摘要
原文 | 英語 |
---|---|
頁(從 - 到) | 40-53 |
頁數 | 14 |
期刊 | Neurobiology of Disease |
卷 | 18 |
發行號 | 1 |
DOIs | |
出版狀態 | 已發佈 - 2005 |
對外發佈 | 是 |
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於: Neurobiology of Disease, 卷 18, 編號 1, 2005, p. 40-53.
研究成果: 雜誌貢獻 › 文章 › 同行評審
}
TY - JOUR
T1 - Skin denervation, neuropathology, and neuropathic pain in a laser-induced focal neuropathy
AU - Chiang, Hou-Yu
AU - Chen, Chin-Tin
AU - Chien, Hsiung-Fei
AU - Hsieh, Sung-Tsang
N1 - 被引用次數:22 Export Date: 16 March 2016 CODEN: NUDIE 通訊地址: Dept. of Anatomy and Cell Biology, Natl. Taiwan Univ. Coll. of Medicine, Taipei 10018, TaiwanTaiwan; 電子郵件: [email protected] 化學物質/CAS: calcitonin gene related peptide, 83652-28-2; cholinesterase, 9001-08-5; substance P, 33507-63-0; Biological Markers; Neuropeptides 參考文獻: Basbaum, A.I., Gautron, M., Jazat, F., Mayes, M., Guilbaud, G., The spectrum of fiber loss in a model of neuropathic pain in the rat: An electron microscopic study (1991) Pain, 47, pp. 359-367; Bennett, G.J., Xie, Y.K., A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man (1988) Pain, 33, pp. 87-107; Chaplan, S.R., Bach, F.W., Pogrel, J.W., Chung, J.M., Yaksh, T.L., Quantitative assessment of tactile allodynia in the rat paw (1994) J. Neurosci. Methods, 53, pp. 55-63; Craig, A.D., Pain mechanisms: Labeled lines versus convergence in central processing (2003) Annu. Rev. 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(1999) Neurology, 53, pp. 1614-1615; Ko, M.H., Chen, W.P., Lin-Shiau, S.Y., Hsieh, S.T., Age-dependent acrylamide neurotoxicity in mice: Morphology, physiology, and function (1999) Exp. Neurol., 158, pp. 37-46; Kupers, R.C., Nuytten, D., Castro-Costa, M., Gybels, J.M., A time course analysis of the changes in spontaneous and evoked behaviour in a rat model of neuropathic pain (1992) Pain, 50, pp. 101-111; Kupers, R., Yu, W., Persson, J.K., Xu, X.J., Wiesenfeld-Hallin, Z., Photochemically-induced ischemia of the rat sciatic nerve produces a dose-dependent and highly reproducible mechanical, heat and cold allodynia, and signs of spontaneous pain (1998) Pain, 76, pp. 45-59; Lin, W.M., Hsieh, S.T., Huang, I.T., Griffin, J.W., Chen, W.P., Ultrastructural localization and regulation of protein gene product 9.5 (1997) NeuroReport, 8, pp. 2999-3004; Lin, Y.W., Tseng, T.J., Lin, W.M., Hsieh, S.T., Cutaneous nerve terminal degeneration in painful mononeuropathy (2001) Exp. Neurol., 170, pp. 290-296; Lindenlaub, T., Sommer, C., Epidermal innervation density after partial sciatic nerve lesion and pain-related behavior in the rat (2002) Acta. Neuropathol. (Berl.), 104, pp. 137-143; Ma, W., Bisby, M.A., Calcitonin gene-related peptide, substance P and protein gene product 9.5 immunoreactive axonal fibers in the rat footpad skin following partial sciatic nerve injuries (2000) J. Neurocytol., 29, pp. 249-262; Malmberg, A.B., Basbaum, A.I., Partial sciatic nerve injury in the mouse as a model of neuropathic pain: Behavioral and neuroanatomical correlates (1998) Pain, 76, pp. 215-222; Menovsky, T., Van Den Berghweerman, M., Beek, J.F., Effect of CO 2 milliwatt laser on peripheral nerves: Part I. A dose-response study (1996) Microsurgery, 17, pp. 562-567; Menovsky, T., Van Den Berghweerman, M., Beek, J.F., Effect of CO 2 milliwatt laser on peripheral nerves: Part II. A histological and functional study (2000) Microsurgery, 20, pp. 150-155; Morris, S.J., Kunzek, S., Shore, A.C., The effect of acetylcholine on finger capillary pressure and capillary flow in healthy volunteers (1996) J. Physiol., 494, pp. 307-313; Myers, R.R., James, H.E., Powell, H.C., Laser injury of peripheral nerve: A model for focal endoneurial damage (1985) J. Neurol. Neurosurg. Psychiatry, 48, pp. 1265-1268; Myers, R.R., Heckman, H.M., Powell, H.C., Axonal viability and the persistence of thermal hyperalgesia after partial freeze lesions of nerve (1996) J. Neurol. Sci., 139, pp. 28-38; Nakuda, H., Lynch, C.D.P., McMorran, P.D., Aggravated reperfusion injury in STZ-diabetic nerve (2002) J. Peripher. Nerv. Syst., 