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Neurotensin Modulates Pacemaker Activity in Interstitial Cells of Cajal from the Mouse Small Intestine
Neurotensin, a tridecapeptide localized in the gut to discrete enteroendocrine cells of the small bowel mucosa, is a hormone that plays an important role in gastrointestinal secretion, growth, and motility. Neurotensin has inhibitory and excitatory effects on peristaltic activity and produces contra...
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Published in: | Molecules and cells 2012, 33(5), , pp.509-516 |
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creator | Lee, J., Chosun University, Gwangju, Republic of Korea Kim, Y.D., Chosun University, Gwangju, Republic of Korea Park, C.G., Chosun University, Gwangju, Republic of Korea Kim, M.Y., Chosun University, Gwangju, Republic of Korea Chang, I.Y., Chosun University, Gwangju, Republic of Korea Zuo, Dong Chuan, Chosun University, Gwangju, Republic of Korea Shahi, Pawan Kumar, Chosun University, Gwangju, Republic of Korea Choi, S., Chosun University, Gwangju, Republic of Korea Yeum, C.H., Chosun University, Gwangju, Republic of Korea Jun, J.Y., Chosun University, Gwangju, Republic of Korea |
description | Neurotensin, a tridecapeptide localized in the gut to discrete enteroendocrine cells of the small bowel mucosa, is a hormone that plays an important role in gastrointestinal secretion, growth, and motility. Neurotensin has inhibitory and excitatory effects on peristaltic activity and produces contractile and relaxant responses in intestinal smooth muscle. Our objective in this study is to investigate the effects of neurotensin in small intestinal interstitial cells of Cajal (ICC) and elucidate the mechanism. To determine the electrophysiological effects of neurotensin on ICC, whole-cell patch clamp recordings were performed in cultured ICC from the small intestine. Exposure to neurotensin depolarized the membrane of pacemaker cells and produced tonic inward pacemaker currents. Only neurotensin receptor1 was identified when RT-PCR and immunocytochemistry were performed with mRNA isolated from small intestinal ICC and c-Kit positive cells. Neurotensin-induced tonic inward pacemaker currents were blocked by external Na+-free solution and in the presence of flufenamic acid, an inhibitor of non-selective cation channels. Furthermore, neurotensin-induced action is blocked either by treatment with U73122, a phospholipase C inhibitor, or thapsigargin, a Ca²+-ATPase inhibitor in ICC. We found that neurotensin increased spontaneous intracellular Ca²+ oscillations as seen with fluo4/AM recording. These results suggest that neurotensin modulates pacemaker currents via the activation of non-selective cation channels by intracellular Ca²+-release through neurotensin receptor1. |
doi_str_mv | 10.1007/s10059-012-2290-5 |
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Neurotensin has inhibitory and excitatory effects on peristaltic activity and produces contractile and relaxant responses in intestinal smooth muscle. Our objective in this study is to investigate the effects of neurotensin in small intestinal interstitial cells of Cajal (ICC) and elucidate the mechanism. To determine the electrophysiological effects of neurotensin on ICC, whole-cell patch clamp recordings were performed in cultured ICC from the small intestine. Exposure to neurotensin depolarized the membrane of pacemaker cells and produced tonic inward pacemaker currents. Only neurotensin receptor1 was identified when RT-PCR and immunocytochemistry were performed with mRNA isolated from small intestinal ICC and c-Kit positive cells. Neurotensin-induced tonic inward pacemaker currents were blocked by external Na+-free solution and in the presence of flufenamic acid, an inhibitor of non-selective cation channels. Furthermore, neurotensin-induced action is blocked either by treatment with U73122, a phospholipase C inhibitor, or thapsigargin, a Ca²+-ATPase inhibitor in ICC. We found that neurotensin increased spontaneous intracellular Ca²+ oscillations as seen with fluo4/AM recording. These results suggest that neurotensin modulates pacemaker currents via the activation of non-selective cation channels by intracellular Ca²+-release through neurotensin receptor1.