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制川乌及其活性成分新乌头碱可能减轻奥沙利铂诱导的外周神经性疼痛。

Processed aconite root and its active ingredient neoline may alleviate oxaliplatin-induced peripheral neuropathic pain.

作者信息

Suzuki Toshiaki, Miyamoto Keisuke, Yokoyama Naomi, Sugi Mayuko, Kagioka Akina, Kitao Yuka, Adachi Takumi, Ohsawa Masahiro, Mizukami Hajime, Makino Toshiaki

机构信息

Department of Pharmacognosy, Graduate School of Pharmaceutical Sciences, Nagoya City University, 3-1 Tanabe-Dori, Mizuho-ku, Nagoya 467-8603, Japan; Department of Cellular Pharmacology, Graduate School of Pharmaceutical Sciences, Nagoya University, Nagoya 464-8601, Japan.

Department of Neuropharmacology, Graduate School of Pharmaceutical Sciences, Nagoya City University, 3-1 Tanabe-Dori, Mizuho-ku, Nagoya 467-8603, Japan.

出版信息

J Ethnopharmacol. 2016 Jun 20;186:44-52. doi: 10.1016/j.jep.2016.03.056. Epub 2016 Mar 30.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Processed aconite root (PA, the root of Aconitum carmichaeli, Ranunculaceae) is a crude drug used in traditional Chinese or Japanese kampo medicine to generate heat in the body and to treat pain associated with coldness. Oxaliplatin (L-OHP) is a platinum-based anticancer drug that frequently causes acute and chronic peripheral neuropathies, including cold and mechanical hyperalgesia.

AIM OF THE STUDY

We investigated the effects of PA on L-OHP-induced peripheral neuropathies and identified the active ingredient within PA extract.

MATERIALS AND METHODS

L-OHP was intraperitoneally injected into mice, and PA boiled water extract was orally administered. Cold and mechanical hyperalgesia were evaluated using the acetone test and the von Frey filament method, respectively. Dorsal root ganglion (DRG) neurons were isolated from normal mice and cultured with L-OHP with or without PA extract. Cell viability and neurite elongation were evaluated.

RESULTS

PA extract significantly attenuated cold and mechanical hyperalgesia induced by L-OHP in mice. In cultured DRG neurons, L-OHP reduced cell viability and neurite elongation in a dose-dependent manner. Treatment with PA extract significantly alleviated the L-OHP-induced reduction of neurite elongation, while the cytotoxicity of L-OHP was not affected. Using activity-guided fractionation, we isolated neoline from PA extract as the active ingredient. Neoline significantly alleviated L-OHP-induced reduction of neurite elongation in cultured DRG neurons in a concentration-dependent manner. Moreover, subcutaneous injection of neoline attenuated cold and mechanical hyperalgesia in L-OHP-treated mice. PA extract and neoline did not show sedation and motor impairment.

CONCLUSIONS

The present study indicates that PA and its active ingredient neoline are promising agents to alleviate L-OHP-induced neuropathic pain.

摘要

民族药理学相关性

制川乌(PA,毛茛科乌头属植物乌头的根)是一种在传统中医或日本汉方医学中使用的草药,用于在体内产生热量并治疗与寒冷相关的疼痛。奥沙利铂(L-OHP)是一种铂类抗癌药物,经常引起急性和慢性周围神经病变,包括冷觉和机械性痛觉过敏。

研究目的

我们研究了制川乌对奥沙利铂诱导的周围神经病变的影响,并确定了制川乌提取物中的活性成分。

材料与方法

将奥沙利铂腹腔注射到小鼠体内,并口服制川乌水煮提取物。分别使用丙酮试验和von Frey细丝法评估冷觉和机械性痛觉过敏。从正常小鼠中分离背根神经节(DRG)神经元,并用奥沙利铂加或不加制川乌提取物进行培养。评估细胞活力和神经突伸长。

结果

制川乌提取物显著减轻了奥沙利铂诱导的小鼠冷觉和机械性痛觉过敏。在培养的DRG神经元中,奥沙利铂以剂量依赖性方式降低细胞活力和神经突伸长。制川乌提取物处理显著减轻了奥沙利铂诱导的神经突伸长减少,而奥沙利铂的细胞毒性不受影响。通过活性导向分级分离,我们从制川乌提取物中分离出新乌头碱作为活性成分。新乌头碱以浓度依赖性方式显著减轻了培养的DRG神经元中奥沙利铂诱导的神经突伸长减少。此外,皮下注射新乌头碱减轻了奥沙利铂处理小鼠的冷觉和机械性痛觉过敏。制川乌提取物和新乌头碱未表现出镇静和运动障碍。

结论

本研究表明,制川乌及其活性成分新乌头碱有望缓解奥沙利铂诱导的神经性疼痛。

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