Progesterone restores retrograde labeling of cervical motoneurons in Wobbler mouse motoneuron disease
The Wobbler mouse, a mutant characterized by motoneuron degeneration in the cervical spinal cord, has been used to test the efficacy of novel treatments for human motoneuron diseases (HMD). Previous reports have shown that slow axonal transport is impaired in Wobblers and other models of HMD. Since...
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description | The Wobbler mouse, a mutant characterized by motoneuron degeneration in the cervical spinal cord, has been used to test the efficacy of novel treatments for human motoneuron diseases (HMD). Previous reports have shown that slow axonal transport is impaired in Wobblers and other models of HMD. Since progesterone (PROG) corrects some morphological, molecular, and functional abnormalities of Wobbler mice, we studied if steroid exposure for 8 weeks restored retrograde axonal transport by measuring motoneuron labeling after injection of fluorogold into the limb muscles. The dye was injected into forelimb biceps bracchii and flexor or into the rearlimb gastrocnemius muscles; 6 days later, the number of fluorescent motoneurons and the total number of cresyl violet stained motoneurons were counted in the cervical (C5–T1) or lumbar (L3–L5) spinal cord regions. A pronounced reduction (− 42.2%) of the percent of fluorescent motoneurons in Wobbler mice cervical cord was noted, which was significantly corrected after PROG treatment. In contrast, labeling of lumbar motoneurons was not reduced in Wobbler mice and was not affected by PROG treatment. In no case PROG showed an effect in control mice. Concomitantly, PROG slightly but significantly increased biceps weight of Wobbler mice. Behaviorally, PROG-treated Wobblers performed better on a motor test (hanging time from a horizontal rope) compared to untreated counterparts. We postulate a dual role for PROG in the Wobbler mouse, in part by prevention of motoneuron degeneration and also by enhancement of axonal transport. The latter mechanism could improve the traffic of neurotrophic factors from the forelimb muscles into the ailing motoneurons, improving neuromuscular function in this murine model of HMD. |
doi_str_mv | 10.1016/j.expneurol.2005.06.015 |
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Previous reports have shown that slow axonal transport is impaired in Wobblers and other models of HMD. Since progesterone (PROG) corrects some morphological, molecular, and functional abnormalities of Wobbler mice, we studied if steroid exposure for 8 weeks restored retrograde axonal transport by measuring motoneuron labeling after injection of fluorogold into the limb muscles. The dye was injected into forelimb biceps bracchii and flexor or into the rearlimb gastrocnemius muscles; 6 days later, the number of fluorescent motoneurons and the total number of cresyl violet stained motoneurons were counted in the cervical (C5–T1) or lumbar (L3–L5) spinal cord regions. A pronounced reduction (− 42.2%) of the percent of fluorescent motoneurons in Wobbler mice cervical cord was noted, which was significantly corrected after PROG treatment. In contrast, labeling of lumbar motoneurons was not reduced in Wobbler mice and was not affected by PROG treatment. In no case PROG showed an effect in control mice. Concomitantly, PROG slightly but significantly increased biceps weight of Wobbler mice. Behaviorally, PROG-treated Wobblers performed better on a motor test (hanging time from a horizontal rope) compared to untreated counterparts. We postulate a dual role for PROG in the Wobbler mouse, in part by prevention of motoneuron degeneration and also by enhancement of axonal transport. The latter mechanism could improve the traffic of neurotrophic factors from the forelimb muscles into the ailing motoneurons, improving neuromuscular function in this murine model of HMD.</description><identifier>ISSN: 0014-4886</identifier><identifier>EISSN: 1090-2430</identifier><identifier>DOI: 10.1016/j.expneurol.2005.06.015</identifier><identifier>PMID: 16095593</identifier><identifier>CODEN: EXNEAC</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Animals ; Axonal transport ; Axonal Transport - drug effects ; Behavior, Animal ; Biological and medical sciences ; Cervical Vertebrae - pathology ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Disease Models, Animal ; Female ; Fluorogold ; Male ; Medical sciences ; Mice ; Mice, Neurologic Mutants ; Motoneuron degeneration ; Motor Neuron Disease - drug therapy ; Motor Neuron Disease - physiopathology ; Motor Neurons - drug effects ; Neurology ; Orthopedic surgery ; Progesterone ; Progestins - blood ; Progestins - therapeutic use ; Spinal cord ; Spinal Cord - pathology ; Stilbamidines - metabolism ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Upper Extremity - physiopathology ; Wobbler mouse</subject><ispartof>Experimental neurology, 2005-10, Vol.195 (2), p.518-523</ispartof><rights>2005 Elsevier Inc.