</description><identifier>ISSN: 1016-8478</identifier><identifier>EISSN: 0219-1032</identifier><identifier>DOI: 10.1007/s10059-012-2290-5</identifier><identifier>PMID: 22441675</identifier><language>eng</language><publisher>Springer: Korean Society for Molecular and Cellular Biology</publisher><subject>Animals ; Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Biotechnology ; Calcium - metabolism ; Calcium-Transporting ATPases - antagonists & inhibitors ; Calcium-Transporting ATPases - metabolism ; Cell Biology ; Cells, Cultured ; Endoplasmic Reticulum - metabolism ; Female ; GASTROINTESTINAL MOTILITY ; In Vitro Techniques ; interstitial cells of Cajal ; Interstitial Cells of Cajal - drug effects ; Interstitial Cells of Cajal - metabolism ; Intestine, Small - cytology ; Intestine, Small - drug effects ; Intestine, Small - metabolism ; Ion Channels - metabolism ; Life Sciences ; Male ; Membrane Potentials - physiology ; Mice ; Mice, Inbred BALB C ; MOTRICITE GASTRO-INTESTINALE ; MOVILIDAD GASTROINTESTINAL ; Muscle, Smooth - metabolism ; neurotensin ; Neurotensin - metabolism ; Neurotensin - pharmacology ; neurotensin receptor1 ; Receptors, Neurotensin - metabolism ; Sodium - metabolism ; Type C Phospholipases - antagonists & inhibitors ; Type C Phospholipases - metabolism ; 생물학</subject><ispartof>Molecules and Cells, 2012, 33(5), , pp.509-516</ispartof><rights>The Korean Society for Molecular and Cellular Biology and Springer Netherlands 2012</rights><rights>The Korean Society for Molecular and Cellular Biology. All rights reserved. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c524t-a0ab63f57d0ef24e54aa982d8f59a8f51b14c8e231dc8b7bab8ed3dafaac73423</citedby><cites>FETCH-LOGICAL-c524t-a0ab63f57d0ef24e54aa982d8f59a8f51b14c8e231dc8b7bab8ed3dafaac73423</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3887726/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3887726/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22441675$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001660809$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, J., Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Kim, Y.D., Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Park, C.G., Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Kim, M.Y., Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Chang, I.Y., Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Zuo, Dong Chuan, Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Shahi, Pawan Kumar, Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Choi, S., Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Yeum, C.H., Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Jun, J.Y., Chosun University, Gwangju, Republic of Korea</creatorcontrib><title>Neurotensin Modulates Pacemaker Activity in Interstitial Cells of Cajal from the Mouse Small Intestine</title><title>Molecules and cells</title><addtitle>Mol Cells</addtitle><addtitle>Mol Cells</addtitle><description>Neurotensin, a tridecapeptide localized in the gut to discrete enteroendocrine cells of the small bowel mucosa, is a hormone that plays an important role in gastrointestinal secretion, growth, and motility. Neurotensin has inhibitory and excitatory effects on peristaltic activity and produces contractile and relaxant responses in intestinal smooth muscle. Our objective in this study is to investigate the effects of neurotensin in small intestinal interstitial cells of Cajal (ICC) and elucidate the mechanism. To determine the electrophysiological effects of neurotensin on ICC, whole-cell patch clamp recordings were performed in cultured ICC from the small intestine. Exposure to neurotensin depolarized the membrane of pacemaker cells and produced tonic inward pacemaker currents. Only neurotensin receptor1 was identified when RT-PCR and immunocytochemistry were performed with mRNA isolated from small intestinal ICC and c-Kit positive cells. Neurotensin-induced tonic inward pacemaker currents were blocked by external Na+-free solution and in the presence of flufenamic acid, an inhibitor of non-selective cation channels. Furthermore, neurotensin-induced action is blocked either by treatment with U73122, a phospholipase C inhibitor, or thapsigargin, a Ca²+-ATPase inhibitor in ICC. We found that neurotensin increased spontaneous intracellular Ca²+ oscillations as seen with fluo4/AM recording. These results suggest that neurotensin modulates pacemaker currents via the activation of non-selective cation channels by intracellular Ca²+-release through neurotensin receptor1.