New Insights in Understanding and Treating Bone Fracture Pain

被引:75
|
作者
Mitchell, Stefanie A. T. [1 ]
Majuta, Lisa A. [1 ]
Mantyh, Patrick W. [1 ,2 ]
机构
[1] Univ Arizona, Dept Pharmacol, 1501 N Campbell Ave,POB 245050, Tucson, AZ 85724 USA
[2] Univ Arizona, Canc Ctr, Tucson, AZ 85724 USA
来源
CURRENT OSTEOPOROSIS REPORTS | 2018年 / 16卷 / 04期
关键词
Skeletal; Nociceptors; Nerve growth factor; Pediatric; Genetic disorders; Geriatric; NERVE GROWTH-FACTOR; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; NONMALIGNANT SKELETAL PAIN; CANCER PAIN; SENSORY FIBERS; CENTRAL SENSITIZATION; SCLEROSTIN ANTIBODY; SUSTAINED BLOCKADE; MOUSE FEMUR; RAT MODEL;
D O I
10.1007/s11914-018-0446-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This paper describes recent advances in understanding the mechanisms that drive fracture pain and how these findings are helping develop new therapies to treat fracture pain. Immediately following fracture, mechanosensitive nerve fibers that innervate bone are mechanically distorted. This results in these nerve fibers rapidly discharging and signaling the initial sharp fracture pain to the brain. Within minutes to hours, a host of neurotransmitters, cytokines, and nerve growth factor are released by cells at the fracture site. These factors stimulate, sensitize, and induce ectopic nerve sprouting of the sensory and sympathetic nerve fibers which drive the sharp pain upon movement and the dull aching pain at rest. If rapid and effective healing of the fracture occurs, these factors return to baseline and the pain subsides, but if not, these factors can drive chronic bone pain. New mechanism-based therapies have the potential to fundamentally change the way acute and chronic fracture pain is managed.
引用
收藏
页码:325 / 332
页数:8
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