Reinnervation of transplanted vas deferens by cholinergic nerves normally supplying skeletal muscle

The rat vas deferens was removed and either transplanted alongside the soleus muscle or into the bed of the soleus muscle that had previously been removed, and in this case the soleus nerve was connected to the transplant. The vas deferens reinnervated by the somatomotor nerve recovered the best. Co...

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Veröffentlicht in:Experimental neurology 2009-02, Vol.215 (2), p.264-270
Hauptverfasser: Vrbová, G., Burnstock, G.
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description The rat vas deferens was removed and either transplanted alongside the soleus muscle or into the bed of the soleus muscle that had previously been removed, and in this case the soleus nerve was connected to the transplant. The vas deferens reinnervated by the somatomotor nerve recovered the best. Contractions to transmural electrical stimulation could not be elicited from the denervated vas deferens, although noradrenaline and acetylcholine elicited contractions. The reinnervated vas deferens produced good contractile responses to transmural stimulation, and these were substantially reduced by a cholinergic muscarinic blocking agent, hyoscine, as compared to only a small reduction in the control vas deferens. Neostigmine potentiated the contraction of the transplanted vas deferens to a greater extent than that of the control. This indicated that a substantial component of the contractile response was produced by cholinergic fibres. Consistent with this was the finding that, while guanethidine blocked a greater proportion of the contraction in the control vas deferens, the contraction of the reinnervated transplant was less affected. Acetylcholine elicited a strong contraction in control vas deferens, but only a small response was obtained in the reinnervated transplant. However, the response to noradrenaline was greater in the transplant than in the control vas deferens. These results indicate that cholinergic nerves normally supplying skeletal muscle can reinnervate smooth muscle and that the alien somatomotor innervation altered the responsiveness of the smooth muscle of the vas deferens. Morphological studies confirm the shift from adrenergic to cholinergic fibres in the reinnervated vas deferens.
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The vas deferens reinnervated by the somatomotor nerve recovered the best. Contractions to transmural electrical stimulation could not be elicited from the denervated vas deferens, although noradrenaline and acetylcholine elicited contractions. The reinnervated vas deferens produced good contractile responses to transmural stimulation, and these were substantially reduced by a cholinergic muscarinic blocking agent, hyoscine, as compared to only a small reduction in the control vas deferens. Neostigmine potentiated the contraction of the transplanted vas deferens to a greater extent than that of the control. This indicated that a substantial component of the contractile response was produced by cholinergic fibres. Consistent with this was the finding that, while guanethidine blocked a greater proportion of the contraction in the control vas deferens, the contraction of the reinnervated transplant was less affected. Acetylcholine elicited a strong contraction in control vas deferens, but only a small response was obtained in the reinnervated transplant. However, the response to noradrenaline was greater in the transplant than in the control vas deferens. These results indicate that cholinergic nerves normally supplying skeletal muscle can reinnervate smooth muscle and that the alien somatomotor innervation altered the responsiveness of the smooth muscle of the vas deferens. 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Diseases due to physical agents ; Male ; Medical sciences ; Microscopy, Electron, Transmission - methods ; Muscle, Skeletal - innervation ; Muscle, Skeletal - ultrastructure ; Neostigmine - pharmacology ; Neurology ; Noradrenaline ; Norepinephrine - pharmacology ; Rats ; Rats, Sprague-Dawley ; Reinnervation ; Scopolamine Hydrobromide - pharmacology ; Soleus muscle ; Time Factors ; Traumas. 