Loading…

Effects of lipase inhibition on gastric emptying of, and on the glycaemic, insulin and cardiovascular responses to, a high-fat/carbohydrate meal in type 2 diabetes

We examined the effects of lipase inhibition with orlistat on (i) gastric emptying of, and (ii) the glycaemic, glucagon-like peptide-1 (GLP-1) and cardiovascular responses to, a high-fat/carbohydrate meal in type 2 diabetic patients. Eight type 2 diabetic patients, who were aged 62 years (median ran...

Full description

Saved in:
Bibliographic Details
Published in:Diabetologia 2004-12, Vol.47 (12), p.2208-2214
Main Authors: ODONOVAN, D, HOROWITZ, M, RUSSO, A, FEINLE-BISSET, C, MUROLO, N, GENTILCORE, D, WISHART, J. M, MORRIS, H. A, JONES, K. L
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c465t-5242a880f868852a078a89e10c996db4d6a068e5cbc3ad8469f30898f8d7d433
cites cdi_FETCH-LOGICAL-c465t-5242a880f868852a078a89e10c996db4d6a068e5cbc3ad8469f30898f8d7d433
container_end_page 2214
container_issue 12
container_start_page 2208
container_title Diabetologia
container_volume 47
creator ODONOVAN, D
HOROWITZ, M
RUSSO, A
FEINLE-BISSET, C
MUROLO, N
GENTILCORE, D
WISHART, J. M
MORRIS, H. A
JONES, K. L
description We examined the effects of lipase inhibition with orlistat on (i) gastric emptying of, and (ii) the glycaemic, glucagon-like peptide-1 (GLP-1) and cardiovascular responses to, a high-fat/carbohydrate meal in type 2 diabetic patients. Eight type 2 diabetic patients, who were aged 62 years (median range: 49-68 years) and managed by diet alone, consumed a meal containing 65 g powdered potato, 20 g glucose reconstituted with 200 ml water (labelled with 20 MBq (99m)Tc-sulphur-colloid) and 45 g margarine. They did this on two separate occasions, with and without 120 mg orlistat, and while in the seated position with their back against a gamma camera. Venous blood samples for measurement of blood glucose, plasma insulin and GLP-1 were obtained immediately before the meal and at regular intervals afterwards. Blood pressure (systolic and diastolic) and heart rate were measured using an automated device. Gastric emptying of the meal was faster after orlistat than without orlistat (50% emptying time [mean +/- SEM], 61+/-8 min vs 98+/-5 min; p=0.0001). In the first 60 min after the meal blood glucose (p=0.001) and plasma insulin (p=0.01) concentrations were higher in patients who had taken orlistat; between 60 and 180 min plasma GLP-1 (p=0.02) concentrations were lower after orlistat than without orlistat. Between 0 and 30 min systolic blood pressure (p=0.003) was lower, and heart rate (p=0.03) greater in subjects who had taken orlistat than in those who had not. Inhibition of fat digestion by orlistat may-as a result of more rapid gastric emptying-exacerbate postprandial glycaemia and the postprandial fall in blood pressure in patients with type 2 diabetes after ingestion of meals containing fat and carbohydrate.
