Histamine induces postprandial tachycardia through a direct effect on cardiac H2-receptors in pythons
1 Zoophysiology, Department of Biological Sciences, University of Aarhus, Denmark; and 2 Department of Molecular Biology, University of Aarhus, Denmark Submitted 31 May 2008 ; accepted in final form 13 December 2008 The intrinsic heart rate of most vertebrates studied, including humans, is elevated...
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creator | Skovgaard, Nini Moller, Kate Gesser, Hans Wang, Tobias |
description | 1 Zoophysiology, Department of Biological Sciences, University of Aarhus, Denmark; and 2 Department of Molecular Biology, University of Aarhus, Denmark
Submitted 31 May 2008
; accepted in final form 13 December 2008
The intrinsic heart rate of most vertebrates studied, including humans, is elevated during digestion, suggesting that a nonadrenergic-noncholinergic factor contributes to the postprandial tachycardia. The regulating factor, however, remains elusive and difficult to identify. Pythons can ingest very large meals, and digestion is associated with a marked rise in metabolism that is sustained for several days. The metabolic rise causes more than a doubling of heart rate and a fourfold rise in cardiac output. This makes the python an interesting model to investigate the postprandial tachycardia. We measured blood pressure and heart rate in fasting Python regius , and at 24 and 48 h after ingestion of a meal amounting to 25% of body wt. Digestion caused heart rate to increase from 25 to 56 min, whereas blood pressure was unchanged. The postprandial rise in heart rate was partially due to a doubling of intrinsic heart rate. The H 2 -antagonist did not affect heart rate of fasting snakes but decreased heart rate by 15–20 min at 24 h into digestion, whereas it had no effects at 48 h. Thus, the histaminergic tone on the heart rose from none to 30% at 24 h but vanished after 48 h. In anesthetized snakes, histamine caused a systemic vasodilatation and a marked increase in heart rate and cardiac output mediated through a direct effect on H 2 - receptors. Our study strongly indicates that histamine regulates heart rate during the initial phase of digestion in pythons. This study describes a novel regulation of the vertebrate heart.
reptile; digestion; heart rate; blood flow; blood pressure
Address for reprint requests and other correspondence: N. Skovgaard, Zoophysiology, Dept. of Biological Sciences, Univ. of Aarhus, Bldg. 1131, 8000 Aarhus C, Denmark (e-mail: nini.jensen{at}biology.au.dk ) |
doi_str_mv | 10.1152/ajpregu.90466.2008 |
format | Article |
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Submitted 31 May 2008
; accepted in final form 13 December 2008
The intrinsic heart rate of most vertebrates studied, including humans, is elevated during digestion, suggesting that a nonadrenergic-noncholinergic factor contributes to the postprandial tachycardia. The regulating factor, however, remains elusive and difficult to identify. Pythons can ingest very large meals, and digestion is associated with a marked rise in metabolism that is sustained for several days. The metabolic rise causes more than a doubling of heart rate and a fourfold rise in cardiac output. This makes the python an interesting model to investigate the postprandial tachycardia. We measured blood pressure and heart rate in fasting Python regius , and at 24 and 48 h after ingestion of a meal amounting to 25% of body wt. Digestion caused heart rate to increase from 25 to 56 min, whereas blood pressure was unchanged. The postprandial rise in heart rate was partially due to a doubling of intrinsic heart rate. The H 2 -antagonist did not affect heart rate of fasting snakes but decreased heart rate by 15–20 min at 24 h into digestion, whereas it had no effects at 48 h. Thus, the histaminergic tone on the heart rose from none to 30% at 24 h but vanished after 48 h. In anesthetized snakes, histamine caused a systemic vasodilatation and a marked increase in heart rate and cardiac output mediated through a direct effect on H 2 - receptors. Our study strongly indicates that histamine regulates heart rate during the initial phase of digestion in pythons. This study describes a novel regulation of the vertebrate heart.
