Abstract
Given
that many fundamental questions in neuroscience are still open, it
seems pertinent to explore whether the brain might use other physical
modalities than the ones that have been discovered so far. In particular
it is well established that neurons can emit photons, which prompts the
question whether these biophotons could serve as signals between
neurons, in addition to the well-known electro-chemical signals. For
such communication to be targeted, the photons would need to travel in
waveguides. Here we show, based on detailed theoretical modeling, that
myelinated axons could serve as photonic waveguides, taking into account
realistic optical imperfections. We propose experiments, both in vivo and in vitro,
to test our hypothesis. We discuss the implications of our results,
including the question whether photons could mediate long-range quantum
entanglement in the brain.
Introduction
The
human brain is a dynamic physical system of unparalleled complexity.
While neuroscience has made great strides, many fundamental questions
are still unanswered, including the processes underlying memory formation, the working principle of anesthesia, and–most fundamentally–the generation of conscious experience.
It therefore seems pertinent to explore whether the brain might
generate, transmit and store information using other physical modalities
than the ones that have been discovered so far.
In the present work we focus on the question whether biophotons could serve as a supplementary information carrier in the brain in addition to the well established electro-chemical signals. Biophotons are the quanta of light spanning the near-UV to near-IR frequency range. They are produced mostly by electronically excited molecular species in a variety of oxidative metabolic processes in cells. They may play a role in cell to cell communication, and have been observed in many organisms, including humans, and in different parts of the body, including the brain. Photons in the brain could serve as ideal candidates for information transfer. 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, even if they were just the by–products of metabolism to begin with. Most of the required molecular machinery seems to exist in living cells such as neurons. Mitochondrial respiration or lipid oxidation could serve as sources, and centrosomes or chromophores in the mitochondria could serve as detectors.
However, one crucial element for optical communication is not well established, namely the existence of physical links to connect all of these spatially separated agents in a selective way. The only viable way to achieve targeted optical communication in the dense and (seemingly) disordered brain environment is for the photons to travel in waveguides. Mitochondria and microtubules in neurons have been hypothesized to serve as waveguides. However, these structures are too small and inhomogeneous to guide light efficiently over significant distances.
Here we propose myelinated axons as potential biophoton waveguides in the brain, and we support this hypothesis with detailed theoretical modeling. These axons are tightly wrapped by a lamellar structure called the myelin sheath, which has a higher refractive index than both the inside of the axon and the interstitial fluid outside (see Fig. 1a). This compact sheath could therefore also serve as a waveguide, in addition to increasing the propagation speed of an action potential (via saltatory conduction) based on its insulating property. There is some indirect experimental evidence for light conduction by axons, including the observation of increased transmission along the axes of the white matter tracts, which consist of myelinated axons. Myelin is formed in the central nervous system (CNS) by a kind of glia cell called oligodendrocyte. Interestingly, certain glia cells, known as Müller cells, have been shown to guide light in mammalian eyes.
An
interesting feature of photonic communication channels is that they can
transmit quantum information as well. The potential role of quantum
effects in biological systems is currently being investigated in several
areas, including olfaction, avian magnetoreception, and photosynthesis.
There is also growing speculation about the role of fundamental quantum
features such as superposition and entanglement in certain higher level
brain functions.
Of particular relevance is the “binding problem” of consciousness,
which questions how a single integrated experience arises from the
activities of individual molecules in billions of neurons. The answer to
this question might be provided by quantum entanglement, where the whole is more than the sum of its parts in a well-defined physical and mathematical sense.
The main challenge in envisioning a “quantum brain” is environmental decoherence, which destroys quantum effects very rapidly at room temperature for most physical degrees of freedom. However, nuclear spins can have coherence times of tens of milliseconds in the brain, and much longer times are imaginable. Long-lived nuclear spin entanglement has also been demonstrated in other condensed-matter systems at room temperature. A recent proposal on “quantum cognition” is based on nuclear spins, but relies on the physical transport of molecules to carry quantum information, which is very slow. In contrast, photons are well suited for transmitting quantum information over long distances, which is why currently envisioned man-made quantum networks rely on optical communication channels (typically optical fibers) between spins.
Efficient light guidance therefore seems necessary for both classical and quantum optical networks in the brain. Is this possible in myelinated axons with all their “imperfections” from a waveguide perspective? In an attempt to answer this question, we have developed a detailed theoretical model of light guidance in axons. We show in the next section that the answer seems to be in the affirmative.
In the present work we focus on the question whether biophotons could serve as a supplementary information carrier in the brain in addition to the well established electro-chemical signals. Biophotons are the quanta of light spanning the near-UV to near-IR frequency range. They are produced mostly by electronically excited molecular species in a variety of oxidative metabolic processes in cells. They may play a role in cell to cell communication, and have been observed in many organisms, including humans, and in different parts of the body, including the brain. Photons in the brain could serve as ideal candidates for information transfer. 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, even if they were just the by–products of metabolism to begin with. Most of the required molecular machinery seems to exist in living cells such as neurons. Mitochondrial respiration or lipid oxidation could serve as sources, and centrosomes or chromophores in the mitochondria could serve as detectors.
However, one crucial element for optical communication is not well established, namely the existence of physical links to connect all of these spatially separated agents in a selective way. The only viable way to achieve targeted optical communication in the dense and (seemingly) disordered brain environment is for the photons to travel in waveguides. Mitochondria and microtubules in neurons have been hypothesized to serve as waveguides. However, these structures are too small and inhomogeneous to guide light efficiently over significant distances.
Here we propose myelinated axons as potential biophoton waveguides in the brain, and we support this hypothesis with detailed theoretical modeling. These axons are tightly wrapped by a lamellar structure called the myelin sheath, which has a higher refractive index than both the inside of the axon and the interstitial fluid outside (see Fig. 1a). This compact sheath could therefore also serve as a waveguide, in addition to increasing the propagation speed of an action potential (via saltatory conduction) based on its insulating property. There is some indirect experimental evidence for light conduction by axons, including the observation of increased transmission along the axes of the white matter tracts, which consist of myelinated axons. Myelin is formed in the central nervous system (CNS) by a kind of glia cell called oligodendrocyte. Interestingly, certain glia cells, known as Müller cells, have been shown to guide light in mammalian eyes.
The main challenge in envisioning a “quantum brain” is environmental decoherence, which destroys quantum effects very rapidly at room temperature for most physical degrees of freedom. However, nuclear spins can have coherence times of tens of milliseconds in the brain, and much longer times are imaginable. Long-lived nuclear spin entanglement has also been demonstrated in other condensed-matter systems at room temperature. A recent proposal on “quantum cognition” is based on nuclear spins, but relies on the physical transport of molecules to carry quantum information, which is very slow. In contrast, photons are well suited for transmitting quantum information over long distances, which is why currently envisioned man-made quantum networks rely on optical communication channels (typically optical fibers) between spins.
Efficient light guidance therefore seems necessary for both classical and quantum optical networks in the brain. Is this possible in myelinated axons with all their “imperfections” from a waveguide perspective? In an attempt to answer this question, we have developed a detailed theoretical model of light guidance in axons. We show in the next section that the answer seems to be in the affirmative.