Bilateral cervical contusion spinal cord injury in rats

There is increasing motivation to develop clinically relevant experimental models for cervical SCI in rodents and techniques to assess deficits in forelimb function. Here we describe a bilateral cervical contusion model in rats. Female Sprague–Dawley rats received mild or moderate cervical contusion...

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Veröffentlicht in:Experimental neurology 2009-11, Vol.220 (1), p.9-22
Hauptverfasser: Anderson, Kim D., Sharp, Kelli G., Steward, Oswald
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description There is increasing motivation to develop clinically relevant experimental models for cervical SCI in rodents and techniques to assess deficits in forelimb function. Here we describe a bilateral cervical contusion model in rats. Female Sprague–Dawley rats received mild or moderate cervical contusion injuries (using the Infinite Horizons device) at C5, C6, or C7/8. Forelimb motor function was assessed using a grip strength meter (GSM); sensory function was assessed by the von Frey hair test; the integrity of the corticospinal tract (CST) was assessed by biotinylated dextran amine (BDA) tract tracing. Mild contusions caused primarily dorsal column (DC) and gray matter (GM) damage while moderate contusions produced additional damage to lateral and ventral tissue. Forelimb and hindlimb function was severely impaired immediately post-injury, but all rats regained the ability to use their hindlimbs for locomotion. Gripping ability was abolished immediately after injury but recovered partially, depending upon the spinal level and severity of the injury. Rats exhibited a loss of sensation in both fore- and hindlimbs that partially recovered, and did not exhibit allodynia. Tract tracing revealed that the main contingent of CST axons in the DC was completely interrupted in all but one animal whereas the dorsolateral CST (dlCST) was partially spared, and dlCST axons gave rise to axons that arborized in the GM caudal to the injury. Our data demonstrate that rats can survive significant bilateral cervical contusion injuries at or below C5 and that forepaw gripping function recovers after mild injuries even when the main component of CST axons in the dorsal column is completely interrupted.
doi_str_mv 10.1016/j.expneurol.2009.06.012
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Here we describe a bilateral cervical contusion model in rats. Female Sprague–Dawley rats received mild or moderate cervical contusion injuries (using the Infinite Horizons device) at C5, C6, or C7/8. Forelimb motor function was assessed using a grip strength meter (GSM); sensory function was assessed by the von Frey hair test; the integrity of the corticospinal tract (CST) was assessed by biotinylated dextran amine (BDA) tract tracing. Mild contusions caused primarily dorsal column (DC) and gray matter (GM) damage while moderate contusions produced additional damage to lateral and ventral tissue. Forelimb and hindlimb function was severely impaired immediately post-injury, but all rats regained the ability to use their hindlimbs for locomotion. Gripping ability was abolished immediately after injury but recovered partially, depending upon the spinal level and severity of the injury. Rats exhibited a loss of sensation in both fore- and hindlimbs that partially recovered, and did not exhibit allodynia. Tract tracing revealed that the main contingent of CST axons in the DC was completely interrupted in all but one animal whereas the dorsolateral CST (dlCST) was partially spared, and dlCST axons gave rise to axons that arborized in the GM caudal to the injury. Our data demonstrate that rats can survive significant bilateral cervical contusion injuries at or below C5 and that forepaw gripping function recovers after mild injuries even when the main component of CST axons in the dorsal column is completely interrupted.</description><identifier>ISSN: 0014-4886</identifier><identifier>EISSN: 1090-2430</identifier><identifier>DOI: 10.1016/j.expneurol.2009.06.012</identifier><identifier>PMID: 19559699</identifier><identifier>CODEN: EXNEAC</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Animals ; Axotomy - methods ; Biological and medical sciences ; Biotin - analogs &amp; derivatives ; Cervical injury ; Cervical Vertebrae ; Contusion ; Corticospinal tract ; Dextrans ; Digital flexors ; Disease Models, Animal ; Female ; Forelimb ; Forelimb - innervation ; Forelimb - physiopathology ; Functional Laterality - physiology ; Grip strength ; Growth Cones - physiology ; Growth Cones - ultrastructure ; Hand Strength - physiology ; Injuries of the nervous system and the skull. Diseases due to physical agents ; Lameness, Animal - etiology ; Lameness, Animal - pathology ; Lameness, Animal - physiopathology ; Medical sciences ; Movement Disorders - etiology ; Movement Disorders - pathology ; Movement Disorders - physiopathology ; Muscle Strength Dynamometer ; Nerve Regeneration - physiology ; Neurologic Examination ; Neurology ; Neuronal Plasticity - physiology ; Physical Stimulation ; Pyramidal Tracts - injuries ; Pyramidal Tracts - pathology ; Pyramidal Tracts - physiopathology ; Rats ; Rats, Sprague-Dawley ; Recovery of Function - physiology ; Sensation Disorders - etiology ; Sensation Disorders - pathology ; Sensation Disorders - physiopathology ; Spinal Cord Injuries - complications ; Spinal Cord Injuries - pathology ; Spinal Cord Injuries - physiopathology ; Staining and Labeling ; Traumas. 