Insulin Knockout Mice Have Extended Survival but Volatile Blood Glucose Levels on Leptin Therapy
Leptin can reverse hyperglycemia in rodent models of type 1 diabetes. However, these models have used chemical or immune mediated β-cell destruction where insulin depletion is incomplete. Thus it is unknown which actions of leptin are entirely insulin independent, versus those which require insulin....
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Veröffentlicht in: | Endocrinology (Philadelphia) 2016-03, Vol.157 (3), p.1007-1012 |
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description | Leptin can reverse hyperglycemia in rodent models of type 1 diabetes. However, these models have used chemical or immune mediated β-cell destruction where insulin depletion is incomplete. Thus it is unknown which actions of leptin are entirely insulin independent, versus those which require insulin. To directly assess this we maximized blockage of insulin action using an insulin receptor antagonist in combination with streptozotocin-diabetic mice; leptin treatment was still able to reduce blood glucose. Next, we leptin-treated adult insulin knockout (InsKO) mice. Remarkably, leptin-treated InsKO mice were viable for up to 3 weeks without insulin therapy. Leptin treatment reduced plasma corticosterone, glucagon, β-hydroxybutyrate, triglycerides, cholesterol, fatty acids and glycerol. However, leptin-treated InsKO mice exhibited overt fed hyperglycemia and severe fasting hypoglycemia. Therefore, leptin can normalize many metabolic parameters in the complete absence of insulin, but blood glucose levels are volatile and the length of survival finite. |
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However, these models have used chemical or immune mediated β-cell destruction where insulin depletion is incomplete. Thus it is unknown which actions of leptin are entirely insulin independent, versus those which require insulin. To directly assess this we maximized blockage of insulin action using an insulin receptor antagonist in combination with streptozotocin-diabetic mice; leptin treatment was still able to reduce blood glucose. Next, we leptin-treated adult insulin knockout (InsKO) mice. Remarkably, leptin-treated InsKO mice were viable for up to 3 weeks without insulin therapy. Leptin treatment reduced plasma corticosterone, glucagon, β-hydroxybutyrate, triglycerides, cholesterol, fatty acids and glycerol. However, leptin-treated InsKO mice exhibited overt fed hyperglycemia and severe fasting hypoglycemia. Therefore, leptin can normalize many metabolic parameters in the complete absence of insulin, but blood glucose levels are volatile and the length of survival finite.</description><identifier>ISSN: 0013-7227</identifier><identifier>EISSN: 1945-7170</identifier><identifier>DOI: 10.1210/en.2015-1890</identifier><identifier>PMID: 26696124</identifier><language>eng</language><publisher>United States: Endocrine Society</publisher><subject>3-Hydroxybutyric Acid - blood ; Animal models ; Animals ; Beta cells ; Blood ; Blood glucose ; Blood Glucose - drug effects ; Blood Glucose - metabolism ; Blood levels ; Cell culture ; Cholesterol ; Cholesterol - blood ; Corticosterone ; Corticosterone - blood ; Diabetes mellitus (insulin dependent) ; Diabetes Mellitus, Experimental - metabolism ; Diabetes Mellitus, Type 1 - metabolism ; Fatty Acids - blood ; Glucagon ; Glucagon - blood ; Glucagon - drug effects ; Glucose ; Glycerol - blood ; Hyperglycemia ; Hypoglycemia ; Insulin ; Insulin - genetics ; Leptin ; Leptin - pharmacology ; Mice ; Mice, Knockout ; Peptides - pharmacology ; Receptor, Insulin - antagonists & inhibitors ; Streptozocin ; Survival ; Triglycerides ; Triglycerides - blood</subject><ispartof>Endocrinology (Philadelphia), 2016-03, Vol.157 (3), p.1007-1012</ispartof><rights>Copyright © 2016 by the Endocrine Society</rights><rights>Copyright © 2016 by the Endocrine Society 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c532t-642e96a46d07a3a72a80ee999d7b87834108aeaa25f2a30164a3e1db9931a3b83</citedby><cites>FETCH-LOGICAL-c532t-642e96a46d07a3a72a80ee999d7b87834108aeaa25f2a30164a3e1db9931a3b83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26696124$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Neumann, Ursula