Modulation by oxytocin of ATP-activated currents in rat dorsal root ganglion neurons

The modulatory effect of oxytocin (OT) on ATP-activated currents (I ATP) was studied in freshly isolated dorsal root ganglion (DRG) neurons of rats using whole cell clamp technique. In most of the neurons examined (50/70, 71.4%) extracellular application of OT (10 −9–10 −5 mol/L) suppressed I ATP wh...

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Veröffentlicht in:Neuropharmacology 2002-10, Vol.43 (5), p.910-916
Hauptverfasser: Yang, Qing, Wu, Zi-Zhen, Li, Xiao, Li, Zhi-Wang, Wei, Jin-Bo, Hu, Qi-Sheng
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container_issue 5
container_start_page 910
container_title Neuropharmacology
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creator Yang, Qing
Wu, Zi-Zhen
Li, Xiao
Li, Zhi-Wang
Wei, Jin-Bo
Hu, Qi-Sheng
description The modulatory effect of oxytocin (OT) on ATP-activated currents (I ATP) was studied in freshly isolated dorsal root ganglion (DRG) neurons of rats using whole cell clamp technique. In most of the neurons examined (50/70, 71.4%) extracellular application of OT (10 −9–10 −5 mol/L) suppressed I ATP while in the rest (20/70, 28.6%) no modulatory effect was observed. OT shifted the ATP concentration-response curve downwards with a decrease of 39.8±4.2% in the maximal current response and with no significant change of Kd value. This OT-induced inhibition of I ATP showed no voltage dependence, and could be blocked by [d(CH 2) 5,Tyr(Me) 2,Thr 4,Tyr-NH 2 9]-OVT (d(CH 2) 5-OVT) (10 −8 mol/L), a specific OT receptor antagonist. Intracellular application of H-9 (4×10 −5 mol/L, an inhibitor of protein kinase A) ( n=12), BAPTA (10 −2 mol/L, a chelator of calcium ions) ( n=4) could reverse the inhibitory effect of extracellular OT (10 −7 mol), while inclusion of H-7 (2×10 −5 mol/L, a protein kinase C inhibitior) ( n=8) and KN-93 (10 −5 mol/L, an inhibitor of CaMKII) ( n=9) in the recording pipette did not affect this effect. The results suggested that OT inhibition on ATP-activated currents was mediated by OT receptors in the membrane of DRG neurons; and this inhibitory effect involved the transduction of intracellular cAMP-PKA and Ca 2+.
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In most of the neurons examined (50/70, 71.4%) extracellular application of OT (10 −9–10 −5 mol/L) suppressed I ATP while in the rest (20/70, 28.6%) no modulatory effect was observed. OT shifted the ATP concentration-response curve downwards with a decrease of 39.8±4.2% in the maximal current response and with no significant change of Kd value. This OT-induced inhibition of I ATP showed no voltage dependence, and could be blocked by [d(CH 2) 5,Tyr(Me) 2,Thr 4,Tyr-NH 2 9]-OVT (d(CH 2) 5-OVT) (10 −8 mol/L), a specific OT receptor antagonist. Intracellular application of H-9 (4×10 −5 mol/L, an inhibitor of protein kinase A) ( n=12), BAPTA (10 −2 mol/L, a chelator of calcium ions) ( n=4) could reverse the inhibitory effect of extracellular OT (10 −7 mol), while inclusion of H-7 (2×10 −5 mol/L, a protein kinase C inhibitior) ( n=8) and KN-93 (10 −5 mol/L, an inhibitor of CaMKII) ( n=9) in the recording pipette did not affect this effect. 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In most of the neurons examined (50/70, 71.4%) extracellular application of OT (10 −9–10 −5 mol/L) suppressed I ATP while in the rest (20/70, 28.6%) no modulatory effect was observed. OT shifted the ATP concentration-response curve downwards with a decrease of 39.8±4.2% in the maximal current response and with no significant change of Kd value. This OT-induced inhibition of I ATP showed no voltage dependence, and could be blocked by [d(CH 2) 5,Tyr(Me) 2,Thr 4,Tyr-NH 2 9]-OVT (d(CH 2) 5-OVT) (10 −8 mol/L), a specific OT receptor antagonist. Intracellular application of H-9 (4×10 −5 mol/L, an inhibitor of protein kinase A) ( n=12), BAPTA (10 −2 mol/L, a chelator of calcium ions) ( n=4) could reverse the inhibitory effect of extracellular OT (10 −7 mol), while inclusion of H-7 (2×10 −5 mol/L, a protein kinase C inhibitior) ( n=8) and KN-93 (10 −5 mol/L, an inhibitor of CaMKII) ( n=9) in the recording pipette did not affect this effect. 