Scientific Reports (Dec 2023)

Information encoded in volumes and areas of dendritic spines is nearly maximal across mammalian brains

  • Jan Karbowski,
  • Paulina Urban

DOI
https://doi.org/10.1038/s41598-023-49321-9
Journal volume & issue
Vol. 13, no. 1
pp. 1 – 29

Abstract

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Abstract Many experiments suggest that long-term information associated with neuronal memory resides collectively in dendritic spines. However, spines can have a limited size due to metabolic and neuroanatomical constraints, which should effectively limit the amount of encoded information in excitatory synapses. This study investigates how much information can be stored in the population of sizes of dendritic spines, and whether it is optimal in any sense. It is shown here, using empirical data for several mammalian brains across different regions and physiological conditions, that dendritic spines nearly maximize entropy contained in their volumes and surface areas for a given mean size in cortical and hippocampal regions. Although both short- and heavy-tailed fitting distributions approach $$90-100\%$$ 90 - 100 % of maximal entropy in the majority of cases, the best maximization is obtained primarily for short-tailed gamma distribution. We find that most empirical ratios of standard deviation to mean for spine volumes and areas are in the range $$1.0\pm 0.3$$ 1.0 ± 0.3 , which is close to the theoretical optimal ratios coming from entropy maximization for gamma and lognormal distributions. On average, the highest entropy is contained in spine length ( $$4-5$$ 4 - 5 bits per spine), and the lowest in spine volume and area ( $$2-3$$ 2 - 3 bits), although the latter two are closer to optimality. In contrast, we find that entropy density (entropy per spine size) is always suboptimal. Our results suggest that spine sizes are almost as random as possible given the constraint on their size, and moreover the general principle of entropy maximization is applicable and potentially useful to information and memory storing in the population of cortical and hippocampal excitatory synapses, and to predicting their morphological properties.