The brain has an enormous capacity to adapt to its environment. This ability to continuously learn and form new memories thanks to its malleability, is known as brain plasticity.
One of the most important
mechanisms behind brain plasticity is the change in both the structure and
function of synapses, the points of contact between neurons where communication
happens. These sites of synaptic contact occur through microscopic protrusions
on the branches of neurons, called dendritic spines. Dendritic spines are very
dynamic, changing their shape and size in response to stimuli.
Previous studies have shown
that alterations in synaptic plasticity occur in various animal models of brain
diseases. However, it remains unclear whether human cortical neurons express
synaptic plasticity similarly to those in the rodent brain.
Recently, a derivative of
vitamin A has been linked to synaptic plasticity. In addition, several studies
have evaluated the effects of this derivative in patients with cognitive
dysfunctions, including Alzheimer’s disease, Fragile X syndrome, and
depression.
However, there is no direct
experimental evidence for synaptic plasticity in the adult human cerebral
cortex related to vitamin A signaling and metabolism.
To investigate this, Lenz et
al. used human cortical slices prepared from neurosurgical resections and
treated them with a solution of the vitamin A derivative all-trans retinoic
acid for 6-10 hours. Lenz et al. employed a variety of techniques, including
patch-clamp recordings to measure neuron function as well as different types of
microscopy to evaluate structural changes in dendritic spines.
These experiments
demonstrated that the derivative promoted the synaptic plasticity in the adult
human cortex. Specifically, it increased the size of the dendritic spines and
strengthened their ability to transmit signals. In addition, Lenz et al. found
that the spine apparatus organelle – a structure found in some dendritic spines
– was a target of the vitamin A derivative and promoted synaptic plasticity.
These findings advance the
understanding of the pathways through which vitamin A derivatives affect
synaptic plasticity, which may aide the development of new therapeutic
strategies for brain diseases. More generally, the results contribute to the
identification of key mechanisms of synaptic plasticity in the adult human
brain.
Source: https://elifesciences.org/articles/63026
Image credit: The Center for
Sleep and Consciousness, University of Wisconsin-Madison School of Medicine
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