</description><subject>Animals</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Biotechnology</subject><subject>Calcium - metabolism</subject><subject>Calcium-Transporting ATPases - antagonists & inhibitors</subject><subject>Calcium-Transporting ATPases - metabolism</subject><subject>Cell Biology</subject><subject>Cells, Cultured</subject><subject>Endoplasmic Reticulum - metabolism</subject><subject>Female</subject><subject>GASTROINTESTINAL MOTILITY</subject><subject>In Vitro Techniques</subject><subject>interstitial cells of Cajal</subject><subject>Interstitial Cells of Cajal - drug effects</subject><subject>Interstitial Cells of Cajal - metabolism</subject><subject>Intestine, Small - cytology</subject><subject>Intestine, Small - drug effects</subject><subject>Intestine, Small - metabolism</subject><subject>Ion Channels - metabolism</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Membrane Potentials - physiology</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>MOTRICITE GASTRO-INTESTINALE</subject><subject>MOVILIDAD GASTROINTESTINAL</subject><subject>Muscle, Smooth - metabolism</subject><subject>neurotensin</subject><subject>Neurotensin - metabolism</subject><subject>Neurotensin - pharmacology</subject><subject>neurotensin receptor1</subject><subject>Receptors, Neurotensin - metabolism</subject><subject>Sodium - metabolism</subject><subject>Type C Phospholipases - antagonists & inhibitors</subject><subject>Type C Phospholipases - metabolism</subject><subject>생물학</subject><issn>1016-8478</issn><issn>0219-1032</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp1kktv1DAUhSMEotPCD2ABisQCNgE_4tjZVBqNKIwoD5Wytm4ce-qZxC62U6n_Hs-kVAWJja-s-51j-x4XxQuM3mGE-PuYV9ZWCJOKkBZV7FGxQAS3FUaUPC4WGOGmEjUXR8VxjFuEMG-IeFocEVLXuOFsUZivego-aRetK7_4fhog6Vh-B6VH2OlQLlWyNzbdlrm_dkmHmGyyMJQrPQyx9KZcwTZvTfBjma50NpmiLn-MMAwHQeadflY8MTBE_fyunhQ_zz5crj5V598-rlfL80oxUqcKEHQNNYz3SBtSa1YDtIL0wrAW8oI7XCuhCcW9Eh3voBO6pz0YAMVpTehJ8Wb2dcHInbLSgz3UjZe7IJcXl2vJMW9RJk9n8nrqRt0r7VKAQV4HO0K4Pej-7jh7lV1uJBWCc9Jkg7d3BsH_mvIz5WijykMBp_MIZB4-Qy1rCc3o63_QrZ-Cy4M4UA3lNdsb4plSwccYtLm_DEZyn7ec85Y5b7nPW7KsefXwFfeKPwFngMxAzC230eHh0f93fTmLDHgJm2Cj_HxBEKb7H0Q4_Q0Imr_6</recordid><startdate>20120501</startdate><enddate>20120501</enddate><creator>Lee, J., Chosun University, Gwangju, Republic of Korea</creator><creator>Kim, Y.D., Chosun University, Gwangju, Republic of Korea</creator><creator>Park, C.G., Chosun University, Gwangju, Republic of Korea</creator><creator>Kim, M.Y., Chosun University, Gwangju, Republic of Korea</creator><creator>Chang, I.Y., Chosun University, Gwangju, Republic of Korea</creator><creator>Zuo, Dong Chuan, Chosun University, Gwangju, Republic of Korea</creator><creator>Shahi, Pawan Kumar, Chosun University, Gwangju, Republic of Korea</creator><creator>Choi, S., Chosun University, Gwangju, Republic of Korea</creator><creator>Yeum, C.H., Chosun University, Gwangju, Republic of Korea</creator><creator>Jun, J.Y., Chosun University, Gwangju, Republic of Korea</creator><general>Korean Society for Molecular and Cellular Biology</general><general>Korea Society for Molecular and Cellular Biology</general><general>한국분자세포생물학회</general><scope>FBQ</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BVBZV</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>ACYCR</scope></search><sort><creationdate>20120501</creationdate><title>Neurotensin Modulates Pacemaker Activity in Interstitial Cells of Cajal from the Mouse Small Intestine</title><author>Lee, J., Chosun University, Gwangju, Republic of Korea ; Kim, Y.D., Chosun University, Gwangju, Republic of Korea ; Park, C.G., Chosun University, Gwangju, Republic of Korea ; Kim, M.Y., Chosun University, Gwangju, Republic of Korea ; Chang, I.Y., Chosun University, Gwangju, Republic of Korea ; Zuo, Dong Chuan, Chosun University, Gwangju, Republic of Korea ; Shahi, Pawan Kumar, Chosun University, Gwangju, Republic of Korea ; Choi, S., Chosun University, Gwangju, Republic of Korea ; Yeum, C.H., Chosun University, Gwangju, Republic of Korea ; Jun, J.Y., Chosun University, Gwangju, Republic of Korea</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c524t-a0ab63f57d0ef24e54aa982d8f59a8f51b14c8e231dc8b7bab8ed3dafaac73423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Biotechnology</topic><topic>Calcium - 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pharmacology</topic><topic>neurotensin receptor1</topic><topic>Receptors, Neurotensin - metabolism</topic><topic>Sodium - metabolism</topic><topic>Type C Phospholipases - antagonists & inhibitors</topic><topic>Type C Phospholipases - metabolism</topic><topic>생물학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, J., Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Kim, Y.D., Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Park, C.G., Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Kim, M.Y., Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Chang, I.Y., Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Zuo, Dong Chuan, Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Shahi, Pawan