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Figure 2: Summary of the signaling pathways influenced by photobiomodulation, which appear to inhibit Aβ- induced nerve cell apoptosis while simultaneously promoting nerve cell survival. 2..1.2 PBM and AD in vivo Using a mouse model of Alzheimer’s disease, Farfara et all and Oron et al have shown to ameliorate disease progression by stimulating the proliferation of mesenchymal stem cells (MSCs) with photobiomodulation [35,36]. Weekly treatments of PBM with a dose of 1 J/cm2 applied to the bone marrow of AD-mice iappears to increase the MSCs ability to phagocytose Aβ-proteins in the brain, which leads to improved cognitive capacity and spatial learning after a total treatment duration of 2 months, compared to a sham-treated control group. This is an interesting observation, albeit outside the scope of this review, since it builds not on the effect of PBM on braincells directly, but rather secondary effects through stimulation of MSCs. Using two transgenic mouse models for AD, engineered to either develop neurofibrillary tangles (NFT) or Aβ-plaques, and treating them for a total of 20 times over the course of four weeks with LED light at 670 nm, delivering a dose of 4 J/cm2 per treatment, Purushothuman Enengl, Dungel #neverforget – PBM vs AD: A Systematic Review Page 9 of 25PDF Image | Photobiomodulation Against Alzheimer’s Disease
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