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Deteriorated glucose metabolism with a high-protein, low-carbohydrate diet in db mice, an animal model of type 2 diabetes, might be caused by insufficient insulin secretion
Purpose We previously showed the deleterious effects of increased dietary protein on renal manifestations and glucose metabolism in leptin receptor-deficient ( db ) mice. Here, we further examined its effects on glucose metabolism, including urinary C-peptide. We also orally administered mixtures co...
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Published in: | European journal of nutrition 2017-02, Vol.56 (1), p.237-246 |
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creator | Arimura, Emi Pulong, Wijang Pralampita Marchianti, Ancah Caesarina Novi Nakakuma, Miwa Abe, Masaharu Ushikai, Miharu Horiuchi, Masahisa |
description | Purpose
We previously showed the deleterious effects of increased dietary protein on renal manifestations and glucose metabolism in leptin receptor-deficient (
db
) mice. Here, we further examined its effects on glucose metabolism, including urinary C-peptide. We also orally administered mixtures corresponding to low- or high-protein diets to diabetic mice.
Methods
In diet experiments, under pair-feeding (equivalent energy and fat) conditions using a metabolic cage, mice were fed diets with different protein content (L diet: 12 % protein, 71 % carbohydrate, 17 % fat; H diet: 24 % protein, 59 % carbohydrate, 17 % fat) for 15 days. In oral administration experiments, the respective mixtures (L mixture: 12 % proline, 71 % maltose or starch, 17 % linoleic acid; H mixture: 24 % proline, 59 % maltose or starch, 17 % linoleic acid) were supplied to mice. Biochemical parameters related to glucose metabolism were measured.
Results
The
db–H
diet mice showed significantly higher water intake, urinary volume, and glucose levels than
db–L
diet mice but similar levels of excreted urinary C-peptide. In contrast, control-H diet mice showed significantly higher C-peptide excretion than control-L diet mice. Both types of mice fed H diet excreted high levels of urinary albumin. When maltose mixtures were administered,
db–L
mixture mice showed significantly higher blood glucose after 30 min than
db–H
mixture mice. However,
db
mice administered starch–H mixture showed significantly higher blood glucose 120–300 min post-administration than
db–L
mixture mice, although both groups exhibited similar insulin levels.
Conclusions
High-protein, low-carbohydrate diets deteriorated diabetic conditions and were associated with insufficient insulin secretion in
db
mice. Our findings may have implications for dietary management of diabetic symptoms in human patients. |
doi_str_mv | 10.1007/s00394-015-1075-y |
format | article |
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We previously showed the deleterious effects of increased dietary protein on renal manifestations and glucose metabolism in leptin receptor-deficient (
db
) mice. Here, we further examined its effects on glucose metabolism, including urinary C-peptide. We also orally administered mixtures corresponding to low- or high-protein diets to diabetic mice.
Methods
In diet experiments, under pair-feeding (equivalent energy and fat) conditions using a metabolic cage, mice were fed diets with different protein content (L diet: 12 % protein, 71 % carbohydrate, 17 % fat; H diet: 24 % protein, 59 % carbohydrate, 17 % fat) for 15 days. In oral administration experiments, the respective mixtures (L mixture: 12 % proline, 71 % maltose or starch, 17 % linoleic acid; H mixture: 24 % proline, 59 % maltose or starch, 17 % linoleic acid) were supplied to mice. Biochemical parameters related to glucose metabolism were measured.
Results
The
db–H
diet mice showed significantly higher water intake, urinary volume, and glucose levels than
db–L
diet mice but similar levels of excreted urinary C-peptide. In contrast, control-H diet mice showed significantly higher C-peptide excretion than control-L diet mice. Both types of mice fed H diet excreted high levels of urinary albumin. When maltose mixtures were administered,
db–L
mixture mice showed significantly higher blood glucose after 30 min than
db–H
mixture mice. However,
db
mice administered starch–H mixture showed significantly higher blood glucose 120–300 min post-administration than
db–L
mixture mice, although both groups exhibited similar insulin levels.