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Here we describe a bilateral cervical contusion model in rats. Female Sprague–Dawley rats received mild or moderate cervical contusion injuries (using the Infinite Horizons device) at C5, C6, or C7/8. Forelimb motor function was assessed using a grip strength meter (GSM); sensory function was assessed by the von Frey hair test; the integrity of the corticospinal tract (CST) was assessed by biotinylated dextran amine (BDA) tract tracing. Mild contusions caused primarily dorsal column (DC) and gray matter (GM) damage while moderate contusions produced additional damage to lateral and ventral tissue. Forelimb and hindlimb function was severely impaired immediately post-injury, but all rats regained the ability to use their hindlimbs for locomotion. Gripping ability was abolished immediately after injury but recovered partially, depending upon the spinal level and severity of the injury. Rats exhibited a loss of sensation in both fore- and hindlimbs that partially recovered, and did not exhibit allodynia. Tract tracing revealed that the main contingent of CST axons in the DC was completely interrupted in all but one animal whereas the dorsolateral CST (dlCST) was partially spared, and dlCST axons gave rise to axons that arborized in the GM caudal to the injury. Our data demonstrate that rats can survive significant bilateral cervical contusion injuries at or below C5 and that forepaw gripping function recovers after mild injuries even when the main component of CST axons in the dorsal column is completely interrupted.</description><subject>Animals</subject><subject>Axotomy - methods</subject><subject>Biological and medical sciences</subject><subject>Biotin - analogs &amp; derivatives</subject><subject>Cervical injury</subject><subject>Cervical Vertebrae</subject><subject>Contusion</subject><subject>Corticospinal tract</subject><subject>Dextrans</subject><subject>Digital flexors</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Forelimb</subject><subject>Forelimb - innervation</subject><subject>Forelimb - physiopathology</subject><subject>Functional Laterality - physiology</subject><subject>Grip strength</subject><subject>Growth Cones - physiology</subject><subject>Growth Cones - ultrastructure</subject><subject>Hand Strength - physiology</subject><subject>Injuries of the nervous system and the skull. Diseases due to physical agents</subject><subject>Lameness, Animal - etiology</subject><subject>Lameness, Animal - pathology</subject><subject>Lameness, Animal - physiopathology</subject><subject>Medical sciences</subject><subject>Movement Disorders - etiology</subject><subject>Movement Disorders - pathology</subject><subject>Movement Disorders - physiopathology</subject><subject>Muscle Strength Dynamometer</subject><subject>Nerve Regeneration - physiology</subject><subject>Neurologic Examination</subject><subject>Neurology</subject><subject>Neuronal Plasticity - physiology</subject><subject>Physical Stimulation</subject><subject>Pyramidal Tracts - injuries</subject><subject>Pyramidal Tracts - pathology</subject><subject>Pyramidal Tracts - physiopathology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Recovery of Function - physiology</subject><subject>Sensation Disorders - etiology</subject><subject>Sensation Disorders - pathology</subject><subject>Sensation Disorders - physiopathology</subject><subject>Spinal Cord Injuries - complications</subject><subject>Spinal Cord Injuries - pathology</subject><subject>Spinal Cord Injuries - physiopathology</subject><subject>Staining and Labeling</subject><subject>Traumas. Diseases due to physical agents</subject><issn>0014-4886</issn><issn>1090-2430</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkT1v2zAQhomiQe2k_QuJl2aTcqQoSlwCJEY-CgTIks4ERZ1aGjLpkJIR__vQseGmk6cjyOcO7_Eh5IJCToGKq0WObyuHY_B9zgBkDiIHyr6QKQUJGeMFfCVTAMozXtdiQk5jXEACOau-kQmVZSmFlFNS3dpeDxh0PzMY1tZsD94NY7TezeLKuo-L0M6sW4xhk8os6CF-Jyed7iP-2Ncz8vv-7mX-mD09P_ya3zxlRgAMWQGaS41MFoBMNx2KhrLaGA1lQyUi8tIUQFvGm7IzLSDWuqUcW2qaiouqOCPXu7mrsVlia9ANKataBbvUYaO8tur_F2f_qj9-rVglKJcyDbjcDwj-dcQ4qKWNBvteO_RjVKISNRNwHGSUFkzwOoHVDjTBxxiwO6ShoLZ21EId7KitHQVCJTup8_zzMv_69joS8HMP6JhMdEE7Y-OBYwzKmnOeuJsdh-nr1xaDisaiM9jagGZQrbdHw7wDXUa0Wg</recordid><startdate>20091101</startdate><enddate>20091101</enddate><creator>Anderson, Kim D.</creator><creator>Sharp, Kelli G.