Betel nut (Areca catechu) consumption and the induction of glucose intolerance in adult CD1 mice and in their F1 and F2 offspring

Many mutagenic nitroso compounds are also diabetogenic. Betel-nut (Areca catechu) chewing populations have an increased incidence of foregut cancers related to betel-nut nitrosamines which suggests that betel consumption could be diabetogenic. Young adult CD1 mice with a low spontaneous incidence of...

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Veröffentlicht in:Diabetologia 1994, Vol.37 (1), p.49-55
Hauptverfasser: BOUCHER, B. J, EWEN, S. W. B, STOWERS, J. M
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STOWERS, J. M
description Many mutagenic nitroso compounds are also diabetogenic. Betel-nut (Areca catechu) chewing populations have an increased incidence of foregut cancers related to betel-nut nitrosamines which suggests that betel consumption could be diabetogenic. Young adult CD1 mice with a low spontaneous incidence of diabetes were fed betel nut in standard feed for 2-6 days. Single point (90 min) intra-peritoneal glucose tolerance tests were used to follow glucose tolerance up to 6 months of age. Glucose intolerance was defined as over 3 SD above mean control values. Glucose intolerance was found in 3 of 51 male and 4 of 33 female adult mice which were fed the betel diet (p < 0.01). Studies on the progeny of these mice are presented separately for animals studied in Aberdeen (Group 1) and London (Group 2). In matings of Group 1 betel-fed parents glucose intolerance was found in 4 of 25 male and 1 of 22 female F1 offspring, with significant hyperglycaemia in F1 males born to hyperglycaemic but not to normoglycaemic mothers (p < 0.01). In the F2 generation 4 of 23 males and 1 of 16 females and in the F3 generation 1 of 16 males and 0 of 20 females were glucose intolerant. In the Group 2 studies where betel-fed parents were mated to normal controls glucose intolerance was found in 10 of 35 male and 10 of 33 female F1 progeny (p < 0.005), and mean islet areas were increased in offspring of betel-fed parents (p < 0.001).
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J</creatorcontrib><creatorcontrib>EWEN, S. W. B</creatorcontrib><creatorcontrib>STOWERS, J. M</creatorcontrib><title>Betel nut (Areca catechu) consumption and the induction of glucose intolerance in adult CD1 mice and in their F1 and F2 offspring</title><title>Diabetologia</title><addtitle>Diabetologia</addtitle><description>Many mutagenic nitroso compounds are also diabetogenic. Betel-nut (Areca catechu) chewing populations have an increased incidence of foregut cancers related to betel-nut nitrosamines which suggests that betel consumption could be diabetogenic. Young adult CD1 mice with a low spontaneous incidence of diabetes were fed betel nut in standard feed for 2-6 days. Single point (90 min) intra-peritoneal glucose tolerance tests were used to follow glucose tolerance up to 6 months of age. Glucose intolerance was defined as over 3 SD above mean control values. Glucose intolerance was found in 3 of 51 male and 4 of 33 female adult mice which were fed the betel diet (p &lt; 0.01). Studies on the progeny of these mice are presented separately for animals studied in Aberdeen (Group 1) and London (Group 2). In matings of Group 1 betel-fed parents glucose intolerance was found in 4 of 25 male and 1 of 22 female F1 offspring, with significant hyperglycaemia in F1 males born to hyperglycaemic but not to normoglycaemic mothers (p &lt; 0.01). In the F2 generation 4 of 23 males and 1 of 16 females and in the F3 generation 1 of 16 males and 0 of 20 females were glucose intolerant. In the Group 2 studies where betel-fed parents were mated to normal controls glucose intolerance was found in 10 of 35 male and 10 of 33 female F1 progeny (p &lt; 0.005), and mean islet areas were increased in offspring of betel-fed parents (p &lt; 0.001).</description><subject>Animals</subject><subject>Areca</subject><subject>Biological and medical sciences</subject><subject>Crosses, Genetic</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Female</subject><subject>Glucose Intolerance - etiology</subject><subject>Glucose Intolerance - genetics</subject><subject>Glucose Tolerance Test</subject><subject>Islets of Langerhans - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Nitrosamines - toxicity</subject><subject>Nuts</subject><subject>Pancreatic Diseases - etiology</subject><subject>Pancreatic Diseases - pathology</subject><subject>Plants, Medicinal</subject><subject>Reference Values</subject><subject>Sex Factors</subject><issn>0012-186X</issn><issn>1432-0428</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFUDtPwzAQthColMLCjuSBAZACfjV2x7YQQKrE0oEtss92Ccqjip2BkX9O0lZlurvvcaf7ELqm5JESIp8WGSGCKSnlCRpTwVkyjKdoTAhlCVXp5zm6COGbEMKnIh2hkaJTwjgZo9-Fi67EdRfx3bx1oDHo6OCru8fQ1KGrtrFoaqxri-OXw0VtO9ghjcebsoMmDGBsStfqGoYea9uVES-fKa6KHhmsPdq7ixZndDdnrPf7sG2LenOJzrwug7s61AlaZy_r5Vuy-nh9X85XCXAhY-Jlapx1nqWgpTBsBsYYBp47JQ1MlfVKSSqsM0R7BzPrreMauPdM6KnnE_SwXwttE0LrfN5fr3T7k1OSDynm_yn24pu9eNuZytmj9BBbz98eeB1Al374vQhHGVczIZXgf3pae0Q</recordid><startdate>1994</startdate><enddate>1994</enddate><creator>BOUCHER, B. 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Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Female</topic><topic>Glucose Intolerance - etiology</topic><topic>Glucose Intolerance - genetics</topic><topic>Glucose Tolerance Test</topic><topic>Islets of Langerhans - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Nitrosamines - toxicity</topic><topic>Nuts</topic><topic>Pancreatic Diseases - etiology</topic><topic>Pancreatic Diseases - pathology</topic><topic>Plants, Medicinal</topic><topic>Reference Values</topic><topic>Sex Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BOUCHER, B. J</creatorcontrib><creatorcontrib>EWEN, S. W. B</creatorcontrib><creatorcontrib>STOWERS, J. 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In the Group 2 studies where betel-fed parents were mated to normal controls glucose intolerance was found in 10 of 35 male and 10 of 33 female F1 progeny (p &lt; 0.005), and mean islet areas were increased in offspring of betel-fed parents (p &lt; 0.001).</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>8150230</pmid><doi>10.1007/BF00428777</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Areca
Biological and medical sciences
Crosses, Genetic
Diabetes. Impaired glucose tolerance
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Etiopathogenesis. Screening. Investigations. Target tissue resistance
Female
Glucose Intolerance - etiology
Glucose Intolerance - genetics
Glucose Tolerance Test
Islets of Langerhans - pathology
Male
Medical sciences
Mice
Mice, Inbred Strains
Nitrosamines - toxicity
Nuts
Pancreatic Diseases - etiology
Pancreatic Diseases - pathology
Plants, Medicinal
Reference Values
Sex Factors
title Betel nut (Areca catechu) consumption and the induction of glucose intolerance in adult CD1 mice and in their F1 and F2 offspring
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