Effects of FKBP-12 ligands following tibial nerve injury in rats

被引:35
作者
Becker, DB [1 ]
Jensen, JN [1 ]
Myckatyn, TM [1 ]
Doolabh, VB [1 ]
Hunter, DA [1 ]
Mackinnon, SE [1 ]
机构
[1] Washington Univ, Sch Med, Div Plast & Reconstruct Surg, St Louis, MO 63110 USA
关键词
D O I
10.1055/s-2000-9379
中图分类号
R61 [外科手术学];
学科分类号
摘要
The neuroregenerative properties of FK506, an FKBP-12 ligand that inhibits calcineurin, and V-10,367, an FKBP-12 ligand that does not inhibit calcineurin, were evaluated in crush and transection models. Rats were randomly assigned to one of seven groups, including untreated controls and FK506- or V-10,367-treated experimental groups. Following crush or transection nerve injury, animals were assessed with walking tracks, and histomorphometry FK506-treated animals demonstrated significant functional recovery 11 days following crush and 18 days following transection injury. In untreated and V-10,367 treated animals, nerves recovered 13 days following crush injury, but did not improve significantly prior to sacrifice at 28 days in animals sustaining a transection injury. No statistically significant differences in histomorphometric parameters were identified between any of the groups, The study confirms that FK506 accelerates recovery from tibial nerve injury.
引用
收藏
页码:613 / 620
页数:8
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