P2X3 expression is not altered by lingual nerve injury

被引:9
作者
Biggs, James E. [1 ,2 ]
Yates, Julian M. [2 ]
Loescher, Alison R. [2 ]
Clayton, Nick M. [3 ]
Robinson, Peter P. [2 ]
Boissonade, Fiona M. [2 ]
机构
[1] Univ Alberta, Dept Pharmacol, Edmonton, AB T6G 2H7, Canada
[2] Univ Sheffield, Dept Oral & Maxillofacial Surg, Sch Clin Dent, Sheffield S10 2TN, S Yorkshire, England
[3] GlaxoSmithKline Inc, Neurol & GI CEDD, London, England
基金
英国医学研究理事会;
关键词
lingual nerve; trigeminal ganglion; P2X(3); neuropathic pain; dysaesthesia;
D O I
10.1016/j.neulet.2008.05.118
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We have investigated a possible role for the ATP receptor subunit P2X(3), in the development of neuropathic pain following injury to a peripheral branch of the trigeminal nerve. In nine anaesthetised adult ferrets the left lingual nerve was sectioned and recovery permitted for 3 days, 3 weeks or 3 months (3 ferrets per group). A retrograde tracer, fluorogold, was applied to the nerve to allow identification of cell bodies in the trigeminal ganglion with axons in the injured nerve. Indirect immunofluorescence for P2X(3) and image analysis was used to quantify the percentage area of staining at the site of injury. Additionally, the proportion of fluorogold-positive cells that expressed P2X(3) was determined and compared with expression in non-fluorogold containing cells in another part of the ganglion. Comparisons were made with results from control animals that only received the tracer injection. After lingual nerve injury there was no significant change in P2X(3) expression at the site of nerve injury or within cell bodies linked to either injured (lingual) or uninjured (ophthalmic) axons, at any of the time periods investigated. Overall, this study suggests that P2X(3) expression at these sites is not involved in the development of neuropathic pain following lingual nerve injury. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:110 / 114
页数:5
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