</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-26d66976ee4ad0c07b29e3dfc00b866631d3662b8a7bb8b56e24891407d9eb073</citedby><cites>FETCH-LOGICAL-c448t-26d66976ee4ad0c07b29e3dfc00b866631d3662b8a7bb8b56e24891407d9eb073</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0014488605002232$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17126715$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16095593$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gonzalez Deniselle, Maria Claudia</creatorcontrib><creatorcontrib>Garay, Laura</creatorcontrib><creatorcontrib>Gonzalez, Susana</creatorcontrib><creatorcontrib>Guennoun, Rachida</creatorcontrib><creatorcontrib>Schumacher, Michael</creatorcontrib><creatorcontrib>De Nicola, Alejandro F.</creatorcontrib><title>Progesterone restores retrograde labeling of cervical motoneurons in Wobbler mouse motoneuron disease</title><title>Experimental neurology</title><addtitle>Exp Neurol</addtitle><description>The Wobbler mouse, a mutant characterized by motoneuron degeneration in the cervical spinal cord, has been used to test the efficacy of novel treatments for human motoneuron diseases (HMD). Previous reports have shown that slow axonal transport is impaired in Wobblers and other models of HMD. Since progesterone (PROG) corrects some morphological, molecular, and functional abnormalities of Wobbler mice, we studied if steroid exposure for 8 weeks restored retrograde axonal transport by measuring motoneuron labeling after injection of fluorogold into the limb muscles. The dye was injected into forelimb biceps bracchii and flexor or into the rearlimb gastrocnemius muscles; 6 days later, the number of fluorescent motoneurons and the total number of cresyl violet stained motoneurons were counted in the cervical (C5–T1) or lumbar (L3–L5) spinal cord regions. A pronounced reduction (− 42.2%) of the percent of fluorescent motoneurons in Wobbler mice cervical cord was noted, which was significantly corrected after PROG treatment. In contrast, labeling of lumbar motoneurons was not reduced in Wobbler mice and was not affected by PROG treatment. In no case PROG showed an effect in control mice. Concomitantly, PROG slightly but significantly increased biceps weight of Wobbler mice. Behaviorally, PROG-treated Wobblers performed better on a motor test (hanging time from a horizontal rope) compared to untreated counterparts. We postulate a dual role for PROG in the Wobbler mouse, in part by prevention of motoneuron degeneration and also by enhancement of axonal transport. The latter mechanism could improve the traffic of neurotrophic factors from the forelimb muscles into the ailing motoneurons, improving neuromuscular function in this murine model of HMD.</description><subject>Animals</subject><subject>Axonal transport</subject><subject>Axonal Transport - drug effects</subject><subject>Behavior, Animal</subject><subject>Biological and medical sciences</subject><subject>Cervical Vertebrae - pathology</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Fluorogold</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Neurologic Mutants</subject><subject>Motoneuron degeneration</subject><subject>Motor Neuron Disease - drug therapy</subject><subject>Motor Neuron Disease - physiopathology</subject><subject>Motor Neurons - drug effects</subject><subject>Neurology</subject><subject>Orthopedic surgery</subject><subject>Progesterone</subject><subject>Progestins - blood</subject><subject>Progestins - therapeutic use</subject><subject>Spinal cord</subject><subject>Spinal Cord - pathology</subject><subject>Stilbamidines - metabolism</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Upper Extremity - physiopathology</subject><subject>Wobbler mouse</subject><issn>0014-4886</issn><issn>1090-2430</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtP3DAQgC1EVZbHX6C5wC3p2HH8OCIEbSWk9tCqR8uPCfIqG2_tLKL_voZdld56sUfjbx7-CPlAoaNAxcd1h8_bGXc5TR0DGDoQHdDhiKwoaGgZ7-GYrAAob7lS4oSclrIGAM2ZfE9OqAA9DLpfEfyW0yOWBXOasck1SvWowVLz2QZsJutwivNjk8bGY36K3k7NJi3pdfxcmjg3P5NzE-aa3hX857EJsaAteE7ejXYqeHG4z8iP-7vvt5_bh6-fvtzePLSec7W0TAQhtBSI3AbwIB3T2IfRAzglhOhp6IVgTlnpnHKDQMaVphxk0OhA9mfket93m9OvXf2M2cTicZrsjHU1I9SgqWSqgnIP-pxKyTiabY4bm38bCubFsFmbv4bNi2EDwlTDtfLyMGLnNhje6g5KK3B1AGypqsZsZx_LGycpE_K10c2ewyrkKWI2xUecPYaY0S8mpPjfZf4AeYCgqg</recordid><startdate>20051001</startdate><enddate>20051001</enddate><creator>Gonzalez Deniselle, Maria Claudia</creator><creator>Garay, Laura</creator><creator>Gonzalez, Susana</creator><creator>Guennoun, Rachida</creator><creator>Schumacher, Michael</creator><creator>De Nicola, Alejandro F.