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...
Gespeichert in:
Veröffentlicht in: | Neuropharmacology 2002-10, Vol.43 (5), p.910-916 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 916 |
---|---|
container_issue | 5 |
container_start_page | 910 |
container_title | Neuropharmacology |
container_volume | 43 |
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+. |
doi_str_mv | 10.1016/S0028-3908(02)00127-2 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_72189248</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0028390802001272</els_id><sourcerecordid>18645582</sourcerecordid><originalsourceid>FETCH-LOGICAL-c488t-f74c31aec22f1c876191028c9060d61ecf1ee89a74166f587d4e2f8cd3c7f87a3</originalsourceid><addsrcrecordid>eNqFkMtuFDEQRS0EIkPgE0DegGDRwXZ7bPcqiiJeUqIgMawtp1yOjHrsYLsj5u_TnRmRZVa1qHNvlQ4hbzk74Yyrz78YE6brB2Y-MvGJMS50J56RFTe67zRT8jlZ_UeOyKta_zDGpOHmJTniojeSa7Uim8vsp9G1mBO93tH8b9cyxERzoGebn52DFu9cQ09hKgVTq3ReFteoz6W6kZacG71x6WZcGhJOJaf6mrwIbqz45jCPye-vXzbn37uLq28_zs8uOpDGtC5oCT13CEIEDkYrPvD5YxiYYl5xhMARzeC05EqFtdFeoggGfA86GO36Y_Jh33tb8t8Ja7PbWAHH0SXMU7VacDMIaZ4EuVFyvTZiBtd7EEqutWCwtyVuXdlZzuzi3T54t4tUy4R98G6X3LvDgel6i_4xdRA9A-8PgKvgxlBcglgfuX5Qg1BL0emew9nbXcRiK0RMgD4WhGZ9jk-8cg9mNZ8e</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>18645582</pqid></control><display><type>article</type><title>Modulation by oxytocin of ATP-activated currents in rat dorsal root ganglion neurons</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Yang, Qing ; Wu, Zi-Zhen ; Li, Xiao ; Li, Zhi-Wang ; Wei, Jin-Bo ; Hu, Qi-Sheng</creator><creatorcontrib>Yang, Qing ; Wu, Zi-Zhen ; Li, Xiao ; Li, Zhi-Wang ; Wei, Jin-Bo ; Hu, Qi-Sheng</creatorcontrib><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+.</description><identifier>ISSN: 0028-3908</identifier><identifier>EISSN: 1873-7064</identifier><identifier>DOI: 10.1016/S0028-3908(02)00127-2</identifier><identifier>PMID: 12384176</identifier><identifier>CODEN: NEPHBW</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>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</subject><ispartof>Neuropharmacology, 2002-10, Vol.43 (5), p.910-916</ispartof><rights>2002 Elsevier Science Ltd</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c488t-f74c31aec22f1c876191028c9060d61ecf1ee89a74166f587d4e2f8cd3c7f87a3</citedby><cites>FETCH-LOGICAL-c488t-f74c31aec22f1c876191028c9060d61ecf1ee89a74166f587d4e2f8cd3c7f87a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0028390802001272$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13969262$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12384176$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Modulation by oxytocin of ATP-activated currents in rat dorsal root ganglion neurons</title><title>Neuropharmacology</title><addtitle>Neuropharmacology</addtitle><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+.</description><subject>1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine - pharmacology</subject><subject>Adenosine Triphosphate - physiology</subject><subject>Animals</subject><subject>ATP</subject><subject>Biological and medical sciences</subject><subject>Calcium Signaling - drug effects</subject><subject>Calcium Signaling - physiology</subject><subject>Calcium-Calmodulin-Dependent Protein Kinase Type 2</subject><subject>Calcium-Calmodulin-Dependent Protein Kinases - antagonists & inhibitors</subject><subject>Central nervous system</subject><subject>Central neurotransmission. Neuromudulation. Pathways and receptors</subject><subject>Dorsal root ganglion</subject><subject>Electrophysiology</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Ganglia, Spinal - cytology</subject><subject>Ganglia, Spinal - drug effects</subject><subject>Ganglia, Spinal - metabolism</subject><subject>Hormones and neuropeptides. Regulation</subject><subject>Hypothalamus. Hypophysis. Epiphysis. 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 & inhibitors</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Oxytocin - antagonists & 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 & inhibitors</topic><topic>Central nervous system</topic><topic>Central neurotransmission. Neuromudulation. Pathways and receptors</topic><topic>Dorsal root ganglion</topic><topic>Electrophysiology</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Ganglia, Spinal - cytology</topic><topic>Ganglia, Spinal - drug effects</topic><topic>Ganglia, Spinal - metabolism</topic><topic>Hormones and neuropeptides. Regulation</topic><topic>Hypothalamus. Hypophysis. Epiphysis. 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 & inhibitors</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Oxytocin - antagonists & 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> |
fulltext | fulltext |
identifier | ISSN: 0028-3908 |
ispartof | Neuropharmacology, 2002-10, Vol.43 (5), p.910-916 |
issn | 0028-3908 1873-7064 |
language | eng |
recordid | cdi_proquest_miscellaneous_72189248 |
source | MEDLINE; Elsevier ScienceDirect Journals |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T15%3A44%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Modulation%20by%20oxytocin%20of%20ATP-activated%20currents%20in%20rat%20dorsal%20root%20ganglion%20neurons&rft.jtitle=Neuropharmacology&rft.au=Yang,%20Qing&rft.date=2002-10-01&rft.volume=43&rft.issue=5&rft.spage=910&rft.epage=916&rft.pages=910-916&rft.issn=0028-3908&rft.eissn=1873-7064&rft.coden=NEPHBW&rft_id=info:doi/10.1016/S0028-3908(02)00127-2&rft_dat=%3Cproquest_cross%3E18645582%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=18645582&rft_id=info:pmid/12384176&rft_els_id=S0028390802001272&rfr_iscdi=true |