Mdivi1 prevents early-stage induction of mitophagy and accelerated cell death in a rat model of moderate controlled cortical impact brain injury.

BACKGROUND: Growing evidences have implicated dysfunctional mitochondria in the pathophysiology of neurodegenerative disorders. Selective degradation of dysfunctional mitochondria is termed mitophagy and constitutes a pivotal component of mitochondrial quality control to maintain cellular homeostasis. Mitochondrial fission plays prominent roles in controlling mitochondrial shape and function. However, it is unclear whether mitochondrial fission in the context of eliminating damaged mitochondria is involved in traumatic brain injury (TBI). The objective of this study was to examine the role of mitochondrial division inhibitor 1 (Mdivi1), a small-molecule inhibitor of dynamin-related protein (Drp1), in general autophagy and mitophagy after controlled cortical impact (CCI).

METHODS: Mitophagy and the role of Drp1 in this process after CCI were examined using western blotting, electron microscopy, double immunofluorescence staining, neurological severity scores (NSS), and hematoxylin and eosin (HE) staining. Statistical analysis was performed using one-way ANOVA followed by the least significant difference (LSD) test or the Games-Howell test.

RESULTS: Animals exposed to CCI exhibited induction of mitophagy and fragmentation of mitochondria. When fission was blocked with Mdivi1, the mitochondria became excessively long and interconnected. Inhibition of Drp1 blocked the induction of mitophagy specifically, which aggravated neurological manifestations and neuronal apoptosis. Mdivi1 activated caspase-3 and caspase-9, implying that selective degradation of damaged mitochondria by autophagy markedly decreased cell apoptosis induced by TBI and thus promoted cell survival.

CONCLUSIONS: This study supports the hypothesis that Drp1-dependent mitochondrial fission contributes to mitophagy in TBI, and further understanding the regulatory mechanisms of Drp1 will provide opportunities to develop novel strategies against TBI.