Correlated oscillations in glucose consumption, oxygen consumption, and intracellular free Ca(2+) in single islets of Langerhans
Micron-sized sensors were used to monitor glucose and oxygen levels in the extracellular space of single islets of Langerhans in real-time. At 10 mM glucose, oscillations in intraislet glucose concentration were readily detected. Changes in glucose level correspond to changes in glucose consumption...
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Veröffentlicht in: | The Journal of biological chemistry 2000-03, Vol.275 (9), p.6642-6650 |
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description | Micron-sized sensors were used to monitor glucose and oxygen levels in the extracellular space of single islets of Langerhans in real-time. At 10 mM glucose, oscillations in intraislet glucose concentration were readily detected. Changes in glucose level correspond to changes in glucose consumption by glycolysis balanced by mass transport into the islet. Oscillations had a period of 3.1 +/- 0.2 min and amplitude of 0.8 +/- 0.1 mM glucose (n = 21). Superimposed on these oscillations were faster fluctuations in glucose level during the periods of low glucose consumption. Oxygen level oscillations that were out of phase with the glucose oscillations were also detected. Oscillations in both oxygen and glucose consumption were strongly dependent upon extracellular Ca(2+) and sensitive to nifedipine. Simultaneous measurements of glucose with intracellular Ca(2+) ([Ca(2+)](i)) revealed that decreases in [Ca(2+)](i) preceded increases in glucose consumption by 7.4 +/- 2.1 s during an oscillation (n = 9). Conversely, increases in [Ca(2+)](i) preceded increases in oxygen consumption by 1.5 +/- 0.2 s (n = 4). These results suggest that during oscillations, bursts of glycolysis begin after Ca(2+) has stopped entering the cell. Glycolysis stimulates further Ca(2+) entry, which in turn stimulates increases in respiration. The data during oscillation are in contrast to the time course of events during initial exposure to glucose. Under these conditions, a burst of oxygen consumption precedes the initial rise in [Ca(2+)](i). A model to explain these results is described. |
doi_str_mv | 10.1074/jbc.275.9.6642 |
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At 10 mM glucose, oscillations in intraislet glucose concentration were readily detected. Changes in glucose level correspond to changes in glucose consumption by glycolysis balanced by mass transport into the islet. Oscillations had a period of 3.1 +/- 0.2 min and amplitude of 0.8 +/- 0.1 mM glucose (n = 21). Superimposed on these oscillations were faster fluctuations in glucose level during the periods of low glucose consumption. Oxygen level oscillations that were out of phase with the glucose oscillations were also detected. Oscillations in both oxygen and glucose consumption were strongly dependent upon extracellular Ca(2+) and sensitive to nifedipine. Simultaneous measurements of glucose with intracellular Ca(2+) ([Ca(2+)](i)) revealed that decreases in [Ca(2+)](i) preceded increases in glucose consumption by 7.4 +/- 2.1 s during an oscillation (n = 9). Conversely, increases in [Ca(2+)](i) preceded increases in oxygen consumption by 1.5 +/- 0.2 s (n = 4). These results suggest that during oscillations, bursts of glycolysis begin after Ca(2+) has stopped entering the cell. Glycolysis stimulates further Ca(2+) entry, which in turn stimulates increases in respiration. The data during oscillation are in contrast to the time course of events during initial exposure to glucose. Under these conditions, a burst of oxygen consumption precedes the initial rise in [Ca(2+)](i). A model to explain these results is described.</description><identifier>ISSN: 0021-9258</identifier><identifier>DOI: 10.1074/jbc.275.9.6642</identifier><identifier>PMID: 10692473</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Biosensing Techniques ; Calcium - metabolism ; Cell Respiration ; Glucose - metabolism ; Glycolysis ; Islets of Langerhans - metabolism ; Mice ; Microelectrodes ; Models, Biological ; Nifedipine - pharmacology ; Oxygen Consumption</subject><ispartof>The Journal of biological chemistry, 2000-03, Vol.275 (9), p.6642-6650</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10692473$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jung, S K</creatorcontrib><creatorcontrib>Kauri, L M</creatorcontrib><creatorcontrib>Qian, W J</creatorcontrib><creatorcontrib>Kennedy, R T</creatorcontrib><title>Correlated oscillations in glucose consumption, oxygen consumption, and intracellular free Ca(2+) in single islets of Langerhans</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Micron-sized sensors were used to monitor glucose and oxygen levels in the extracellular space of single islets of Langerhans in real-time. At 10 mM glucose, oscillations in intraislet glucose concentration were readily detected. Changes in glucose level correspond to changes in glucose consumption by glycolysis balanced by mass transport into the islet. Oscillations had a period of 3.1 +/- 0.2 min and amplitude of 0.8 +/- 0.1 mM glucose (n = 21). Superimposed on these oscillations were faster fluctuations in glucose level during the periods of low glucose consumption. Oxygen level oscillations that were out of phase with the glucose oscillations were also detected. Oscillations in both oxygen and glucose consumption were strongly dependent upon extracellular Ca(2+) and sensitive to nifedipine. Simultaneous measurements of glucose with intracellular Ca(2+) ([Ca(2+)](i)) revealed that decreases in [Ca(2+)](i) preceded increases in glucose consumption by 7.4 +/- 2.1 s during an oscillation (n = 9). Conversely, increases in [Ca(2+)](i) preceded increases in oxygen consumption by 1.5 +/- 0.2 s (n = 4). These results suggest that during oscillations, bursts of glycolysis begin after Ca(2+) has stopped entering the cell. Glycolysis stimulates further Ca(2+) entry, which in turn stimulates increases in respiration. The data during oscillation are in contrast to the time course of events during initial exposure to glucose. Under these conditions, a burst of oxygen consumption precedes the initial rise in [Ca(2+)](i). A model to explain these results is described.