118-OR: Activation of Dopamine Signaling in the Brain Causes HAAF
Hypoglycemia-associated autonomic failure (HAAF) is comprised of both a blunted counterregulatory response to hypoglycemia and hypoglycemia unawareness. We previously demonstrated that both these aspects of HAAF can be reversed by treatment with the dopamine receptor antagonist, metoclopramide. Thes...
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Veröffentlicht in: | Diabetes (New York, N.Y.) N.Y.), 2019-06, Vol.68 (Supplement_1) |
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creator | DE ABREU, ADRIANA VIEIRA AGRAWAL, RAHUL MEIER, ETHAN R. CHAN, OWEN FISHER, SIMON |
description | Hypoglycemia-associated autonomic failure (HAAF) is comprised of both a blunted counterregulatory response to hypoglycemia and hypoglycemia unawareness. We previously demonstrated that both these aspects of HAAF can be reversed by treatment with the dopamine receptor antagonist, metoclopramide. These findings suggest that repetitive activation of the dopaminergic system may contribute to HAAF. We now evaluate whether both the blunted counterregulatory response to hypoglycemia and hypoglycemia unawareness are mediated by repeated activation of brain dopaminergic receptors. To test this hypothesis, male Sprague-Dawley rats were randomized to receive either the dopamine receptor agonist, bromocriptine, (Bromo; 20 µg/d) intracerebroventricularly (ICV) for 3 consecutive days or recurrent ICV saline (controls). On the fourth day, all rats underwent either, 1) a hyperinsulinemic (50 mU/kg/min) hypoglycemic (∼50 mg/dl) clamp to assess counterregulation, or 2) had food consumption measured in response to insulin-induced (15 U/kg; SQ) hypoglycemia (∼40 mg/dl) to assess hypoglycemia awareness. In response to hypoglycemia, antecedent Bromo blunted, 1) the epinephrine response by 86%* (see Fig), 2) the glucagon response by 56%§, and 3) hypoglycemia awareness by 37%§, as compared to controls (*p |
doi_str_mv | 10.2337/db19-118-OR |
format | Article |
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We previously demonstrated that both these aspects of HAAF can be reversed by treatment with the dopamine receptor antagonist, metoclopramide. These findings suggest that repetitive activation of the dopaminergic system may contribute to HAAF. We now evaluate whether both the blunted counterregulatory response to hypoglycemia and hypoglycemia unawareness are mediated by repeated activation of brain dopaminergic receptors. To test this hypothesis, male Sprague-Dawley rats were randomized to receive either the dopamine receptor agonist, bromocriptine, (Bromo; 20 µg/d) intracerebroventricularly (ICV) for 3 consecutive days or recurrent ICV saline (controls). On the fourth day, all rats underwent either, 1) a hyperinsulinemic (50 mU/kg/min) hypoglycemic (∼50 mg/dl) clamp to assess counterregulation, or 2) had food consumption measured in response to insulin-induced (15 U/kg; SQ) hypoglycemia (∼40 mg/dl) to assess hypoglycemia awareness. In response to hypoglycemia, antecedent Bromo blunted, 1) the epinephrine response by 86%* (see Fig), 2) the glucagon response by 56%§, and 3) hypoglycemia awareness by 37%§, as compared to controls (*p<0.01, §p<0.05). These findings demonstrate that dopaminergic signaling in the central nervous system contributes to the development of HAAF.</description><identifier>ISSN: 0012-1797</identifier><identifier>EISSN: 1939-327X</identifier><identifier>DOI: 10.2337/db19-118-OR</identifier><language>eng</language><publisher>New York: American Diabetes Association</publisher><subject>Bromocriptine ; Central nervous system ; Dopamine ; Dopamine receptors ; Epinephrine ; Food consumption ; Glucagon ; Glucose ; Hypoglycemia ; Insulin ; Metoclopramide ; Rodents</subject><ispartof>Diabetes (New York, N.Y.), 2019-06, Vol.68 (Supplement_1)</ispartof><rights>Copyright American Diabetes Association Jun 1, 2019</rights><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>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>DE ABREU, ADRIANA VIEIRA</creatorcontrib><creatorcontrib>AGRAWAL, RAHUL</creatorcontrib><creatorcontrib>MEIER, ETHAN R.</creatorcontrib><creatorcontrib>CHAN, OWEN</creatorcontrib><creatorcontrib>FISHER, SIMON</creatorcontrib><title>118-OR: Activation of Dopamine Signaling in the Brain Causes HAAF</title><title>Diabetes (New York, N.Y.)</title><description>Hypoglycemia-associated autonomic failure (HAAF) is comprised of both a blunted counterregulatory response to hypoglycemia and hypoglycemia unawareness. We previously demonstrated that both these aspects of HAAF can be reversed by treatment with the dopamine receptor antagonist, metoclopramide. These findings suggest that repetitive activation of the dopaminergic system may contribute to HAAF. We now evaluate whether both the blunted counterregulatory response to hypoglycemia and hypoglycemia unawareness are mediated by repeated activation of brain dopaminergic receptors. To test this hypothesis, male Sprague-Dawley rats were randomized to receive either the dopamine receptor agonist, bromocriptine, (Bromo; 20 µg/d) intracerebroventricularly (ICV) for 3 consecutive days or recurrent ICV saline (controls). On the fourth day, all rats underwent either, 1) a hyperinsulinemic (50 mU/kg/min) hypoglycemic (∼50 mg/dl) clamp to assess counterregulation, or 2) had food consumption measured in response to insulin-induced (15 U/kg; SQ) hypoglycemia (∼40 mg/dl) to assess hypoglycemia awareness. In response to hypoglycemia, antecedent Bromo blunted, 1) the epinephrine response by 86%* (see Fig), 2) the glucagon response by 56%§, and 3) hypoglycemia awareness by 37%§, as compared to controls (*p<0.01, §p<0.05). These findings demonstrate that dopaminergic signaling in the central nervous system contributes to the development of HAAF.