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DOI 10.1016/j.jphotobiol.2013.02.005

Медицинская библиотека · Journal of photochemistry and photobiology. B, Biology · 2013

In vitro and in vivo evaluation of inhibition activity of lotus (Nelumbo nucifera Gaertn.) leaves against ultraviolet B-induced phototoxicity.

Huang Bo, Zhu Ling, Liu Song, Li Dong, Chen Yuxin, Ma Bingxin, Wang Youwei

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Lotus (Nelumbo nucifera Gaertn.), an aquatic vegetable, is extensively cultivated in eastern Asia, particularly in China. Our previous study showed that lotus leaf extracts (LLEs) have strong antioxidant effects in vitro and in vivo. The main antioxidants in lotus leaf have been identified via liquid chromatography-mass spectrometry. Ultraviolet B (UVB) protective effects have been associated with plant extracts rich in antioxidants. The current study focuses on the mitochondria model to evaluate the potent inhibition activity of LLE against UVB-induced phototoxicity. The level of thiobarbituric acid reactive substances, glutathione, lipid hydroperoxide, conjugated diene, and 4-hydroxynonenal were measured. The in vivo activity of LLE was also investigated in mice model. The results showed that all concentrations of LLE (10, 100, and 1000μg/ml) possessed strong protective effect against UVB-induced phototoxicity in the mitochondria model. The in vivo test showed that LLE have significant protective effects on the level of superoxide dismutase, catalase, and glutathione peroxidase, as well as the contents of hydroxyproline and malondialdehyde in the skin samples. This study would provide a foundation for broadening the applications of lotus leaf in both the medical and food industries.

Для цитирования: Huang Bo, Zhu Ling, Liu Song, Li Dong, Chen Yuxin, Ma Bingxin, Wang Youwei. In vitro and in vivo evaluation of inhibition activity of lotus (Nelumbo nucifera Gaertn.) leaves against ultraviolet B-induced phototoxicity.. Journal of photochemistry and photobiology. B, Biology. 2013. DOI: 10.1016/j.jphotobiol.2013.02.005.

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