Neuronal pathways in tendon healing

被引:42
作者
Ackermann, Paul W. [1 ]
Salo, Paul T. [2 ]
Hart, David A. [2 ]
机构
[1] Karolinska Inst, Dept Mol Med & Surg, Orthoped Lab, Stockholm, Sweden
[2] Univ Calgary, Dept Surg, McCaig Inst Bone & Joint Hlth, Calgary, AB, Canada
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2009年 / 14卷
关键词
Neurotransmitters; Neuropeptides; Glutamate; Opioids; Tendon; Healing; Pain; Tendinopathy; Review; GENE-RELATED PEPTIDE; VASOACTIVE-INTESTINAL-PEPTIDE; NERVE-GROWTH-FACTOR; LOCAL CATECHOLAMINE PRODUCTION; IN-SITU HYBRIDIZATION; SUBSTANCE-P; NEUROPEPTIDE-Y; ACHILLES-TENDON; CONNECTIVE-TISSUE; MESSENGER-RNA;
D O I
10.2741/3593
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The regulatory mechanisms involved in tendon homeostasis and repair are not fully understood. Accumulating data, however, demonstrate that the nervous system, in addition to afferent (sensory) functions, through efferent neuronal pathways plays an active role in regulating pain, inflammation, and tissue repair processes. Thus, in normal-, healing- and tendinopathic tendons three major neuronal signalling pathways consisting of autonomic, sensory and glutamatergic neuromediators have been established. In healthy tendons, these neural elements are found in the paratenon, whereas the proper tendon is practically devoid of nerves, reflecting that normally tendon homeostasis is regulated by pro- and anti-inflammatory mediators from the tendon surroundings. During tendon repair, however, there is extensive nerve ingrowth into the tendon proper and subsequent time-dependent appearance of sensory, autonomic and glutamatergic mediators, which amplify and fine-tune inflammation and tendon regeneration. In tendinopathy excessive and protracted sensory and glutamatergic signalling may be involved in inflammatory, painful and hypertrophic tissue reactions. In a future perspective, neuronal mediators may prove to be useful in targeted pharmacotherapy and tissue engineering in painful, degenerative and traumatic tendon disorders.
引用
收藏
页码:5165 / 5187
页数:23
相关论文
共 150 条
[61]   Denervation impairs healing of the rabbit medial collateral ligament [J].
Ivie, TJ ;
Bray, RC ;
Salo, PT .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2002, 20 (05) :990-995
[62]   Inhibitory neurogenic modulation of histamine-induced cutaneous plasma extravasation in the pigeon [J].
Jancsó, G ;
Sántha, P ;
Horváth, V ;
Pierau, FK .
REGULATORY PEPTIDES, 2000, 95 (1-3) :75-80
[63]   Calcitonin gene related peptide and neuropeptide Y in skeletal muscle after eccentric exercise: a microdialysis study [J].
Jonhagen, S ;
Ackermann, P ;
Saartok, T ;
Renstrom, PA .
BRITISH JOURNAL OF SPORTS MEDICINE, 2006, 40 (03) :264-267
[64]  
KARANTH SS, 1990, HISTOCHEMISTRY, V94, P659
[65]   REINNERVATION AND NEUROPEPTIDES IN MOUSE SKIN FLAPS [J].
KARANTH, SS ;
DHITAL, S ;
SPRINGALL, DR ;
POLAK, JM .
JOURNAL OF THE AUTONOMIC NERVOUS SYSTEM, 1990, 31 (02) :127-134
[66]   Substance P augments fibrogenic cytokine-induced fibroblast proliferation: possible involvement of neuropeptide in tissue fibrosis [J].
Katayama, I ;
Nishioka, K .
JOURNAL OF DERMATOLOGICAL SCIENCE, 1997, 15 (03) :201-206
[67]  
Kim Lincoln R., 1998, Wound Repair and Regeneration, V6, P194, DOI 10.1046/j.1524-475X.1998.60305.x
[69]   Impaired angiogenesis in neuropeptide Y (NPY)-Y2 receptor knockout mice [J].
Lee, EW ;
Grant, DS ;
Movafagh, S ;
Zukowska, Z .
PEPTIDES, 2003, 24 (01) :99-106
[70]   INHIBITION OF NEUROGENIC VASODILATATION AND PLASMA EXTRAVASATION BY SUBSTANCE-P ANTAGONISTS, SOMATOSTATIN AND [D-MET2,PRO5]ENKEPHALINAMIDE [J].
LEMBECK, F ;
DONNERER, J ;
BARTHO, L .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1982, 85 (02) :171-176