, 2009). Instead, these athletes have subconcussive or concussive impact to the brain, due to acceleration/deceleration forces with diffuse axonal injury. For this reason, it is questionable whether animal models based on direct crush or compression injury are relevant models to study the neurobiology MDV3100 cost of mild TBI. Closed head injury with acceleration and deceleration forces to the brain causes a multifaceted cascade of neurochemical changes that affect brain function (see Figure 1).
Although detailed understanding of the pathophysiology of concussion is lacking, studies using the mild fluid percussion model support the idea that the initiating event is stretching and disrupting of neuronal and axonal cell membranes, while cell bodies and myelin sheaths are less affected (Spain et al., 2010). Resulting membrane defects cause a deregulated flux of ions, including an efflux of potassium and influx of calcium. These events precipitate enhanced release of excitatory
neurotransmitters, particularly glutamate. Binding glutamate to N-methyl-D-aspartate (NMDA) receptors results in further depolarization, influx of calcium ions, and widespread suppression of neurons with glucose hypometabolism ( Giza and Hovda, 2001; Barkhoudarian et al., 2011). Increased activity in membrane pumps (to restore ionic balance) raises glucose consumption, depletes energy stores, causes calcium influx into mitochondria, and impairs oxidative metabolism and consequently learn more anaerobic glycolysis with lactate production, which might cause acidosis and edema ( Giza and Hovda, 2001; Barkhoudarian
Adenosine et al., 2011). DAI, caused by shearing of fragile axons by acceleration/deceleration forces from the trauma, is the primary neuropathology of TBI (Adams et al., 1989; Alexander, 1995; Meythaler et al., 2001; Johnson et al., 2012). DAI is present also in patients with mild TBI (Oppenheimer, 1968), and the severity of DAI is proportional to the deceleration force (Elson and Ward, 1994). In patients with TBI, DAI is notoriously difficult to identify using CT and conventional MRI, although MRI is more sensitive (Kim and Gean, 2011). However, novel MRI techniques such as diffusion tensor imaging (DTI) have been shown to be useful to asses axonal integrity and to identify DAI in patients with mild TBI (Bazarian et al., 2007; Mayer et al., 2010; Miles et al., 2008) and also in athletes with mild sports-related concussive or subconcussive TBI (Bazarian et al., 2012). By histological techniques, DAI can be identified very early (hours) after trauma and is characterized by sequential changes with an acute shearing of axons, which leads to disrupted axonal transport with axonal swellings and thereafter secondary disconnection and in the end Wallerian degeneration (Johnson et al., 2012).
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