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Urophysis</subject><subject>Intracellular dialysis</subject><subject>Ion Channels - drug effects</subject><subject>Ion Channels - metabolism</subject><subject>Membrane Potentials - drug effects</subject><subject>Membrane Potentials - physiology</subject><subject>Neurons, Afferent - drug effects</subject><subject>Neurons, Afferent - metabolism</subject><subject>Oxytocin</subject><subject>Oxytocin - pharmacology</subject><subject>Patch-Clamp Techniques</subject><subject>Protein Kinase C - antagonists &amp; inhibitors</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Oxytocin - antagonists &amp; inhibitors</subject><subject>Signal Transduction - drug effects</subject><subject>Vertebrates: endocrinology</subject><subject>Vertebrates: nervous system and sense organs</subject><subject>Whole cell recording</subject><issn>0028-3908</issn><issn>1873-7064</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtuFDEQRS0EIkPgE0DegGDRwXZ7bPcqiiJeUqIgMawtp1yOjHrsYLsj5u_TnRmRZVa1qHNvlQ4hbzk74Yyrz78YE6brB2Y-MvGJMS50J56RFTe67zRT8jlZ_UeOyKta_zDGpOHmJTniojeSa7Uim8vsp9G1mBO93tH8b9cyxERzoGebn52DFu9cQ09hKgVTq3ReFteoz6W6kZacG71x6WZcGhJOJaf6mrwIbqz45jCPye-vXzbn37uLq28_zs8uOpDGtC5oCT13CEIEDkYrPvD5YxiYYl5xhMARzeC05EqFtdFeoggGfA86GO36Y_Jh33tb8t8Ja7PbWAHH0SXMU7VacDMIaZ4EuVFyvTZiBtd7EEqutWCwtyVuXdlZzuzi3T54t4tUy4R98G6X3LvDgel6i_4xdRA9A-8PgKvgxlBcglgfuX5Qg1BL0emew9nbXcRiK0RMgD4WhGZ9jk-8cg9mNZ8e</recordid><startdate>20021001</startdate><enddate>20021001</enddate><creator>Yang, Qing</creator><creator>Wu, Zi-Zhen</creator><creator>Li, Xiao</creator><creator>Li, Zhi-Wang</creator><creator>Wei, Jin-Bo</creator><creator>Hu, Qi-Sheng</creator><general>Elsevier Ltd</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>20021001</creationdate><title>Modulation by oxytocin of ATP-activated currents in rat dorsal root ganglion neurons</title><author>Yang, Qing ; Wu, Zi-Zhen ; Li, Xiao ; Li, Zhi-Wang ; Wei, Jin-Bo ; Hu, Qi-Sheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c488t-f74c31aec22f1c876191028c9060d61ecf1ee89a74166f587d4e2f8cd3c7f87a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine - pharmacology</topic><topic>Adenosine Triphosphate - physiology</topic><topic>Animals</topic><topic>ATP</topic><topic>Biological and medical sciences</topic><topic>Calcium Signaling - drug effects</topic><topic>Calcium Signaling - physiology</topic><topic>Calcium-Calmodulin-Dependent Protein Kinase Type 2</topic><topic>Calcium-Calmodulin-Dependent Protein Kinases - antagonists &amp; inhibitors</topic><topic>Central nervous system</topic><topic>Central neurotransmission. 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Urophysis</topic><topic>Intracellular dialysis</topic><topic>Ion Channels - drug effects</topic><topic>Ion Channels - metabolism</topic><topic>Membrane Potentials - drug effects</topic><topic>Membrane Potentials - physiology</topic><topic>Neurons, Afferent - drug effects</topic><topic>Neurons, Afferent - metabolism</topic><topic>Oxytocin</topic><topic>Oxytocin - pharmacology</topic><topic>Patch-Clamp Techniques</topic><topic>Protein Kinase C - antagonists &amp; inhibitors</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Oxytocin - antagonists &amp; inhibitors</topic><topic>Signal Transduction - drug effects</topic><topic>Vertebrates: endocrinology</topic><topic>Vertebrates: nervous system and sense organs</topic><topic>Whole cell