Maqui berry (Aristotelia chilensis) and the constituent delphinidin glycoside inhibit photoreceptor cell death induced by visible light

• Published in: Food chemistry 2013-08, Vol.139 (1-4), p.129-137
• Main Authors: Tanaka, Junji, Kadekaru, Takashi, Ogawa, Kenjirou, Hitoe, Shoketsu, Shimoda, Hiroshi, Hara, Hideaki
• Format: Article
• Language: English
• Subjects: Anthocyanin; Anthocyanins - pharmacology; Biological and medical sciences; Cell Death - radiation effects; Cell Survival - drug effects; Down-Regulation - radiation effects; Elaeocarpaceae - chemistry; Food industries; Fruit - chemistry; Fruit and vegetable industries; Fundamental and applied biological sciences. Psychology; Glycosides - pharmacology; Humans; Light - adverse effects; Maqui berry extract; Photoreceptor; Photoreceptor Cells - cytology; Photoreceptor Cells - metabolism; Photoreceptor Cells - radiation effects; Plant Extracts - pharmacology; Reactive oxygen species; Reactive Oxygen Species - metabolism
• ISSN: 0308-8146; 1873-7072
• DOI: 10.1016/j.foodchem.2013.01.036

► Maqui berry extract (MBE) contains delphinidin glycosides as major ingredients. ► MBE and its constituent inhibit light-induced photoreceptor cell (661W) death. ► MBE and its constituent inhibit light-induced ROS production in 661W. ► MBE inhibit light-induced phosphorylation of p38 in 661W. ► MBE was much stronger than those of other berry extracts. The protective effects of maqui berry (Aristotelia chilensis) extract (MBE) and its major anthocyanins [delphinidin 3,5-O-diglucoside (D3G5G) and delphinidin 3-O-sambubioside-5-O-glucoside (D3S5G)] against light-induced murine photoreceptor cells (661W) death were evaluated. Viability of 661W after light treatment for 24h, assessed by the tetrazolium salt (WST-8) assay and Hoechst 33342 nuclear staining, was improved by addition of MBE, D3G5G, and D3S5G. Intracellular radical activation in 661W, evaluated using the reactive oxygen species (ROS)-sensitive probe 5-(and-6)-chloromethyl-2,7-dichlorodihydro fluorescein diacetate acetyl ester (CM-H2DCFDA), was reduced by MBE and its anthocyanins. The anti-apoptosis mechanism of MBE was evaluated by light-induced phosphorylation of p38. MBE significantly suppressed the light-induced phosphorylation of p38. These findings indicate that MBE and its anthocyanidins suppress the light-induced photoreceptor cell death by inhibiting ROS production, suggesting that the inhibition of phosphorylated-p38 may be involved in the underlying mechanism.