摘要
原文 | 英語 |
---|---|
頁(從 - 到) | 576-587 |
頁數 | 12 |
期刊 | Journal of Neuropathology and Experimental Neurology |
卷 | 64 |
發行號 | 7 |
出版狀態 | 已發佈 - 2005 |
對外發佈 | 是 |
指紋
深入研究「Reinnervation of muscular targets by nerve regeneration through guidance conduits」主題。共同形成了獨特的指紋。引用此
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於: Journal of Neuropathology and Experimental Neurology, 卷 64, 編號 7, 2005, p. 576-587.
研究成果: 雜誌貢獻 › 文章 › 同行評審
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TY - JOUR
T1 - Reinnervation of muscular targets by nerve regeneration through guidance conduits
AU - Chiang, Hou-Yu
AU - Chien, Hsiung-Fei
AU - Shen, Hsin-Hsin
AU - Yang, Jean-Dean
AU - Chen, Yu-Hua
AU - Chen, Jui-Hsiang
AU - Hsieh, Sung-Tsang
N1 - 被引用次數:20 Export Date: 16 March 2016 CODEN: JNENA 通訊地址: Hsieh, S.-T.; Department of Anatomy and Cell Biology, National Taiwan University College of Medicine, No. 1 Jen-Ai Rd., Sec. 1, Taipei 10063, Taiwan; 電子郵件: [email protected] 化學物質/CAS: cholinesterase, 9001-08-5; polycaprolactone, 24980-41-4, 25248-42-4; aquaplast, caprolactone, 24980-41-4; Biocompatible Materials; Cholinesterases, EC 3.1.1.8; Polyesters 參考文獻: Bisby, M.A., Regeneration of peripheral nervous system axons (1995) The Axons: Structure, Function and Pathophysiology, pp. 553-577. , Waxman SG, Kocsis JD, Stys PK, eds. New York: Oxford University Press; Griffin, J.W., Hoffman, P.N., Degeneration and regeneration in the peripheral nervous system (1993) Peripheral Neuropathy, pp. 361-375. , Dyck PJ, ed. Philadelphia: W.B. 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Rodriguez, F.J., Gomez, N., Perego, G., Navarro, X., Highly permeable polylactide-caprolactone nerve guides enhance peripheral nerve regeneration through long gaps (1999) Biomaterials, 20, pp. 1489-1500; Ceballos, D., Navarro, X., Dubey, N., Wendelschafer-Crabb, G., Kennedy, W.R., Tranquillo, R.T., Magnetically aligned collagen gel filling a collagen nerve guide improves peripheral nerve regeneration (1999) Exp Neurol, 158, pp. 290-300; Dubey, N., Letourneau, P.C., Tranquillo, R.T., Guided neurite elongation and Schwann cell invasion into magnetically aligned collagen in simulated peripheral nerve regeneration (1999) Exp Neurol, 158, pp. 338-350; Rangappa, N., Romero, A., Nelson, K.D., Eberhart, R.C., Smith, G.M., Laminin-coated poly (L-lactide) filaments induce robust neurite growth while providing directional orientation (2000) J Biomed Mater Res, 51, pp. 625-634; Yoshii, S., Oka, M., Collagen filaments as a scaffold for nerve regeneration (2001) J Biomed Mater Res, 56, pp. 400-405; Terada, N., Bjursten, L.M., Papaloizis, M., Lundborg, G., Resorbable filament structures as a scaffold for matrix formation and axonal growth in bioartificial nerve grafts: Long term observations (1997) Restor Neurol Neurosci, 11, pp. 65-69; Varejao, A.S.P., Cabrita, A.M., Meek, M.F., Fornaro, M., Geuna, S., Giacobini-Robecchi, M.G., Morphology of nerve fiber regeneration along a biodegradable poly (DLLA-ε-CL) nerve guide filled with fresh skeletal muscle (2003) Microsurgery, 23, pp. 338-345; Varejao, A.S.P., Cabrita, A.M., Geuna, S., Functional assessment of sciatic nerve recovery: Biodegradable poly (DLLA-ε-CL) nerve guide filled with fresh skeletal muscle (2003) Microsurgery, 23, pp. 346-353; (1985) Guide for the Care and Use of Lab Animals, , Washington, D.C.: US Department of Health and Human Services; 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; 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; Zhao, Q.Z., Drott, J., Laurell, T., Rat sciatic nerve regeneration through a micromachined silicon chip (1997) Biomaterials, 18, pp. 75-80; Hadlock, T.A., Sundback, C.A., Hunter, D.A., Vacanti, J.P., Cheney, M.L., A new artificial nerve graft containing rolled Schwann cell monolayers (2001) Microsurgery, 21, pp. 96-101; Sondell, M., Lundborg, G., Kanje, M., Vascular endothelial growth factor stimulates Schwann cells invasion and neovascularization of acellular nerve grafts (1999) Brain Res, 846, pp. 