Literature DB >> 15048938

Subcutaneous tri-block copolymer produces recovery from spinal cord injury.

Richard B Borgens1, Debbie Bohnert, Brad Duerstock, Daniel Spomar, Raphael C Lee.   

Abstract

We have studied the ability of nonionic detergents and hydrophilic polymers to seal permeabilized membranes of damaged cells, rescuing them from progressive dissolution, degeneration, and death. We report that a single subcutaneous injection of the tri-block copolymer, Poloxamer 188 (P188) 6 hr after a severe compression of the adult guinea pig spinal cord is able to: (1). preserve the anatomic integrity of the cord; (2). produce a rapid recovery of nerve impulse conduction through the lesion; and (3). produce a behavioral recovery of a spinal cord dependent long tract spinal cord reflex. These observations stood out against a control group in blinded evaluation. Conduction through the lesion was monitored by stimulating the tibial nerve of the hind limb, and measuring the arrival of evoked potentials at the contralateral sensory cortex of the brain (somatosensory evoked potentials; SSEP). Behavioral recovery was determined by a return of sensitivity of formerly areflexic receptive fields of the cutaneous trunchi muscle (CTM) reflex. This contraction of back skin in response to tactile stimulation is totally dependent on the integrity of an identified bilateral column of ascending long tract axons. A statistically significant recovery of both SSEP conduction through the lesion and the CTM reflex occurred in P188-treated animals compared to vehicle-treated controls. Quantitative 3D computer reconstruction of the lesioned vertebral segment of spinal cord revealed a statistically significant sparing of spinal cord parenchyma and a significant reduction in cavitation of the spinal cord compared to control animals We determined that the proportion of P188-treated animals that recovered evoked potentials were nearly identical to that produced by a subcutaneous injection of polyethylene glycol (PEG). In contrast, P188 was not as effective as PEG in producing a recovery of CTM functioning. We discuss the likely differences in the mechanisms of action of these two polymers, and the possibilities inherent in a combined treatment. Copyright 2004 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15048938     DOI: 10.1002/jnr.20053

Source DB:  PubMed          Journal:  J Neurosci Res        ISSN: 0360-4012            Impact factor:   4.164


  14 in total

1.  Amphiphilic copolymers reduce aggregation of unfolded lysozyme more effectively than polyethylene glycol.

Authors:  Jaemin Chin; Devkumar Mustafi; Michael J Poellmann; Raphael C Lee
Journal:  Phys Biol       Date:  2017-02-08       Impact factor: 2.583

2.  Neuroprotective ferulic acid (FA)-glycol chitosan (GC) nanoparticles for functional restoration of traumatically injured spinal cord.

Authors:  Wei Wu; Seung-Young Lee; Xiangbing Wu; Jacqueline Y Tyler; He Wang; Zheng Ouyang; Kinam Park; Xiao-Ming Xu; Ji-Xin Cheng
Journal:  Biomaterials       Date:  2013-12-12       Impact factor: 12.479

3.  PEO-PPO Diblock Copolymers Protect Myoblasts from Hypo-Osmotic Stress In Vitro Dependent on Copolymer Size, Composition, and Architecture.

Authors:  Mihee Kim; Karen J Haman; Evelyne M Houang; Wenjia Zhang; Demetris Yannopoulos; Joseph M Metzger; Frank S Bates; Benjamin J Hackel
Journal:  Biomacromolecules       Date:  2017-06-14       Impact factor: 6.988

4.  Poloxamer 188 Attenuates Cerebral Hypoxia/Ischemia Injury in Parallel with Preventing Mitochondrial Membrane Permeabilization and Autophagic Activation.

Authors:  Chengliang Luo; Qianqian Li; Yuan Gao; Xi Shen; Lu Ma; Qiong Wu; Zufeng Wang; Mingyang Zhang; Ziqin Zhao; Xiping Chen; Luyang Tao
Journal:  J Mol Neurosci       Date:  2015-05-13       Impact factor: 3.444

5.  Kollidon VA64, a membrane-resealing agent, reduces histopathology and improves functional outcome after controlled cortical impact in mice.

Authors:  Lamin H Mbye; Eyup Keles; Luyang Tao; Jimmy Zhang; Joonyong Chung; Mykol Larvie; Rajani Koppula; Eng H Lo; Michael J Whalen
Journal:  J Cereb Blood Flow Metab       Date:  2011-11-16       Impact factor: 6.200

6.  Poloxamer-188 can attenuate blood-brain barrier damage to exert neuroprotective effect in mice intracerebral hemorrhage model.

Authors:  Tao Wang; Xiping Chen; Zufeng Wang; Mingyang Zhang; Huanhuan Meng; Yuan Gao; Bin Luo; Luyang Tao; Yijiu Chen
Journal:  J Mol Neurosci       Date:  2014-04-29       Impact factor: 3.444

Review 7.  Poloxamer 188 (p188) as a membrane resealing reagent in biomedical applications.

Authors:  Joseph G Moloughney; Noah Weisleder
Journal:  Recent Pat Biotechnol       Date:  2012-12

8.  Mechanical membrane injury induces axonal beading through localized activation of calpain.

Authors:  Devrim Kilinc; Gianluca Gallo; Kenneth A Barbee
Journal:  Exp Neurol       Date:  2009-07-18       Impact factor: 5.330

9.  Poloxamer 188 reduces the contraction-induced force decline in lumbrical muscles from mdx mice.

Authors:  Rainer Ng; Joseph M Metzger; Dennis R Claflin; John A Faulkner
Journal:  Am J Physiol Cell Physiol       Date:  2008-05-21       Impact factor: 4.249

10.  Effective repair of traumatically injured spinal cord by nanoscale block copolymer micelles.

Authors:  Yunzhou Shi; Sungwon Kim; Terry B Huff; Richard B Borgens; Kinam Park; Riyi Shi; Ji-Xin Cheng
Journal:  Nat Nanotechnol       Date:  2009-11-08       Impact factor: 39.213

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.