</creator><creator>Steward, Oswald</creator><general>Elsevier Inc</general><general>Elsevier</general><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>7TK</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20091101</creationdate><title>Bilateral cervical contusion spinal cord injury in rats</title><author>Anderson, Kim D. ; Sharp, Kelli G. ; Steward, Oswald</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c600t-30a49ae2930e2abfe6b128cca05b19eee45c301d24b5fcd0ee8ad14ed1cb74673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Axotomy - methods</topic><topic>Biological and medical sciences</topic><topic>Biotin - analogs &amp; derivatives</topic><topic>Cervical injury</topic><topic>Cervical Vertebrae</topic><topic>Contusion</topic><topic>Corticospinal tract</topic><topic>Dextrans</topic><topic>Digital flexors</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Forelimb</topic><topic>Forelimb - innervation</topic><topic>Forelimb - physiopathology</topic><topic>Functional Laterality - physiology</topic><topic>Grip strength</topic><topic>Growth Cones - physiology</topic><topic>Growth Cones - ultrastructure</topic><topic>Hand Strength - physiology</topic><topic>Injuries of the nervous system and the skull. Diseases due to physical agents</topic><topic>Lameness, Animal - etiology</topic><topic>Lameness, Animal - pathology</topic><topic>Lameness, Animal - physiopathology</topic><topic>Medical sciences</topic><topic>Movement Disorders - etiology</topic><topic>Movement Disorders - pathology</topic><topic>Movement Disorders - physiopathology</topic><topic>Muscle Strength Dynamometer</topic><topic>Nerve Regeneration - physiology</topic><topic>Neurologic Examination</topic><topic>Neurology</topic><topic>Neuronal Plasticity - physiology</topic><topic>Physical Stimulation</topic><topic>Pyramidal Tracts - injuries</topic><topic>Pyramidal Tracts - pathology</topic><topic>Pyramidal Tracts - physiopathology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Recovery of Function - physiology</topic><topic>Sensation Disorders - etiology</topic><topic>Sensation Disorders - pathology</topic><topic>Sensation Disorders - physiopathology</topic><topic>Spinal Cord Injuries - complications</topic><topic>Spinal Cord Injuries - pathology</topic><topic>Spinal Cord Injuries - physiopathology</topic><topic>Staining and Labeling</topic><topic>Traumas. Diseases due to physical agents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Anderson, Kim D.</creatorcontrib><creatorcontrib>Sharp, Kelli G.</creatorcontrib><creatorcontrib>Steward, Oswald</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Experimental neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Anderson, Kim D.</au><au>Sharp, Kelli G.</au><au>Steward, Oswald</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bilateral cervical contusion spinal cord injury in rats</atitle><jtitle>Experimental neurology</jtitle><addtitle>Exp Neurol</addtitle><date>2009-11-01</date><risdate>2009</risdate><volume>220</volume><issue>1</issue><spage>9</spage><epage>22</epage><pages>9-22</pages><issn>0014-4886</issn><eissn>1090-2430</eissn><coden>EXNEAC</coden><abstract>There is increasing motivation to develop clinically relevant experimental models for cervical SCI in rodents and techniques to assess deficits in forelimb function. 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Rats exhibited a loss of sensation in both fore- and hindlimbs that partially recovered, and did not exhibit allodynia. Tract tracing revealed that the main contingent of CST axons in the DC was completely interrupted in all but one animal whereas the dorsolateral CST (dlCST) was partially spared, and dlCST axons gave rise to axons that arborized in the GM caudal to the injury. Our data demonstrate that rats can survive significant bilateral cervical contusion injuries at or below C5 and that forepaw gripping function recovers after mild injuries even when the main component of CST axons in the dorsal column is completely interrupted.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>19559699</pmid><doi>10.1016/j.expneurol.2009.06.012</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Axotomy - methods
Biological and medical sciences
Biotin - analogs & derivatives
Cervical injury
Cervical Vertebrae
Contusion
Corticospinal tract
Dextrans
Digital flexors
Disease Models, Animal
Female
Forelimb
Forelimb - innervation
Forelimb - physiopathology
Functional Laterality - physiology
Grip strength
Growth Cones - physiology
Growth Cones - ultrastructure
Hand Strength - physiology
Injuries of the nervous system and the skull. Diseases due to physical agents
Lameness, Animal - etiology
Lameness, Animal - pathology
Lameness, Animal - physiopathology
Medical sciences
Movement Disorders - etiology
Movement Disorders - pathology
Movement Disorders - physiopathology
Muscle Strength Dynamometer
Nerve Regeneration - physiology
Neurologic Examination
Neurology
Neuronal Plasticity - physiology
Physical Stimulation
Pyramidal Tracts - injuries
Pyramidal Tracts - pathology
Pyramidal Tracts - physiopathology
Rats
Rats, Sprague-Dawley
Recovery of Function - physiology
Sensation Disorders - etiology
Sensation Disorders - pathology
Sensation Disorders - physiopathology
Spinal Cord Injuries - complications
Spinal Cord Injuries - pathology
Spinal Cord Injuries - physiopathology
Staining and Labeling
Traumas. Diseases due to physical agents
title Bilateral cervical contusion spinal cord injury in rats
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