Preferential expression of IGF-I in small DRG neurons and down-regulation following injury

被引:63
作者
Craner, MJ
Klein, JP
Black, JA
Waxman, SG
机构
[1] Yale Univ, Sch Med, Dept Neurol, LCI 707, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, PVA EPVA Ctr Neurosci & Regenerat Res, New Haven, CT 06510 USA
[3] VA Connecticut Healthcare Syst, Rehabil Res Ctr, West Haven, CT 06516 USA
关键词
Axotomy; diabetes; growth factor; hyperexcitability; neuropathy; nociception; sodium channel;
D O I
10.1097/00001756-200209160-00016
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In this study, we examined the expression of insulin-like growth factor I (IGF-I) and its receptor (IGF-IR) in dorsal root ganglia (DRG) neurons in two rodent models of nerve injury: sciatic nerve axotomy and streptozotocin-induced (STZ) painful diabetic neuropathy. We demonstrate that IGF-I and its receptor are preferentially expressed in small (< 25 mu m diameter) DRG neurons. There is a significant down-regulation in the expression of IGF-I and IGF-IR in the small DRG neurons of STZ rats by 59% and 71%, respectively. A parallel reduction in expression is shown in axotomized < 25 mum diameter DRG neurons for IGF-I (47%) but not for IGF-IR. The loss of IGF-I support to a population of predominantly nociceptive neurons may contribute to neuropathic pain observed in these models.
引用
收藏
页码:1649 / 1652
页数:4
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