7, pp. 37-43; Nuytten, D., Kupers, R., Lammens, M., Dom, R., Van Hees, J., Gybels, J., Further evidence for myelinated as well as unmyelinated fibre damage in a rat model of neuropathic pain (1992) Exp. Brain Res., 91, pp. 73-78; Oaklander, A.L., Romans, K., Horasek, S., Stocks, A., Hauer, P., Meyer, R.A., Unilateral postherpetic neuralgia is associated with bilateral sensory neuron damage (1998) Ann. Neurol., 44, pp. 789-795; Parry, G.J., Brown, M.J., Selective fiber vulnerability in acute ischemic neuropathy (1982) Ann. Neurol., 11, pp. 147-154; Periquet, M.I., Novak, V., Collins, M.P., Nagaraja, H.N., Erdem, S., Nash, S.M., Freimer, M.L., Mendell, J.R., Painful sensory neuropathy: Prospective evaluation using skin biopsy (1999) Neurology, 53, pp. 1641-1647; Rosen, E.D., Raymond, S., Zollman, A., Noria, F., Sandoval-Cooper, M., Shulman, A., Merz, J.L., Castellino, F.J., Laser-induced noninvasive vascular injury models in mice generate platelet- and coagulation-dependent thrombi (2001) Am. J. 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PY - 2005
Y1 - 2005
N2 - Small-diameter sensory nerves innervating the skin are responsive to noxious stimuli, and an injury to these nerves is presumably related to neuropathic pain. Injury-induced neuropathic pain in animals can be produced by laser irradiation, which usually requires concomitant use of photosensitive dyes, known as the photochemical approach. It is not clear whether laser irradiation alone can induce neuropathic pain. In addition, two issues are important to apply these approaches: the relationship between the extent of laser irradiation and the occurrence of neuropathic pain, and the susceptibility of small-diameter sensory nerves in the skin to laser-induced neuropathic pain. To address these issues, we designed a new model of focal neuropathy by applying a diode laser of 532 nm (100 mW) to the sciatic nerve and evaluated small-diameter nerves by quantifying skin innervation and large-diameter nerves by measuring amplitudes of the compound muscle action potential (CMAP). Immediately after laser irradiation, epineurial vessels were occluded due to the formation of thrombi, and the blood flow through these vessels was markedly reduced. On postoperative day (POD) 2, animals developed characteristic manifestations of neuropathic pain, including spontaneous pain behaviors, thermal hyperalgesia, and mechanical allodynia. These phenomena peaked during PODs 7-21, and lasted for 3-6 weeks. The neuropathology at the irradiated site of the sciatic nerve included a focal area of axonal degeneration surrounded by demyelination and endoneurial edema. The extent of damage to large-diameter motor and sensory nerves after laser irradiation was evaluated by nerve conduction studies. On the irradiated sides, amplitudes of the compound muscle action potentials and sensory nerve action potentials (SNAPs) were reduced to 65.0% (P <0.0001) and 42.5% (P <0.01) of those on the control sides, respectively. Motor innervation of the neuromuscular junctions (NMJs) on plantar muscles was examined by combined cholinesterase histochemistry and immunohistochemistry. The ratio of innervated NMJs on the operated sides decreased to 76.3% of that on the control side. Skin innervation in the territory of the irradiated sciatic nerves was evaluated by immunohistochemistry with neuronal markers. Among these markers, epidermal nerve densities for protein gene product (PGP) 9.5, calcitonin gene-related peptide (CGRP), and substance P (SP) were significantly lower on the irradiated sides than the control sides with a different degree of loss for each marker (42.1-53.1%, P <0.05). Results suggest that laser-induced focal neuropathy provides a new system for studying neuropathic pain. With this approach, the extent of nerve injury can be quantified. Both small-diameter epidermal nerves and large-diameter sensory and motor nerves are susceptible to laser-induced injury of different degrees. © 2004 Elsevier Inc. All rights reserved.
