Xanthohumol induces generation of reactive oxygen species and triggers apoptosis through inhibition of mitochondrial electron transfer chain complex I

• Published in: Free radical biology & medicine Vol. 89; pp. 486 - 497
• Main Authors: Zhang, Bo, Chu, Wei, Wei, Peng, Liu, Ying, Wei, Taotao
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.12.2015
• Subjects: Antineoplastic Agents - pharmacology; Apoptosis - drug effects; Blotting, Western; Cell Line, Tumor; Cell Survival - drug effects; Complex I; Electron Transport Complex I - drug effects; Flavonoids - pharmacology; Flow Cytometry; Humans; Membrane Potential, Mitochondrial - drug effects; Mitochondria; Neoplasms - metabolism; Oxidative Phosphorylation; Propiophenones - pharmacology; Reactive Oxygen Species; Reactive Oxygen Species - metabolism; Xanthohumol; Mito-CP; Reactive Oxygen Species; Xanthohumol; α-TOS; OXPHOS; FCCP; H2DCFDA; TMPD; GPDH; G-3-P; α-TEA; DMEM; Mitochondria; TMRM; WST-8; SDH; Mito-Q; CCK-8; AA; NBT; DCA; BN-PAGE; TCA cycle; Oxidative Phosphorylation; 2-DG; 8-PN; Complex I; MitoVES; ECAR; NAD; MMP; NAC; ETC; Rot; XN; ROS; PI; BNG; IXN; OCR; Oligo
• ISSN: 0891-5849; 1873-4596
• DOI: 10.1016/j.freeradbiomed.2015.09.021

Xanthohumol is a prenylflavonoid extracted from hops (Humulus lupulus). It possesses anti-cancer and anti-inflammatory activities in vitro and in vivo, and offers therapeutic benefits for treatment of metabolic syndromes. However, the precise mechanisms underlying its pharmacological effects remain to be elucidated, together with its cellular target. Here, we provide evidence that xanthohumol directly interacts with the mitochondrial electron transfer chain complex I (NADH dehydrogenase), inhibits the oxidative phosphorylation, triggers the production of reactive oxygen species, and induces apoptosis. In addition, we show that as a result of the inhibition of the mitochondrial oxidative phosphorylation, xanthohumol exposure causes a rapid decrease of mitochondrial transmembrane potential. Furthermore, we showed that xanthohumol up-regulates the glycolytic capacity in cells, and thus compensates cellular ATP generation. Dissection of the multiple steps of aerobic respiration by extracellular flux assays revealed that xanthohumol specifically inhibits the activity of mitochondrial complex I, but had little effect on that of complex II, III and IV. Inhibition of complex I by xanthohumol caused the overproduction of reactive oxygen species, which are responsible for the induction of apoptosis in cancer cells. We also found that isoxanthohumol, the structural isomer of xanthohumol, is inactive to cells, suggesting that the reactive 2-hydroxyl group of xanthohumol is crucial for its targeting to the mitochondrial complex I. Together, the remodeling of cell metabolism revealed here has therapeutic potential for the use of xanthohumol. [Display omitted] •Xanthohumol directly interacts with the mitochondrial electron transfer chain complex I.•Xanthohumol inhibits the oxidative phosphorylation and remodels cell metabolism.•Xanthohumol triggers the production of reactive oxygen species and induces apoptosis.