Literature DB >> 11893023

A mouse model of acute ischemic spinal cord injury.

Manuel Gaviria1, Henri Haton, Françoise Sandillon, Alain Privat.   

Abstract

Mice models of spinal cord injury (SCI) should improve our knowledge of the mechanisms of injury and repair of the nervous tissue. They represent a powerful tool for the development of therapeutic strategies in the fields of pharmacological, cellular, and genetic approaches of neurotrauma. We demonstrate here that the photochemical graded ischemic spinal cord injury model, described in rats, can be successfully adapted in mice, in a reliable and reproducible manner. Following the intravenous injection of Rose Bengal, the translucent dorsal surface of the T9 vertebral laminae of C57BL/6 female mice was irradiated with a 560-nm wavelength-light (3-8 min depending on the experimental group). Animals were sacrificed at 1 day or 7 days after injury. Functional tests were performed daily for motor, sensory, autonomic, and reflex responses. Lesion histopathology was assessed for lesion length, percentage of residual white matter, and astrocytic reactivity. Experimental groups demonstrated a functional deficit, which was correlated to the increase of the irradiation time and, therefore, to the severity of the injury. Histopathological and immunocytochemical data were reliable morphological measurements characterizing the degree of injury, which were strongly correlated to the severity of the functional impairment. Despite differences in the mechanism of injury, the wound healing response described in other traumatic SCI mice models was confirmed (no cavitation and, conversely, the formation of a dense connective tissue matrix). In this context, the precise understanding of the mechanisms of healing response after SCI in mice and of neurochemical kinetics appear to be crucial in the development of therapeutic strategies of CNS repair. Thus, the possible use of an increasing collection of transgenic mice offers a new dimension for experimental research in this area. The ischemic photochemical model of SCI in mice represents a relevant model that can play a key role in this new era of neurotrauma research.

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Year:  2002        PMID: 11893023     DOI: 10.1089/08977150252806965

Source DB:  PubMed          Journal:  J Neurotrauma        ISSN: 0897-7151            Impact factor:   5.269


  12 in total

1.  Axonal plasticity and functional recovery after spinal cord injury in mice deficient in both glial fibrillary acidic protein and vimentin genes.

Authors:  V Menet; M Prieto; A Privat; M Giménez y Ribotta
Journal:  Proc Natl Acad Sci U S A       Date:  2003-07-14       Impact factor: 11.205

Review 2.  Animal models of spinal cord injury: a systematic review.

Authors:  M Sharif-Alhoseini; M Khormali; M Rezaei; M Safdarian; A Hajighadery; M M Khalatbari; M Safdarian; S Meknatkhah; M Rezvan; M Chalangari; P Derakhshan; V Rahimi-Movaghar
Journal:  Spinal Cord       Date:  2017-01-24       Impact factor: 2.772

3.  Development of a simplified spinal cord ischemia model in mice.

Authors:  Zhengfeng Wang; Wei Yang; Gavin W Britz; Frederick W Lombard; David S Warner; Huaxin Sheng
Journal:  J Neurosci Methods       Date:  2010-04-13       Impact factor: 2.390

Review 4.  Animal models of spinal injury for studying back pain and SCI.

Authors:  Shakti A Goel; Vicky Varghese; Tyfik Demir
Journal:  J Clin Orthop Trauma       Date:  2020-07-08

Review 5.  The animal model of spinal cord injury as an experimental pain model.

Authors:  Aya Nakae; Kunihiro Nakai; Kenji Yano; Ko Hosokawa; Masahiko Shibata; Takashi Mashimo
Journal:  J Biomed Biotechnol       Date:  2011-03-07

6.  Grafted human embryonic progenitors expressing neurogenin-2 stimulate axonal sprouting and improve motor recovery after severe spinal cord injury.

Authors:  Florence E Perrin; Guillaume Boniface; Che Serguera; Nicolas Lonjon; Angeline Serre; Monica Prieto; Jacques Mallet; Alain Privat
Journal:  PLoS One       Date:  2010-12-30       Impact factor: 3.240

7.  Behavioral improvement and regulation of molecules related to neuroplasticity in ischemic rat spinal cord treated with PEDF.

Authors:  Chary Marquez Batista; Leonardo Luis Torres Bianqui; Bruno Bonganha Zanon; Mauricio Menezes Aben Athar Ivo; Gabriela Pintar de Oliveira; Jessica Ruivo Maximino; Gerson Chadi
Journal:  Neural Plast       Date:  2014-07-03       Impact factor: 3.599

8.  Flufenamic acid inhibits secondary hemorrhage and BSCB disruption after spinal cord injury.

Authors:  Yingtao Yao; Jianyi Xu; Tingting Yu; Zhilong Chen; Zhiyong Xiao; Jiedong Wang; Yiqiang Hu; Yongchao Wu; Dan Zhu
Journal:  Theranostics       Date:  2018-07-30       Impact factor: 11.556

Review 9.  Functional Test Scales for Evaluating Cell-Based Therapies in Animal Models of Spinal Cord Injury.

Authors:  Woon Ryoung Kim; Minjin Kang; Heejoo Park; Hyun-Joo Ham; Hyunji Lee; Dongho Geum
Journal:  Stem Cells Int       Date:  2017-10-04       Impact factor: 5.443

10.  Perturbing chondroitin sulfate proteoglycan signaling through LAR and PTPσ receptors promotes a beneficial inflammatory response following spinal cord injury.

Authors:  Scott Dyck; Hardeep Kataria; Arsalan Alizadeh; Kallivalappil T Santhosh; Bradley Lang; Jerry Silver; Soheila Karimi-Abdolrezaee
Journal:  J Neuroinflammation       Date:  2018-03-20       Impact factor: 8.322

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