Conclusions
High-protein, low-carbohydrate diets deteriorated diabetic conditions and were associated with insufficient insulin secretion in
db
mice. Our findings may have implications for dietary management of diabetic symptoms in human patients.</description><identifier>ISSN: 1436-6207</identifier><identifier>EISSN: 1436-6215</identifier><identifier>EISSN: 1435-1293</identifier><identifier>DOI: 10.1007/s00394-015-1075-y</identifier><identifier>PMID: 26497335</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Albuminuria - metabolism ; Animals ; Blood Glucose - metabolism ; Body Weight ; C-Peptide - urine ; Carbohydrate Metabolism ; Chemistry ; Chemistry and Materials Science ; Diabetes Mellitus, Experimental - physiopathology ; Diabetes Mellitus, Type 2 - physiopathology ; Diet, Carbohydrate-Restricted ; Dietary Carbohydrates - administration & dosage ; Dietary Proteins - administration & dosage ; Dietary Proteins - analysis ; Insulin - blood ; Insulin - metabolism ; Insulin Secretion ; Leptin - blood ; Male ; Maltose - administration & dosage ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Nutrition ; Original Contribution ; Starch - administration & dosage</subject><ispartof>European journal of nutrition, 2017-02, Vol.56 (1), p.237-246</ispartof><rights>Springer-Verlag Berlin Heidelberg 2015</rights><rights>European Journal of Nutrition is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-6050e3df5e5c24121b83691efc4d150c4707ecf9928fb8a2304cf4d3927822143</citedby><cites>FETCH-LOGICAL-c405t-6050e3df5e5c24121b83691efc4d150c4707ecf9928fb8a2304cf4d3927822143</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26497335$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arimura, Emi</creatorcontrib><creatorcontrib>Pulong, Wijang Pralampita</creatorcontrib><creatorcontrib>Marchianti, Ancah Caesarina Novi</creatorcontrib><creatorcontrib>Nakakuma, Miwa</creatorcontrib><creatorcontrib>Abe, Masaharu</creatorcontrib><creatorcontrib>Ushikai, Miharu</creatorcontrib><creatorcontrib>Horiuchi, Masahisa</creatorcontrib><title>Deteriorated glucose metabolism with a high-protein, low-carbohydrate diet in db mice, an animal model of type 2 diabetes, might be caused by insufficient insulin secretion</title><title>European journal of nutrition</title><addtitle>Eur J Nutr</addtitle><addtitle>Eur J Nutr</addtitle><description>Purpose
We previously showed the deleterious effects of increased dietary protein on renal manifestations and glucose metabolism in leptin receptor-deficient (
db
) mice. Here, we further examined its effects on glucose metabolism, including urinary C-peptide. We also orally administered mixtures corresponding to low- or high-protein diets to diabetic mice.
Methods
In diet experiments, under pair-feeding (equivalent energy and fat) conditions using a metabolic cage, mice were fed diets with different protein content (L diet: 12 % protein, 71 % carbohydrate, 17 % fat; H diet: 24 % protein, 59 % carbohydrate, 17 % fat) for 15 days. In oral administration experiments, the respective mixtures (L mixture: 12 % proline, 71 % maltose or starch, 17 % linoleic acid; H mixture: 24 % proline, 59 % maltose or starch, 17 % linoleic acid) were supplied to mice. Biochemical parameters related to glucose metabolism were measured.
Results
The
db–H
diet mice showed significantly higher water intake, urinary volume, and glucose levels than
db–L
diet mice but similar levels of excreted urinary C-peptide. In contrast, control-H diet mice showed significantly higher C-peptide excretion than control-L diet mice. Both types of mice fed H diet excreted high levels of urinary albumin. When maltose mixtures were administered,
db–L
mixture mice showed significantly higher blood glucose after 30 min than
db–H
mixture mice. However,
db
mice administered starch–H mixture showed significantly higher blood glucose 120–300 min post-administration than
db–L
mixture mice, although both groups exhibited similar insulin levels.
