Insulin Reduces Contraction and Intracellular Calcium Concentration in Vascular Smooth Muscle
Resistance to insulin-induced glucose disposal is associated with hypertension, in accord with recent reports that insulin-induced vasodilation is impaired in men with resistance to insulin-induced glucose disposal. Nevertheless, the mechanism of insulin-induced vasodilation is not known. We wished...
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Veröffentlicht in: | Hypertension (Dallas, Tex. 1979) Tex. 1979), 1993-11, Vol.22 (5), p.735-742 |
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creator | Kahn, Andrew M Seidel, Charles L Allen, Julius C OʼNeil, Roger G Shelat, Harnath Song, Tom |
description | Resistance to insulin-induced glucose disposal is associated with hypertension, in accord with recent reports that insulin-induced vasodilation is impaired in men with resistance to insulin-induced glucose disposal. Nevertheless, the mechanism of insulin-induced vasodilation is not known. We wished to determine whether a physiological concentration of insulin inhibits agonist-induced contraction at the level of the individual vascular smooth muscle cell, and if so, how. Dispersed vascular smooth muscle cells from dog femoral artery were grown on collagen gels for 4 to 8 days. Contraction and intracellular Ca concentration of individual cells were measured by photomicroscopy and fura 2 epifluorescence microscopy, respectively. Serotonin and angiotensin II contracted cells in a dose-dependent manner. Preincubation of cells for 20 minutes (short-term) or 7 days (long-term) with insulin (40 μU/mL) inhibited serotonin- and angiotensin II–induced contractions by approximately 50%. Insulin (10 μU/mL) acutely inhibited serotonin-induced contraction by 34%. The maximal effect of high extracellular K–induced contraction was not affected by short-term insulin exposure, but the ED50 for extracellular K–induced contraction was increased from 7.6±2.5 to 16.0±3.9 mmol/L (P |
doi_str_mv | 10.1161/01.HYP.22.5.735 |
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Nevertheless, the mechanism of insulin-induced vasodilation is not known. We wished to determine whether a physiological concentration of insulin inhibits agonist-induced contraction at the level of the individual vascular smooth muscle cell, and if so, how. Dispersed vascular smooth muscle cells from dog femoral artery were grown on collagen gels for 4 to 8 days. Contraction and intracellular Ca concentration of individual cells were measured by photomicroscopy and fura 2 epifluorescence microscopy, respectively. Serotonin and angiotensin II contracted cells in a dose-dependent manner. Preincubation of cells for 20 minutes (short-term) or 7 days (long-term) with insulin (40 μU/mL) inhibited serotonin- and angiotensin II–induced contractions by approximately 50%. Insulin (10 μU/mL) acutely inhibited serotonin-induced contraction by 34%. The maximal effect of high extracellular K–induced contraction was not affected by short-term insulin exposure, but the ED50 for extracellular K–induced contraction was increased from 7.6±2.5 to 16.0±3.9 mmol/L (P <.05). Short-term insulin exposure also attenuated the peak rise of the serotonin-induced intracellular Ca transient and increased the rate constant for intracellular Ca decline. Verapamil and ouabain completely blocked the attenuation of agonist-induced contraction by short-term insulin exposure, indicating the importance of voltage-operated Ca channels and the Na-K pump for this effect. We conclude that a physiological insulin concentration inhibits extracellular K– and agonist-induced contractions at the level of the vascular smooth muscle cell and attenuates the intracellular Ca transient in agonist-stimulated cells. Insulin may stimulate Na-K pump activity, which hyperpolarizes the cell, thereby decreasing Ca influx via voltage-operated channels.</description><identifier>ISSN: 0194-911X</identifier><identifier>EISSN: 1524-4563</identifier><identifier>DOI: 10.1161/01.HYP.22.5.735</identifier><identifier>PMID: 8225533</identifier><language>eng</language><publisher>United States: American Heart Association, Inc</publisher><subject>Angiotensin II - pharmacology ; Animals ; Calcium - metabolism ; Cells, Cultured ; Dogs ; Dose-Response Relationship, Drug ; Female ; Femoral Artery - drug effects ; Femoral Artery - metabolism ; Femoral Artery - physiology ; In Vitro Techniques ; Insulin - pharmacology ; Kinetics ; Male ; Muscle Contraction - drug effects ; Muscle, Smooth, Vascular - drug effects ; Muscle, Smooth, Vascular - metabolism ; Muscle, Smooth, Vascular - physiology ; Ouabain - pharmacology ; Potassium - pharmacology ; Serotonin - pharmacology ; Vasodilation - drug effects ; Verapamil - pharmacology</subject><ispartof>Hypertension (Dallas, Tex. 1979), 1993-11, Vol.22 (5), p.735-742</ispartof><rights>1993 American