recording</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Qing</creatorcontrib><creatorcontrib>Wu, Zi-Zhen</creatorcontrib><creatorcontrib>Li, Xiao</creatorcontrib><creatorcontrib>Li, Zhi-Wang</creatorcontrib><creatorcontrib>Wei, Jin-Bo</creatorcontrib><creatorcontrib>Hu, Qi-Sheng</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>Neuropharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Qing</au><au>Wu, Zi-Zhen</au><au>Li, Xiao</au><au>Li, Zhi-Wang</au><au>Wei, Jin-Bo</au><au>Hu, Qi-Sheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modulation by oxytocin of ATP-activated currents in rat dorsal root ganglion neurons</atitle><jtitle>Neuropharmacology</jtitle><addtitle>Neuropharmacology</addtitle><date>2002-10-01</date><risdate>2002</risdate><volume>43</volume><issue>5</issue><spage>910</spage><epage>916</epage><pages>910-916</pages><issn>0028-3908</issn><eissn>1873-7064</eissn><coden>NEPHBW</coden><abstract>The modulatory effect of oxytocin (OT) on ATP-activated currents (I ATP) was studied in freshly isolated dorsal root ganglion (DRG) neurons of rats using whole cell clamp technique. In most of the neurons examined (50/70, 71.4%) extracellular application of OT (10 −9–10 −5 mol/L) suppressed I ATP while in the rest (20/70, 28.6%) no modulatory effect was observed. OT shifted the ATP concentration-response curve downwards with a decrease of 39.8±4.2% in the maximal current response and with no significant change of Kd value. This OT-induced inhibition of I ATP showed no voltage dependence, and could be blocked by [d(CH 2) 5,Tyr(Me) 2,Thr 4,Tyr-NH 2 9]-OVT (d(CH 2) 5-OVT) (10 −8 mol/L), a specific OT receptor antagonist. Intracellular application of H-9 (4×10 −5 mol/L, an inhibitor of protein kinase A) ( n=12), BAPTA (10 −2 mol/L, a chelator of calcium ions) ( n=4) could reverse the inhibitory effect of extracellular OT (10 −7 mol), while inclusion of H-7 (2×10 −5 mol/L, a protein kinase C inhibitior) ( n=8) and KN-93 (10 −5 mol/L, an inhibitor of CaMKII) ( n=9) in the recording pipette did not affect this effect. The results suggested that OT inhibition on ATP-activated currents was mediated by OT receptors in the membrane of DRG neurons; and this inhibitory effect involved the transduction of intracellular cAMP-PKA and Ca 2+.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>12384176</pmid><doi>10.1016/S0028-3908(02)00127-2</doi><tpages>7</tpages></addata></record>
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subjects 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine - pharmacology
Adenosine Triphosphate - physiology
Animals
ATP
Biological and medical sciences
Calcium Signaling - drug effects
Calcium Signaling - physiology
Calcium-Calmodulin-Dependent Protein Kinase Type 2
Calcium-Calmodulin-Dependent Protein Kinases - antagonists & inhibitors
Central nervous system
Central neurotransmission. Neuromudulation. Pathways and receptors
Dorsal root ganglion
Electrophysiology
Enzyme Inhibitors - pharmacology
Fundamental and applied biological sciences. Psychology
Ganglia, Spinal - cytology
Ganglia, Spinal - drug effects
Ganglia, Spinal - metabolism
Hormones and neuropeptides. Regulation
Hypothalamus. Hypophysis. Epiphysis. Urophysis
Intracellular dialysis
Ion Channels - drug effects
Ion Channels - metabolism
Membrane Potentials - drug effects
Membrane Potentials - physiology
Neurons, Afferent - drug effects
Neurons, Afferent - metabolism
Oxytocin
Oxytocin - pharmacology
Patch-Clamp Techniques
Protein Kinase C - antagonists & inhibitors
Rats
Rats, Sprague-Dawley
Receptors, Oxytocin - antagonists & inhibitors
Signal Transduction - drug effects
Vertebrates: endocrinology
Vertebrates: nervous system and sense organs
Whole cell recording
title Modulation by oxytocin of ATP-activated currents in rat dorsal root ganglion neurons
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