Antagonism of Nerve Growth Factor-TrkA Signaling and the Relief of Pain

被引:299
作者
Mantyh, Patrick W. [1 ]
Koltzenburg, Martin [1 ]
Mendell, Lorne M. [1 ]
Tive, Leslie [1 ]
Shelton, David L. [1 ]
机构
[1] Univ Arizona, Dept Pharmacol, Coll Med, Tucson, AZ USA
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
DORSAL-ROOT GANGLION; PRIMARY SENSORY NEURONS; GENE-RELATED PEPTIDE; EXPERIMENTAL AUTOIMMUNE MODEL; FACTOR INDUCED HYPERALGESIA; NONMALIGNANT SKELETAL PAIN; P75 NEUROTROPHIN RECEPTOR; NGF-INDUCED HYPERALGESIA; RAT SCIATIC-NERVE; ADULT-RAT;
D O I
10.1097/ALN.0b013e31821b1ac5
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
Nerve growth factor (NGF) was originally discovered as a neurotrophic factor essential for the survival of sensory and sympathetic neurons during development. However, in the adult NGF has been found to play an important role in nociceptor sensitization after tissue injury. The authors outline mechanisms by which NGF activation of its cognate receptor, tropomyosin-related kinase A receptor, regulates a host of ion channels, receptors, and signaling molecules to enhance acute and chronic pain. The authors also document that peripherally restricted antagonism of NGF-tropomyosin-related kinase A receptor signaling is effective for controlling human pain while appearing to maintain normal nociceptor function. Understanding whether there are any unexpected adverse events and how humans may change their behavior and use of the injured/degenerating tissue after significant pain relief without sedation will be required to fully appreciate the patient populations that may benefit from these therapies targeting NGF.
引用
收藏
页码:189 / 204
页数:16
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