doi_str_mv 10.1007/s00125-004-1591-4
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67223210</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>783184691</sourcerecordid><originalsourceid>FETCH-LOGICAL-c465t-5242a880f868852a078a89e10c996db4d6a068e5cbc3ad8469f30898f8d7d433</originalsourceid><addsrcrecordid>eNpdkcuKFDEYhYMoTs_oA7iRIOhqysm9U0sZxlEYcDMLd-GvXLoz1M0kJdTz-KKm7IYBIZDF-c4h5EPoHSWfKSH7m0wIZbIhRDRUtrQRL9COCs4aIph-iXZb3FCtfl6gy5yfCCFcCvUaXVCpFJNS79CfuxC8LRlPAfdxhuxxHI-xiyVOI67nALmkaLEf5rLG8VDBawyj27Jy9PjQrxb8EO11Lealj-O_1EJycfoN2S49JJx8nqcx-4zLVOv4GA_HJkC5qVw3HVeXoHg8eOjrCi7r7DHDLkLni89v0KsAffZvz_cVevx693j7rXn4cf_99stDY4WSpZFMMNCaBK20lgzIXoNuPSW2bZXrhFNAlPbSdpaD00K1gRPd6qDd3gnOr9Cn0-ycpl-Lz8UMMVvf9zD6aclG7RnjjJIKfvgPfJqWNNanGUa5Fq0UG0RPkE1TzskHM6c4QFoNJWazZ072TLVnNntG1M778_DSDd49N866KvDxDNSPhT4kGG3Mz5zibasp538BUvqjPg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>213849540</pqid></control><display><type>article</type><title>Effects of lipase inhibition on gastric emptying of, and on the glycaemic, insulin and cardiovascular responses to, a high-fat/carbohydrate meal in type 2 diabetes</title><source>Springer Nature</source><creator>ODONOVAN, D ; HOROWITZ, M ; RUSSO, A ; FEINLE-BISSET, C ; MUROLO, N ; GENTILCORE, D ; WISHART, J. M ; MORRIS, H. A ; JONES, K. L</creator><creatorcontrib>ODONOVAN, D ; HOROWITZ, M ; RUSSO, A ; FEINLE-BISSET, C ; MUROLO, N ; GENTILCORE, D ; WISHART, J. M ; MORRIS, H. A ; JONES, K. L</creatorcontrib><description>We examined the effects of lipase inhibition with orlistat on (i) gastric emptying of, and (ii) the glycaemic, glucagon-like peptide-1 (GLP-1) and cardiovascular responses to, a high-fat/carbohydrate meal in type 2 diabetic patients. Eight type 2 diabetic patients, who were aged 62 years (median range: 49-68 years) and managed by diet alone, consumed a meal containing 65 g powdered potato, 20 g glucose reconstituted with 200 ml water (labelled with 20 MBq (99m)Tc-sulphur-colloid) and 45 g margarine. They did this on two separate occasions, with and without 120 mg orlistat, and while in the seated position with their back against a gamma camera. Venous blood samples for measurement of blood glucose, plasma insulin and GLP-1 were obtained immediately before the meal and at regular intervals afterwards. Blood pressure (systolic and diastolic) and heart rate were measured using an automated device. Gastric emptying of the meal was faster after orlistat than without orlistat (50% emptying time [mean +/- SEM], 61+/-8 min vs 98+/-5 min; p=0.0001). In the first 60 min after the meal blood glucose (p=0.001) and plasma insulin (p=0.01) concentrations were higher in patients who had taken orlistat; between 60 and 180 min plasma GLP-1 (p=0.02) concentrations were lower after orlistat than without orlistat. Between 0 and 30 min systolic blood pressure (p=0.003) was lower, and heart rate (p=0.03) greater in subjects who had taken orlistat than in those who had not. Inhibition of fat digestion by orlistat may-as a result of more rapid gastric emptying-exacerbate postprandial glycaemia and the postprandial fall in blood pressure in patients with type 2 diabetes after ingestion of meals containing fat and carbohydrate.</description><identifier>ISSN: 0012-186X</identifier><identifier>EISSN: 1432-0428</identifier><identifier>DOI: 10.1007/s00125-004-1591-4</identifier><identifier>PMID: 15662558</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Aged ; Biological and medical sciences ; Blood Glucose - drug effects ; Blood Glucose - metabolism ; Blood pressure ; Blood Pressure - drug effects ; Carbohydrates ; Diabetes ; Diabetes Mellitus, Type 2 - blood ; Diabetes Mellitus, Type 2 - physiopathology ; Diabetes. Impaired glucose tolerance ; Dietary Carbohydrates - pharmacology ; Dietary Fats - pharmacology ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Enzyme Inhibitors - pharmacology ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Female ; Gastric Emptying - drug effects ; Gastric Emptying - physiology ; Glucagon ; Glucagon - blood ; Glucagon-Like Peptide 1 ; Glucose ; Heart rate ; Heart Rate - drug effects ; Hemoglobin ; Humans ; Insulin ; Insulin - blood ; Insulin - metabolism ; Insulin Secretion ; Lactones - pharmacology ; Lipase - antagonists &amp; inhibitors ; Male ; Medical sciences ; Middle Aged ; Orlistat ; Peptide Fragments - blood ; Plasma ; Polypeptides ; Protein Precursors - blood</subject><ispartof>Diabetologia, 2004-12, Vol.47 (12), p.2208-2214</ispartof><rights>2005 INIST-CNRS</rights><rights>Copyright Springer-Verlag 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-5242a880f868852a078a89e10c996db4d6a068e5cbc3ad8469f30898f8d7d433</citedby><cites>FETCH-LOGICAL-c465t-5242a880f868852a078a89e10c996db4d6a068e5cbc3ad8469f30898f8d7d433</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16399813$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15662558$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ODONOVAN, D</creatorcontrib><creatorcontrib>HOROWITZ, M</creatorcontrib><creatorcontrib>RUSSO, A</creatorcontrib><creatorcontrib>FEINLE-BISSET, C</creatorcontrib><creatorcontrib>MUROLO, N</creatorcontrib><creatorcontrib>GENTILCORE, D</creatorcontrib><creatorcontrib>WISHART, J. M</creatorcontrib><creatorcontrib>MORRIS, H. A</creatorcontrib><creatorcontrib>JONES, K. L</creatorcontrib><title>Effects of lipase inhibition on gastric emptying of, and on the glycaemic, insulin and cardiovascular responses to, a high-fat/carbohydrate meal in type 2 diabetes</title><title>Diabetologia</title><addtitle>Diabetologia</addtitle><description>We examined the effects of lipase inhibition with orlistat on (i) gastric emptying of, and (ii) the glycaemic, glucagon-like peptide-1 (GLP-1) and cardiovascular responses to, a high-fat/carbohydrate meal in type 2 diabetic patients. Eight type 2 diabetic patients, who were aged 62 years (median range: 49-68 years) and managed by diet alone, consumed a meal containing 65 g powdered potato, 20 g glucose reconstituted with 200 ml water (labelled with 20 MBq (99m)Tc-sulphur-colloid) and 45 g margarine. They did this on two separate occasions, with and without 120 mg orlistat, and while in the seated position with their back against a gamma camera. Venous blood samples for measurement of blood glucose, plasma insulin and GLP-1 were obtained immediately before the meal and at regular intervals afterwards. Blood pressure (systolic and diastolic) and heart rate were measured using an automated device. Gastric emptying of the meal was faster after orlistat than without orlistat (50% emptying time [mean +/- SEM], 61+/-8 min vs 98+/-5 min; p=0.0001). In the first 60 min after the meal blood glucose (p=0.001) and plasma insulin (p=0.01) concentrations were higher in patients who had taken orlistat; between 60 and 180 min plasma GLP-1 (p=0.02) concentrations were lower after orlistat than without orlistat. Between 0 and 30 min systolic blood pressure (p=0.003) was lower, and heart rate (p=0.03) greater in subjects who had taken orlistat than in those who had not. Inhibition of fat digestion by orlistat may-as a result of more rapid gastric emptying-exacerbate postprandial glycaemia and the postprandial fall in blood pressure in patients with type 2 diabetes after ingestion of meals containing fat and carbohydrate.</description><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Blood Glucose - drug effects</subject><subject>Blood Glucose - metabolism</subject><subject>Blood pressure</subject><subject>Blood Pressure - drug effects</subject><subject>Carbohydrates</subject><subject>Diabetes</subject><subject>Diabetes Mellitus, Type 2 - blood</subject><subject>Diabetes Mellitus, Type 2 - physiopathology</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Dietary Carbohydrates - pharmacology</subject><subject>Dietary Fats - pharmacology</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Female</subject><subject>Gastric Emptying - drug effects</subject><subject>Gastric Emptying - physiology</subject><subject>Glucagon</subject><subject>Glucagon - blood</subject><subject>Glucagon-Like Peptide 1</subject><subject>Glucose</subject><subject>Heart rate</subject><subject>Heart Rate - drug effects</subject><subject>Hemoglobin</subject><subject>Humans</subject><subject>Insulin</subject><subject>Insulin - blood</subject><subject>Insulin - metabolism</subject><subject>Insulin