mTOR/ α-ketoglutarate-mediated signaling pathways in the context of brain neurodegeneration and neuroprotection

被引:6
|
作者
Kostiuchenko, Olha [1 ,2 ]
Lushnikova, Iryna [1 ]
Kowalczyk, Magdalena [2 ]
Skibo, Galyna [1 ]
机构
[1] Natl Acad Sci Ukraine, Bogomoletz Inst Physiol, UA-01024 Kiev, Ukraine
[2] Inst Biochem & Biophys, Polish Acad Sci, PL-02106 Warsaw, Poland
来源
BBA ADVANCES | 2022年 / 2卷
关键词
mTOR; alpha-ketoglutarate (AKG); Metabolism; Autophagy; Aging; Neurodegeneration; Neuroprotection; LIFE-SPAN; IN-VITRO; METABOLISM; AUTOPHAGY; TRANSPORT; ISCHEMIA; PROTEIN; GROWTH; ACID; 2-OXOGLUTARATE;
D O I
10.1016/j.bbadva.2022.100066
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
Cerebral disorders are largely associated with impaired cellular metabolism, despite the regulatory mechanisms designed to ensure cell viability and adequate brain function. Mechanistic target of rapamycin (mTOR) signaling is one of the most crucial factors in the regulation of energy homeostasis and its imbalance is linked with a variety of neurodegenerative diseases. Recent advances in the metabolic pathways' modulation indicate the role of alpha-ketoglutarate (AKG) as a major signaling hub, additionally highlighting its anti -aging and neuroprotective properties, but the mechanisms of its action are not entirely clear. In this review, we analyzed the physiological and pathophysiological aspects of mTOR in the brain. We also discussed AKG's multifunctional properties, as well as mTOR/AKG-mediated functional communications in cellular metabolism. Thus, this article provides a broad overview of the mTOR/AKG-mediated signaling pathways, in the context of neurodegeneration and endogenous neuroprotection, with the aim to find novel therapeutic strategies.
引用
收藏
页数:10
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