Photons guided by axons may enable backpropagation-based learning in the brain

TL;DR

This paper proposes that biophotons guided by axons could serve as a biological mechanism for backpropagation-like learning in the brain, demonstrated through a neural network model that learns MNIST digit classification.

Contribution

It introduces a novel hypothesis that biophotons can enable backward information transmission in the brain, facilitating backpropagation-like learning.

Findings

Neural network successfully learns MNIST with photonic feedback.

System remains effective with low biophoton emission rates and noise.

Biophotons may serve a functional role in brain learning mechanisms.

Abstract

Despite great advances in explaining synaptic plasticity and neuron function, a complete understanding of the brain's learning algorithms is still missing. Artificial neural networks provide a powerful learning paradigm through the backpropagation algorithm which modifies synaptic weights by using feedback connections. Backpropagation requires extensive communication of information back through the layers of a network. This has been argued to be biologically implausible and it is not clear whether backpropagation can be realized in the brain. Here we suggest that biophotons guided by axons provide a potential channel for backward transmission of information in the brain. Biophotons have been experimentally shown to be produced in the brain, yet their purpose is not understood. We propose that biophotons can propagate from each post-synaptic neuron to its pre-synaptic one to carry the required information backward. To reflect the stochastic character of biophoton emissions, our model includes the stochastic backward transmission of teaching signals. We demonstrate that a three-layered network of neurons can learn the MNIST handwritten digit classification task using our proposed backpropagation-like algorithm with stochastic photonic feedback. We model realistic restrictions and show that our system still learns the task for low rates of biophoton emission, information-limited (one bit per photon) backward transmission, and in the presence of noise photons. Our results suggest a new functionality for biophotons and provide an alternate mechanism for backward transmission in the brain.