Possibility of QX-314 as a novel therapeutic drug for neuropathic pain
Project/Area Number |
22659367
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Research Category |
Grant-in-Aid for Challenging Exploratory Research
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Allocation Type | Single-year Grants |
Research Field |
Surgical dentistry
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Research Institution | Niigata University |
Principal Investigator |
SEO Kenji 新潟大学, 医歯学系, 教授 (40242440)
|
Co-Investigator(Kenkyū-buntansha) |
MAEDA Takeyasu 新潟大学, 医歯学系, 教授 (40183941)
KITAGAWA Jyunichi 新潟大学, 医歯学系, 准教授 (50373006)
FUJIWARA Naoshi 新潟大学, 医歯学系, 教授 (70181419)
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Project Period (FY) |
2010 – 2012
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Project Status |
Completed (Fiscal Year 2012)
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Budget Amount *help |
¥3,220,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥420,000)
Fiscal Year 2012: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2011: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2010: ¥1,400,000 (Direct Cost: ¥1,400,000)
|
Keywords | QX-314, リドカイン / ニューロパチー / TRPV1 / PAIN / 三叉神経 / QX-314 / カプサイシン / 末梢神経 / 知覚 / 神経因性疼痛 / 下歯槽神経 / 神経切断 / TRPV1チャネル / ラット / 触覚 / 三叉神経脊髄路核 / 侵害刺激 / 膜電位 / C-繊維 |
Research Abstract |
A novel local anesthetic, QX-314 is known to have an effect of Na+ channel blockade.This action requires it to enter through TRIPV1 channel on the surface of the neuron and make a blockade action inside the neuron. Thus, we aimed to study the possibility of QX-314 in anti-nociceptive effect and investigated the effects of QX-314 on the withdraw threshold which was decreased by a resection of inferior alveolar nerve in the rats. The results were that QX-314 using together with capsaicin, the threshold became to be elevated. This was consistent with histological findings that TRIPV1channels increased in the injured trigeminal nerve. These suggested that QX-314 has a potential to be used as a therapeutic tool for neuropathic pain.
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Report
(4 results)
Research Products
(2 results)
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[Journal Article] Expression of TRPV1 channels after nerve injury provides an essential delivery tool for neuropathic pain attenuation2012
Author(s)
Zakir HM, Mostafeezur RM, Suzuki A, Hitomi S, Suzuki I, Maeda T, Seo K, Yamada Y, Yamamura K, Lev S, Binshtok AM, Iwata K, Kitagawa J
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Journal Title
Related Report
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