Evidence for purinergic neurotransmission in the urinary bladder of pithed rats

The purpose of this study was to investigate the contribution of adenosine-5′-triphosphate (ATP) to segmental (L6-S2) spinal electrical stimulation evoked increases in intra-vesical pressure in pithed rats. Exogenous ATP and substance P produced dose-dependent increases in intra-vesical pressure (ED...

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Veröffentlicht in:European journal of pharmacology 1998-05, Vol.349 (1), p.75-82
Hauptverfasser: Hegde, Sharath S, Mandel, Dan A, Wilford, Mary R, Briaud, Stephanie, Ford, Anthony P.D.W, Eglen, Richard M
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container_title European journal of pharmacology
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creator Hegde, Sharath S
Mandel, Dan A
Wilford, Mary R
Briaud, Stephanie
Ford, Anthony P.D.W
Eglen, Richard M
description The purpose of this study was to investigate the contribution of adenosine-5′-triphosphate (ATP) to segmental (L6-S2) spinal electrical stimulation evoked increases in intra-vesical pressure in pithed rats. Exogenous ATP and substance P produced dose-dependent increases in intra-vesical pressure (ED 10 mmHg (dose required to elicit 10 mmHg increase in intra-vesical pressure)=1.7 mg/kg and 1.1 μg/kg, i.v., respectively). Desensitisation (or antagonism) of P 2x purinoceptors with α, β-methylene ATP ( α, β-meATP; 30 μg/kg per min, i.v.) or pyridoxalphosphate-6-azophenyl-2′,4′-disulfonic acid (PPADS; 10 mg/kg, i.v.) significantly ( p8 and 3.6-fold increase in ED 10 mmHg, respectively) but had no significant effect on intra-vesical pressure responses to substance P. Spinal stimulation evoked frequency-dependent increases in intra-vesical pressure (EF 20 mmHg (frequency required to produce 20 mmHg increase in intra-vesical pressure)=3.4 Hz). Blockade of muscarinic cholinoceptors and adrenoceptors with atropine (3 mg/kg, i.v.), propranolol (3 mg/kg, i.v.) and phentolamine (10 mg/kg, i.v.) produced marginal attenuation of the intra-vesical pressure responses to spinal stimulation indicating a major non-adrenergic non-cholinergic (NANC) component in the overall response. The NANC responses were significantly ( p2.6-fold increase in EF 20 mmHg), consistent with involvement of a purinergic neurotransmitter, presumably ATP. Comparative studies in young (4–6 months) and old (21–23 months) Fischer rats revealed no age-dependent changes in the relative contribution of the cholinergic and purinergic systems, with the latter being the dominant one. These findings suggest that purinergic neurotransmission, presumably mediated by ATP acting via P 2x purinoceptors, represents a major component of excitatory innervation to the urinary bladder in pithed rats.
doi_str_mv 10.1016/S0014-2999(98)00173-3
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Exogenous ATP and substance P produced dose-dependent increases in intra-vesical pressure (ED 10 mmHg (dose required to elicit 10 mmHg increase in intra-vesical pressure)=1.7 mg/kg and 1.1 μg/kg, i.v., respectively). Desensitisation (or antagonism) of P 2x purinoceptors with α, β-methylene ATP ( α, β-meATP; 30 μg/kg per min, i.v.) or pyridoxalphosphate-6-azophenyl-2′,4′-disulfonic acid (PPADS; 10 mg/kg, i.v.) significantly ( p&lt;0.05) antagonized the intra-vesical pressure responses to ATP (&gt;8 and 3.6-fold increase in ED 10 mmHg, respectively) but had no significant effect on intra-vesical pressure responses to substance P. Spinal stimulation evoked frequency-dependent increases in intra-vesical pressure (EF 20 mmHg (frequency required to produce 20 mmHg increase in intra-vesical pressure)=3.4 Hz). Blockade of muscarinic cholinoceptors and adrenoceptors with atropine (3 mg/kg, i.v.), propranolol (3 