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米诺环素可预防长春新碱诱导的周围神经病变小鼠模型中机械性异常性疼痛的发生。

Minocycline Prevents the Development of Mechanical Allodynia in Mouse Models of Vincristine-Induced Peripheral Neuropathy.

作者信息

Starobova H, Mueller A, Allavena R, Lohman R J, Sweet M J, Vetter I

机构信息

Centre for Pain Research, Institute for Molecular Bioscience, The University of Queensland, Saint Lucia, QLD, Australia.

School of Veterinary Science, The University of Queensland, Gatton, QLD, Australia.

出版信息

Front Neurosci. 2019 Jun 27;13:653. doi: 10.3389/fnins.2019.00653. eCollection 2019.

Abstract

Vincristine is an antineoplastic substance that is part of many chemotherapy regimens, used especially for the treatment of a variety of pediatric cancers including leukemias and brain tumors. Unfortunately, many vincristine-treated patients develop peripheral neuropathy, a side effect characterized by sensory, motoric, and autonomic symptoms. The sensory symptoms include pain, in particular hypersensitivity to light touch, as well as loss of sensory discrimination to detect vibration and touch. The symptoms of vincristine-induced neuropathy are only poorly controlled by currently available analgesics and therefore often necessitate dose reductions or even cessation of treatment. The aim of this study was to identify new therapeutic targets for the treatment of vincristine-induced peripheral neuropathy (VIPN) by combining behavioral experiments, histology, and pharmacology after vincristine treatment. Local intraplantar injection of vincristine into the hind paw caused dose- and time-dependent mechanical hypersensitivity that developed into mechanical hyposensitivity at high doses, and lead to a pronounced, dose-dependent infiltration of immune cells at the site of injection. Importantly, administration of minocycline effectively prevented the development of mechanical hypersensitivity and infiltration of immune cells in mouse models of vincristine induce peripheral neuropathy (VIPN) based on intraperitoneal or intraplantar administration of vincristine. Similarly, Toll-like receptor 4 knockout mice showed diminished vincristine-induced mechanical hypersensitivity and immune cell infiltration, while treatment with the anti-inflammatory meloxicam had no effect. These results provide evidence for the involvement of Toll-like receptor 4 in the development of VIPN and suggest that minocycline and/or direct Toll-like receptor 4 antagonists may be an effective preventative treatment for patients receiving vincristine.

摘要

长春新碱是一种抗肿瘤物质,是许多化疗方案的组成部分,尤其用于治疗包括白血病和脑肿瘤在内的多种儿科癌症。不幸的是,许多接受长春新碱治疗的患者会出现周围神经病变,这是一种以感觉、运动和自主神经症状为特征的副作用。感觉症状包括疼痛,特别是对轻触的超敏反应,以及检测振动和触觉的感觉辨别能力丧失。目前可用的镇痛药对长春新碱引起的神经病变症状控制不佳,因此常常需要减少剂量甚至停止治疗。本研究的目的是通过在长春新碱治疗后结合行为实验、组织学和药理学方法,确定治疗长春新碱引起的周围神经病变(VIPN)的新治疗靶点。将长春新碱局部足底内注射到后爪会引起剂量和时间依赖性的机械性超敏反应,在高剂量时会发展为机械性低敏反应,并导致注射部位免疫细胞明显的剂量依赖性浸润。重要的是,基于腹腔内或足底内注射长春新碱的长春新碱诱导的周围神经病变(VIPN)小鼠模型中,给予米诺环素可有效预防机械性超敏反应的发展和免疫细胞浸润。同样,Toll样受体4基因敲除小鼠显示长春新碱诱导的机械性超敏反应和免疫细胞浸润减弱,而用抗炎药美洛昔康治疗则无效。这些结果为Toll样受体4参与VIPN的发展提供了证据,并表明米诺环素和/或直接的Toll样受体4拮抗剂可能是接受长春新碱治疗患者的一种有效预防性治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/898b/6610325/a6e400f44b50/fnins-13-00653-g001.jpg

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