Paclitaxel-induced peripheral neuropathy in male rats attenuated by calmangafodipir, a superoxide dismutase mimetic

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Takehiro Kawashiri , Kohei Mori , Haruna Ishida , Mami Ueda , Kozo Yao , Fumiko Nagahama , Keisuke Mine , Yusuke Mori , Yusuke Koura , Shunsuke Fujita , Takao Shimazoe , Daisuke Kobayashi
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引用次数: 0

Abstract

Paclitaxel induces peripheral neuropathy, which is considered a dose-limiting factor. However, appropriate prophylactic agents are currently unavailable. We investigated the prophylactic effects of calmangafodipir, a superoxide dismutase mimetic, on paclitaxel-induced peripheral neuropathy using a male rat model. Repeated administration of paclitaxel (6 mg/kg, intraperitoneal, once weekly for 4 weeks) resulted in mechanical allodynia in the von Frey test and axonal degeneration in the sciatic nerve. Conversely, calmangafodipir (1–10 mg/kg, intravenous, thrice weekly for 4 weeks) prevented mechanical allodynia and axonal degeneration induced by paclitaxel. These results suggest that calmangafodipir may inhibit paclitaxel-induced peripheral neuropathy.
紫杉醇诱导的雄性大鼠外周神经病变可通过超氧化物歧化酶模拟物卡马福地平(Calangafodipir)得到缓解
紫杉醇会诱发周围神经病变,这被认为是一个剂量限制因素。然而,目前还没有合适的预防药物。我们以雄性大鼠为模型,研究了超氧化物歧化酶模拟物钙拮抗剂对紫杉醇诱导的周围神经病变的预防作用。重复给予紫杉醇(6 毫克/千克,腹腔注射,每周一次,连续 4 周)会导致 von Frey 试验中的机械异感和坐骨神经轴突变性。相反,卡马福迪皮(1-10 毫克/千克,静脉注射,每周三次,连续 4 周)可防止紫杉醇引起的机械异感和轴突变性。这些结果表明,钙泊三醇可抑制紫杉醇诱导的周围神经病变。
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来源期刊
CiteScore
6.20
自引率
2.90%
发文量
104
审稿时长
31 days
期刊介绍: Journal of Pharmacological Sciences (JPS) is an international open access journal intended for the advancement of pharmacological sciences in the world. The Journal welcomes submissions in all fields of experimental and clinical pharmacology, including neuroscience, and biochemical, cellular, and molecular pharmacology for publication as Reviews, Full Papers or Short Communications. Short Communications are short research article intended to provide novel and exciting pharmacological findings. Manuscripts concerning descriptive case reports, pharmacokinetic and pharmacodynamic studies without pharmacological mechanism and dose-response determinations are not acceptable and will be rejected without peer review. The ethnopharmacological studies are also out of the scope of this journal. Furthermore, JPS does not publish work on the actions of biological extracts unknown chemical composition.
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