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Review
. 2006;28(1):65-76.
doi: 10.1385/jmn:28:1:65.

Neuroactive steroids: A therapeutic approach to maintain peripheral nerve integrity during neurodegenerative events

Affiliations
Review

Neuroactive steroids: A therapeutic approach to maintain peripheral nerve integrity during neurodegenerative events

Emanuela Leonelli et al. J Mol Neurosci. 2006.

Abstract

It is now well known that peripheral nerves are a target for the action of neuroactive steroids. This review summarizes observations obtained so far, indicating that through the interaction with classical and nonclassical steroid receptors, neuroactive steroids (e.g., progesterone, testosterone and their derivatives, estrogens, etc.) are able to influence several parameters of the peripheral nervous system, particularly its glial compartment (i.e., Schwann cells). Interestingly, some of these neuroactive steroids might be considered as promising neuroprotective agents. They are able to counteract neurodegenerative events of rat peripheral nerves occurring after experimental physical trauma, during the aging process, or in hereditary demyelinating diseases. On this basis, the hypothesis that neuroactive steroids might represent a new therapeutic strategy for peripheral neuropathy is proposed.

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References

    1. Nat Med. 2004 Jul;10(7):704-11 - PubMed
    1. Mol Hum Reprod. 2002 Jul;8(7):644-50 - PubMed
    1. J Neurosci. 2003 May 1;23(9):3572-6 - PubMed
    1. Brain Res Mol Brain Res. 2004 Jul 5;126(1):67-73 - PubMed
    1. J Steroid Biochem Mol Biol. 2001 Nov;78(5):401-7 - PubMed

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