219-222; Hobson, M.I., Green, C.J., Terenghi, G., VEGF enhances intraneural angiogenesis and improves nerve regeneration after axotomy (2000) J Anat, 197, pp. 591-605; Tseng, C.Y., Hu, G., Ambron, R.T., Chiu, D.T., Histologic analysis of Schwann cell migration and peripheral nerve regeneration in the autogenous venous nerve conduit (AVNC) (2003) J Reconstr Microsurg, 19, pp. 331-340; Taniuchi, M., Clark, H.B., Schweitzer, J.B., Johnson Jr., E.M., Induction of nerve growth factor receptor in Schwann cells after axotomy (1986) Proc Natl Acad Sci USA, 83, pp. 4094-4098; Taniuchi, M., Clark, H.B., Schweitzer, J.B., Johnson Jr., E.M., Expression of nerve growth factor receptors by Schwann cells of axotomized peripheral nerves: Ultrastructural location, suppression by axonal contact, and binding properties (1988) J Neurosci, 8, pp. 664-681; You, S., Petrov, T., Chung, P.H., Gordon, T., The expression of the low affinity nerve growth factor receptor in long-term denervated Schwann cells (1997) Glia, 20, pp. 87-100; Hall, S.M., The biology of chronically denervated Schwann cells (1999) Ann NY Acad Sci, 883, pp. 215-233; Chamberlain, L.J., Yannas, I.V., Hsu, H.P., Strichatrz, G.R., Spector, M., Collagen-GAG substrate enhances the quality of nerve regeneration through collagen tubes up to level of autograft (1998) Exp Neurol, 154, pp. 315-329; Mligiliche, N.L., Tabata, Y., Kitada, M., Poly lactic acid-caprolactone copolymer tube with a denatured skeletal muscle segment inside as a guide for peripheral nerve regeneration: A morphological and electrophysiological evaluation of the regenerated nerves (2003) Anat Sci Int, 78, pp. 156-161; Chamberlain, L.J., Yannas, I.V., Hsu, H.P., Strichatrz, G.R., Spector, M., Near-terminus axonal structure and function following rat sciatic nerve regeneration through a collagen-GAG matrix in a ten-millimeter gap (2000) J Neurosci Res, 60, pp. 666-677; Matsumoto, K., Ohnishi, K., Kiyotani, T., Peripheral nerve regeneration across an 80-mm gap bridged by a polyglycolic acid (PGA)-collagen tube filled with laminin-coated collagen fibers: A histological and electrophysiological evaluation of regenerated nerves (2000) Brain Res, 868, pp. 315-328; Verdu, E., Navarro, X., Comparison of immunohistochemical and functional reinnervation (1997) Exp Neurol, 146, pp. 187-198; Chiang, H.Y., Chen, C.T., Chien, H.F., Hsieh, S.T., Skin denervation, neuropathology, and neuropathic pain in a laser-induced focal neuropathy (2005) Neurobiol Dis, 18, pp. 40-53
PY - 2005
Y1 - 2005
N2 - We established histopathologic and neurophysiologic approaches to examine whether different designs of polycaprolactone-engineered nerve conduits (hollow vs. laminated) could promote nerve regeneration as autologous grafts after transection of sciatic nerves. The assessments included morphometric analysis at the level of sciatic nerve, neuromuscular junction (NMJ) and gastrocnemius muscle, and nerve conduction studies on sciatic nerves. Six months after nerve grafting, the nerve fiber density in the hollow-conduit group was similar to that in the autologous-graft group; the laminated-conduit group only achieved ∼20% of these values. The consequences of these differences were reflected in nerve growth into muscular targets; this was demonstrated by combined cholinesterase histochemistry for NMJ and immunohistochemistry for nerve fibers innervating NMJ with an axonal marker, protein gene product 9.5. Hollow conduits had similar index of NMJ innervation as autologous grafts; the values were higher than those of laminated conduits. Among the 3 groups there were same patterns of differences in the cross-sectional area of muscle fibers and amplitudes of compound muscle action potential. These results indicate that hollow conduits were as efficient as autologous grafts to facilitate nerve regeneration, and provide a multidisciplinary approach to quantitatively evaluate muscular reinnervation after nerve injury. Copyright © 2005 by the American Association of Neuropathologists, Inc.