Conclusions
High-protein, low-carbohydrate diets deteriorated diabetic conditions and were associated with insufficient insulin secretion in
db
mice. Our findings may have implications for dietary management of diabetic symptoms in human patients.</description><subject>Albuminuria - metabolism</subject><subject>Animals</subject><subject>Blood Glucose - metabolism</subject><subject>Body Weight</subject><subject>C-Peptide - urine</subject><subject>Carbohydrate Metabolism</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Diabetes Mellitus, Experimental - physiopathology</subject><subject>Diabetes Mellitus, Type 2 - physiopathology</subject><subject>Diet, Carbohydrate-Restricted</subject><subject>Dietary Carbohydrates - administration & dosage</subject><subject>Dietary Proteins - administration & dosage</subject><subject>Dietary Proteins - analysis</subject><subject>Insulin - blood</subject><subject>Insulin - metabolism</subject><subject>Insulin Secretion</subject><subject>Leptin - blood</subject><subject>Male</subject><subject>Maltose - administration & dosage</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Nutrition</subject><subject>Original Contribution</subject><subject>Starch - administration & dosage</subject><issn>1436-6207</issn><issn>1436-6215</issn><issn>1435-1293</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqNkdGK1TAQhoso7rLuA3gjAW-8ONVJmqTppezqKix4o9clSSenkbY5JilL32kf0hzPuoggCIFkyDf_z8xfVS8pvKUA7bsE0HS8BipqCq2otyfVOeWNrCWj4unjG9qz6jIlbwCUAKFU-7w6Y5J3bdOI8-r-GjNGH6LOOJD9tNqQkMyYtQmTTzO583kkmox-P9aHGDL6ZUemcFdbHU0Yt-HYSQaPmfiFDIbM3uKO6KUcP-uJzGHAiQRH8nZAwgqqTfFMu0Lux0wMEqvXVNzNViTS6py3Hpf8q5iKaEIbMfuwvKieOT0lvHy4L6pvHz98vfpU3365-Xz1_ra2HESuJQjAZnAChWWcMmpUIzuKzvKBCrC8hRat6zqmnFGaNcCt40PTsVYxVvZ2Ub056ZaBf6yYcj_7ZHGa9IJhTT1VUjUAnRL_gTIpuWpVV9DXf6HfwxqXMshRUDChpGSFoifKxpBSRNcfYtlj3HoK_TH4_hR8X4Lvj8H3W-l59aC8mhmHx47fMReAnYBUvpY9xj-s_6n6Ex8Vuco</recordid><startdate>20170201</startdate><enddate>20170201</enddate><creator>Arimura, Emi</creator><creator>Pulong, Wijang Pralampita</creator><creator>Marchianti, Ancah Caesarina Novi</creator><creator>Nakakuma, Miwa</creator><creator>Abe, Masaharu</creator><creator>Ushikai, Miharu</creator><creator>Horiuchi, Masahisa</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</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>3V.</scope><scope>7QP</scope><scope>7RQ</scope><scope>7RV</scope><scope>7TS</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>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20170201</creationdate><title>Deteriorated glucose metabolism with a high-protein, low-carbohydrate diet in db mice, an animal model of type 2 diabetes, might be caused by insufficient insulin secretion</title><author>Arimura, Emi ; Pulong, Wijang Pralampita ; Marchianti, Ancah Caesarina Novi ; Nakakuma, Miwa ; Abe, Masaharu ; Ushikai, Miharu ; Horiuchi, Masahisa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-6050e3df5e5c24121b83691efc4d150c4707ecf9928fb8a2304cf4d3927822143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Albuminuria - metabolism</topic><topic>Animals</topic><topic>Blood Glucose - metabolism</topic><topic>Body Weight</topic><topic>C-Peptide - urine</topic><topic>Carbohydrate Metabolism</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Diabetes Mellitus, Experimental - physiopathology</topic><topic>Diabetes Mellitus, Type 2 - physiopathology</topic><topic>Diet, Carbohydrate-Restricted</topic><topic>Dietary Carbohydrates - administration & dosage</topic><topic>Dietary Proteins - administration & dosage</topic><topic>Dietary Proteins - analysis</topic><topic>Insulin - blood</topic><topic>Insulin - metabolism</topic><topic>Insulin Secretion</topic><topic>Leptin - blood</topic><topic>Male</topic><topic>Maltose - administration & dosage</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Nutrition</topic><topic>Original Contribution</topic><topic>Starch - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arimura, Emi</creatorcontrib><creatorcontrib>Pulong, Wijang Pralampita</creatorcontrib><creatorcontrib>Marchianti, Ancah Caesarina