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The vas deferens reinnervated by the somatomotor nerve recovered the best. Contractions to transmural electrical stimulation could not be elicited from the denervated vas deferens, although noradrenaline and acetylcholine elicited contractions. The reinnervated vas deferens produced good contractile responses to transmural stimulation, and these were substantially reduced by a cholinergic muscarinic blocking agent, hyoscine, as compared to only a small reduction in the control vas deferens. Neostigmine potentiated the contraction of the transplanted vas deferens to a greater extent than that of the control. This indicated that a substantial component of the contractile response was produced by cholinergic fibres. Consistent with this was the finding that, while guanethidine blocked a greater proportion of the contraction in the control vas deferens, the contraction of the reinnervated transplant was less affected. Acetylcholine elicited a strong contraction in control vas deferens, but only a small response was obtained in the reinnervated transplant. However, the response to noradrenaline was greater in the transplant than in the control vas deferens. These results indicate that cholinergic nerves normally supplying skeletal muscle can reinnervate smooth muscle and that the alien somatomotor innervation altered the responsiveness of the smooth muscle of the vas deferens. Morphological studies confirm the shift from adrenergic to cholinergic fibres in the reinnervated vas deferens.</description><subject>Acetylcholine</subject><subject>Acetylcholine - metabolism</subject><subject>Acetylcholine - pharmacology</subject><subject>Adrenergic Agents - pharmacology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cholinergic Antagonists - pharmacology</subject><subject>Cholinergic Fibers - physiology</subject><subject>Cholinesterase Inhibitors - pharmacology</subject><subject>Denervation</subject><subject>Electric Stimulation</subject><subject>Guanethidine - pharmacology</subject><subject>Injuries of the nervous system and the skull. Diseases due to physical agents</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microscopy, Electron, Transmission - methods</subject><subject>Muscle, Skeletal - innervation</subject><subject>Muscle, Skeletal - ultrastructure</subject><subject>Neostigmine - pharmacology</subject><subject>Neurology</subject><subject>Noradrenaline</subject><subject>Norepinephrine - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reinnervation</subject><subject>Scopolamine Hydrobromide - pharmacology</subject><subject>Soleus muscle</subject><subject>Time Factors</subject><subject>Traumas. Diseases due to physical agents</subject><subject>Vas deferens</subject><subject>Vas Deferens - innervation</subject><subject>Vas Deferens - physiology</subject><subject>Vas Deferens - transplantation</subject><subject>Vas Deferens - ultrastructure</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>eNqFkc1u3CAUhVHVqJmmfYWWTbvz5AIejJdRlP5IkSpV6RphfEmZYuyCPeq8fbBmlC6zuhL3O3A4h5CPDLYMmLzeb_HfFHFJY9hyAFVOt8DYK7Jh0ELFawGvyQaA1VWtlLwkb3PeA0Bb8-YNuWQtcM5rtSH2J_oYMR3M7MdIR0fnZGKegokz9vRgMu3RYcKYaXek9vcYfMEfvaWrCjONYxpMCEeal2kKRx8faf6DAWcT6LBkG_AduXAmZHx_nlfk15e7h9tv1f2Pr99vb-4rKxo5V67hVsmd6HZcYd1L61wnalRCtIK5WrgGleIOmHIcGzDKtLzrWmF2YBkTvbgin0_3Tmn8u2Ce9eCzxVD-guOStZRKyJLBiyAHoQrIC9icQJvGnBM6PSU_mHTUDPRahN7r5yL0WsS6KEUU5YfzE0s3YP9fd06-AJ_OgMnWBFdStz4_c5wxDpKvXm9OHJbkDh6TztZjtNj7hHbW_ehfNPMEzZ-tKQ</recordid><startdate>20090201</startdate><enddate>20090201</enddate><creator>Vrbová, G.</creator><creator>Burnstock, G.</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></search><sort><creationdate>20090201</creationdate><title>Reinnervation of transplanted vas deferens by cholinergic nerves normally supplying skeletal muscle</title><author>Vrbová, G. ; Burnstock, G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c376t-f72c8653b528e4d6cffb34e833931f43f7e882f018f2e70a8a92bb93a50c113d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Acetylcholine</topic><topic>Acetylcholine - metabolism</topic><topic>Acetylcholine - pharmacology</topic><topic>Adrenergic Agents - pharmacology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cholinergic Antagonists - pharmacology</topic><topic>Cholinergic Fibers - physiology</topic><topic>Cholinesterase Inhibitors - pharmacology</topic><topic>Denervation</topic><topic>Electric Stimulation</topic><topic>Guanethidine - pharmacology</topic><topic>Injuries of the nervous system and the skull. Diseases due to physical