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纤维蛋白凝胶中 ABC 软骨素酶的控释可降低损伤脊髓中抑制性糖胺聚糖链的水平。

Controlled release of chondroitinase ABC from fibrin gel reduces the level of inhibitory glycosaminoglycan chains in lesioned spinal cord.

机构信息

Centre for Brain Repair, University of Cambridge, Robinson Way, Cambridge CB2 0PY, United Kingdom.

出版信息

J Control Release. 2010 Oct 1;147(1):24-9. doi: 10.1016/j.jconrel.2010.06.026. Epub 2010 Jul 8.

Abstract

Chondroitinase ABC (ChABC) is a bacterial enzyme that can enhance plasticity following injury to the central nervous system (CNS) by degrading the glycosaminoglycan (GAG) side chains of proteoglycans. CNS lesions treated with ChABC often show enhanced axonal sprouting and improved functional recovery and there is therefore much interest in the potential use of ChABC as a clinical treatment in humans. When highly concentrated fibrin gel containing ChABC was implanted adjacent to a spinal cord lesion, bioactive ChABC was detectable in the spinal cord for at least three weeks. Nearly six times more bioactive ChABC was detected in the spinal cord 3 weeks after injury when the fibrin delivery system was used vs. an intraspinal injection of ChABC (61+/-30 mU vs. 11+/-4 mU). Furthermore, 3 weeks after injury the level of inhibitory GAG found in injured spinal cord treated with the delivery system was 37% lower than the level of GAG in spinal cord treated with an injection of ChABC. When using the delivery system, 24.4% of the initial ChABC dose could still be detected in the lesion after 3 weeks, compared to just 4.4% when using an intraspinal injection of ChABC.

摘要

软骨素酶 ABC(ChABC)是一种细菌酶,可通过降解蛋白聚糖(PG)的糖胺聚糖(GAG)侧链来增强中枢神经系统(CNS)损伤后的可塑性。用 ChABC 治疗的 CNS 损伤常显示出增强的轴突发芽和改善的功能恢复,因此人们对 ChABC 作为人类临床治疗的潜在用途非常感兴趣。当将含有 ChABC 的高浓度纤维蛋白凝胶植入脊髓损伤部位附近时,可在脊髓中检测到至少 3 周的生物活性 ChABC。与 ChABC 椎管内注射(61+/-30 mU 比 11+/-4 mU)相比,在损伤后 3 周时,纤维蛋白递送系统的生物活性 ChABC 检测值增加了近 6 倍(61+/-30 mU 比 11+/-4 mU)。此外,在损伤后 3 周时,用递送系统治疗的损伤脊髓中抑制性 GAG 的水平比用 ChABC 注射治疗的脊髓中的 GAG 水平低 37%。使用递送系统时,在 3 周后仍可在损伤部位检测到初始 ChABC 剂量的 24.4%,而用 ChABC 椎管内注射时仅为 4.4%。

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