Abating progressive tissue injury and preserving function after CNS trauma: The role of inflammation modulatory therapies.

Damien Pearse, Kurt Jarnagin
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Abstract

Brain and spinal cord injuries result in cognitive and/or sensorimotor impairments that can significantly diminish the quality of life for the patient and their carers, and result in healthcare system costs totaling in the billions. The current gold-standard of acute care for spinal cord injury is to administer high doses of glucocorticoids within 8 h of injury; administration after 8 h may be without effect or detrimental to the outcome of the patient. Therefore, improved pharmacological approaches for limiting the extent of tissue damage and neurological dysfunction in the acute injury setting are urgently needed. Early intervention in CNS injury by antagonizing or controlling the post-injury inflammatory process with pharmaceutical agents is a major focus of current clinical and preclinical investigations. In this editorial overview, recent clinical trials and preclinical studies of brain and spinal cord injuries are discussed, including studies focusing on the use of broad-spectrum immunosuppressive drugs (eg, minocycline); growth factors (eg, erythropoietin); dual anti-inflammatory and anti-vasospasm drugs, such as Rho and ROCK kinase inhibitors; and broad-spectrum anti-inflammatory drugs, such as PDE4 inhibitors. These new approaches hold great promise to improve outcomes for patients with brain and spinal injuries.

减轻中枢神经系统损伤后进行性组织损伤并保持功能:炎症调节疗法的作用。
脑和脊髓损伤会导致认知和/或感觉运动障碍,这可能会显著降低患者及其护理人员的生活质量,并导致总计数十亿美元的医疗保健系统成本。目前脊髓损伤急性护理的黄金标准是在损伤后8小时内给予高剂量糖皮质激素;8小时后给药可能对患者的预后没有影响或有害。因此,迫切需要改进的药理学方法来限制急性损伤环境中组织损伤和神经功能障碍的程度。通过药物拮抗或控制损伤后炎症过程来早期干预中枢神经系统损伤是当前临床和临床前研究的主要焦点。在这篇社论概述中,讨论了最近的脑和脊髓损伤的临床试验和临床前研究,包括集中于使用广谱免疫抑制药物(如米诺环素)的研究;生长因子(如促红细胞生成素);双重抗炎和抗血管痉挛药物,如Rho和ROCK激酶抑制剂;以及广谱抗炎药物,如PDE4抑制剂。这些新方法有望改善脑和脊髓损伤患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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