Light promotes regeneration and functional recovery and alters the immune response after spinal cord injury

被引:273
作者
Byrnes, KR
Waynant, RW
Ilev, IK
Wu, XJ
Barna, L
Smith, K
Heckert, R
Gerst, H
Anders, JJ
机构
[1] Uniformed Serv Univ Hlth Sci, Dept Anat Physiol & Genet, Bethesda, MD 20814 USA
[2] US FDA, Ctr Devices & Radiol Hlth, ElectroOpt Branch, Rockville, MD 20857 USA
关键词
astrocytes; corticospinal tract; footprint analysis; low power laser irradiation; macrophage; microglia; photobiomodulation; rat; retrograde and anterograde tract tracing;
D O I
10.1002/lsm.20143
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background and Objectives: Photobiomodulation (PBM) has been proposed as a potential therapy for spinal cord injury (SCI). We aimed to demonstrate that 810 nm light can penetrate deep into the body and promote neuronal regeneration and functional recovery. Study Design/Materials and Methods: Adult rats underwent a T9 dorsal hemisection, followed by treatment with an 810 nm, 150 mW diode laser (dosage = 1,589 J/cm(2)). Axonal regeneration and functional recovery were assessed using single and double label tract tracing and various locomotor tasks. The immune response within the spinal cord was also assessed. Results: PBM, with 6% power penetration to the spinal cord depth, significantly increased axonal number and distance of regrowth (P < 0.001). PBM also returned aspects of function to baseline levels and significantly suppressed immune cell activation and cytokine/chemokine expression. Conclusion: Our results demonstrate that light, delivered transcutaneously, improves recovery after injury and suggests that light will be a useful treatment for human SCI.
引用
收藏
页码:171 / 185
页数:15
相关论文
共 110 条
[1]   LOW-POWER LASER IRRADIATION ALTERS THE RATE OF REGENERATION OF THE RAT FACIAL-NERVE [J].
ANDERS, JJ ;
BORKE, RC ;
WOOLERY, SK ;
VANDEMERWE, WP .
LASERS IN SURGERY AND MEDICINE, 1993, 13 (01) :72-82
[2]   Neural repair of the injured spinal cord by grafting: comparison between peripheral nerve segments and embryonic homologous structures as a conduit of CNS axons [J].
Asada, Y ;
Kawaguchi, S ;
Hayashi, H ;
Nakamura, T .
NEUROSCIENCE RESEARCH, 1998, 31 (03) :241-249
[3]   Peroxynitrite generated in the rat spinal cord induces neuron death and neurological deficits [J].
Bao, F ;
Liu, D .
NEUROSCIENCE, 2002, 115 (03) :839-849
[4]   Expression of pro-inflammatory cytokine and chemokine mRNA upon experimental spinal cord injury in mouse: An in situ hybridization study [J].
Bartholdi, D ;
Schwab, ME .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1997, 9 (07) :1422-1438
[5]   CONTRIBUTION OF THE MITOCHONDRIAL COMPARTMENT TO THE OPTICAL-PROPERTIES OF THE RAT-LIVER - A THEORETICAL AND PRACTICAL APPROACH [J].
BEAUVOIT, B ;
KITAI, T ;
CHANCE, B .
BIOPHYSICAL JOURNAL, 1994, 67 (06) :2501-2510
[6]   2 NEW FLUORESCENT RETROGRADE NEURONAL TRACERS WHICH ARE TRANSPORTED OVER LONG DISTANCES [J].
BENTIVOGLIO, M ;
KUYPERS, HGJM ;
CATSMANBERREVOETS, CE ;
LOEWE, H ;
DANN, O .
NEUROSCIENCE LETTERS, 1980, 18 (01) :25-30
[7]   INFLAMMATORY CYTOKINES WITHIN THE CENTRAL-NERVOUS-SYSTEM - SOURCES, FUNCTION, AND MECHANISM OF ACTION [J].
BENVENISTE, EN .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (01) :C1-C16
[8]   Axotomized rubrospinal neurons rescued by fetal spinal cord transplants maintain axon collaterals to rostral CNS targets [J].
BernsteinGoral, H ;
Bregman, BS .
EXPERIMENTAL NEUROLOGY, 1997, 148 (01) :13-25
[9]   Intercostal nerve implants transduced with an adenoviral vector encoding neurotrophin-3 promote regrowth of injured rat corticospinal tract fibers and improve hindlimb function [J].
Blits, P ;
Dijkhuizen, PA ;
Boer, GJ ;
Verhaagen, J .
EXPERIMENTAL NEUROLOGY, 2000, 164 (01) :25-37
[10]  
Bregman B. S., 1994, FUNCTIONAL NEURAL TR, P489