</description><subject>Bromocriptine</subject><subject>Central nervous system</subject><subject>Dopamine</subject><subject>Dopamine receptors</subject><subject>Epinephrine</subject><subject>Food consumption</subject><subject>Glucagon</subject><subject>Glucose</subject><subject>Hypoglycemia</subject><subject>Insulin</subject><subject>Metoclopramide</subject><subject>Rodents</subject><issn>0012-1797</issn><issn>1939-327X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNotkEFLxDAUhIMoWFdP_oGAR4m-JG3aeKvVdYWFwroHbyFtkzXLbluTVvDf26XyDvMOH8PMIHRL4YFxnj42FZWE0oyUmzMUUckl4Sz9PEcRAGWEpjK9RFch7AFATBehfKafcF4P7kcPrmtxZ_FL1-ujaw3-cLtWH1y7w67Fw5fBz15PX6HHYAJe5fnyGl1YfQjm5l8XaLt83RYrsi7f3ot8TWoRJ6SRQkMsACzQStQWuDWQxBWLgYHIUpsZXSeGMcoTY3SlqWFV3dhKQyLBCr5Ad7Nt77vv0YRB7bvRT9mCYizOJhuZJRN1P1O170Lwxqreu6P2v4qCOk2kThOpqbQqN_wPC_1Wxw</recordid><startdate>20190601</startdate><enddate>20190601</enddate><creator>DE ABREU, ADRIANA VIEIRA</creator><creator>AGRAWAL, RAHUL</creator><creator>MEIER, ETHAN R.</creator><creator>CHAN, OWEN</creator><creator>FISHER, SIMON</creator><general>American Diabetes Association</general><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>NAPCQ</scope></search><sort><creationdate>20190601</creationdate><title>118-OR: Activation of Dopamine Signaling in the Brain Causes HAAF</title><author>DE ABREU, ADRIANA VIEIRA ; AGRAWAL, RAHUL ; MEIER, ETHAN R. ; CHAN, OWEN ; FISHER, SIMON</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c645-d96a04600f01b6cf03fe054b24020687f8eac5e22135eeaba1e2bcdfba0590f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Bromocriptine</topic><topic>Central nervous system</topic><topic>Dopamine</topic><topic>Dopamine receptors</topic><topic>Epinephrine</topic><topic>Food consumption</topic><topic>Glucagon</topic><topic>Glucose</topic><topic>Hypoglycemia</topic><topic>Insulin</topic><topic>Metoclopramide</topic><topic>Rodents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DE ABREU, ADRIANA VIEIRA</creatorcontrib><creatorcontrib>AGRAWAL, RAHUL</creatorcontrib><creatorcontrib>MEIER, ETHAN R.</creatorcontrib><creatorcontrib>CHAN, OWEN</creatorcontrib><creatorcontrib>FISHER, SIMON</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><jtitle>Diabetes (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DE ABREU, ADRIANA VIEIRA</au><au>AGRAWAL, RAHUL</au><au>MEIER, ETHAN R.</au><au>CHAN, OWEN</au><au>FISHER, SIMON</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>118-OR: Activation of Dopamine Signaling in the Brain Causes HAAF</atitle><jtitle>Diabetes (New York, N.Y.)</jtitle><date>2019-06-01</date><risdate>2019</risdate><volume>68</volume><issue>Supplement_1</issue><issn>0012-1797</issn><eissn>1939-327X</eissn><abstract>Hypoglycemia-associated autonomic failure (HAAF) is comprised of both a blunted counterregulatory response to hypoglycemia and hypoglycemia unawareness. We previously demonstrated that both these aspects of HAAF can be reversed by treatment with the dopamine receptor antagonist, metoclopramide. These findings suggest that repetitive activation of the dopaminergic system may contribute to HAAF. We now evaluate whether both the blunted counterregulatory response to hypoglycemia and hypoglycemia unawareness are mediated by repeated activation of brain dopaminergic receptors. To test this hypothesis, male Sprague-Dawley rats were randomized to receive either the dopamine receptor agonist, bromocriptine, (Bromo; 20 µg/d) intracerebroventricularly (ICV) for 3 consecutive days or recurrent ICV saline (controls). On the fourth day, all rats underwent either, 1) a hyperinsulinemic (50 mU/kg/min) hypoglycemic (∼50 mg/dl) clamp to assess counterregulation, or 2) had food consumption measured in response to insulin-induced (15 U/kg; SQ) hypoglycemia (∼40 mg/dl) to assess hypoglycemia awareness. In response to hypoglycemia, antecedent Bromo blunted, 1) the epinephrine response by 86%* (see Fig), 2) the glucagon response by 56%§, and 3) hypoglycemia awareness by 37%§, as compared to controls (*p<0.01, §p<0.05). These findings demonstrate that dopaminergic signaling in the central nervous system contributes to the development of HAAF.</abstract><cop>New York</cop><pub>American Diabetes Association</pub><doi>10.2337/db19-118-OR</doi></addata></record> |
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subjects | Bromocriptine Central nervous system Dopamine Dopamine receptors Epinephrine Food consumption Glucagon Glucose Hypoglycemia Insulin Metoclopramide Rodents |
title | 118-OR: Activation of Dopamine Signaling in the Brain Causes HAAF |
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