Biophotons: A Mechanism Connecting Human Consciousness to Light
Despite the innovations of human intelligence and advancements in neuroscience, the origin of consciousness and subjective experience itself remains elusive and uncharted territory. Our knowledge of the mechanisms through which anesthesia functions, as well as the processes responsible for establishment of memory and conscious perception are rudimentary at best (25).
Because biophotons have been found in the brain and are hypothesized to be quintessential to neurological activity, scientists are exploring the possibility that neurons communicate via photonic emissions in addition to the classic electro-chemical signaling comprised of neural impulses and neurotransmitters (20). Biophotons are optimal candidates, as “They travel tens of millions of times faster than a typical electrical neural signal and are not prone to thermal noise at body temperature owing to their relatively high energies. It is conceivable that evolution might have found a way to utilize these precious high-energy resources for information transfer” (25).
Not only that, but axons, the projecting appendages of nerve cells that conduct electrical impulses away from the neuronal cell body, which are surrounded by an insulating fatty myelin sheath, may serve as waveguides for biophotons to travel between neurons (20). Myelin sheaths are created by specialized glial cells in the central nervous system known as oligodendrocytes, which lends credence to the idea of biophoton-mediated neural communication since another kind of glial cell called the Müller cell has been proven to guide light in mammalian eyes (30, 31).
Myelin sheaths rectify the problem of communication across spatially separated agents in the nervous system since the insulating property of myelin increases the propagation speed of action potentials (the electrical spikes that occur when a neuron sends information down its axon to another neuron) (25). This theory is also supported by the observation that light conduction is enhanced along white matter tracts comprised of myelinated axons (32).
References
1. Mothersill, C. et al. (2013). Transmission of signals from rats receiving high doses of microbeam radiation to cage mates: an inter-mammal bystander effect. Dose Response, 12(1), 72—92. doi: 10.2203/dose-response.13-011.Mothersill.
2. Mothersill, C., & Seymour, C. (1997). Medium from irradiated human epithelial cells but not human fibroblasts reduces the clonogenic survival of unirradiated cells. International Journal of Radiation Biology, 71, 421–427.
3. Azzam, E.I., de Toledo, S.M., & Little, J.B. (2001). Direct evidence for the participation of gap junction-mediated intercellular communication in the transmission of damage signals from alpha -particle irradiated to nonirradiated cells. Proceedings of the National Academy of Sciences (USA), 98, 473–478.
4. Kaminski, J.M. et al. (2005). The controversial abscopal effect. Cancer Treatment Reviews, 31 ,159–172.
5. Kroemer, G., & Zitvogel, L. (2012). Abscopal but desirable: The contribution of immune responses to the efficacy of radiotherapy. Oncoimmunology, 1, 407–408.
6. Lakshmanagowda, P.B. et al. (2009). Abscopal effect in a patient with chronic lymphocytic leukemia during radiation therapy: a case report. Cases Journal, 2, 204. doi: 10.1186/1757-1626-2-204.
7. Faguet, G.B., Reichard, S.M., & Welter, D.A. (1984). Radiation-induced clastogenic plasma factors. Cancer Genetics and Cytogenetics, 12, 73–83.
8. Youssefi, A.A., Arutyunyan, R., & Emerit, I. (1994). Chromosome damage in PUVA-treated human lymphocytes is related to active oxygen species and clastogenic factors. Mutation Research, 309, 185–191.
9. Audette-Stuart, M., & Yankovich, T. (2011). Bystander effects in Bullfrog tadpoles. Radioprotection, 46, S497–S497.
10. Isaeva, V.G., & Surinov, B.P. (2007). Postradiation volatile secretion and development of immunosu-pression effectes by laboratory mice with various genotype. Radiatsionnaia biologiia, radioecologiia, 47, 10–16.
11. Mothersill, C. et al. (2006). Communication of radiation-induced stress or bystander signals between fish in vivo. Environmental Science Technology, 40, 6859–6864.
12. Mothersill, C. et al. (2007). Characterization of a radiation-induced stress response communicated in vivo between zebrafish. Environmental Science Technology, 41, 3382–3387.
13. Mothersill, C. et al. (2009). Communication of radiation-induced signals in vivo between DNA repair deficient and proficient medaka (Oryzias latipes). Environmental Science Technology, 43, 3335–3342.
