Brain-derived TNFα:: involvement in neuroplastic changes implicated in the conscious perception of persistent pain

被引:92
作者
Covey, WC
Ignatowski, TA
Knight, PR
Spengler, RN
机构
[1] SUNY Buffalo, Sch Med & Biomed Sci, Dept Pathol, Buffalo, NY 14214 USA
[2] SUNY Buffalo, Sch Med & Biomed Sci, Dept Anesthesiol, Buffalo, NY 14214 USA
关键词
tumor necrosis factor; adrenergic; pain; central nervous system; brain;
D O I
10.1016/S0006-8993(00)01965-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The pleiotropic cytokine tumor necrosis factor-alpha (TNF alpha) is implicated in the development of persistent pain through its actions in the periphery and in the central nervous system (CNS). Activation of the alpha(2)-adrenergic receptor is associated with modulation of pain, possibly through its autoregulatory effect on norepinephrine (NE) release in the CNS. The present study employs a chronic constriction nerve injury (CCI) pain model to demonstrate the interactive role of presynaptic sensitivity to TNF alpha and the alpha(2)-adrenergic autoreceptor in the pathogenesis of neuropathic pain. Accumulation of TNF alpha is increased initially in a region of the brain containing the locus coeruleus (LC) at day 4 post-ligature placement, followed by an increase in TNF alpha in the hippocampus at day 8 post-ligature placement, coincident with hyperalgesia. Levels of TNF alpha in the thoraco-lumbar spinal cord are also increased at day 8 post-ligature placement. Concurrently, alpha(2)-adrenergic receptor and TNF alpha-induced inhibition of NE release are increased, and stimulated NE release is decreased in superfused hippocampal slices isolated at day 8 post-ligature placement. Stimulated NE release is also decreased in spinal cord slices (lumbar region) from animals undergoing CCI, although in contrast to that which occurs in the hippocampus, alpha(2)-adrenergic receptor inhibition of NE release is not changed. These results indicate an important role that TNF alpha plays in adrenergic neuroplastic changes in a region of the brain that, among its many functions, appears to be a crucial link in the conscious perception of pain. We predict that neuroplastic changes, involving increased functional responses of alpha(2)-adrenergic autoreceptors and increased presynaptic sensitivity to TNF alpha, culminate in decreased NE release in the CNS. These neuroplastic changes provide a mechanism for the role of CNS-derived TNF alpha in the pathogenesis of persistent pain. (C) 2000 Elsevier Science B.V. All rights reserved.
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页码:113 / 122
页数:10
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