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The Metabolic and Endocrine Effects of a 12-Week Allulose-Rich Diet
The global rise in type 2 diabetes (T2D) and obesity necessitates innovative dietary interventions. This study investigates the effects of allulose, a rare sugar shown to reduce blood glucose, in a rat model of diet-induced obesity and T2D. Over 12 weeks, we hypothesized that allulose supplementatio...
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Published in: | Nutrients 2024-06, Vol.16 (12), p.1821 |
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creator | Cayabyab, Kevin B Shin, Marley J Heimuli, Micah S Kim, Iris J D'Agostino, Dominic P Johnson, Richard J Koutnik, Andrew P Bellissimo, Nick Diamond, David M Norwitz, Nicholas G Arroyo, Juan A Reynolds, Paul R Bikman, Benjamin T |
description | The global rise in type 2 diabetes (T2D) and obesity necessitates innovative dietary interventions. This study investigates the effects of allulose, a rare sugar shown to reduce blood glucose, in a rat model of diet-induced obesity and T2D. Over 12 weeks, we hypothesized that allulose supplementation would improve body weight, insulin sensitivity, and glycemic control. Our results showed that allulose mitigated the adverse effects of high-fat, high-sugar diets, including reduced body weight gain and improved insulin resistance. The allulose group exhibited lower food consumption and increased levels of glucagon-like peptide-1 (GLP-1), enhancing glucose regulation and appetite control. Additionally, allulose prevented liver triglyceride accumulation and promoted mitochondrial uncoupling in adipose tissue. These findings suggest that allulose supplementation can improve metabolic health markers, making it a promising dietary component for managing obesity and T2D. Further research is needed to explore the long-term benefits and mechanisms of allulose in metabolic disease prevention and management. This study supports the potential of allulose as a safe and effective intervention for improving metabolic health in the context of dietary excess. |
doi_str_mv | 10.3390/nu16121821 |
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This study investigates the effects of allulose, a rare sugar shown to reduce blood glucose, in a rat model of diet-induced obesity and T2D. Over 12 weeks, we hypothesized that allulose supplementation would improve body weight, insulin sensitivity, and glycemic control. Our results showed that allulose mitigated the adverse effects of high-fat, high-sugar diets, including reduced body weight gain and improved insulin resistance. The allulose group exhibited lower food consumption and increased levels of glucagon-like peptide-1 (GLP-1), enhancing glucose regulation and appetite control. Additionally, allulose prevented liver triglyceride accumulation and promoted mitochondrial uncoupling in adipose tissue. These findings suggest that allulose supplementation can improve metabolic health markers, making it a promising dietary component for managing obesity and T2D. Further research is needed to explore the long-term benefits and mechanisms of allulose in metabolic disease prevention and management. 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Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2024 by the authors. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c466t-4d929cfea2c9be4d5a64474c1d39b385ae19e951b26f391fb7f2f168a970f0523</cites><orcidid>0000-0003-4155-8687 ; 0000-0001-9652-181X ; 0000-0002-0931-3025</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3072617231/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3072617231?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38931176$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cayabyab, Kevin B</creatorcontrib><creatorcontrib>Shin, Marley J</creatorcontrib><creatorcontrib>Heimuli, Micah S</creatorcontrib><creatorcontrib>Kim, Iris J</creatorcontrib><creatorcontrib>D'Agostino, Dominic P</creatorcontrib><creatorcontrib>Johnson, Richard J</creatorcontrib><creatorcontrib>Koutnik, Andrew P</creatorcontrib><creatorcontrib>Bellissimo, Nick</creatorcontrib><creatorcontrib>Diamond, David M</creatorcontrib><creatorcontrib>Norwitz, Nicholas G</creatorcontrib><creatorcontrib>Arroyo, Juan A</creatorcontrib><creatorcontrib>Reynolds, Paul R</creatorcontrib><creatorcontrib>Bikman, Benjamin T</creatorcontrib><title>The Metabolic and Endocrine Effects of a 12-Week Allulose-Rich Diet</title><title>Nutrients</title><addtitle>Nutrients</addtitle><description>The global rise in type 2 diabetes (T2D) and obesity necessitates innovative dietary interventions. This study investigates the effects of allulose, a rare sugar shown to reduce blood glucose, in a rat model of diet-induced obesity and T2D. Over 12 weeks, we hypothesized that allulose supplementation would improve body weight, insulin sensitivity, and glycemic control. Our results showed that allulose mitigated the adverse effects of high-fat, high-sugar diets, including reduced body weight gain and improved insulin resistance. The allulose group exhibited lower food consumption and increased levels of glucagon-like peptide-1 (GLP-1), enhancing glucose regulation and appetite control. Additionally, allulose prevented liver triglyceride accumulation and promoted mitochondrial uncoupling in adipose tissue. These findings suggest that allulose supplementation can improve metabolic health markers, making it a promising dietary component for managing obesity and T2D. Further research is needed to explore the long-term benefits and mechanisms of allulose in metabolic disease prevention and management. This study supports the potential of allulose as a safe and effective intervention for improving metabolic health in the context of dietary excess.