reptile; digestion; heart rate; blood flow; blood pressure
Address for reprint requests and other correspondence: N. Skovgaard, Zoophysiology, Dept. of Biological Sciences, Univ. of Aarhus, Bldg. 1131, 8000 Aarhus C, Denmark (e-mail: nini.jensen{at}biology.au.dk )</description><identifier>ISSN: 0363-6119</identifier><identifier>EISSN: 1522-1490</identifier><identifier>DOI: 10.1152/ajpregu.90466.2008</identifier><identifier>PMID: 19091908</identifier><language>eng</language><publisher>United States</publisher><subject>Anesthesia ; Animals ; Blood Pressure - drug effects ; Boidae - physiology ; Female ; Histamine - blood ; Histamine - pharmacology ; Histamine Agonists - pharmacology ; Histamine H1 Antagonists - pharmacology ; Histamine H2 Antagonists - pharmacology ; Male ; Postprandial Period - drug effects ; Postprandial Period - physiology ; Receptors, Histamine H1 - drug effects ; Receptors, Histamine H2 - drug effects ; Regional Blood Flow - drug effects ; Sinoatrial Node - drug effects ; Tachycardia - chemically induced ; Tachycardia - physiopathology</subject><ispartof>American journal of physiology. Regulatory, integrative and comparative physiology, 2009-03, Vol.296 (3), p.R774</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/19091908$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Skovgaard, Nini</creatorcontrib><creatorcontrib>Moller, Kate</creatorcontrib><creatorcontrib>Gesser, Hans</creatorcontrib><creatorcontrib>Wang, Tobias</creatorcontrib><title>Histamine induces postprandial tachycardia through a direct effect on cardiac H2-receptors in pythons</title><title>American journal of physiology. Regulatory, integrative and comparative physiology</title><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><description>1 Zoophysiology, Department of Biological Sciences, University of Aarhus, Denmark; and 2 Department of Molecular Biology, University of Aarhus, Denmark
Submitted 31 May 2008
; accepted in final form 13 December 2008
The intrinsic heart rate of most vertebrates studied, including humans, is elevated during digestion, suggesting that a nonadrenergic-noncholinergic factor contributes to the postprandial tachycardia. The regulating factor, however, remains elusive and difficult to identify. Pythons can ingest very large meals, and digestion is associated with a marked rise in metabolism that is sustained for several days. The metabolic rise causes more than a doubling of heart rate and a fourfold rise in cardiac output. This makes the python an interesting model to investigate the postprandial tachycardia. We measured blood pressure and heart rate in fasting Python regius , and at 24 and 48 h after ingestion of a meal amounting to 25% of body wt. Digestion caused heart rate to increase from 25 to 56 min, whereas blood pressure was unchanged. The postprandial rise in heart rate was partially due to a doubling of intrinsic heart rate. The H 2 -antagonist did not affect heart rate of fasting snakes but decreased heart rate by 15–20 min at 24 h into digestion, whereas it had no effects at 48 h. Thus, the histaminergic tone on the heart rose from none to 30% at 24 h but vanished after 48 h. In anesthetized snakes, histamine caused a systemic vasodilatation and a marked increase in heart rate and cardiac output mediated through a direct effect on H 2 - receptors. Our study strongly indicates that histamine regulates heart rate during the initial phase of digestion in pythons. This study describes a novel regulation of the vertebrate heart.
reptile; digestion; heart rate; blood flow; blood pressure
Address for reprint requests and other correspondence: N. Skovgaard, Zoophysiology, Dept. of Biological Sciences, Univ. of Aarhus, Bldg. 1131, 8000 Aarhus C, Denmark (e-mail: nini.jensen{at}biology.au.dk )</description><subject>Anesthesia</subject><subject>Animals</subject><subject>Blood Pressure - drug effects</subject><subject>Boidae - physiology</subject><subject>Female</subject><subject>Histamine - blood</subject><subject>Histamine - pharmacology</subject><subject>Histamine Agonists - pharmacology</subject><subject>Histamine H1 Antagonists - pharmacology</subject><subject>Histamine H2 Antagonists - pharmacology</subject><subject>Male</subject><subject>Postprandial Period - drug effects</subject><subject>Postprandial Period - physiology</subject><subject>Receptors, Histamine H1 - drug effects</subject><subject>Receptors, Histamine H2 - drug effects</subject><subject>Regional Blood Flow - drug effects</subject><subject>Sinoatrial Node - drug effects</subject><subject>Tachycardia - chemically induced</subject><subject>Tachycardia - physiopathology</subject><issn>0363-6119</issn><issn>1522-1490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kN1KAzEQhYMotlZfwAvJC2zNX7O7lyJqhYIger1k87NJaTchySL79kZaYYaP4RwOnAHgHqM1xhvyKPYh6mFat4hxviYINRdgWQRSYdaiS7BElNOKY9wuwE1Ke4QQo4xegwVuUVu2WQK9dSmLoxs1dKOapE4w-JRDFKNy4gCzkHaWIpYDZhv9NFgooHJRywy1MX_wIzw5JNySqig6ZB9TCYRhztaP6RZcGXFI-u7MFfh-ffl63la7j7f356ddZTEnudIYC0JrgttaYdFLJiVTdW8a3TRMkzKYKCMNR8SIXhmCGBYFwuh6w5GgK_Bwyg1Tf9SqC9EdRZy7_77FUJ0M1g32p7Togp2T8wc_zN35nx1peUe7z7pm9Bd1uGwK</recordid><startdate>20090301</startdate><enddate>20090301</enddate><creator>Skovgaard, Nini</creator><creator>Moller, Kate</creator><creator>Gesser, Hans</creator><creator>Wang, Tobias</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20090301</creationdate><title>Histamine