AB - Small-diameter sensory nerves innervating the skin are responsive to noxious stimuli, and an injury to these nerves is presumably related to neuropathic pain. Injury-induced neuropathic pain in animals can be produced by laser irradiation, which usually requires concomitant use of photosensitive dyes, known as the photochemical approach. It is not clear whether laser irradiation alone can induce neuropathic pain. In addition, two issues are important to apply these approaches: the relationship between the extent of laser irradiation and the occurrence of neuropathic pain, and the susceptibility of small-diameter sensory nerves in the skin to laser-induced neuropathic pain. To address these issues, we designed a new model of focal neuropathy by applying a diode laser of 532 nm (100 mW) to the sciatic nerve and evaluated small-diameter nerves by quantifying skin innervation and large-diameter nerves by measuring amplitudes of the compound muscle action potential (CMAP). Immediately after laser irradiation, epineurial vessels were occluded due to the formation of thrombi, and the blood flow through these vessels was markedly reduced. On postoperative day (POD) 2, animals developed characteristic manifestations of neuropathic pain, including spontaneous pain behaviors, thermal hyperalgesia, and mechanical allodynia. These phenomena peaked during PODs 7-21, and lasted for 3-6 weeks. The neuropathology at the irradiated site of the sciatic nerve included a focal area of axonal degeneration surrounded by demyelination and endoneurial edema. The extent of damage to large-diameter motor and sensory nerves after laser irradiation was evaluated by nerve conduction studies. On the irradiated sides, amplitudes of the compound muscle action potentials and sensory nerve action potentials (SNAPs) were reduced to 65.0% (P <0.0001) and 42.5% (P <0.01) of those on the control sides, respectively. Motor innervation of the neuromuscular junctions (NMJs) on plantar muscles was examined by combined cholinesterase histochemistry and immunohistochemistry. The ratio of innervated NMJs on the operated sides decreased to 76.3% of that on the control side. Skin innervation in the territory of the irradiated sciatic nerves was evaluated by immunohistochemistry with neuronal markers. Among these markers, epidermal nerve densities for protein gene product (PGP) 9.5, calcitonin gene-related peptide (CGRP), and substance P (SP) were significantly lower on the irradiated sides than the control sides with a different degree of loss for each marker (42.1-53.1%, P <0.05). Results suggest that laser-induced focal neuropathy provides a new system for studying neuropathic pain. With this approach, the extent of nerve injury can be quantified. Both small-diameter epidermal nerves and large-diameter sensory and motor nerves are susceptible to laser-induced injury of different degrees. © 2004 Elsevier Inc. All rights reserved.
KW - Epidermal nerves
KW - Ischemic neuropathy
KW - Laser irradiation
KW - Neuropathic pain
KW - Protein gene product 9.5
KW - Skin innervation
KW - Ubiquitin
KW - biochemical marker
KW - calcitonin gene related peptide
KW - cholinesterase
KW - gene product
KW - substance P
KW - allodynia
KW - amplitude modulation
KW - animal experiment
KW - animal model
KW - animal tissue
KW - article
KW - blood vessel
KW - controlled study
KW - demyelination
KW - denervation
KW - diode laser
KW - edema
KW - enzyme histochemistry
KW - experimental model
KW - hyperalgesia
KW - immunohistochemistry
KW - ischemia
KW - male
KW - motor nerve
KW - muscle action potential
KW - muscle innervation
KW - nerve conduction
KW - nerve fiber degeneration
KW - nerve injury
KW - neuromuscular synapse
KW - neuropathic pain
KW - neuropathology
KW - nonhuman
KW - peripheral neuropathy
KW - plantaris muscle
KW - priority journal
KW - rat
KW - sciatic nerve
KW - sciatic neuropathy
KW - sensory nerve
KW - skin nerve
KW - statistical significance
KW - thrombogenesis
KW - Animals
KW - Biological Markers
KW - Blood Vessels
KW - Denervation
KW - Disease Models, Animal
KW - Disease Susceptibility
KW - Lasers
KW - Male
KW - Nerve Fibers, Myelinated
KW - Nerve Fibers, Unmyelinated
KW - Neural Conduction
KW - Neuralgia
KW - Neuropeptides
KW - Nociceptors
KW - Peripheral Nervous System Diseases
KW - Rats
KW - Rats, Sprague-Dawley
KW - Receptors, Sensory
KW - Sciatic Nerve
KW - Sciatic Neuropathy
KW - Skin
KW - Wallerian Degeneration
U2 - 10.1016/j.nbd.2004.09.006
DO - 10.1016/j.nbd.2004.09.006
M3 - Article
SN - 0969-9961
VL - 18
SP - 40
EP - 53
JO - Neurobiology of Disease
JF - Neurobiology of Disease
IS - 1
ER -