Physiological Reports, Volume (12), No (1), Year (2024-1)

Title : ( Iron role paradox in nerve degeneration and regeneration )

Authors: Samira Bolandghamat , Morteza Behnam Rassouli ,

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Abstract

Iron accumulates in the neural tissue during peripheral nerve degeneration. Some studies have already been suggested that iron facilitates Wallerian degeneration (WD) events such as Schwann cell de-differentiation. On the other hand, intracellular iron levels remain elevated during nerve regeneration and gradually decrease. Iron enhances Schwann cell differentiation and axonal outgrowth. Therefore, there seems to be a paradox in the role of iron during nerve degeneration and regeneration. We explain this contradiction by suggesting that the increase in intracellular iron concentration during peripheral nerve degeneration is likely to prepare neural cells for the initiation of regeneration. Changes in iron levels are the result of changes in the expression of iron homeostasis proteins. In this review, we will first discuss the changes in the iron/iron homeostasis protein levels during peripheral nerve degeneration and regeneration and then explain how iron is related to nerve regeneration. This data may help better understand the mechanisms of peripheral nerve repair and find a solution to prevent or slow the progression of peripheral neuropathies.

Keywords

, iron homeostasis, nerve degeneration, nerve regeneration, nerve repair, peripheral nerve, peripheral neuropathy
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@article{paperid:1097290,
author = {Bolandghamat, Samira and Behnam Rassouli, Morteza},
title = {Iron role paradox in nerve degeneration and regeneration},
journal = {Physiological Reports},
year = {2024},
volume = {12},
number = {1},
month = {January},
issn = {2051-817X},
keywords = {iron homeostasis; nerve degeneration; nerve regeneration; nerve repair; peripheral nerve; peripheral neuropathy},
}

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%0 Journal Article
%T Iron role paradox in nerve degeneration and regeneration
%A Bolandghamat, Samira
%A Behnam Rassouli, Morteza
%J Physiological Reports
%@ 2051-817X
%D 2024

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