Capsaicin may have important potential for promoting vascular and metabolic health

被引:93
作者
McCarty, Mark F. [1 ]
DiNicolantonio, James J. [2 ]
O'Keefe, James H. [2 ]
机构
[1] Catalyt Longev, Encinitas, CA 92007 USA
[2] St Lukes Hosp, Mid Amer Heart Inst, Kansas City, MO 64111 USA
关键词
D O I
10.1136/openhrt-2015-000262
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Capsaicin, the phytochemical responsible for the spiciness of peppers, has the potential to modulate metabolism via activation of transient receptor potential vanilloid 1 (TRPV1) receptors, which are found not only on nociceptive sensory neurons, but also in a range of other tissues. TRPV1 activation induces calcium influx, and in certain tissues this is associated with increased activation or expression of key proteins such as endothelial nitric oxide synthase (eNOS), uncoupling protein 2 (UCP2), KLF2, PPARdelta, PPARgamma, and LXRa. The calcium influx triggered by TRPV1 activation in endothelial cells mimics the impact of shear stress in this regard, activating and increasing the expression of eNOS-but also increasing expression of cox-2, thrombomodulin, and nrf2-responsive antioxidant enzymes, while decreasing expression of proinflammatory proteins. Hence, dietary capsaicin has favourably impacted endothelium-dependent vasodilation in rodents. TRPV1-mediated induction of LXRa in foam cells promotes cholesterol export, antagonising plaque formation. Capsaicin-mediated activation of TRPV1expressing neurons in the gastrointestinal tract promotes sympathetically mediated stimulation of brown fat, raising metabolic rate. The increased expression of UCP2 induced by TRPV1 activation exerts a protective antioxidant effect on the liver in non-alcoholic fatty liver disease, and on vascular endothelium in the context of hyperglycaemia. In rodent studies, capsaicin-rich diets have shown favourable effects on atherosclerosis, metabolic syndrome, diabetes, obesity, non-alcoholic fatty liver, cardiac hypertrophy, hypertension and stroke risk. Clinically, ingestion of capsaicin-or its less stable non-pungent analogue capsiate-has been shown to boost metabolic rate modestly. Topical application of capsaicin via patch was found to increase exercise time to ischaemic threshold in patients with angina. Further clinical studies with capsaicin administered in food, capsules, or via patch, are needed to establish protocols that are tolerable for most patients, and to evaluate the potential of capsaicin for promoting vascular and metabolic health.
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页数:7
相关论文
共 78 条
[1]   A Comprehensive Review of the Carcinogenic and Anticarcinogenic Potential of Capsaicin [J].
Bley, Keith ;
Boorman, Gary ;
Mohammad, Bashir ;
McKenzie, Donald ;
Babbar, Sunita .
TOXICOLOGIC PATHOLOGY, 2012, 40 (06) :847-873
[2]   Impaired capsaicin-induced relaxation of coronary arteries in a porcine model of the metabolic syndrome [J].
Bratz, Ian N. ;
Dick, Gregory M. ;
Tune, Johnathan D. ;
Edwards, Jason M. ;
Neeb, Zachary P. ;
Dincer, U. Deniz ;
Sturek, Michael .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2008, 294 (06) :H2489-H2496
[3]  
Chaiyasit Kamon, 2009, Journal of the Medical Association of Thailand, V92, P108
[4]   Activation of TRPV1 channel by dietary capsaicin improves visceral fat remodeling through connexin43-mediated Ca2+ Influx [J].
Chen, Jian ;
Li, Li ;
Li, Yingsha ;
Liang, Xia ;
Sun, Qianqian ;
Yu, Hao ;
Zhong, Jian ;
Ni, Yinxing ;
Chen, Jing ;
Zhao, Zhigang ;
Gao, Peng ;
Wang, Bin ;
Liu, Daoyan ;
Zhu, Zhiming ;
Yan, Zhencheng .
CARDIOVASCULAR DIABETOLOGY, 2015, 14
[5]   The common-866G>A variant in the promoter of UCP2 is associated with decreased risk of coronary artery disease in type 2 diabetic men [J].
Cheurfa, Nadir ;
Dubois-Laforgue, Daniele ;
Ferrarezi, Daniela A. F. ;
Reis, Andre F. ;
Brenner, Guilherme M. ;
Bouche, Clara ;
Le Feuvre, Claude ;
Fumeron, Frederic ;
Timsit, Jose ;
Marre, Michel ;
Velho, Gilberto .
DIABETES, 2008, 57 (04) :1063-1068
[6]   Molecular mechanisms of activation of endothelial nitric oxide synthase mediated by transient receptor potential vanilloid type 1 [J].
Ching, Li-Chieh ;
Kou, Yu Ru ;
Shyue, Song-Kun ;
Su, Kuo-Hui ;
Wei, Jeng ;
Cheng, Li-Ching ;
Yu, Yuan-Bin ;
Pan, Ching-Chian ;
Lee, Tzong-Shyuan .
CARDIOVASCULAR RESEARCH, 2011, 91 (03) :492-501
[7]   Structure-activity relationships of vanilloid receptor agonists for arteriolar TRPV1 [J].
Czikora, A. ;
Lizanecz, E. ;
Bako, P. ;
Rutkai, I. ;
Ruzsnavszky, F. ;
Magyar, J. ;
Porszasz, R. ;
Kark, T. ;
Facsko, A. ;
Papp, Z. ;
Edes, I. ;
Toth, A. .
BRITISH JOURNAL OF PHARMACOLOGY, 2012, 165 (06) :1801-1812
[8]   Different Desensitization Patterns for Sensory and Vascular TRPV1 Populations in the Rat: Expression, Localization and Functional Consequences [J].
Czikora, Agnes ;
Rutkai, Ibolya ;
Pasztor, Eniko T. ;
Szalai, Andrea ;
Porszasz, Robert ;
Boczan, Judit ;
Edes, Istvan ;
Papp, Zoltan ;
Toth, Attila .
PLOS ONE, 2013, 8 (11)
[9]  
D'Elia L, 2014, CANCER TREAT RES, V159, P83, DOI 10.1007/978-3-642-38007-5_6
[10]   Mechanisms underlying the hypertensive response induced by capsaicin [J].
Dutta, Abhaya ;
Deshpande, Shripad B. .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2010, 145 (02) :358-359