Literature DB >> 8944316

Axotomy as an experimental model of neuronal injury and cell death.

V E Koliatsos1, D L Price.   

Abstract

Axonal transection provides very useful paradigms to study cellular responses to injury, mechanisms of regeneration and plasticity, and processes that lead to nerve cell degeneration. Moreover, models of axotomy are valuable for testing experimental therapeutic approaches. Lesions can be made with great precision, and, depending on the neural system, location of the lesion, and age of the animal, these models allow the opportunity to examine a range of neuronal responses. Many parameters influence the character, evolution, and outcomes of axotomy-related processes. The most severe outcome of axotomy is cell death, very common in lesions of neurons of the central nervous system (CNS), although neurons of the peripheral nervous system (PNS) may also die if the transection is sufficiently close to the neuronal cell body or if lesions are performed in young animals. Studies of axotomy models have provided clues into the cellular/molecular events associated with neuronal death and the ways in which interventions can delay or prevent processes that lead to cell death. In this review, we select examples, primarily from our own work, to illustrate how axotomy models have enhanced our understanding of neuronal responses to injury, clarified mechanisms of both regeneration/plasticity and degeneration/ cell death, and allowed assessments of the utility of therapeutic approaches.

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Year:  1996        PMID: 8944316     DOI: 10.1111/j.1750-3639.1996.tb00875.x

Source DB:  PubMed          Journal:  Brain Pathol        ISSN: 1015-6305            Impact factor:   6.508


  8 in total

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Authors:  Vassilis E Koliatsos; Athanasios S Alexandris
Journal:  Curr Opin Neurol       Date:  2019-12       Impact factor: 5.710

2.  Long-term effects of a lumbosacral ventral root avulsion injury on axotomized motor neurons and avulsed ventral roots in a non-human primate model of cauda equina injury.

Authors:  M Ohlsson; J H Nieto; K L Christe; L A Havton
Journal:  Neuroscience       Date:  2013-07-02       Impact factor: 3.590

3.  Cortical interneurons become activated by deafferentation and instruct the apoptosis of pyramidal neurons.

Authors:  V E Koliatsos; T M Dawson; A Kecojevic; Yueping Zhou; Yi-Feei Wang; K-X Huang
Journal:  Proc Natl Acad Sci U S A       Date:  2004-09-20       Impact factor: 11.205

4.  FK506 protects neurons following peripheral nerve injury via immunosuppression.

Authors:  Kapil Saxena; Nisha Patro; Ishan Patro
Journal:  Cell Mol Neurobiol       Date:  2007-12-14       Impact factor: 5.046

5.  Paclitaxel alters the evoked release of calcitonin gene-related peptide from rat sensory neurons in culture.

Authors:  Sherry K Pittman; Neilia G Gracias; Michael R Vasko; Jill C Fehrenbacher
Journal:  Exp Neurol       Date:  2013-12-26       Impact factor: 5.330

6.  Degeneration of axotomized projection neurons in the rat dLGN: temporal progression of events and their mitigation by a single administration of FGF2.

Authors:  Michael L Hendrickson; Changying Ling; Ronald E Kalil
Journal:  PLoS One       Date:  2012-11-05       Impact factor: 3.240

7.  Minocycline Increases in-vitro Cortical Neuronal Cell Survival after Laser Induced Axotomy.

Authors:  Burak Yulug; Mehmet Ozansoy; Merve Alokten; Muzaffer B C Ozansoy; Seyda Cankaya; Lutfu Hanoglu; Ulkan Kilic; Ertugrul Kilic
Journal:  Curr Clin Pharmacol       Date:  2020

8.  Upregulation of Nucleotide-Binding Oligomerization Domain-, LRR- and Pyrin Domain-Containing Protein 3 in Motoneurons Following Peripheral Nerve Injury in Mice.

Authors:  Bernát Nógrádi; Ádám Nyúl-Tóth; Mihály Kozma; Kinga Molnár; Roland Patai; László Siklós; Imola Wilhelm; István A Krizbai
Journal:  Front Pharmacol       Date:  2020-11-26       Impact factor: 5.810

  8 in total

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