Novi</creatorcontrib><creatorcontrib>Nakakuma, Miwa</creatorcontrib><creatorcontrib>Abe, Masaharu</creatorcontrib><creatorcontrib>Ushikai, Miharu</creatorcontrib><creatorcontrib>Horiuchi, Masahisa</creatorcontrib><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>Calcium & Calcified Tissue Abstracts</collection><collection>Career & Technical Education Database</collection><collection>Nursing & Allied Health Database</collection><collection>Physical Education Index</collection><collection>Health & Medical Collection</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 Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arimura, Emi</au><au>Pulong, Wijang Pralampita</au><au>Marchianti, Ancah Caesarina Novi</au><au>Nakakuma, Miwa</au><au>Abe, Masaharu</au><au>Ushikai, Miharu</au><au>Horiuchi, Masahisa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Deteriorated glucose metabolism with a high-protein, low-carbohydrate diet in db mice, an animal model of type 2 diabetes, might be caused by insufficient insulin secretion</atitle><jtitle>European journal of nutrition</jtitle><stitle>Eur J Nutr</stitle><addtitle>Eur J Nutr</addtitle><date>2017-02-01</date><risdate>2017</risdate><volume>56</volume><issue>1</issue><spage>237</spage><epage>246</epage><pages>237-246</pages><issn>1436-6207</issn><eissn>1436-6215</eissn><eissn>1435-1293</eissn><abstract>Purpose
We previously showed the deleterious effects of increased dietary protein on renal manifestations and glucose metabolism in leptin receptor-deficient (
db
) mice. Here, we further examined its effects on glucose metabolism, including urinary C-peptide. We also orally administered mixtures corresponding to low- or high-protein diets to diabetic mice.
Methods
In diet experiments, under pair-feeding (equivalent energy and fat) conditions using a metabolic cage, mice were fed diets with different protein content (L diet: 12 % protein, 71 % carbohydrate, 17 % fat; H diet: 24 % protein, 59 % carbohydrate, 17 % fat) for 15 days. In oral administration experiments, the respective mixtures (L mixture: 12 % proline, 71 % maltose or starch, 17 % linoleic acid; H mixture: 24 % proline, 59 % maltose or starch, 17 % linoleic acid) were supplied to mice. Biochemical parameters related to glucose metabolism were measured.
Results
The
db–H
diet mice showed significantly higher water intake, urinary volume, and glucose levels than
db–L
diet mice but similar levels of excreted urinary C-peptide. In contrast, control-H diet mice showed significantly higher C-peptide excretion than control-L diet mice. Both types of mice fed H diet excreted high levels of urinary albumin. When maltose mixtures were administered,
db–L
mixture mice showed significantly higher blood glucose after 30 min than
db–H
mixture mice. However,
db
mice administered starch–H mixture showed significantly higher blood glucose 120–300 min post-administration than
db–L
mixture mice, although both groups exhibited similar insulin levels.
Conclusions
High-protein, low-carbohydrate diets deteriorated diabetic conditions and were associated with insufficient insulin secretion in
db
mice. Our findings may have implications for dietary management of diabetic symptoms in human patients.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>26497335</pmid><doi>10.1007/s00394-015-1075-y</doi><tpages>10</tpages></addata></record> |
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source | EBSCOhost SPORTDiscus with Full Text; Springer Nature |
subjects | Albuminuria - metabolism Animals Blood Glucose - metabolism Body Weight C-Peptide - urine Carbohydrate Metabolism Chemistry Chemistry and Materials Science Diabetes Mellitus, Experimental - physiopathology Diabetes Mellitus, Type 2 - physiopathology Diet, Carbohydrate-Restricted Dietary Carbohydrates - administration & dosage Dietary Proteins - administration & dosage Dietary Proteins - analysis Insulin - blood Insulin - metabolism Insulin Secretion Leptin - blood Male Maltose - administration & dosage Mice Mice, Inbred C57BL Mice, Knockout Nutrition Original Contribution Starch - administration & dosage |
title | Deteriorated glucose metabolism with a high-protein, low-carbohydrate diet in db mice, an animal model of type 2 diabetes, might be caused by insufficient insulin secretion |
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