Kumar, Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Choi, S., Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Yeum, C.H., Chosun University, Gwangju, Republic of Korea</creatorcontrib><creatorcontrib>Jun, J.Y., Chosun University, Gwangju, Republic of Korea</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>East & South Asia Database</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Korean Citation Index</collection><jtitle>Molecules and cells</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, J., Chosun University, Gwangju, Republic of Korea</au><au>Kim, Y.D., Chosun University, Gwangju, Republic of Korea</au><au>Park, C.G., Chosun University, Gwangju, Republic of Korea</au><au>Kim, M.Y., Chosun University, Gwangju, Republic of Korea</au><au>Chang, I.Y., Chosun University, Gwangju, Republic of Korea</au><au>Zuo, Dong Chuan, Chosun University, Gwangju, Republic of Korea</au><au>Shahi, Pawan Kumar, Chosun University, Gwangju, Republic of Korea</au><au>Choi, S., Chosun University, Gwangju, Republic of Korea</au><au>Yeum, C.H., Chosun University, Gwangju, Republic of Korea</au><au>Jun, J.Y., Chosun University, Gwangju, Republic of Korea</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neurotensin Modulates Pacemaker Activity in Interstitial Cells of Cajal from the Mouse Small Intestine</atitle><jtitle>Molecules and cells</jtitle><stitle>Mol Cells</stitle><addtitle>Mol Cells</addtitle><date>2012-05-01</date><risdate>2012</risdate><volume>33</volume><issue>5</issue><spage>509</spage><epage>516</epage><pages>509-516</pages><issn>1016-8478</issn><eissn>0219-1032</eissn><abstract>Neurotensin, a tridecapeptide localized in the gut to discrete enteroendocrine cells of the small bowel mucosa, is a hormone that plays an important role in gastrointestinal secretion, growth, and motility. Neurotensin has inhibitory and excitatory effects on peristaltic activity and produces contractile and relaxant responses in intestinal smooth muscle. Our objective in this study is to investigate the effects of neurotensin in small intestinal interstitial cells of Cajal (ICC) and elucidate the mechanism. To determine the electrophysiological effects of neurotensin on ICC, whole-cell patch clamp recordings were performed in cultured ICC from the small intestine. Exposure to neurotensin depolarized the membrane of pacemaker cells and produced tonic inward pacemaker currents. Only neurotensin receptor1 was identified when RT-PCR and immunocytochemistry were performed with mRNA isolated from small intestinal ICC and c-Kit positive cells. Neurotensin-induced tonic inward pacemaker currents were blocked by external Na+-free solution and in the presence of flufenamic acid, an inhibitor of non-selective cation channels. Furthermore, neurotensin-induced action is blocked either by treatment with U73122, a phospholipase C inhibitor, or thapsigargin, a Ca²+-ATPase inhibitor in ICC. We found that neurotensin increased spontaneous intracellular Ca²+ oscillations as seen with fluo4/AM recording. These results suggest that neurotensin modulates pacemaker currents via the activation of non-selective cation channels by intracellular Ca²+-release through neurotensin receptor1.</abstract><cop>Springer</cop><pub>Korean Society for Molecular and Cellular Biology</pub><pmid>22441675</pmid><doi>10.1007/s10059-012-2290-5</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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recordid | cdi_nrf_kci_oai_kci_go_kr_ARTI_71790 |
source | Elsevier ScienceDirect Journals; PubMed Central |
subjects | Animals Biochemistry Biomedical and Life Sciences Biomedicine Biotechnology Calcium - metabolism Calcium-Transporting ATPases - antagonists & inhibitors Calcium-Transporting ATPases - metabolism Cell Biology Cells, Cultured Endoplasmic Reticulum - metabolism Female GASTROINTESTINAL MOTILITY In Vitro Techniques interstitial cells of Cajal Interstitial Cells of Cajal - drug effects Interstitial Cells of Cajal - metabolism Intestine, Small - cytology Intestine, Small - drug effects Intestine, Small - metabolism Ion Channels - metabolism Life Sciences Male Membrane Potentials - physiology Mice Mice, Inbred BALB C MOTRICITE GASTRO-INTESTINALE MOVILIDAD GASTROINTESTINAL Muscle, Smooth - metabolism neurotensin Neurotensin - metabolism Neurotensin - pharmacology neurotensin receptor1 Receptors, Neurotensin - metabolism Sodium - metabolism Type C Phospholipases - antagonists & inhibitors Type C Phospholipases - metabolism 생물학 |
title | Neurotensin Modulates Pacemaker Activity in Interstitial Cells of Cajal from the Mouse Small Intestine |
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