaaki, Nakamura, Kae, Kajiyama, Hiroaki, Kano, Hiroyuki, Uchida, Koji, Kikkawa, Fumitaka, Hori, Masaru, Toyokuni, Shinya
• Format: Article
• Language: English
• Subjects: 8-OHdG; electron spin resonance spin-trapping; HNE-modified protein; non-equilibrium atmospheric pressure plasma; Original
• ISSN: 0912-0009; 1880-5086
• DOI: 10.3164/jcbn.14-40

Thermal plasmas and lasers are used in medicine to cut and ablate tissues and for coagulation. Non-equilibrium atmospheric pressure plasma (NEAPP) is a recently developed, non-thermal technique with possible biomedical applications. Although NEAPP reportedly generates reactive oxygen/nitrogen species, electrons, positive ions, and ultraviolet radiation, little research has been done into the use of this technique for conventional free radical biology. Recently, we developed a NEAPP device with high electron density. Electron spin resonance spin-trapping revealed •OH as a major product. To obtain evidence of NEAPP-induced oxidative modifications in biomolecules and standardize them, we evaluated lipid peroxidation and DNA modifications in various in vitro and ex vivo experiments. Conjugated dienes increased after exposure to linoleic and α-linolenic acids. An increase in 2-thiobarbituric acid-reactive substances was also observed after exposure to phosphatidylcholine, liposomes or liver homogenate. Direct exposure to rat liver in saline produced immunohistochemical evidence of 4-hydroxy-2-nonenal- and acrolein-modified proteins. Exposure to plasmid DNA induced dose-dependent single/double strand breaks and increased the amounts of 8-hydroxy-2'-deoxyguanosine and cyclobutane pyrimidine dimers. These results indicate that oxidative biomolecular damage by NEAPP is dose-dependent and thus can be controlled in a site-specific manner. Simultaneous oxidative and UV-specific DNA damage may be useful in cancer treatment.