agents</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microscopy, Electron, Transmission - methods</topic><topic>Muscle, Skeletal - innervation</topic><topic>Muscle, Skeletal - ultrastructure</topic><topic>Neostigmine - pharmacology</topic><topic>Neurology</topic><topic>Noradrenaline</topic><topic>Norepinephrine - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reinnervation</topic><topic>Scopolamine Hydrobromide - pharmacology</topic><topic>Soleus muscle</topic><topic>Time Factors</topic><topic>Traumas. Diseases due to physical agents</topic><topic>Vas deferens</topic><topic>Vas Deferens - innervation</topic><topic>Vas Deferens - physiology</topic><topic>Vas Deferens - transplantation</topic><topic>Vas Deferens - ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vrbová, G.</creatorcontrib><creatorcontrib>Burnstock, G.</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><jtitle>Experimental neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vrbová, G.</au><au>Burnstock, G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reinnervation of transplanted vas deferens by cholinergic nerves normally supplying skeletal muscle</atitle><jtitle>Experimental neurology</jtitle><addtitle>Exp Neurol</addtitle><date>2009-02-01</date><risdate>2009</risdate><volume>215</volume><issue>2</issue><spage>264</spage><epage>270</epage><pages>264-270</pages><issn>0014-4886</issn><eissn>1090-2430</eissn><coden>EXNEAC</coden><abstract>The rat vas deferens was removed and either transplanted alongside the soleus muscle or into the bed of the soleus muscle that had previously been removed, and in this case the soleus nerve was connected to the transplant. The vas deferens reinnervated by the somatomotor nerve recovered the best. Contractions to transmural electrical stimulation could not be elicited from the denervated vas deferens, although noradrenaline and acetylcholine elicited contractions. The reinnervated vas deferens produced good contractile responses to transmural stimulation, and these were substantially reduced by a cholinergic muscarinic blocking agent, hyoscine, as compared to only a small reduction in the control vas deferens. Neostigmine potentiated the contraction of the transplanted vas deferens to a greater extent than that of the control. This indicated that a substantial component of the contractile response was produced by cholinergic fibres. Consistent with this was the finding that, while guanethidine blocked a greater proportion of the contraction in the control vas deferens, the contraction of the reinnervated transplant was less affected. Acetylcholine elicited a strong contraction in control vas deferens, but only a small response was obtained in the reinnervated transplant. However, the response to noradrenaline was greater in the transplant than in the control vas deferens. These results indicate that cholinergic nerves normally supplying skeletal muscle can reinnervate smooth muscle and that the alien somatomotor innervation altered the responsiveness of the smooth muscle of the vas deferens. Morphological studies confirm the shift from adrenergic to cholinergic fibres in the reinnervated vas deferens.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>19022248</pmid><doi>10.1016/j.expneurol.2008.10.011</doi><tpages>7</tpages></addata></record>
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subjects Acetylcholine
Acetylcholine - metabolism
Acetylcholine - pharmacology
Adrenergic Agents - pharmacology
Animals
Biological and medical sciences
Cholinergic Antagonists - pharmacology
Cholinergic Fibers - physiology
Cholinesterase Inhibitors - pharmacology
Denervation
Electric Stimulation
Guanethidine - pharmacology
Injuries of the nervous system and the skull. Diseases due to physical agents
Male
Medical sciences
Microscopy, Electron, Transmission - methods
Muscle, Skeletal - innervation
Muscle, Skeletal - ultrastructure
Neostigmine - pharmacology
Neurology
Noradrenaline
Norepinephrine - pharmacology
Rats
Rats, Sprague-Dawley
Reinnervation
Scopolamine Hydrobromide - pharmacology
Soleus muscle
Time Factors
Traumas. Diseases due to physical agents
Vas deferens
Vas Deferens - innervation
Vas Deferens - physiology
Vas Deferens - transplantation
Vas Deferens - ultrastructure
title Reinnervation of transplanted vas deferens by cholinergic nerves normally supplying skeletal muscle
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