mg/kg, i.v.) and phentolamine (10 mg/kg, i.v.) produced marginal attenuation of the intra-vesical pressure responses to spinal stimulation indicating a major non-adrenergic non-cholinergic (NANC) component in the overall response. The NANC responses were significantly ( p&lt;0.05) antagonized by α, β-meATP (30 μg/kg per min, i.v.) and PPADS (10 mg/kg, i.v.) (&gt;2.6-fold increase in EF 20 mmHg), consistent with involvement of a purinergic neurotransmitter, presumably ATP. Comparative studies in young (4–6 months) and old (21–23 months) Fischer rats revealed no age-dependent changes in the relative contribution of the cholinergic and purinergic systems, with the latter being the dominant one. 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Exogenous ATP and substance P produced dose-dependent increases in intra-vesical pressure (ED 10 mmHg (dose required to elicit 10 mmHg increase in intra-vesical pressure)=1.7 mg/kg and 1.1 μg/kg, i.v., respectively). Desensitisation (or antagonism) of P 2x purinoceptors with α, β-methylene ATP ( α, β-meATP; 30 μg/kg per min, i.v.) or pyridoxalphosphate-6-azophenyl-2′,4′-disulfonic acid (PPADS; 10 mg/kg, i.v.) significantly ( p&lt;0.05) antagonized the intra-vesical pressure responses to ATP (&gt;8 and 3.6-fold increase in ED 10 mmHg, respectively) but had no significant effect on intra-vesical pressure responses to substance P. Spinal stimulation evoked frequency-dependent increases in intra-vesical pressure (EF 20 mmHg (frequency required to produce 20 mmHg increase in intra-vesical pressure)=3.4 Hz). Blockade of muscarinic cholinoceptors and adrenoceptors with atropine (3 mg/kg, i.v.), propranolol (3 mg/kg, i.v.) and phentolamine (10 mg/kg, i.v.) produced marginal attenuation of the intra-vesical pressure responses to spinal stimulation indicating a major non-adrenergic non-cholinergic (NANC) component in the overall response. The NANC responses were significantly ( p&lt;0.05) antagonized by α, β-meATP (30 μg/kg per min, i.v.) and PPADS (10 mg/kg, i.v.) (&gt;2.6-fold increase in EF 20 mmHg), consistent with involvement of a purinergic neurotransmitter, presumably ATP. Comparative studies in young (4–6 months) and old (21–23 months) Fischer rats revealed no age-dependent changes in the relative contribution of the cholinergic and purinergic systems, with the latter being the dominant one. 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Psychology</subject><subject>Ganglionic Blockers - pharmacology</subject><subject>Muscarinic Antagonists - pharmacology</subject><subject>Muscle, Smooth - drug effects</subject><subject>Muscle, Smooth - innervation</subject><subject>Muscle, Smooth - physiology</subject><subject>Peripheral nervous system. Autonomic nervous system. Neuromuscular transmission. Ganglionic transmission. Electric organ</subject><subject>PPADS (pyridoxalphosphate-6-azophenyl-2′,4′-disulfonic acid), α, β-methylene ATP</subject><subject>Pressure</subject><subject>Purinergic</subject><subject>Purinergic P2 Receptor Antagonists</subject><subject>Purinoceptor</subject><subject>Pyridoxal Phosphate - analogs &amp; derivatives</subject><subject>Pyridoxal Phosphate - pharmacology</subject><subject>Rats</subject><subject>Rats, Inbred F344</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Purinergic - physiology</subject><subject>Spinal Nerves - physiology</subject><subject>Substance P - pharmacology</subject><subject>Synaptic Transmission - drug effects</subject><subject>Synaptic Transmission - physiology</subject><subject>Urinary Bladder - drug effects</subject><subject>Urinary Bladder - innervation</subject><subject>Urinary Bladder - physiology</subject><subject>Vertebrates: nervous system and sense organs</subject><subject>Vertebrates: urinary