Neuroplasticity and Repair in Rodent Neurotoxic Models of Spinal Motoneuron Disease

Retrogradely transported toxins are widely used to set up protocols for selective lesioning of the nervous system. These methods could be collectively named "molecular neurosurgery" because they are able to destroy specific types of neurons by using targeted neurotoxins. Lectins such as ri...

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Détails bibliographiques
Publié dans:Neural plasticity. - 1998. - 2016(2016) vom: 10., Seite 2769735
Auteur principal: Gulino, Rosario (Auteur)
Format: Article en ligne
Langue:English
Publié: 2016
Accès à la collection:Neural plasticity
Sujets:Journal Article Review Ribosome Inactivating Proteins, Type 1 Ribosome Inactivating Proteins, Type 2 cholera toxin B-saporin conjugate Cholera Toxin 9012-63-9 volkensin 91933-11-8 Saporins EC 3.2.2.22
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Résumé:Retrogradely transported toxins are widely used to set up protocols for selective lesioning of the nervous system. These methods could be collectively named "molecular neurosurgery" because they are able to destroy specific types of neurons by using targeted neurotoxins. Lectins such as ricin, volkensin, or modeccin and neuropeptide- or antibody-conjugated saporin represent the most effective toxins used for neuronal lesioning. Some of these specific neurotoxins could be used to induce selective depletion of spinal motoneurons. In this review, we extensively describe two rodent models of motoneuron degeneration induced by volkensin or cholera toxin-B saporin. In particular, we focus on the possible experimental use of these models to mimic neurodegenerative diseases, to dissect the molecular mechanisms of neuroplastic changes underlying the spontaneous functional recovery after motoneuron death, and finally to test different strategies of neural repair. The potential clinical applications of these approaches are also discussed
Description:Date Completed 04.11.2016
Date Revised 02.12.2018
published: Print-Electronic
Citation Status MEDLINE
ISSN:1687-5443
DOI:10.1155/2016/2769735