TABLE 2.
Human | Rodent | |
Presynaptic changes | ||
Active zone density | Unknown | Decreases (Chen et al., 2012) |
Active zone-specific proteins | Unknown | Selective degeneration of bassoon, piccolo and P/Q type VGCC protein level and density per synapse (Chen et al., 2012; Nishimune et al., 2012; Nishimune et al., 2016) |
Synaptic vesicle density | Unknown | Decreases (Fahim and Robbins, 1982; Banker et al., 1983) |
Nerve terminal branching | Increases (Oda, 1984), no change (Gambino et al., 1990) | Increases (Fahim et al., 1983; Li et al., 2011; Valdez et al., 2012) |
Denervation | Increases in intercoastal (Oda, 1984) and VL muscles (Lexell and Downham, 1991; Mosole et al., 2014; Zampieri et al., 2016), no change in the peroneus longus muscle (Jones et al., 2017) | Increases in TA, plantaris, and EDL muscle (Fahim and Robbins, 1982; Deschenes et al., 2010; Valdez et al., 2010; Chai et al., 2011) |
Postsynaptic changes | ||
NMJ fragmentation | No change in the peroneus longus muscle (Jones et al., 2017) | Increases in the EDL, diaphragm, soleus, sternomastoid, and TA muscles (Andonian and Fahim, 1988; Valdez et al., 2010; Li et al., 2011; Willadt et al., 2016) |
Endplate area | Increases (Oda, 1984) and no change (Wokke et al., 1990) in intercostal muscles. No change in the peroneus longus muscle (Jones et al., 2017) | No change in the EDC, EDL, GM, and soleus muscles (Banker et al., 1983) |
Postsynaptic folds number and regularity | Decreases (Arizono et al., 1984; Wokke et al., 1990) | Decreases (Fahim and Robbins, 1982) |
The age range for human studies is 4–95 years, and the age range for rodent studies is 21 days to 33 months (mice) and 56 days to 24 months (rats). EDC, extensor digitorum communis; EDL, extensor digitorum longus; GM, gluteus maximus; NMJ, neuromuscular junction; TA, tibialis anterior; VGCC, voltage-gated calcium channel; VL, vastus lateralis.