Short- and long-term peripheral nerve regeneration using a poly-lactic-co-glycolic-acid scaffold containing nerve growth factor and glial cell line-derived neurotrophic factor releasing microspheres
Addition of neural growth factors to bioengineered scaffolds may improve peripheral nerve regeneration. The aim of this study is to evaluate the short‐ and long term effect of microsphere delivered nerve growth factor (NGF) and glial cell derived neurotrophic factor (GDNF) in the 10 mm rat sciatic n...
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Veröffentlicht in: | Journal of biomedical materials research. Part A 2012-08, Vol.100A (8), p.2139-2146 |
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creator | de Boer, Ralph Borntraeger, Andreas Knight, Andrew M. Hébert-Blouin, Marie-Noëlle Spinner, Robert J. Malessy, Martijn J. A. Yaszemski, Michael J. Windebank, Anthony J. |
description | Addition of neural growth factors to bioengineered scaffolds may improve peripheral nerve regeneration. The aim of this study is to evaluate the short‐ and long term effect of microsphere delivered nerve growth factor (NGF) and glial cell derived neurotrophic factor (GDNF) in the 10 mm rat sciatic nerve gap. Eighty‐four rats were assigned to seven groups (n = 6) at two endpoints (6 and 16 weeks): saline, saline NGF, saline NGF‐microspheres, saline GDNF, saline GDNF‐microspheres, saline blank microspheres, and autologous nerve graft. Total fascicular area and total number of myelinated fibers at mid‐tube increased in all conduit groups between 6 and 16 weeks. Autologous, saline NGF‐microsphere and saline GDNF‐microsphere groups reached maximal histomorphometric values by 6 weeks (p < 0.05). Compound muscle action potentials returned after 6 weeks for the autologous graft and continued to increase to a level of 3.6 ± 1.9 mV at endpoint. No significant differences were found between study groups as measured by ankle angle. These experiments show an initial beneficial effect of incorporation of NGF‐ or GDNF‐microspheres in a PLGA 85/15 nerve conduit, since histomorphometric values reached their maximum by 6 weeks compared to control groups. These results do not yet extrapolate into improved electrophysiological or functional improvement. © 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2012. |
doi_str_mv | 10.1002/jbm.a.34088 |
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Autologous, saline NGF‐microsphere and saline GDNF‐microsphere groups reached maximal histomorphometric values by 6 weeks (p < 0.05). Compound muscle action potentials returned after 6 weeks for the autologous graft and continued to increase to a level of 3.6 ± 1.9 mV at endpoint. No significant differences were found between study groups as measured by ankle angle. These experiments show an initial beneficial effect of incorporation of NGF‐ or GDNF‐microspheres in a PLGA 85/15 nerve conduit, since histomorphometric values reached their maximum by 6 weeks compared to control groups. These results do not yet extrapolate into improved electrophysiological or functional improvement. © 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2012.</description><identifier>ISSN: 1549-3296</identifier><identifier>EISSN: 1552-4965</identifier><identifier>DOI: 10.1002/jbm.a.34088</identifier><identifier>PMID: 22615148</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Action Potentials - drug effects ; Animals ; Biological and medical sciences ; GDNF ; Glial Cell Line-Derived Neurotrophic Factor - pharmacology ; Lactic Acid - chemistry ; Medical sciences ; Microspheres ; Motor Neurons - drug effects ; Motor Neurons - physiology ; Movement - drug effects ; Muscles - drug effects ; Muscles - physiology ; Nerve Regeneration - drug effects ; Neurosurgery ; NGF ; Peripheral Nerves - drug effects ; Peripheral Nerves - physiology ; PLGA ; Polyglycolic Acid - chemistry ; Rats ; Rats, Sprague-Dawley ; regeneration ; scaffold ; sciatic nerve ; Surgery (general aspects). Transplantations, organ and tissue grafts. 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A.</creatorcontrib><creatorcontrib>Yaszemski, Michael J.</creatorcontrib><creatorcontrib>Windebank, Anthony J.</creatorcontrib><title>Short- and long-term peripheral nerve regeneration using a poly-lactic-co-glycolic-acid scaffold containing nerve growth factor and glial cell line-derived neurotrophic factor releasing microspheres</title><title>Journal of biomedical materials research. Part A</title><addtitle>J. Biomed. Mater. Res</addtitle><description>Addition of neural growth factors to bioengineered scaffolds may improve peripheral nerve regeneration. The aim of this study is to evaluate the short‐ and long term effect of microsphere delivered nerve growth factor (NGF) and glial cell derived neurotrophic factor (GDNF) in the 10 mm rat sciatic nerve gap. Eighty‐four rats were assigned to seven groups (n = 6) at two endpoints (6 and 16 weeks): saline, saline NGF, saline NGF‐microspheres, saline GDNF, saline GDNF‐microspheres, saline blank microspheres, and autologous nerve graft. Total fascicular area and total number of myelinated fibers at mid‐tube increased in all conduit groups between 6 and 16 weeks. Autologous, saline NGF‐microsphere and saline GDNF‐microsphere groups reached maximal histomorphometric values by 6 weeks (p < 0.05). Compound muscle action potentials returned after 6 weeks for the autologous graft and continued to increase to a level of 3.6 ± 1.9 mV at endpoint. No significant differences were found between study groups as measured by ankle angle. These experiments show an initial beneficial effect of incorporation of NGF‐ or GDNF‐microspheres in a PLGA 85/15 nerve conduit, since histomorphometric values reached their maximum by 6 weeks compared to control groups. These results do not yet extrapolate into improved electrophysiological or functional improvement. © 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2012.