AB - We established histopathologic and neurophysiologic approaches to examine whether different designs of polycaprolactone-engineered nerve conduits (hollow vs. laminated) could promote nerve regeneration as autologous grafts after transection of sciatic nerves. The assessments included morphometric analysis at the level of sciatic nerve, neuromuscular junction (NMJ) and gastrocnemius muscle, and nerve conduction studies on sciatic nerves. Six months after nerve grafting, the nerve fiber density in the hollow-conduit group was similar to that in the autologous-graft group; the laminated-conduit group only achieved ∼20% of these values. The consequences of these differences were reflected in nerve growth into muscular targets; this was demonstrated by combined cholinesterase histochemistry for NMJ and immunohistochemistry for nerve fibers innervating NMJ with an axonal marker, protein gene product 9.5. Hollow conduits had similar index of NMJ innervation as autologous grafts; the values were higher than those of laminated conduits. Among the 3 groups there were same patterns of differences in the cross-sectional area of muscle fibers and amplitudes of compound muscle action potential. These results indicate that hollow conduits were as efficient as autologous grafts to facilitate nerve regeneration, and provide a multidisciplinary approach to quantitatively evaluate muscular reinnervation after nerve injury. Copyright © 2005 by the American Association of Neuropathologists, Inc.
KW - Innervation
KW - Nerve conduits
KW - Nerve graft
KW - Nerve regeneration
KW - Neuromuscular junctions
KW - Polycaprolactone
KW - Ubiquitin
KW - cholinesterase
KW - gene product
KW - polycaprolactone
KW - protein gene product 9.5
KW - unclassified drug
KW - animal experiment
KW - animal model
KW - animal tissue
KW - article
KW - autograft
KW - controlled study
KW - gastrocnemius muscle
KW - histochemistry
KW - histopathology
KW - immunohistochemistry
KW - male
KW - morphometrics
KW - muscle action potential
KW - muscle cell
KW - muscle reinnervation
KW - nerve conduction
KW - nerve fiber
KW - nerve graft
KW - nerve growth
KW - nerve injury
KW - nerve regeneration
KW - nerve transection
KW - neuromuscular synapse
KW - nonhuman
KW - priority journal
KW - quantitative analysis
KW - rat
KW - sciatic nerve
KW - Action Potentials
KW - Animals
KW - Biocompatible Materials
KW - Cholinesterases
KW - Electrophysiology
KW - Immunohistochemistry
KW - Male
KW - Microscopy, Electron, Transmission
KW - Muscle, Skeletal
KW - Nerve Regeneration
KW - Neuromuscular Junction
KW - Polyesters
KW - Prostheses and Implants
KW - Rats
KW - Rats, Sprague-Dawley
KW - Sciatic Nerve
KW - Transplantation, Homologous
M3 - Article
SN - 0022-3069
VL - 64
SP - 576
EP - 587
JO - Journal of Neuropathology and Experimental Neurology
JF - Journal of Neuropathology and Experimental Neurology
IS - 7
ER -