Secretion</subject><subject>Lactones - pharmacology</subject><subject>Lipase - antagonists &amp; inhibitors</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Orlistat</subject><subject>Peptide Fragments - blood</subject><subject>Plasma</subject><subject>Polypeptides</subject><subject>Protein Precursors - blood</subject><issn>0012-186X</issn><issn>1432-0428</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNpdkcuKFDEYhYMoTs_oA7iRIOhqysm9U0sZxlEYcDMLd-GvXLoz1M0kJdTz-KKm7IYBIZDF-c4h5EPoHSWfKSH7m0wIZbIhRDRUtrQRL9COCs4aIph-iXZb3FCtfl6gy5yfCCFcCvUaXVCpFJNS79CfuxC8LRlPAfdxhuxxHI-xiyVOI67nALmkaLEf5rLG8VDBawyj27Jy9PjQrxb8EO11Lealj-O_1EJycfoN2S49JJx8nqcx-4zLVOv4GA_HJkC5qVw3HVeXoHg8eOjrCi7r7DHDLkLni89v0KsAffZvz_cVevx693j7rXn4cf_99stDY4WSpZFMMNCaBK20lgzIXoNuPSW2bZXrhFNAlPbSdpaD00K1gRPd6qDd3gnOr9Cn0-ycpl-Lz8UMMVvf9zD6aclG7RnjjJIKfvgPfJqWNNanGUa5Fq0UG0RPkE1TzskHM6c4QFoNJWazZ072TLVnNntG1M778_DSDd49N866KvDxDNSPhT4kGG3Mz5zibasp538BUvqjPg</recordid><startdate>20041201</startdate><enddate>20041201</enddate><creator>ODONOVAN, D</creator><creator>HOROWITZ, M</creator><creator>RUSSO, A</creator><creator>FEINLE-BISSET, C</creator><creator>MUROLO, N</creator><creator>GENTILCORE, D</creator><creator>WISHART, J. M</creator><creator>MORRIS, H. A</creator><creator>JONES, K. L</creator><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><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>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20041201</creationdate><title>Effects of lipase inhibition on gastric emptying of, and on the glycaemic, insulin and cardiovascular responses to, a high-fat/carbohydrate meal in type 2 diabetes</title><author>ODONOVAN, D ; HOROWITZ, M ; RUSSO, A ; FEINLE-BISSET, C ; MUROLO, N ; GENTILCORE, D ; WISHART, J. M ; MORRIS, H. A ; JONES, K. L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-5242a880f868852a078a89e10c996db4d6a068e5cbc3ad8469f30898f8d7d433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Blood Glucose - drug effects</topic><topic>Blood Glucose - metabolism</topic><topic>Blood pressure</topic><topic>Blood Pressure - drug effects</topic><topic>Carbohydrates</topic><topic>Diabetes</topic><topic>Diabetes Mellitus, Type 2 - blood</topic><topic>Diabetes Mellitus, Type 2 - physiopathology</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Dietary Carbohydrates - pharmacology</topic><topic>Dietary Fats - pharmacology</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Female</topic><topic>Gastric Emptying - drug effects</topic><topic>Gastric Emptying - physiology</topic><topic>Glucagon</topic><topic>Glucagon - blood</topic><topic>Glucagon-Like Peptide 1</topic><topic>Glucose</topic><topic>Heart rate</topic><topic>Heart Rate - drug effects</topic><topic>Hemoglobin</topic><topic>Humans</topic><topic>Insulin</topic><topic>Insulin - blood</topic><topic>Insulin - metabolism</topic><topic>Insulin Secretion</topic><topic>Lactones - pharmacology</topic><topic>Lipase - antagonists &amp; inhibitors</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Orlistat</topic><topic>Peptide Fragments - blood</topic><topic>Plasma</topic><topic>Polypeptides</topic><topic>Protein Precursors - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ODONOVAN, D</creatorcontrib><creatorcontrib>HOROWITZ, M</creatorcontrib><creatorcontrib>RUSSO, A</creatorcontrib><creatorcontrib>FEINLE-BISSET, C</creatorcontrib><creatorcontrib>MUROLO, N</creatorcontrib><creatorcontrib>GENTILCORE, D</creatorcontrib><creatorcontrib>WISHART, J. M</creatorcontrib><creatorcontrib>MORRIS, H. A</creatorcontrib><creatorcontrib>JONES, K. L</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health &amp; Medical Complete (ProQuest Database)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Diabetologia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ODONOVAN, D</au><au>HOROWITZ, M</au><au>RUSSO, A</au><au>FEINLE-BISSET, C</au><au>MUROLO, N</au><au>GENTILCORE, D</au><au>WISHART, J. M</au><au>MORRIS, H. A</au><au>JONES, K. L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of lipase inhibition on gastric emptying of, and on the glycaemic, insulin and cardiovascular responses to, a high-fat/carbohydrate meal in type 2 