Temporal and Spatial Changes of μ-Opioid Receptors in the Brain, Spinal Cord and Dorsal Root Ganglion in a Rat Lumbar Disc Herniation Model

被引:11
作者
Kaneuchi, Yoichi [1 ]
Sekiguchi, Miho [1 ]
Kameda, Takuya [1 ]
Kobayashi, Yoshihiro [1 ]
Konno, Shin-ichi [1 ]
机构
[1] Fukushima Med Univ, Sch Med, Dept Orthopaed Surg, 1 Hikarigaoka, Fukushima, Fukushima 9601295, Japan
关键词
allodynia; brain; caudate putamen; immunohistochemistry; lumbar disc herniation; mu-opioid receptor; neuropathic pain; nucleus accumbens; opioid; periaqueductal gray matter; western blotting; PAIN-RELATED BEHAVIOR; NECROSIS-FACTOR-ALPHA; AUTOLOGOUS NUCLEUS PULPOSUS; MESSENGER-RNA EXPRESSION; NERVE ROOT; INTERVERTEBRAL DISC; NITRIC-OXIDE; MECHANICAL ALLODYNIA; PHOSPHOLIPASE A(2); IN-VITRO;
D O I
10.1097/BRS.0000000000002776
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study Design. Controlled, interventional, animal study. Objective. To investigate the spatial and temporal changes of mu-opioid receptor (MOR) expression in a rat lumbar disc herniation (LDH) model. Summary of Background Data. MORs widely express in the peripheral and central nervous systems, and opioid drugs produce an analgesic effect through their activation. However, the efficacy of opioid drugs is sometimes inadequate in several pathological conditions of pain. MORs in the brain as well as the spinal cord (SC) and dorsal root ganglion (DRG) are thought to be associated with pain-related behavior, but the underlying mechanisms are not completely understood. Methods. In all, 91 adult female Sprague-Dawley rats were used. Autologous nucleus pulposus (NP) was applied onto the left L5 DRG in the NP group rats. Rats were divided into two surgical groups, the NP and the sham group. The von Frey test of left hind paw was performed before surgery, and 2, 7, 14, 21 and 28 days after surgery. Immunohistochemistry and immunoblotting in the DRG, SC, Caudate putamen, nucleus accumbens (NAc) and periaqueductal grey matter were performed before surgery, and 2, 7, 14, 21 and 28 days after surgery. Results. The thresholds in the NP group were significantly lower than those in the sham group from day 2 onwards. At days 7 and 14, MOR expression in the injured-side SC and DRG were significantly lower than those in the sham group. At day 21, MOR in the NAc was significantly decreased compared to that in the sham group. Conclusion. Changes of MOR expression in the NAc, SC and DRG were associated with pain-related behavior. This result might show the underling pathogenesis of the resistance to MOR agonists in the patient with LDH.
引用
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页码:85 / 95
页数:11
相关论文
共 56 条
[1]   Mu and delta opioid receptor-like immunoreactivity in the cervical spinal cord of the rat after dorsal rhizotomy or neonatal capsaicin: an analysis of pre- and postsynaptic receptor distributions [J].
Abbadie, C ;
Lombard, MC ;
Besson, JM ;
Trafton, JA ;
Basbaum, AI .
BRAIN RESEARCH, 2002, 930 (1-2) :150-162
[2]   Local application of disc-related cytokines on spinal nerve roots [J].
Aoki, Y ;
Rydevik, B ;
Kikuchi, S ;
Olmarker, K .
SPINE, 2002, 27 (15) :1614-1617
[3]  
ARVIDSSON U, 1995, J NEUROSCI, V15, P3328
[4]   Loss of spinal μ-opioid receptor is associated with mechanical allodynia in a rat model of peripheral neuropathy [J].
Back, Seung Keun ;
Lee, Jaehee ;
Hong, Seung Kil ;
Na, Heung Sik .
PAIN, 2006, 123 (1-2) :117-126
[5]   CHANGES OF REFLEXES IN VASOCONSTRICTOR NEURONS SUPPLYING THE CAT HINDLIMB FOLLOWING CHRONIC NERVE LESIONS - A MODEL FOR STUDYING MECHANISMS OF REFLEX SYMPATHETIC DYSTROPHY [J].
BLUMBERG, H ;
JANIG, W .
JOURNAL OF THE AUTONOMIC NERVOUS SYSTEM, 1983, 7 (3-4) :399-411
[6]   Nitric oxide as a mediator of nucleus pulposus-induced effects on spinal nerve roots [J].
Brisby, H ;
Byröd, G ;
Olmarker, K ;
Miller, VM ;
Aoki, Y ;
Rydevik, B .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2000, 18 (05) :815-820
[7]   THE ROLE OF THE BASAL GANGLIA IN NOCICEPTION AND PAIN [J].
CHUDLER, EH ;
DONG, WK .
PAIN, 1995, 60 (01) :3-38
[8]   Identifying brain regions for integrative sensorimotor processing with ankle movements [J].
Ciccarelli, O ;
Toosy, AT ;
Marsden, JF ;
Wheeler-Kingshott, CM ;
Sahyoun, C ;
Matthews, PM ;
Miller, DH ;
Thompson, AJ .
EXPERIMENTAL BRAIN RESEARCH, 2005, 166 (01) :31-42
[9]   Opioid receptors on peripheral sensory axons [J].
Coggeshall, RE ;
Zhou, ST ;
Carlton, SM .
BRAIN RESEARCH, 1997, 764 (1-2) :126-132
[10]   State-dependent opioid control of pain [J].
Fields, H .
NATURE REVIEWS NEUROSCIENCE, 2004, 5 (07) :565-575