Heart Association, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4650-a07e2b015a152da9327e113c5302a6ed52655e778bba816bd5ff28219cfac2ed3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3687,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8225533$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kahn, Andrew M</creatorcontrib><creatorcontrib>Seidel, Charles L</creatorcontrib><creatorcontrib>Allen, Julius C</creatorcontrib><creatorcontrib>OʼNeil, Roger G</creatorcontrib><creatorcontrib>Shelat, Harnath</creatorcontrib><creatorcontrib>Song, Tom</creatorcontrib><title>Insulin Reduces Contraction and Intracellular Calcium Concentration in Vascular Smooth Muscle</title><title>Hypertension (Dallas, Tex. 1979)</title><addtitle>Hypertension</addtitle><description>Resistance to insulin-induced glucose disposal is associated with hypertension, in accord with recent reports that insulin-induced vasodilation is impaired in men with resistance to insulin-induced glucose disposal. Nevertheless, the mechanism of insulin-induced vasodilation is not known. We wished to determine whether a physiological concentration of insulin inhibits agonist-induced contraction at the level of the individual vascular smooth muscle cell, and if so, how. Dispersed vascular smooth muscle cells from dog femoral artery were grown on collagen gels for 4 to 8 days. Contraction and intracellular Ca concentration of individual cells were measured by photomicroscopy and fura 2 epifluorescence microscopy, respectively. Serotonin and angiotensin II contracted cells in a dose-dependent manner. Preincubation of cells for 20 minutes (short-term) or 7 days (long-term) with insulin (40 μU/mL) inhibited serotonin- and angiotensin II–induced contractions by approximately 50%. Insulin (10 μU/mL) acutely inhibited serotonin-induced contraction by 34%. The maximal effect of high extracellular K–induced contraction was not affected by short-term insulin exposure, but the ED50 for extracellular K–induced contraction was increased from 7.6±2.5 to 16.0±3.9 mmol/L (P <.05). Short-term insulin exposure also attenuated the peak rise of the serotonin-induced intracellular Ca transient and increased the rate constant for intracellular Ca decline. Verapamil and ouabain completely blocked the attenuation of agonist-induced contraction by short-term insulin exposure, indicating the importance of voltage-operated Ca channels and the Na-K pump for this effect. We conclude that a physiological insulin concentration inhibits extracellular K– and agonist-induced contractions at the level of the vascular smooth muscle cell and attenuates the intracellular Ca transient in agonist-stimulated cells. Insulin may stimulate Na-K pump activity, which hyperpolarizes the cell, thereby decreasing Ca influx via voltage-operated channels.</description><subject>Angiotensin II - pharmacology</subject><subject>Animals</subject><subject>Calcium - metabolism</subject><subject>Cells, Cultured</subject><subject>Dogs</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Femoral Artery - drug effects</subject><subject>Femoral Artery - metabolism</subject><subject>Femoral Artery - physiology</subject><subject>In Vitro Techniques</subject><subject>Insulin - pharmacology</subject><subject>Kinetics</subject><subject>Male</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle, Smooth, Vascular - drug effects</subject><subject>Muscle, Smooth, Vascular - metabolism</subject><subject>Muscle, Smooth, Vascular - physiology</subject><subject>Ouabain - pharmacology</subject><subject>Potassium - pharmacology</subject><subject>Serotonin - pharmacology</subject><subject>Vasodilation - drug effects</subject><subject>Verapamil - pharmacology</subject><issn>0194-911X</issn><issn>1524-4563</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kMtr3DAQxkVI2G43OedU8Ck3ezV6-HEMS9osbGlI2tAegpDlMetWthPJYsl_H-2DDgzD8P1mmPkIuQaaAeSwpJDd_3nIGMtkVnB5RuYgmUiFzPk5mVOoRFoB_P5EPnv_l1IQQhQzMisZk5LzOXlZDz7YbkgesQkGfbIah8lpM3XjkOihSdaHFq0NVrtkpa3pQr-nDO6VAxfHn7U3B-KpH8dpm3wP3li8JBetth6vTnVBfn29-7m6Tzc_vq1Xt5vUiFzSVNMCWU1B6nh8oyvOCgTgRnLKdI6NZLmUWBRlXesS8rqRbctKBpVptWHY8AW5Oe59deNbQD-pvvP7o_WAY_CqyKmQIj68IMsjaNzovcNWvbqu1-5dAVV7QxUFFQ1VjCmpoqFx4stpdah7bP7zJwejLo76brQTOv_Phh06tUVtp62iMQTLyxSqigPELo0JlH8Aj5qBfA</recordid><startdate>199311</startdate><enddate>199311</enddate><creator>Kahn, Andrew M</creator><creator>Seidel, Charles L</creator><creator>Allen, Julius C</creator><creator>OʼNeil, Roger G</creator><creator>Shelat, Harnath</creator><creator>Song, Tom</creator><general>American Heart Association, Inc</general><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>199311</creationdate><title>Insulin Reduces Contraction and Intracellular Calcium Concentration in Vascular Smooth Muscle</title><author>Kahn, Andrew M ; Seidel, Charles L ; Allen, Julius C ; OʼNeil, Roger G ; Shelat, Harnath ; Song, Tom</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4650-a07e2b015a152da9327e113c5302a6ed52655e778bba816bd5ff28219cfac2ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Angiotensin II - pharmacology</topic><topic>Animals</topic><topic>Calcium - metabolism</topic><topic>Cells, Cultured</topic><topic>Dogs</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Femoral Artery - drug effects</topic><topic>Femoral Artery - metabolism</topic><topic>Femoral Artery - physiology</topic><topic>In Vitro Techniques</topic><topic>Insulin - pharmacology</topic><topic>Kinetics</topic><topic>Male</topic><topic>Muscle Contraction - drug effects</topic><topic>Muscle, Smooth, Vascular - drug effects</topic><topic>Muscle, Smooth, Vascular - metabolism</topic><topic>Muscle, Smooth, Vascular - physiology</topic><topic>Ouabain - pharmacology</topic><topic>Potassium - pharmacology</topic><topic>Serotonin - pharmacology</topic><topic>Vasodilation - drug effects</topic><topic>Verapamil - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kahn, Andrew M</creatorcontrib><creatorcontrib>Seidel, Charles L</creatorcontrib><creatorcontrib>Allen, Julius C</creatorcontrib><creatorcontrib>OʼNeil, Roger G</creatorcontrib><creatorcontrib>Shelat, Harnath</creatorcontrib><creatorcontrib>Song, Tom</creatorcontrib><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>Hypertension (Dallas, Tex. 1979)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kahn, Andrew M</au><au>Seidel, Charles L</au><au>Allen, Julius C</au><au>OʼNeil, Roger G</au><au>Shelat, Harnath</au><au>Song, Tom</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insulin Reduces Contraction and Intracellular Calcium Concentration in Vascular Smooth Muscle</atitle><jtitle>Hypertension (Dallas, Tex. 1979)</jtitle><addtitle>Hypertension</addtitle><date>1993-11</date><risdate>1993</risdate><volume>22</volume><issue>5</issue><spage>735</spage><epage>742</epage><pages>735-742</pages><issn>0194-911X</issn><eissn>1524-4563</eissn><abstract>Resistance to insulin-induced glucose disposal is associated with hypertension, in accord with recent reports that insulin-induced vasodilation is impaired in men with resistance to insulin-induced glucose disposal. Nevertheless, the mechanism of insulin-induced vasodilation is not known. We wished to determine whether a physiological concentration of insulin inhibits agonist-induced contraction at the level of the individual vascular smooth muscle cell, and if so, how. Dispersed vascular smooth muscle cells from dog femoral artery were grown on collagen gels for 4 to 8 days. Contraction and intracellular Ca concentration of individual cells were measured by photomicroscopy and fura 2 epifluorescence microscopy, respectively. Serotonin and angiotensin II contracted cells in a dose-dependent manner. Preincubation of cells for 20 minutes (short-term) or 7 days (long-term) with insulin (40 μU/mL) inhibited serotonin- and angiotensin II–induced contractions by approximately 50%. Insulin (10 μU/mL) acutely inhibited serotonin-induced contraction by 34%. The maximal effect of high extracellular K–induced contraction was not affected by short-term insulin exposure, but the ED50 for extracellular K–induced contraction was increased from 7.6±2.5 to 16.0±3.9 mmol/L (P <.05). Short-term insulin exposure also attenuated the peak rise of the serotonin-induced intracellular Ca transient and increased the rate constant for intracellular Ca decline. Verapamil and ouabain completely blocked the attenuation of agonist-induced contraction by short-term insulin exposure, indicating the importance of voltage-operated Ca channels and the Na-K pump for this effect. We conclude that a physiological insulin concentration inhibits extracellular K– and agonist-induced contractions at the level of the vascular smooth muscle cell and attenuates the intracellular Ca transient in agonist-stimulated cells. Insulin may stimulate Na-K pump activity, which hyperpolarizes the cell, thereby decreasing Ca influx via voltage-operated channels.</abstract><cop>United States</cop><pub>American Heart Association, Inc</pub><pmid>8225533</pmid><doi>10.1161/01.HYP.22.5.735</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Angiotensin II - pharmacology Animals Calcium - metabolism Cells, Cultured Dogs Dose-Response Relationship, Drug Female Femoral Artery - drug effects Femoral Artery - metabolism Femoral Artery - physiology In Vitro Techniques Insulin - pharmacology Kinetics Male Muscle Contraction - drug effects Muscle, Smooth, Vascular - drug effects Muscle, Smooth, Vascular - metabolism Muscle, Smooth, Vascular - physiology Ouabain - pharmacology Potassium - pharmacology Serotonin - pharmacology Vasodilation - drug effects Verapamil - pharmacology |
title | Insulin Reduces Contraction and Intracellular Calcium Concentration in Vascular Smooth Muscle |
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