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本文引用的文献

1
Intraepidermal nerve fiber loss corresponds to the development of taxol-induced hyperalgesia and can be prevented by treatment with minocycline.表皮内神经纤维缺失与紫杉醇诱导的痛觉过敏的发展相对应,并用米诺环素治疗可以预防。
Pain. 2011 Feb;152(2):308-313. doi: 10.1016/j.pain.2010.10.030. Epub 2010 Dec 9.
2
Natural history of cutaneous innervation following herpes zoster.带状疱疹后皮肤神经的自然史。
Pain. 2010 Jul;150(1):75-82. doi: 10.1016/j.pain.2010.04.002. Epub 2010 May 8.
3
Oxaliplatin-induced neuropathy in the rat: involvement of oxalate in cold hyperalgesia but not mechanical allodynia.奥沙利铂诱导的大鼠神经病变:草酸盐在冷觉过敏中的作用,但不在机械性痛觉过敏中。
Pain. 2009 Dec 15;147(1-3):165-74. doi: 10.1016/j.pain.2009.09.003. Epub 2009 Sep 25.
4
Utility of bortezomib retreatment in relapsed or refractory multiple myeloma patients: a multicenter case series.硼替佐米再次治疗复发或难治性多发性骨髓瘤患者的效用:一项多中心病例系列研究
Clin Adv Hematol Oncol. 2008 Oct;6(10):755-60.
5
The effects of thalidomide and minocycline on taxol-induced hyperalgesia in rats.沙利度胺和米诺环素对紫杉醇诱导的大鼠痛觉过敏的影响。
Brain Res. 2008 Sep 10;1229:100-10. doi: 10.1016/j.brainres.2008.07.001. Epub 2008 Jul 9.
6
Skin biopsy for the diagnosis of peripheral neuropathy.用于诊断周围神经病变的皮肤活检。
Histopathology. 2009 Feb;54(3):273-85. doi: 10.1111/j.1365-2559.2008.03096.x. Epub 2008 Jul 15.
7
Minocycline protects Schwann cells from ischemia-like injury and promotes axonal outgrowth in bioartificial nerve grafts lacking Wallerian degeneration.米诺环素可保护雪旺细胞免受缺血样损伤,并促进缺乏华勒变性的生物人工神经移植物中的轴突生长。
Exp Neurol. 2008 Jul;212(1):189-200. doi: 10.1016/j.expneurol.2008.03.028. Epub 2008 Apr 15.
8
A review on oxaliplatin-induced peripheral nerve damage.奥沙利铂所致周围神经损伤的综述
Cancer Treat Rev. 2008 Jun;34(4):368-77. doi: 10.1016/j.ctrv.2008.01.003. Epub 2008 Feb 20.
9
Incidence and characteristics of peripheral neuropathy during oxaliplatin-based chemotherapy for metastatic colon cancer.转移性结肠癌基于奥沙利铂化疗期间周围神经病变的发生率及特征
Acta Oncol. 2007;46(8):1131-7. doi: 10.1080/02841860701355055.
10
Behavioral and pharmacological description of oxaliplatin-induced painful neuropathy in rat.奥沙利铂诱导的大鼠疼痛性神经病变的行为学和药理学描述
Pain. 2007 Apr;128(3):225-234. doi: 10.1016/j.pain.2006.09.016. Epub 2006 Nov 7.

米诺环素预防奥沙利铂诱导的机械性痛觉过敏和表皮内神经纤维丢失。

Protection against oxaliplatin-induced mechanical hyperalgesia and intraepidermal nerve fiber loss by minocycline.

机构信息

Department of Pain Medicine, MD Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030, USA.

出版信息

Exp Neurol. 2011 Jun;229(2):353-7. doi: 10.1016/j.expneurol.2011.02.019. Epub 2011 Mar 5.

DOI:10.1016/j.expneurol.2011.02.019
PMID:21385581
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3100431/
Abstract

Treatment with the chemotherapeutic agent oxaliplatin produces a robust painful neuropathy similar to various other neuropathic conditions which result in loss of nerve fibers innervating the skin. This loss of intraepidermal nerve fibers (IENFs) appears to play an important role in neuropathy, but has yet to be investigated in oxaliplatin-induced neuropathic pain. For this study, mechanical hyperalgesia and IENF density were measured in rats receiving oxaliplatin, given at a dosage of 2 mg/kg every other day for four injections. The immunomodulatory agent minocycline (25 mg/kg) was also administered and was given 24 h prior to the first dose of oxaliplatin and continued throughout oxaliplatin treatment. Immunohistochemistry using the pan-neuronal marker PGP9.5 was used to investigate IENF densities in hind paw skin on Day 15 and Day 30. The results show that a robust mechanical sensitivity developed in oxaliplatin treated animals, as did a pronounced decrease in epidermal nerve fibers, and these outcomes were effectively prevented by minocycline treatment. This is the first study to show changes in IENF density in oxaliplatin treated animals, and confirm not only a relationship between IENF loss and hypersensitivity but also prevention of both with minocycline treatment.

摘要

用化疗药物奥沙利铂进行治疗会产生一种强烈的疼痛性神经病变,类似于其他各种导致支配皮肤的神经纤维丧失的神经病变状况。这种表皮内神经纤维(IENF)的丧失似乎在神经病变中起着重要作用,但在奥沙利铂诱导的神经性疼痛中尚未得到研究。在这项研究中,在接受奥沙利铂治疗的大鼠中测量了机械性痛觉过敏和 IENF 密度,奥沙利铂的剂量为每天 2 毫克/千克,每两天注射一次,共注射四次。还给予免疫调节剂米诺环素(25 毫克/千克),在奥沙利铂的第一剂前 24 小时给予,并在奥沙利铂治疗期间持续给予。使用泛神经元标志物 PGP9.5 进行免疫组织化学染色,以研究第 15 天和第 30 天后爪皮肤中的 IENF 密度。结果表明,奥沙利铂治疗的动物中出现了强烈的机械敏感性,表皮神经纤维也明显减少,米诺环素治疗有效地预防了这两种情况。这是第一项研究表明奥沙利铂治疗动物的 IENF 密度发生变化,并证实 IENF 丧失与过敏之间不仅存在关系,而且米诺环素治疗还可以预防两者。