H</creatorcontrib><creatorcontrib>Denroche, Heather C</creatorcontrib><creatorcontrib>Mojibian, Majid</creatorcontrib><creatorcontrib>Covey, Scott D</creatorcontrib><creatorcontrib>Kieffer, Timothy J</creatorcontrib><title>Insulin Knockout Mice Have Extended Survival but Volatile Blood Glucose Levels on Leptin Therapy</title><title>Endocrinology (Philadelphia)</title><addtitle>Endocrinology</addtitle><description>Leptin can reverse hyperglycemia in rodent models of type 1 diabetes. However, these models have used chemical or immune mediated β-cell destruction where insulin depletion is incomplete. Thus it is unknown which actions of leptin are entirely insulin independent, versus those which require insulin. To directly assess this we maximized blockage of insulin action using an insulin receptor antagonist in combination with streptozotocin-diabetic mice; leptin treatment was still able to reduce blood glucose. Next, we leptin-treated adult insulin knockout (InsKO) mice. Remarkably, leptin-treated InsKO mice were viable for up to 3 weeks without insulin therapy. Leptin treatment reduced plasma corticosterone, glucagon, β-hydroxybutyrate, triglycerides, cholesterol, fatty acids and glycerol. However, leptin-treated InsKO mice exhibited overt fed hyperglycemia and severe fasting hypoglycemia. Therefore, leptin can normalize many metabolic parameters in the complete absence of insulin, but blood glucose levels are volatile and the length of survival finite.</description><subject>3-Hydroxybutyric Acid - blood</subject><subject>Animal models</subject><subject>Animals</subject><subject>Beta cells</subject><subject>Blood</subject><subject>Blood glucose</subject><subject>Blood Glucose - drug effects</subject><subject>Blood Glucose - metabolism</subject><subject>Blood levels</subject><subject>Cell culture</subject><subject>Cholesterol</subject><subject>Cholesterol - blood</subject><subject>Corticosterone</subject><subject>Corticosterone - blood</subject><subject>Diabetes mellitus (insulin dependent)</subject><subject>Diabetes Mellitus, Experimental - metabolism</subject><subject>Diabetes Mellitus, Type 1 - metabolism</subject><subject>Fatty Acids - blood</subject><subject>Glucagon</subject><subject>Glucagon - blood</subject><subject>Glucagon - drug effects</subject><subject>Glucose</subject><subject>Glycerol - blood</subject><subject>Hyperglycemia</subject><subject>Hypoglycemia</subject><subject>Insulin</subject><subject>Insulin - genetics</subject><subject>Leptin</subject><subject>Leptin - pharmacology</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Peptides - pharmacology</subject><subject>Receptor, Insulin - antagonists & inhibitors</subject><subject>Streptozocin</subject><subject>Survival</subject><subject>Triglycerides</subject><subject>Triglycerides - blood</subject><issn>0013-7227</issn><issn>1945-7170</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9vFCEYhonR2G315tmQeKgHp_IBA8PRNv0V13iweh2ZmW_jVBZGGDb2v5fNrpqYNp74yPfkyQsvIS-AnQAH9hb9CWdQV9AY9ogswMi60qDZY7JgDESlOdcH5DCl23KVUoqn5IArZRRwuSBfr33KbvT0vQ_995Bn-mHskV7ZDdLznzP6AQf6KcfNuLGOdmX_JTg7jw7pqQthoJcu9yEhXeIGXaLBl2mai_DmG0Y73T0jT1bWJXy-P4_I54vzm7Oravnx8vrs3bLqa8HnSkmORlmpBqatsJrbhiEaYwbdNboRElhj0Vper7gVDJS0AmHojBFgRdeII_J6551i-JExze16TD06Zz2GnNryPdAoLgD-j2rV1LVWkhX01T_obcjRl4e0AgTTAJzpQr3ZUX0MKUVctVMc1zbetcDabUkt-nZb0jbFVvpyL83dGoc_8O9WCnC8A0KeHlJVe5XYkaWo0MfR4xQxpb8p7w3wC8C6p6w</recordid><startdate>20160301</startdate><enddate>20160301</enddate><creator>Neumann, Ursula H</creator><creator>Denroche, Heather C</creator><creator>Mojibian, Majid</creator><creator>Covey, Scott D</creator><creator>Kieffer, Timothy J</creator><general>Endocrine Society</general><general>Oxford University Press</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>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20160301</creationdate><title>Insulin Knockout Mice Have Extended Survival but Volatile Blood Glucose Levels on Leptin Therapy</title><author>Neumann, Ursula H ; Denroche, Heather C ; Mojibian, Majid ; Covey, Scott D ; Kieffer, Timothy J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c532t-642e96a46d07a3a72a80ee999d7b87834108aeaa25f2a30164a3e1db9931a3b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>3-Hydroxybutyric