“…Regarding nerve regeneration, as suggested by Diker et al [ 36 ], most of the original studies involve animal sciatic nerves, and only a small number investigated the effects of PBM following the injury of the trigeminal nerve branches. Despite not being included in the review process due to nonadherence to many points of the ARRIVE guidelines, nine comparative research articles [ 34 , 35 , 38 , 40 , 42 , 43 , 44 , 45 , 46 ] using a total of 273 rats showed the effects of PBM at different wavelengths and phototherapy parameters on the regeneration of trigeminal nerve branches, neurosensory recovery and pain. These effects are most likely the consequence of cell physiology modulation, resulting in a decrease in substance P (SP), vanilloid transient potential receptor of subtype-1 (TRPV1), peptide related to the calcitonin gene [ 34 ], matrix metalloproteinases [ 35 ], laminin, myelin protein zero, neurofilaments [ 38 ] and brain-derived neurotrophic factor [ 45 ], and an increase in the nerve growth factor level [ 45 ].…”