</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>7X8</scope></search><sort><creationdate>20051001</creationdate><title>Progesterone restores retrograde labeling of cervical motoneurons in Wobbler mouse motoneuron disease</title><author>Gonzalez Deniselle, Maria Claudia ; Garay, Laura ; Gonzalez, Susana ; Guennoun, Rachida ; Schumacher, Michael ; De Nicola, Alejandro F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-26d66976ee4ad0c07b29e3dfc00b866631d3662b8a7bb8b56e24891407d9eb073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Axonal transport</topic><topic>Axonal Transport - drug effects</topic><topic>Behavior, Animal</topic><topic>Biological and medical sciences</topic><topic>Cervical Vertebrae - pathology</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Fluorogold</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Neurologic Mutants</topic><topic>Motoneuron degeneration</topic><topic>Motor Neuron Disease - drug therapy</topic><topic>Motor Neuron Disease - physiopathology</topic><topic>Motor Neurons - drug effects</topic><topic>Neurology</topic><topic>Orthopedic surgery</topic><topic>Progesterone</topic><topic>Progestins - blood</topic><topic>Progestins - therapeutic use</topic><topic>Spinal cord</topic><topic>Spinal Cord - pathology</topic><topic>Stilbamidines - metabolism</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Upper Extremity - physiopathology</topic><topic>Wobbler mouse</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gonzalez Deniselle, Maria Claudia</creatorcontrib><creatorcontrib>Garay, Laura</creatorcontrib><creatorcontrib>Gonzalez, Susana</creatorcontrib><creatorcontrib>Guennoun, Rachida</creatorcontrib><creatorcontrib>Schumacher, Michael</creatorcontrib><creatorcontrib>De Nicola, Alejandro F.</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>MEDLINE - Academic</collection><jtitle>Experimental neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gonzalez Deniselle, Maria Claudia</au><au>Garay, Laura</au><au>Gonzalez, Susana</au><au>Guennoun, Rachida</au><au>Schumacher, Michael</au><au>De Nicola, Alejandro F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Progesterone restores retrograde labeling of cervical motoneurons in Wobbler mouse motoneuron disease</atitle><jtitle>Experimental neurology</jtitle><addtitle>Exp Neurol</addtitle><date>2005-10-01</date><risdate>2005</risdate><volume>195</volume><issue>2</issue><spage>518</spage><epage>523</epage><pages>518-523</pages><issn>0014-4886</issn><eissn>1090-2430</eissn><coden>EXNEAC</coden><abstract>The Wobbler mouse, a mutant characterized by motoneuron degeneration in the cervical spinal cord, has been used to test the efficacy of novel treatments for human motoneuron diseases (HMD). Previous reports have shown that slow axonal transport is impaired in Wobblers and other models of HMD. Since progesterone (PROG) corrects some morphological, molecular, and functional abnormalities of Wobbler mice, we studied if steroid exposure for 8 weeks restored retrograde axonal transport by measuring motoneuron labeling after injection of fluorogold into the limb muscles. The dye was injected into forelimb biceps bracchii and flexor or into the rearlimb gastrocnemius muscles; 6 days later, the number of fluorescent motoneurons and the total number of cresyl violet stained motoneurons were counted in the cervical (C5–T1) or lumbar (L3–L5) spinal cord regions. A pronounced reduction (− 42.2%) of the percent of fluorescent motoneurons in Wobbler mice cervical cord was noted, which was significantly corrected after PROG treatment. In contrast, labeling of lumbar motoneurons was not reduced in Wobbler mice and was not affected by PROG treatment. In no case PROG showed an effect in control mice. Concomitantly, PROG slightly but significantly increased biceps weight of Wobbler mice. Behaviorally, PROG-treated Wobblers performed better on a motor test (hanging time from a horizontal rope) compared to untreated counterparts. We postulate a dual role for PROG in the Wobbler mouse, in part by prevention of motoneuron degeneration and also by enhancement of axonal transport. The latter mechanism could improve the traffic of neurotrophic factors from the forelimb muscles into the ailing motoneurons, improving neuromuscular function in this murine model of HMD.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>16095593</pmid><doi>10.1016/j.expneurol.2005.06.015</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Axonal transport Axonal Transport - drug effects Behavior, Animal Biological and medical sciences Cervical Vertebrae - pathology Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Disease Models, Animal Female Fluorogold Male Medical sciences Mice Mice, Neurologic Mutants Motoneuron degeneration Motor Neuron Disease - drug therapy Motor Neuron Disease - physiopathology Motor Neurons - drug effects Neurology Orthopedic surgery Progesterone Progestins - blood Progestins - therapeutic use Spinal cord Spinal Cord - pathology Stilbamidines - metabolism Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Upper Extremity - physiopathology Wobbler mouse |
title | Progesterone restores retrograde labeling of cervical motoneurons in Wobbler mouse motoneuron disease |
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