Herbal terpenoids activate autophagy and mitophagy through modulation of bioenergetics and protect from metabolic stress, sarcopenia and epigenetic aging

草本萜类化合物通过调节生物能量学激活自噬和线粒体自噬,从而抵御代谢压力、肌肉减少症和表观遗传衰老。

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作者:Gabriele Civiletto ,Dario Brunetti ,Giulia Lizzo ,Kamila Muller ,Guillaume E Jacot ,Ioanna Daskalaki ,Federico Sizzano ,Minji Huh ,Ivano Di Meo ,Maria Nicol Colombo ,José L Sanchez-Garcia ,Bertrand J Bétrisey ,Alix Zollinger ,Patricia Lino ,Christopher Neal ,Anne-Laure Egesipe ,Joy Richard ,Myriam Chimen ,Aurélie Hermant ,Benjamin Brinon ,Lorane Texari ,Sylviane Metairon ,Mohammed Adnan Qureshi ,Dhaval S Patel ,Siva A Vanapalli ,Marco Malavolta ,Arwen W Gao ,Amelia Lalou ,Mauro Provinciali ,Fiorenza Orlando ,Valeria Tiranti ,Robert T Brooke ,Steve Horvath ,Johan Auwerx ,Jerome N Feige ,Philipp Gut

Abstract

Small molecular food components contribute to the health benefits of diets rich in fruits, vegetables, herbs and spices. The cellular mechanisms by which noncaloric bioactives promote healthspan are not well understood, limiting their use in disease prevention. Here, we deploy a whole-organism, high-content screen in zebrafish to profile food-derived compounds for activation of autophagy, a cellular quality control mechanism that promotes healthy aging. We identify thymol and carvacrol as activators of autophagy and mitophagy through a transient dampening of the mitochondrial membrane potential. Chemical stabilization of thymol-induced mitochondrial depolarization blocks mitophagy activation, suggesting a mechanism originating from the mitochondrial membrane. Supplementation with thymol prevents excess liver fat accumulation in a mouse model of diet-induced obesity, improves pink-1-dependent heat stress resilience in Caenorhabditis elegans, and slows the decline of skeletal muscle performance while delaying epigenetic aging in SAMP8 mice. Thus, terpenoids from common herbs promote autophagy during aging and metabolic overload, making them attractive molecules for nutrition-based healthspan promotion.

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