Figure 6
Scheme of the potential molecular/biological processes affected by non-ionizing THz radiation. The activation of the CaN complex occurs swiftly in response to an influx of intracellular calcium (Ca2+), playing a crucial role in the dephosphorylation of various important substrates. CaN is known to dephosphorylate the microtubule-associated proteins Mapt and MAP2. Dephosphorylation of the Tau proteins (Mapt and MAP2) by CaN is associated with cellular response to oxidative stress (Zambrano et al., 2004 ). Mitochondrial translocases 1 and 2 make up part of the mitochondrial permeability transition pore complex (2 out of 7 proteins). Transitional pore openings in the inner mitochondrial membrane are linked to mitochondrial dysfunction caused by mitochondrial depolarization, cessation of ATP synthesis, Ca2+ release, pyridine nucleotide depletion, inhibition of respiration and matrix swelling. Short-term openings may be involved in the physiological regulation of Ca2+ and ROS homeostasis and provide mitochondria with a fast mechanism for Ca2+ release, which could be a possible trigger due to SS THz radiation and as shown by previous findings where THz irradiation drove the activation of voltage-gated calcium (Ca2+) channels. |