14. Mothersill, C. et al. (2012). Transmission of signals from irradiated rats to cage mates: an inter-animal bystander effect. Gliwice Scientific Meetings, Poland.
15. O’Dowd, C. et al. (2006). The release of bystander factor(s) from tissue explant cultures of rainbow trout (Onchorhynchus mykiss) after exposure to gamma radiation. Radiation Research, 166, 611–617.
16. Surinov, B.P., Isaeva, V.G., & Dukhova, N.N. (2004). Postirradiation volatile secretions of mice: syngeneic and allogeneic immune and behavioral effects. Bulletin of Experimental Biology and Medicine, 138, 384–386.
17. Daev, E.V. et al. (2007). Chromosomal abnormalities and splenocyte production in laboratory mouse males after exposure to stress chemosignals. Tsitologiia, 49, 696–701.
18. Ahmad, S-B. et al. (2013). Ultra-violet light emission from HPV-G cells irradiated with low LET radiation from 90Y: Consequences for radiation induced bystander effects. Dose-Response, 11. 498–516.
19. Beloussov, L.V. (1997). Life of Alexander G. Gurwitsch and his relevant contribution to the theory of morphogenetic field. The International Journal of Developmental Biology, 41, 771–777.
20. Zarkeshian, P. et al. (2017). Are there optical communication channels in the brain? Biological Physics. Retrieved from https://arxiv.org/abs/1708.08887
21. Sanders, C.L. (2014). Speculations about Bystander and Biophotons. Dose Response, 12(4), 515-517.
22. Schwabl, H., & Klima, H. (2005). Spontaneous Ultraweak Photon Emission from Biological Systems and the Endogenous Light Field. Forschende Komplementärmedizin / Research in Complementary Medicine, 12(2), 84-89. doi:10.1159/000083960.
23. Yang, M. et al. (2015). Spectral discrimination between healthy people and cold patients using spontaneous photon emission.” Biomedical Optical Express, 6, 1331-1339.
24. Cifra, M. & Pospíšil, P. (2014). Ultra-weak photon emission from biological samples: Definition, mechanisms, properties, detection and applications. Journal of Photochemistry and Photobiology B, 139, 2–10.
25. Kumar, S. et al. (2016). Possible existence of optical communication channels in the brain. Scientific Reports, 6, doi:10.1038/srep36508.
26. Devaraj, B., Usa, M., & Inaba, H. (1997). Biophotons: Ultraweak light emission from living systems. Current Opinions on Solid State Matter Science, 2, 188-193.
27. Hossu, M., & Rupert, R. (2006). Quantum Events of Biophoton Emission Associated with Complementary and Alternative Medicine Therapies: A Descriptive Pilot Study. The Journal of Alternative and Complementary Medicine, 12(2), 119-24. doi:10.1089/acm.2006.12.119.
28. Katoka, Y. et al. (2001). Activity-dependent neural tissue oxidation emits intrinsic ultraweak photons. Biochemistry and Biophysics Research Community, 285, 1007-1011.
29. Rosch, P.J. (2014). Bioelectromagnetic and Subtle Energy Medicine. Boca Raton: CRC Press.
30. Franze, K. et al. (2007). Müller cells are living optical fibers in the vertebrate retina. Proceedings of the National Academy of Science (USA), 104, 8287–8292.
31. Labin, A. M. et al. (2014). Müller cells separate between wavelengths to improve day vision with minimal effect upon night vision. Nature Communications, 5, 4319.
32. Hebeda, K.M. et al. (1994). Light propagation in the brain depends on nerve fiber orientation. Neurosurgery, 35, 722–724.
33. Hiscock, H.G. et al. (2016). The quantum needle of the avian magnetic compass. Proceedings of the National Academy of Sciences (USA), 115, 4634-639.
34. Franco, M.I. et al. (2011). Molecular vibration-sensing component in Drosophila melanogaster olfaction. Proceedings of the National Academy of Sciences (USA), 108, 3797–3802.
35. Romero, E. et al. (2014). Quantum coherence in photosynthesis for efficient solar-energy conversion. Nature Physics, 10, 676–682.
36. Zimmer, C. (2010). Sizing Up Consciousness by Its Bits. The New York Times.
37. Bonilla, E. (2008). [Evidence about the power of intention] [Article in Spanish]. Investigación Clínica 49(4), 595-615.
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