diabetes</atitle><jtitle>Diabetologia</jtitle><addtitle>Diabetologia</addtitle><date>2004-12-01</date><risdate>2004</risdate><volume>47</volume><issue>12</issue><spage>2208</spage><epage>2214</epage><pages>2208-2214</pages><issn>0012-186X</issn><eissn>1432-0428</eissn><abstract>We examined the effects of lipase inhibition with orlistat on (i) gastric emptying of, and (ii) the glycaemic, glucagon-like peptide-1 (GLP-1) and cardiovascular responses to, a high-fat/carbohydrate meal in type 2 diabetic patients. Eight type 2 diabetic patients, who were aged 62 years (median range: 49-68 years) and managed by diet alone, consumed a meal containing 65 g powdered potato, 20 g glucose reconstituted with 200 ml water (labelled with 20 MBq (99m)Tc-sulphur-colloid) and 45 g margarine. They did this on two separate occasions, with and without 120 mg orlistat, and while in the seated position with their back against a gamma camera. Venous blood samples for measurement of blood glucose, plasma insulin and GLP-1 were obtained immediately before the meal and at regular intervals afterwards. Blood pressure (systolic and diastolic) and heart rate were measured using an automated device. Gastric emptying of the meal was faster after orlistat than without orlistat (50% emptying time [mean +/- SEM], 61+/-8 min vs 98+/-5 min; p=0.0001). In the first 60 min after the meal blood glucose (p=0.001) and plasma insulin (p=0.01) concentrations were higher in patients who had taken orlistat; between 60 and 180 min plasma GLP-1 (p=0.02) concentrations were lower after orlistat than without orlistat. Between 0 and 30 min systolic blood pressure (p=0.003) was lower, and heart rate (p=0.03) greater in subjects who had taken orlistat than in those who had not. Inhibition of fat digestion by orlistat may-as a result of more rapid gastric emptying-exacerbate postprandial glycaemia and the postprandial fall in blood pressure in patients with type 2 diabetes after ingestion of meals containing fat and carbohydrate.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>15662558</pmid><doi>10.1007/s00125-004-1591-4</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0012-186X
ispartof Diabetologia, 2004-12, Vol.47 (12), p.2208-2214
issn 0012-186X
1432-0428
language eng
recordid cdi_proquest_miscellaneous_67223210
source Springer Nature
subjects Aged
Biological and medical sciences
Blood Glucose - drug effects
Blood Glucose - metabolism
Blood pressure
Blood Pressure - drug effects
Carbohydrates
Diabetes
Diabetes Mellitus, Type 2 - blood
Diabetes Mellitus, Type 2 - physiopathology
Diabetes. Impaired glucose tolerance
Dietary Carbohydrates - pharmacology
Dietary Fats - pharmacology
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Enzyme Inhibitors - pharmacology
Etiopathogenesis. Screening. Investigations. Target tissue resistance
Female
Gastric Emptying - drug effects
Gastric Emptying - physiology
Glucagon
Glucagon - blood
Glucagon-Like Peptide 1
Glucose
Heart rate
Heart Rate - drug effects
Hemoglobin
Humans
Insulin
Insulin - blood
Insulin - metabolism
Insulin Secretion
Lactones - pharmacology
Lipase - antagonists & inhibitors
Male
Medical sciences
Middle Aged
Orlistat
Peptide Fragments - blood
Plasma
Polypeptides
Protein Precursors - blood
title Effects of lipase inhibition on gastric emptying of, and on the glycaemic, insulin and cardiovascular responses to, a high-fat/carbohydrate meal in type 2 diabetes
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T09%3A39%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effects%20of%20lipase%20inhibition%20on%20gastric%20emptying%20of,%20and%20on%20the%20glycaemic,%20insulin%20and%20cardiovascular%20responses%20to,%20a%20high-fat/carbohydrate%20meal%20in%20type%202%20diabetes&rft.jtitle=Diabetologia&rft.au=ODONOVAN,%20D&rft.date=2004-12-01&rft.volume=47&rft.issue=12&rft.spage=2208&rft.epage=2214&rft.pages=2208-2214&rft.issn=0012-186X&rft.eissn=1432-0428&rft_id=info:doi/10.1007/s00125-004-1591-4&rft_dat=%3Cproquest_cross%3E783184691%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c465t-5242a880f868852a078a89e10c996db4d6a068e5cbc3ad8469f30898f8d7d433%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=213849540&rft_id=info:pmid/15662558&rfr_iscdi=true