Department of Pain Medicine, MD Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030, USA.
Exp Neurol. 2011 Jun;229(2):353-7. doi: 10.1016/j.expneurol.2011.02.019. Epub 2011 Mar 5.
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.
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。