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For instance, astrocytes contain glycogen stores that allow them to maintain ATP production through glycolysis and mitochondrial membrane potential by reversal of the F0-F1-ATPase (EC 3.6.3.14) [48]

With the rapid development of lipidomics technologies, especially the application of MS-based high-throughput analysis platforms and multivariate statistical methods, the identification and quantification of these lipid markers have become feasible

Damaged mitochondria are not removed in time and accumulate to form waste mitochondria, which release more ROS, accelerating muscle atrophy (44)

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In normal cases, PINK1 is degraded by healthy mitochondria, but when mitochondria become dysfunctional or damaged, PINK1 accumulates on their outer membranes, recruiting Parkin to mark the defective organelles for autophagic degradation