Literature DB >> 30598904

Chondroitinase ABC Enzyme: A Potential Treatment Option for Spinal Cord Injury.

Rajiv Mahajan1.   

Abstract

Entities:  

Year:  2018        PMID: 30598904      PMCID: PMC6259299          DOI: 10.4103/ijabmr.IJABMR_336_18

Source DB:  PubMed          Journal:  Int J Appl Basic Med Res        ISSN: 2229-516X


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After spinal cord injury (SCI), axons fail to regenerate in the adult mammalian central nervous system (CNS) leading to permanent paralysis.[1] At the site of injury, glial reaction occurs resulting in the formation of glial scar. Glial reaction results in recruitment of microglia, oligodendrocytes precursors, meningeal cells, astrocytes, and stem cells, besides containing oligodendrocytes and myelin debris. Most of these cells release molecules, inhibitory to axon regeneration, resulting in failure of regeneration. Even remyelination may be unsuccessful in such an environment.[2] Glial scar also contains chondroitin sulfate proteoglycan (CSPG), which along with inflammation, is recovery inhibiting factor.[3] Treatment strategy targeting CSPG using chondroitinase ABC (ChABC) enzyme offers the opportunity to improve the outcome of SCI. ChABC is obtained from Proteus vulgaris and it acts by degrading the glycosaminoglycan side chains of CSPGs.[4] Degradation of CSPG with the use of ChABC removes a regeneration inhibition from the glial scar. The plasticity in the CNS is increased with the removal of perineural nets. The mechanism of action of ChABC is unique and does not overlap with mechanisms of other available treatment options for SCI, thus making ChABC an attractive option for the treatment of SCI in combination with other strategies.[5] Treatment with ChABC has shown promising results in animal models of SCI. In a study in male Wistar rats using combination of low-level laser therapy (LLLT) as anti-inflammatory agent and ChABC as CSPG digesting factor after inducing SCI by “clip compression,” combination of LLLT and ChABC showed more effect on reduction of cavity size, improvement of myelination and number of axons around the cavity and decreasing the expression of glycogen synthase kinase-3 β, CSPG and aquaporin 4 expression compared to LLLT and ChABC alone, resulting in more functional recovery in combination group.[3] In another experiment, ChABC treatment reinstated postsynaptic activity below the lesion as evident to electrical stimulation of corticospinal neurons and promoted functional recovery of locomotor and proprioceptive behaviors in rats.[1] ChABC has also shown to promote functional recovery in acute SCI in rats when used in combination with rehabilitation, even after 4 weeks of spinal injury.[6] In a recently concluded study with dog models of naturally occurring severe chronic spinal cord injuries, intraspinal injections of ChABC have shown favorable results and authors have recommended to start human trials.[7] Although no human trials have been conducted till date, the results in animal studies are promising and points toward the potential benefit of ChABC in SCI.
  4 in total

Review 1.  Molecular approaches for spinal cord injury treatment.

Authors:  Fernanda Martins de Almeida; Suelen Adriani Marques; Anne Caroline Rodrigues Dos Santos; Caio Andrade Prins; Fellipe Soares Dos Santos Cardoso; Luiza Dos Santos Heringer; Henrique Rocha Mendonça; Ana Maria Blanco Martinez
Journal:  Neural Regen Res       Date:  2023-01       Impact factor: 6.058

2.  YsHyl8A, an Alkalophilic Cold-Adapted Glycosaminoglycan Lyase Cloned from Pathogenic Yersinia sp. 298.

Authors:  Shilong Zhang; Yujiao Li; Feng Han; Wengong Yu
Journal:  Molecules       Date:  2022-05-02       Impact factor: 4.927

Review 3.  The role of astrocyte-mediated plasticity in neural circuit development and function.

Authors:  Nelson A Perez-Catalan; Chris Q Doe; Sarah D Ackerman
Journal:  Neural Dev       Date:  2021-01-07       Impact factor: 3.842

4.  Reformation of the chondroitin sulfate glycocalyx enables progression of AR-independent prostate cancer.

Authors:  Chris Kedong Wang; Htoo Zarni Oo; Nader Al-Nakouzi; Irina Nelepcu; Nada Lallous; Charlotte B Spliid; Nastaran Khazamipour; Joey Lo; Sarah Truong; Colin Collins; Desmond Hui; Shaghayegh Esfandnia; Hans Adomat; Thomas Mandel Clausen; Tobias Gustavsson; Swati Choudhary; Robert Dagil; Eva Corey; Yuzhuo Wang; Anne Chauchereau; Ladan Fazli; Jeffrey D Esko; Ali Salanti; Peter S Nelson; Martin E Gleave; Mads Daugaard
Journal:  Nat Commun       Date:  2022-08-13       Impact factor: 17.694

  4 in total

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