induces postprandial tachycardia through a direct effect on cardiac H2-receptors in pythons</title><author>Skovgaard, Nini ; Moller, Kate ; Gesser, Hans ; Wang, Tobias</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h162t-e11a2372197d1abc4cc4d7bf8e884e24e212dfcf602fabdf2041adf2afe7560a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Anesthesia</topic><topic>Animals</topic><topic>Blood Pressure - drug effects</topic><topic>Boidae - physiology</topic><topic>Female</topic><topic>Histamine - blood</topic><topic>Histamine - pharmacology</topic><topic>Histamine Agonists - pharmacology</topic><topic>Histamine H1 Antagonists - pharmacology</topic><topic>Histamine H2 Antagonists - pharmacology</topic><topic>Male</topic><topic>Postprandial Period - drug effects</topic><topic>Postprandial Period - physiology</topic><topic>Receptors, Histamine H1 - drug effects</topic><topic>Receptors, Histamine H2 - drug effects</topic><topic>Regional Blood Flow - drug effects</topic><topic>Sinoatrial Node - drug effects</topic><topic>Tachycardia - chemically induced</topic><topic>Tachycardia - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Skovgaard, Nini</creatorcontrib><creatorcontrib>Moller, Kate</creatorcontrib><creatorcontrib>Gesser, Hans</creatorcontrib><creatorcontrib>Wang, Tobias</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Skovgaard, Nini</au><au>Moller, Kate</au><au>Gesser, Hans</au><au>Wang, Tobias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Histamine induces postprandial tachycardia through a direct effect on cardiac H2-receptors in pythons</atitle><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><date>2009-03-01</date><risdate>2009</risdate><volume>296</volume><issue>3</issue><spage>R774</spage><pages>R774-</pages><issn>0363-6119</issn><eissn>1522-1490</eissn><abstract>1 Zoophysiology, Department of Biological Sciences, University of Aarhus, Denmark; and 2 Department of Molecular Biology, University of Aarhus, Denmark
Submitted 31 May 2008
; accepted in final form 13 December 2008
The intrinsic heart rate of most vertebrates studied, including humans, is elevated during digestion, suggesting that a nonadrenergic-noncholinergic factor contributes to the postprandial tachycardia. The regulating factor, however, remains elusive and difficult to identify. Pythons can ingest very large meals, and digestion is associated with a marked rise in metabolism that is sustained for several days. The metabolic rise causes more than a doubling of heart rate and a fourfold rise in cardiac output. This makes the python an interesting model to investigate the postprandial tachycardia. We measured blood pressure and heart rate in fasting Python regius , and at 24 and 48 h after ingestion of a meal amounting to 25% of body wt. Digestion caused heart rate to increase from 25 to 56 min, whereas blood pressure was unchanged. The postprandial rise in heart rate was partially due to a doubling of intrinsic heart rate. The H 2 -antagonist did not affect heart rate of fasting snakes but decreased heart rate by 15–20 min at 24 h into digestion, whereas it had no effects at 48 h. Thus, the histaminergic tone on the heart rose from none to 30% at 24 h but vanished after 48 h. In anesthetized snakes, histamine caused a systemic vasodilatation and a marked increase in heart rate and cardiac output mediated through a direct effect on H 2 - receptors. Our study strongly indicates that histamine regulates heart rate during the initial phase of digestion in pythons. This study describes a novel regulation of the vertebrate heart.
reptile; digestion; heart rate; blood flow; blood pressure
Address for reprint requests and other correspondence: N. Skovgaard, Zoophysiology, Dept. of Biological Sciences, Univ. of Aarhus, Bldg. 1131, 8000 Aarhus C, Denmark (e-mail: nini.jensen{at}biology.au.dk )</abstract><cop>United States</cop><pmid>19091908</pmid><doi>10.1152/ajpregu.90466.2008</doi></addata></record> |
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source | MEDLINE; American Physiological Society Paid; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Anesthesia Animals Blood Pressure - drug effects Boidae - physiology Female Histamine - blood Histamine - pharmacology Histamine Agonists - pharmacology Histamine H1 Antagonists - pharmacology Histamine H2 Antagonists - pharmacology Male Postprandial Period - drug effects Postprandial Period - physiology Receptors, Histamine H1 - drug effects Receptors, Histamine H2 - drug effects Regional Blood Flow - drug effects Sinoatrial Node - drug effects Tachycardia - chemically induced Tachycardia - physiopathology |
title | Histamine induces postprandial tachycardia through a direct effect on cardiac H2-receptors in pythons |
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