</description><subject>Action Potentials - drug effects</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>GDNF</subject><subject>Glial Cell Line-Derived Neurotrophic Factor - pharmacology</subject><subject>Lactic Acid - chemistry</subject><subject>Medical sciences</subject><subject>Microspheres</subject><subject>Motor Neurons - drug effects</subject><subject>Motor Neurons - physiology</subject><subject>Movement - drug effects</subject><subject>Muscles - drug effects</subject><subject>Muscles - physiology</subject><subject>Nerve Regeneration - drug effects</subject><subject>Neurosurgery</subject><subject>NGF</subject><subject>Peripheral Nerves - drug effects</subject><subject>Peripheral Nerves - physiology</subject><subject>PLGA</subject><subject>Polyglycolic Acid - chemistry</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>regeneration</subject><subject>scaffold</subject><subject>sciatic nerve</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Technology. Biomaterials. Equipments</subject><subject>Time Factors</subject><subject>Tissue Scaffolds - chemistry</subject><issn>1549-3296</issn><issn>1552-4965</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUtv1DAUhSMEog9YsUfeICFVHuJHEmdJK5iCBpBKJZaW49xkXJw42EnL_EF-F85kpuxY-S6-c8_xPUnyiqQrkqb03V3VrdSK8VSIJ8kpyTKKeZlnT-eZl5jRMj9JzkK4i3CeZvR5ckJpTjLCxWny5_vW-REj1dfIur7FI_gODeDNsAWvLOrB3wPy0EKc1Ghcj6Zg-hYpNDi7w1bp0WisHW7tTjsbZ6VNjYJWTeNsjbTrR2X6WbLsar17GLeoiULn98atNdFJg7XImh5wHe3voY785N3o3bA1-sh7sKD2ATqjvQtzTAgvkmeNsgFeHt7z5Pbjh9ura7z5tv509X6DNStLgUVVpXnDWZYToUXJOa8qltEqr6uGFYqURTwZYZQ1REC8KM2zigtaFSrjRQ3sPHm7rB28-zVBGGVnwpxb9eCmIElKSSkIpTyiFws6hwweGjl40ym_i5Cce5OxN6nkvrdIvz4snqoO6kf2WFQE3hwAFS9rG696bcI_LifxVyWNHFm4B2Nh9z9P-fnyy9EcLxoTRvj9qFH-p8wLVmTyx9e1vLze0OKG3Mg1-wsZScOG</recordid><startdate>201208</startdate><enddate>201208</enddate><creator>de Boer, Ralph</creator><creator>Borntraeger, Andreas</creator><creator>Knight, Andrew M.</creator><creator>Hébert-Blouin, Marie-Noëlle</creator><creator>Spinner, Robert J.</creator><creator>Malessy, Martijn J. A.</creator><creator>Yaszemski, Michael J.</creator><creator>Windebank, Anthony J.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201208</creationdate><title>Short- and long-term peripheral nerve regeneration using a poly-lactic-co-glycolic-acid scaffold containing nerve growth factor and glial cell line-derived neurotrophic factor releasing microspheres</title><author>de Boer, Ralph ; Borntraeger, Andreas ; Knight, Andrew M. ; Hébert-Blouin, Marie-Noëlle ; Spinner, Robert J. ; Malessy, Martijn J. 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Eighty‐four rats were assigned to seven groups (n = 6) at two endpoints (6 and 16 weeks): saline, saline NGF, saline NGF‐microspheres, saline GDNF, saline GDNF‐microspheres, saline blank microspheres, and autologous nerve graft. Total fascicular area and total number of myelinated fibers at mid‐tube increased in all conduit groups between 6 and 16 weeks. Autologous, saline NGF‐microsphere and saline GDNF‐microsphere groups reached maximal histomorphometric values by 6 weeks (p < 0.05). Compound muscle action potentials returned after 6 weeks for the autologous graft and continued to increase to a level of 3.6 ± 1.9 mV at endpoint. No significant differences were found between study groups as measured by ankle angle. These experiments show an initial beneficial effect of incorporation of NGF‐ or GDNF‐microspheres in a PLGA 85/15 nerve conduit, since histomorphometric values reached their maximum by 6 weeks compared to control groups. These results do not yet extrapolate into improved electrophysiological or functional improvement. © 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2012.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>22615148</pmid><doi>10.1002/jbm.a.34088</doi><tpages>8</tpages></addata></record> |
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subjects | Action Potentials - drug effects Animals Biological and medical sciences GDNF Glial Cell Line-Derived Neurotrophic Factor - pharmacology Lactic Acid - chemistry Medical sciences Microspheres Motor Neurons - drug effects Motor Neurons - physiology Movement - drug effects Muscles - drug effects Muscles - physiology Nerve Regeneration - drug effects Neurosurgery NGF Peripheral Nerves - drug effects Peripheral Nerves - physiology PLGA Polyglycolic Acid - chemistry Rats Rats, Sprague-Dawley regeneration scaffold sciatic nerve Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Technology. Biomaterials. Equipments Time Factors Tissue Scaffolds - chemistry |
title | Short- and long-term peripheral nerve regeneration using a poly-lactic-co-glycolic-acid scaffold containing nerve growth factor and glial cell line-derived neurotrophic factor releasing microspheres |
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