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

被引:28
作者
Matsumura, Yukiko [1 ]
Yokoyama, Yoshihito [1 ]
Hirakawa, Hachidai [1 ]
Shigeto, Tatsuhiko [1 ]
Futagami, Masayuki [1 ]
Mizunuma, Hideki [1 ]
机构
[1] Hirosaki Grad Sch Med, Dept Obstet & Gynecol, Hirosaki, Aomori 0368562, Japan
来源
MOLECULAR PAIN | 2014年 / 10卷
关键词
Paclitaxel; Goshajinkigan; Peripheral neuropathy; Degeneration of the ganglion cells; TRPV4; GOSHA-JINKI-GAN; RECEPTOR POTENTIAL VANILLOID-4; CLINICAL-PRACTICE GUIDELINE; MICE LACKING TRPV4; HERBAL MEDICINE; OVARIAN-CANCER; CHANNELS; HYPERALGESIA; CHEMOTHERAPY; MULTICENTER;
D O I
10.1186/1744-8069-10-61
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: This study aimed to evaluate the prophylactic effect of goshajinkigan (GJG) on paclitaxel (PTX)-induced neuropathy and to elucidate the mechanism of action. Results: 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. Conclusions: 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.
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页数:8
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