Visioli Francesco, Ingram Avery, Beckman Joseph S, Magnusson Kathy R, Hagen Tory M
Department of Molecular Medicine, University of Padova, Italy; IMDEA-Food, Madrid, Spain.
Linus Pauling Institute, Oregon State University, Corvallis, OR, 97331, USA; Department of Biochemistry and Biophysics, Oregon State University, Corvallis, OR, 97331, USA.
Free Radic Biol Med. 2022 Jan;178:330-346. doi: 10.1016/j.freeradbiomed.2021.12.008. Epub 2021 Dec 8.
Mitochondria serve vital roles critical for overall cellular function outside of energy transduction. Thus, mitochondrial decay is postulated to be a key factor in aging and in age-related diseases. Mitochondria may be targets of their own decay through oxidative damage. However, treating animals with antioxidants has been met with only limited success in rejuvenating mitochondrial function or in increasing lifespan. A host of nutritional strategies outside of using traditional antioxidants have been devised to promote mitochondrial function. Dietary compounds are under study that induce gene expression, enhance mitochondrial biogenesis, mitophagy, or replenish key metabolites that decline with age. Moreover, redox-active compounds may now be targeted to mitochondria which improve their effectiveness. Herein we review the evidence that representative dietary effectors modulate mitochondrial function by stimulating their renewal or reversing the age-related loss of key metabolites. While in vitro evidence continues to accumulate that many of these compounds benefit mitochondrial function and/or prevent their decay, the results using animal models and, in some instances human clinical trials, are more mixed and sometimes even contraindicated. Thus, further research on optimal dosage and age of intervention are warranted before recommending potential mitochondrial rejuvenating compounds for human use.
线粒体在能量转导之外的整体细胞功能中发挥着至关重要的作用。因此,线粒体衰退被认为是衰老及与年龄相关疾病的关键因素。线粒体可能会因氧化损伤而成为自身衰退的靶点。然而,用抗氧化剂治疗动物在恢复线粒体功能或延长寿命方面仅取得了有限的成功。人们已经设计出一系列传统抗氧化剂之外的营养策略来促进线粒体功能。正在研究的膳食化合物可诱导基因表达、增强线粒体生物合成、线粒体自噬,或补充随年龄增长而减少的关键代谢物。此外,具有氧化还原活性的化合物现在可以靶向线粒体,从而提高其有效性。在此,我们综述了相关证据,即代表性膳食效应物通过刺激线粒体更新或逆转与年龄相关的关键代谢物损失来调节线粒体功能。虽然体外证据不断积累,表明许多此类化合物有益于线粒体功能和/或防止其衰退,但动物模型以及某些情况下人体临床试验的结果则较为复杂,有时甚至相互矛盾。因此,在推荐潜在的线粒体恢复活力化合物供人类使用之前,有必要进一步研究最佳剂量和干预年龄。