</description><subject>Animals</subject><subject>Biosensing Techniques</subject><subject>Calcium - metabolism</subject><subject>Cell Respiration</subject><subject>Glucose - metabolism</subject><subject>Glycolysis</subject><subject>Islets of Langerhans - metabolism</subject><subject>Mice</subject><subject>Microelectrodes</subject><subject>Models, Biological</subject><subject>Nifedipine - pharmacology</subject><subject>Oxygen Consumption</subject><issn>0021-9258</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkEtLxDAUhbNQnHF061KyEkVbm0eTZinFFwy40XVJ86gd0mRMWnB2_nQ7qAvv5p57-DgcLgBnqMhRwentplU55mUucsYoPgDLosAoE7isFuA4pU0xDxXoCCxQwQSmnCzBVx1iNE6ORsOQVO9m2QefYO9h5yYVkoFqvqdhu_dvYPjcdcb_96TXMz9GqYxzk5MR2mgMrOUlvr7aJ6Xed87APjkzJhgsXEvfmfgufToBh1a6ZE5_9wq8Pdy_1k_Z-uXxub5bZ1uE8Zi1VGBd8VZIqStKsGGkZRxxRlClKquQoqW1UjPNDWWEkLJVSkppS6I1tpaswMVP7jaGj8mksRn6tO8rvQlTanghSMEFn8HzX3BqB6ObbewHGXfN38_IN0v6bzk</recordid><startdate>20000303</startdate><enddate>20000303</enddate><creator>Jung, S K</creator><creator>Kauri, L M</creator><creator>Qian, W J</creator><creator>Kennedy, R T</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20000303</creationdate><title>Correlated oscillations in glucose consumption, oxygen consumption, and intracellular free Ca(2+) in single islets of Langerhans</title><author>Jung, S K ; Kauri, L M ; Qian, W J ; Kennedy, R T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p122t-b492d87b9aad8432e63b67176318c8fc1c45ffad6d7e463335bccaaaf53dd2ff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animals</topic><topic>Biosensing Techniques</topic><topic>Calcium - metabolism</topic><topic>Cell Respiration</topic><topic>Glucose - metabolism</topic><topic>Glycolysis</topic><topic>Islets of Langerhans - metabolism</topic><topic>Mice</topic><topic>Microelectrodes</topic><topic>Models, Biological</topic><topic>Nifedipine - pharmacology</topic><topic>Oxygen Consumption</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jung, S K</creatorcontrib><creatorcontrib>Kauri, L M</creatorcontrib><creatorcontrib>Qian, W J</creatorcontrib><creatorcontrib>Kennedy, R T</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jung, S K</au><au>Kauri, L M</au><au>Qian, W J</au><au>Kennedy, R T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Correlated oscillations in glucose consumption, oxygen consumption, and intracellular free Ca(2+) in single islets of Langerhans</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2000-03-03</date><risdate>2000</risdate><volume>275</volume><issue>9</issue><spage>6642</spage><epage>6650</epage><pages>6642-6650</pages><issn>0021-9258</issn><abstract>Micron-sized sensors were used to monitor glucose and oxygen levels in the extracellular space of single islets of Langerhans in real-time. At 10 mM glucose, oscillations in intraislet glucose concentration were readily detected. Changes in glucose level correspond to changes in glucose consumption by glycolysis balanced by mass transport into the islet. Oscillations had a period of 3.1 +/- 0.2 min and amplitude of 0.8 +/- 0.1 mM glucose (n = 21). Superimposed on these oscillations were faster fluctuations in glucose level during the periods of low glucose consumption. Oxygen level oscillations that were out of phase with the glucose oscillations were also detected. Oscillations in both oxygen and glucose consumption were strongly dependent upon extracellular Ca(2+) and sensitive to nifedipine. Simultaneous measurements of glucose with intracellular Ca(2+) ([Ca(2+)](i)) revealed that decreases in [Ca(2+)](i) preceded increases in glucose consumption by 7.4 +/- 2.1 s during an oscillation (n = 9). Conversely, increases in [Ca(2+)](i) preceded increases in oxygen consumption by 1.5 +/- 0.2 s (n = 4). These results suggest that during oscillations, bursts of glycolysis begin after Ca(2+) has stopped entering the cell. Glycolysis stimulates further Ca(2+) entry, which in turn stimulates increases in respiration. The data during oscillation are in contrast to the time course of events during initial exposure to glucose. Under these conditions, a burst of oxygen consumption precedes the initial rise in [Ca(2+)](i). A model to explain these results is described.</abstract><cop>United States</cop><pmid>10692473</pmid><doi>10.1074/jbc.275.9.6642</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Biosensing Techniques Calcium - metabolism Cell Respiration Glucose - metabolism Glycolysis Islets of Langerhans - metabolism Mice Microelectrodes Models, Biological Nifedipine - pharmacology Oxygen Consumption |
title | Correlated oscillations in glucose consumption, oxygen consumption, and intracellular free Ca(2+) in single islets of Langerhans |
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