Literature DB >> 23793797

The neuroprotective ability of polyethylene glycol is affected by temperature in ex vivo spinal cord injury model.

Sogolie Kouhzaei1, Iman Rad, Kaveh Khodayari, Hamid Mobasheri.   

Abstract

Immediate membrane sealing after spinal cord injury (SCI) can prevent further degradation and result in ultimate functional recovery. It has been reported that polyethylene glycol (PEG) can repair membrane damage caused by mechanical insults to the spinal cord. Furthermore, membrane fluidity and its sealing process vary at different temperatures. Here, we have assessed the possible synergistic effects of PEG and temperature on the repair of neural membranes in an SCI model. The effects of PEGs (400, 1,000 and 2,000 Da) were studied at different temperatures (25, 37 and 40 °C) by means of compound action potential (CAP) recovery and a lactate dehydrogenase (LDH) assay. Isolated spinal cords were mounted in a double sucrose gap chamber, where the amplitude and area of CAPs were recorded after implementing injury, in the presence and absence of PEG. Moreover, the LDH assay was used to assess the effects of PEG on membrane resealing. Data showed that the least CAP recovery occurred at 25 °C, followed by 37 and 40 °C, in all treated groups. Moreover, maximum CAP amplitude recovery, 65.46 ± 5.04 %, was monitored in the presence of PEG400 at 40 °C, followed by 41.49 ± 2.41 % in PEG1000 and 37.36 ± 1.62 % in PEG2000. Furthermore, raising the temperature from 37 to 40 °C significantly increased CAP recovery in the PEG2000 group. Similar recovery patterns were obtained by CAP area measurements and LDH assay. The results suggest that application of low-molecular weight PEG (PEG400) in mild hyperthermia conditions (40 °C) provides the optimum condition for membrane sealing in SCI model.

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Year:  2013        PMID: 23793797     DOI: 10.1007/s00232-013-9574-3

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  32 in total

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2.  Cellular mechanisms of plasmalemmal sealing and axonal repair by polyethylene glycol and methylene blue.

Authors:  C S Spaeth; T Robison; J D Fan; G D Bittner
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Review 3.  Bioengineered strategies for spinal cord repair.

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Journal:  J Neurotrauma       Date:  2006 Mar-Apr       Impact factor: 5.269

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Authors:  J Pryor; R Shi
Journal:  Spinal Cord       Date:  2006-01-24       Impact factor: 2.772

5.  The increase of reactive oxygen species and their inhibition in an isolated guinea pig spinal cord compression model.

Authors:  J Luo; N Li; J P Robinson; R Shi
Journal:  Spinal Cord       Date:  2002-12       Impact factor: 2.772

6.  Acute repair of crushed guinea pig spinal cord by polyethylene glycol.

Authors:  R Shi; R B Borgens
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Authors: 
Journal:  J Colloid Interface Sci       Date:  1999-11-01       Impact factor: 8.128

8.  Polyethylene glycol enhances axolemmal resealing following transection in cultured cells and in ex vivo spinal cord.

Authors:  Ashley Nehrt; Kristin Hamann; Hui Ouyang; Riyi Shi
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9.  Hypothermia for spinal cord injury.

Authors:  Brian K Kwon; Cody Mann; Hong Moon Sohn; Alan S Hilibrand; Frank M Phillips; Jeffrey C Wang; Michael G Fehlings
Journal:  Spine J       Date:  2008-03-10       Impact factor: 4.166

10.  Behavioral recovery from spinal cord injury following delayed application of polyethylene glycol.

Authors:  Richard B Borgens; Riyi Shi; Debra Bohnert
Journal:  J Exp Biol       Date:  2002-01       Impact factor: 3.312

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  3 in total

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  3 in total

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