system</subject><issn>0014-2999</issn><issn>1879-0712</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1PAyEURYnRaP34CSYsjNHFKAwMAytjmvqRmHShrgkDD8VMZyrMNPHfS23TrStC7nnw7kHonJIbSqi4fSWE8qJUSl0peZ0vNSvYHppQWauC1LTcR5MdcoSOU_oihFSqrA7RoRJCcaUmaD5bBQedBez7iJdjDB3Ej2BxB2Psh2i6tAgphb7DocPDJ-A1YuIPblrjHETce7wMOXA4miGdogNv2gRn2_MEvT_M3qZPxcv88Xl6_1JYJtVQWKIE5Y0wVU1qEFQQY73wFZSV81LyxlScSiV9mduUkjWcVZyXtmaSO-sEO0GXm3eXsf8eIQ06r2mhbU0H_Zi0zF0VFXUGqw1oY59SBK-XMSxyAU2JXovUfyL12pJWUv-J1CzPnW8_GJsFuN3U1lzOL7a5Sda0PpuyIe2wkgnBOMnY3QaDLGMVIOpkw9q3CxHsoF0f_lnkF4C1jyI</recordid><startdate>19980515</startdate><enddate>19980515</enddate><creator>Hegde, Sharath S</creator><creator>Mandel, Dan A</creator><creator>Wilford, Mary R</creator><creator>Briaud, Stephanie</creator><creator>Ford, Anthony P.D.W</creator><creator>Eglen, Richard M</creator><general>Elsevier B.V</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>19980515</creationdate><title>Evidence for purinergic neurotransmission in the urinary bladder of pithed rats</title><author>Hegde, Sharath S ; Mandel, Dan A ; Wilford, Mary R ; Briaud, Stephanie ; Ford, Anthony P.D.W ; Eglen, Richard M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-c09614b6a5707e6160acf6f5e25df884ba541898f2879283b435442c7384dcd63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adenosine Triphosphate - analogs &amp; derivatives</topic><topic>Adenosine Triphosphate - pharmacology</topic><topic>Adenosine Triphosphate - physiology</topic><topic>Adrenergic Antagonists - pharmacology</topic><topic>Aging - physiology</topic><topic>Animals</topic><topic>Atropine - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Bladder</topic><topic>Blood Pressure - drug effects</topic><topic>Decerebrate State</topic><topic>Electric Stimulation</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Ganglionic Blockers - pharmacology</topic><topic>Muscarinic Antagonists - pharmacology</topic><topic>Muscle, Smooth - drug effects</topic><topic>Muscle, Smooth - innervation</topic><topic>Muscle, Smooth - physiology</topic><topic>Peripheral nervous system. Autonomic nervous system. Neuromuscular transmission. Ganglionic transmission. Electric organ</topic><topic>PPADS (pyridoxalphosphate-6-azophenyl-2′,4′-disulfonic acid), α, β-methylene ATP</topic><topic>Pressure</topic><topic>Purinergic</topic><topic>Purinergic P2 Receptor Antagonists</topic><topic>Purinoceptor</topic><topic>Pyridoxal Phosphate - analogs &amp; derivatives</topic><topic>Pyridoxal Phosphate - pharmacology</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Purinergic - physiology</topic><topic>Spinal Nerves - physiology</topic><topic>Substance P - pharmacology</topic><topic>Synaptic Transmission - drug effects</topic><topic>Synaptic Transmission - physiology</topic><topic>Urinary Bladder - drug effects</topic><topic>Urinary Bladder - innervation</topic><topic>Urinary Bladder - physiology</topic><topic>Vertebrates: nervous system and sense organs</topic><topic>Vertebrates: urinary system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hegde, Sharath S</creatorcontrib><creatorcontrib>Mandel, Dan A</creatorcontrib><creatorcontrib>Wilford, Mary R</creatorcontrib><creatorcontrib>Briaud, Stephanie</creatorcontrib><creatorcontrib>Ford, Anthony P.D.W</creatorcontrib><creatorcontrib>Eglen, Richard M</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>European journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hegde, Sharath S</au><au>Mandel, Dan A</au><au>Wilford, Mary R</au><au>Briaud, Stephanie</au><au>Ford, Anthony P.D.W</au><au>Eglen, Richard M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evidence for purinergic neurotransmission in the urinary bladder of pithed rats</atitle><jtitle>European journal of pharmacology</jtitle><addtitle>Eur J