Acid - blood</topic><topic>Animal models</topic><topic>Animals</topic><topic>Beta cells</topic><topic>Blood</topic><topic>Blood glucose</topic><topic>Blood Glucose - drug effects</topic><topic>Blood Glucose - metabolism</topic><topic>Blood levels</topic><topic>Cell culture</topic><topic>Cholesterol</topic><topic>Cholesterol - blood</topic><topic>Corticosterone</topic><topic>Corticosterone - blood</topic><topic>Diabetes mellitus (insulin dependent)</topic><topic>Diabetes Mellitus, Experimental - metabolism</topic><topic>Diabetes Mellitus, Type 1 - metabolism</topic><topic>Fatty Acids - blood</topic><topic>Glucagon</topic><topic>Glucagon - blood</topic><topic>Glucagon - drug effects</topic><topic>Glucose</topic><topic>Glycerol - blood</topic><topic>Hyperglycemia</topic><topic>Hypoglycemia</topic><topic>Insulin</topic><topic>Insulin - genetics</topic><topic>Leptin</topic><topic>Leptin - pharmacology</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Peptides - pharmacology</topic><topic>Receptor, Insulin - antagonists & inhibitors</topic><topic>Streptozocin</topic><topic>Survival</topic><topic>Triglycerides</topic><topic>Triglycerides - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Neumann, Ursula H</creatorcontrib><creatorcontrib>Denroche, Heather C</creatorcontrib><creatorcontrib>Mojibian, Majid</creatorcontrib><creatorcontrib>Covey, Scott D</creatorcontrib><creatorcontrib>Kieffer, Timothy J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Endocrinology (Philadelphia)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Neumann, Ursula H</au><au>Denroche, Heather C</au><au>Mojibian, Majid</au><au>Covey, Scott D</au><au>Kieffer, Timothy J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insulin Knockout Mice Have Extended Survival but Volatile Blood Glucose Levels on Leptin Therapy</atitle><jtitle>Endocrinology (Philadelphia)</jtitle><addtitle>Endocrinology</addtitle><date>2016-03-01</date><risdate>2016</risdate><volume>157</volume><issue>3</issue><spage>1007</spage><epage>1012</epage><pages>1007-1012</pages><issn>0013-7227</issn><eissn>1945-7170</eissn><abstract>Leptin can reverse hyperglycemia in rodent models of type 1 diabetes. However, these models have used chemical or immune mediated β-cell destruction where insulin depletion is incomplete. Thus it is unknown which actions of leptin are entirely insulin independent, versus those which require insulin. To directly assess this we maximized blockage of insulin action using an insulin receptor antagonist in combination with streptozotocin-diabetic mice; leptin treatment was still able to reduce blood glucose. Next, we leptin-treated adult insulin knockout (InsKO) mice. Remarkably, leptin-treated InsKO mice were viable for up to 3 weeks without insulin therapy. Leptin treatment reduced plasma corticosterone, glucagon, β-hydroxybutyrate, triglycerides, cholesterol, fatty acids and glycerol. However, leptin-treated InsKO mice exhibited overt fed hyperglycemia and severe fasting hypoglycemia. Therefore, leptin can normalize many metabolic parameters in the complete absence of insulin, but blood glucose levels are volatile and the length of survival finite.</abstract><cop>United States</cop><pub>Endocrine Society</pub><pmid>26696124</pmid><doi>10.1210/en.2015-1890</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3-Hydroxybutyric Acid - blood Animal models Animals Beta cells Blood Blood glucose Blood Glucose - drug effects Blood Glucose - metabolism Blood levels Cell culture Cholesterol Cholesterol - blood Corticosterone Corticosterone - blood Diabetes mellitus (insulin dependent) Diabetes Mellitus, Experimental - metabolism Diabetes Mellitus, Type 1 - metabolism Fatty Acids - blood Glucagon Glucagon - blood Glucagon - drug effects Glucose Glycerol - blood Hyperglycemia Hypoglycemia Insulin Insulin - genetics Leptin Leptin - pharmacology Mice Mice, Knockout Peptides - pharmacology Receptor, Insulin - antagonists & inhibitors Streptozocin Survival Triglycerides Triglycerides - blood |
title | Insulin Knockout Mice Have Extended Survival but Volatile Blood Glucose Levels on Leptin Therapy |
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