The prophylactic effects of a traditional Japanese medicine, goshajinkigan, on paclitaxel-induced peripheral neuropathy and its mechanism of action.

The prophylactic effects of a traditional Japanese medicine, goshajinkigan, on paclitaxel-induced peripheral neuropathy and its mechanism of action.
复制标题

DOI:
10.1186/1744-8069-10-61
复制
发表时间:
2014-09-21
期刊:
影响因子:
3.3
通讯作者:
Mizunuma H
Mizunuma H
中科院分区:
医学3区
文献类型:
--
作者:
Matsumura Y;Yokoyama Y;Hirakawa H;Shigeto T;Futagami M;Mizunuma H

文献摘要

参考文献

相似文献

本研究旨在评估 goshajinkigan (GJG) 对紫杉醇 (PTX) 诱导的神经病变的预防作用并阐明其作用机制。 PTX 组的疼痛阈值出现时间依赖性不可逆转的下降。在PTX/GJG组中,疼痛阈值的变化与对照组相同。电镜观察显示,对照组和PTX/GJG组神经节细胞正常,但PTX组细胞核变性,线粒体肿胀。 PTX组瞬时受体电位香草酸4(TRPV4)基因的表达较对照组和PTX/GJG组显着升高。在 TRPV4 敲除小鼠中,没有观察到 PTX 诱导的痛觉过敏,并且 3 组之间的疼痛阈值没有显着差异。这些结果表明,PTX 通过增强 TRPV4 表达来诱导痛觉过敏,并表明 GJG 可能通过防止神经节细胞变性和抑制 TRPV4 表达来减轻痛觉过敏。
This study aimed to evaluate the prophylactic effect of goshajinkigan (GJG) on paclitaxel (PTX)-induced neuropathy and to elucidate the mechanism of action. There was a time-dependent irreversible decrease in pain threshold in PTX group. In PTX/GJG group, pain threshold showed changes in the same level as control. Electron microscope showed that although the ganglion cells of control and PTX/GJG groups were normal, degeneration of the nucleus and swelling of the mitochondria were observed in PTX group. Expression of transient receptor potential vanilloid 4 (TRPV4) gene in PTX group significantly increased compared with that in control and PTX/GJG groups. In TRPV4 knock-out mice, no PTX-induced hyperalgesia was observed, and there was no significant difference in pain threshold between the 3 groups. These results showed that PTX induced hyperalgesia by enhancing TRPV4 expression, and suggested that GJG might alleviate hyperalgesia by preventing degeneration of the ganglion cells and suppressing TRPV4 expression.
DOI: 10.1038/375424a0
发表时间: 1995-06-01
期刊: NATURE
影响因子: 64.8
作者:
NOGALES, E;WOLF, SG;DOWNING, KH
通讯作者: DOWNING, KH
DOI: 10.1152/ajpcell.00559.2002
发表时间: 2003-07-01
影响因子: 5.5
作者:
Mizuno, A;Matsumoto, N;Suzuki, M
通讯作者: Suzuki, M
DOI: 10.1007/s00424-011-1071-x
发表时间: 2012-04-01
影响因子: 4.5
作者:
Materazzi, Serena;Fusi, Camilla;Nassini, Romina
通讯作者: Nassini, Romina
DOI: 10.1007/bf00916043
发表时间: 1986-03-01
期刊: INFLAMMATION
影响因子: 5.1
作者:
NIWA, Y;MIYACHI, Y
通讯作者: MIYACHI, Y
DOI: 10.1097/cad.0000000000000022
发表时间: 2014-01-01
期刊: ANTI-CANCER DRUGS
影响因子: 2.3
作者:
Kato, Yoshinori;Tateai, Yoshikazu;Yamada, Harumi
通讯作者: Yamada, Harumi