Pharmacol</addtitle><date>1998-05-15</date><risdate>1998</risdate><volume>349</volume><issue>1</issue><spage>75</spage><epage>82</epage><pages>75-82</pages><issn>0014-2999</issn><eissn>1879-0712</eissn><coden>EJPHAZ</coden><abstract>The purpose of this study was to investigate the contribution of adenosine-5′-triphosphate (ATP) to segmental (L6-S2) spinal electrical stimulation evoked increases in intra-vesical pressure in pithed rats. Exogenous ATP and substance P produced dose-dependent increases in intra-vesical pressure (ED 10 mmHg (dose required to elicit 10 mmHg increase in intra-vesical pressure)=1.7 mg/kg and 1.1 μg/kg, i.v., respectively). Desensitisation (or antagonism) of P 2x purinoceptors with α, β-methylene ATP ( α, β-meATP; 30 μg/kg per min, i.v.) or pyridoxalphosphate-6-azophenyl-2′,4′-disulfonic acid (PPADS; 10 mg/kg, i.v.) significantly ( p&lt;0.05) antagonized the intra-vesical pressure responses to ATP (&gt;8 and 3.6-fold increase in ED 10 mmHg, respectively) but had no significant effect on intra-vesical pressure responses to substance P. Spinal stimulation evoked frequency-dependent increases in intra-vesical pressure (EF 20 mmHg (frequency required to produce 20 mmHg increase in intra-vesical pressure)=3.4 Hz). Blockade of muscarinic cholinoceptors and adrenoceptors with atropine (3 mg/kg, i.v.), propranolol (3 mg/kg, i.v.) and phentolamine (10 mg/kg, i.v.) produced marginal attenuation of the intra-vesical pressure responses to spinal stimulation indicating a major non-adrenergic non-cholinergic (NANC) component in the overall response. The NANC responses were significantly ( p&lt;0.05) antagonized by α, β-meATP (30 μg/kg per min, i.v.) and PPADS (10 mg/kg, i.v.) (&gt;2.6-fold increase in EF 20 mmHg), consistent with involvement of a purinergic neurotransmitter, presumably ATP. Comparative studies in young (4–6 months) and old (21–23 months) Fischer rats revealed no age-dependent changes in the relative contribution of the cholinergic and purinergic systems, with the latter being the dominant one. These findings suggest that purinergic neurotransmission, presumably mediated by ATP acting via P 2x purinoceptors, represents a major component of excitatory innervation to the urinary bladder in pithed rats.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>9669499</pmid><doi>10.1016/S0014-2999(98)00173-3</doi><tpages>8</tpages></addata></record>
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subjects Adenosine Triphosphate - analogs & derivatives
Adenosine Triphosphate - pharmacology
Adenosine Triphosphate - physiology
Adrenergic Antagonists - pharmacology
Aging - physiology
Animals
Atropine - pharmacology
Biological and medical sciences
Bladder
Blood Pressure - drug effects
Decerebrate State
Electric Stimulation
Female
Fundamental and applied biological sciences. Psychology
Ganglionic Blockers - pharmacology
Muscarinic Antagonists - pharmacology
Muscle, Smooth - drug effects
Muscle, Smooth - innervation
Muscle, Smooth - physiology
Peripheral nervous system. Autonomic nervous system. Neuromuscular transmission. Ganglionic transmission. Electric organ
PPADS (pyridoxalphosphate-6-azophenyl-2′,4′-disulfonic acid), α, β-methylene ATP
Pressure
Purinergic
Purinergic P2 Receptor Antagonists
Purinoceptor
Pyridoxal Phosphate - analogs & derivatives
Pyridoxal Phosphate - pharmacology
Rats
Rats, Inbred F344
Rats, Sprague-Dawley
Receptors, Purinergic - physiology
Spinal Nerves - physiology
Substance P - pharmacology
Synaptic Transmission - drug effects
Synaptic Transmission - physiology
Urinary Bladder - drug effects
Urinary Bladder - innervation
Urinary Bladder - physiology
Vertebrates: nervous system and sense organs
Vertebrates: urinary system
title Evidence for purinergic neurotransmission in the urinary bladder of pithed rats
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