Vanilloid receptor agonists and antagonists are mitochondrial inhibitors: How vanilloids cause non-vanilloid receptor mediated cell death

被引:85
作者
Athanasiou, Andriani
Smith, Paul A.
Vakilpour, Sara
Kumaran, Nethia M.
Turner, Amy E.
Bagiokou, Dimitra
Layfield, Robert
Ray, David E.
Westwell, Andrew D.
Alexander, Stephen P. H.
Kendall, David A.
Lobo, Dileep N.
Watson, Susan A.
Lophatanon, Artitaya
Muir, Kenneth A.
Guo, De-an
Bates, Timothy E. [1 ]
机构
[1] Univ Nottingham, Sch Community Hlth Sci, Nottingham NG7 2UH, England
[2] Univ Nottingham, Sch Biomed Sci, Nottingham NG7 2UH, England
[3] Univ Nottingham, MRC Appl Neurosci Grp, Nottingham NG7 2UH, England
[4] Cardiff Univ, Welsh Sch Pharm, Cardiff CF10 3XF, Wales
[5] Univ Nottingham, Sch Med & Surg Sci, Nottingham NG7 2UH, England
[6] Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai Res Ctr TCM Modernizat, Shanghai 201203, Peoples R China
[7] Univ Nottingham, Nottingham UK China Collaborat Complementary & Al, Nottingham NG7 2UH, England
关键词
TRPV1; vanilloid; capsaicin; resiniferatoxin; capsazepine; SB366791; apoptosis; necrosis; mitochondria; cell death; chemotherapy; cancer;
D O I
10.1016/j.bbrc.2006.12.179
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Time-lapse photomicroscopy of human H460 lung cancer cells demonstrated of the transient receptor potential V1 (TRPV1) channel agonists, (E)-capsaicin and resiniferatoxin, and the TRPV1 antagonists, capsazepine, and SB366791, were able to bring about morphological changes characteristic of apoptosis and/or necrosis. Immunoblot analysis identified immunoreactivity for the transient receptor potential V1 (TRPV1) channel in rat brain samples, but not in rat heart mitochondria or in H460 cells. In isolated rat heart mitochondria, all four ligands caused concentration-dependent decreases in oxygen consumption and mitochondrial membrane potential. (E)Capsaicin and capsazepine evoked concentration-dependent increases and decreases, respectively, in mitochondrial hydrogen peroxide production, whilst resiniferatoxin and SB366791 were without significant effect. These data support the hypothesis that (E)-capsaicin, resiniferatoxin, capsazepine, and SB366791 are all mitochondrial inhibitors, able to activate apoptosis and/or necrosis via non-receptor mediated mechanisms, and also support the use of TRPV1 ligands as anti-cancer agents. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:50 / 55
页数:6
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