</description><subject>adipose tissue</subject><subject>Adipose Tissue - metabolism</subject><subject>animal models</subject><subject>Animals</subject><subject>appetite</subject><subject>blood glucose</subject><subject>Blood Glucose - metabolism</subject><subject>body weight changes</subject><subject>Diabetes</subject><subject>Diabetes Mellitus, Type 2 - metabolism</subject><subject>Diabetes Mellitus, Type 2 - prevention & control</subject><subject>Diet</subject><subject>Diet, High-Fat - adverse effects</subject><subject>Disease Models, Animal</subject><subject>disease prevention</subject><subject>food composition</subject><subject>food consumption</subject><subject>Fructose - administration & dosage</subject><subject>glucagon-like peptide 1</subject><subject>Glucagon-Like Peptide 1 - blood</subject><subject>Glucagon-Like Peptide 1 - metabolism</subject><subject>Glucose</subject><subject>glycemic control</subject><subject>Health aspects</subject><subject>Insulin</subject><subject>Insulin Resistance</subject><subject>Laboratory animals</subject><subject>Liver</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Metabolism</subject><subject>mitochondria</subject><subject>noninsulin-dependent diabetes mellitus</subject><subject>Obesity</subject><subject>Obesity - metabolism</subject><subject>Physiological aspects</subject><subject>Proteins</subject><subject>psicose</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Respiration</subject><subject>Rodents</subject><subject>Sucrose</subject><subject>triacylglycerols</subject><subject>Triglycerides - blood</subject><subject>Weight control</subject><subject>Weight Gain</subject><issn>2072-6643</issn><issn>2072-6643</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqFkl1rFDEUhoMotqy98QdIwBsRpuYkM8nkSpZ1-wEVQSpehkzmpJs6m9TJjOC_b7at_RDBnIuEk-e8hDcvIa-BHQqh2Yc4gwQOLYdnZJ8zxSspa_H80XmPHOR8yXZLMSXFS7InWi0AlNwnq_MN0s842S4NwVEbe7qOfXJjiEjX3qObMk2eWgq8-o74gy6HYR5SxuprcBv6KeD0irzwdsh4cLcvyLej9fnqpDr7cny6Wp5VrpZyqupec-08Wu50h3XfWFnXqnbQC92JtrEIGnUDHZdeaPCd8tyDbK1WzLOGiwX5eKt7NXdb7B3GabSDuRrD1o6_TbLBPL2JYWMu0i8DUMxgYqfw7k5hTD9nzJPZhuxwGGzENGcjoBGyabnS_0eLvS1rFZMFffsXepnmMRYrbigJigt4oC7sgCZEn8ob3U7ULJXWshG8fNaCHP6DKtXjNrgU0YfSfzLw_nbAjSnnEf29H8DMLiHmISEFfvPYwXv0Tx7ENdUnsWI</recordid><startdate>20240610</startdate><enddate>20240610</enddate><creator>Cayabyab, Kevin B</creator><creator>Shin, Marley J</creator><creator>Heimuli, Micah S</creator><creator>Kim, Iris J</creator><creator>D'Agostino, Dominic P</creator><creator>Johnson, Richard J</creator><creator>Koutnik, Andrew P</creator><creator>Bellissimo, Nick</creator><creator>Diamond, David M</creator><creator>Norwitz, Nicholas G</creator><creator>Arroyo, Juan A</creator><creator>Reynolds, Paul R</creator><creator>Bikman, Benjamin T</creator><general>MDPI AG</general><general>MDPI</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>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</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>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4155-8687</orcidid><orcidid>https://orcid.org/0000-0001-9652-181X</orcidid><orcidid>https://orcid.org/0000-0002-0931-3025</orcidid></search><sort><creationdate>20240610</creationdate><title>The Metabolic and Endocrine Effects of a 12-Week Allulose-Rich Diet</title><author>Cayabyab, Kevin B ; Shin, Marley J ; Heimuli, Micah S ; Kim, Iris J ; D'Agostino, Dominic P ; Johnson, Richard J ; Koutnik, Andrew P ; Bellissimo, Nick ; Diamond, David M ; Norwitz, Nicholas G ; Arroyo, Juan A ; Reynolds, Paul R ; Bikman, Benjamin T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-4d929cfea2c9be4d5a64474c1d39b385ae19e951b26f391fb7f2f168a970f0523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>adipose tissue</topic><topic>Adipose Tissue - metabolism</topic><topic>animal models</topic><topic>Animals</topic><topic>appetite</topic><topic>blood glucose</topic><topic>Blood Glucose - metabolism</topic><topic>body weight changes</topic><topic>Diabetes</topic><topic>Diabetes Mellitus, Type 2 - metabolism</topic><topic>Diabetes Mellitus, Type 2 - prevention & control</topic><topic>Diet</topic><topic>Diet, High-Fat - adverse effects</topic><topic>Disease Models, Animal</topic><topic>disease prevention</topic><topic>food composition</topic><topic>food consumption</topic><topic>Fructose - administration & dosage</topic><topic>glucagon-like peptide 1</topic><topic>Glucagon-Like Peptide 1 - blood</topic><topic>Glucagon-Like Peptide 1 - metabolism</topic><topic>Glucose</topic><topic>glycemic control</topic><topic>Health aspects</topic><topic>Insulin</topic><topic>Insulin Resistance</topic><topic>Laboratory animals</topic><topic>Liver</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>Metabolism</topic><topic>mitochondria</topic><topic>noninsulin-dependent diabetes mellitus</topic><topic>Obesity</topic><topic>Obesity - 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Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nutrients</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cayabyab, Kevin B</au><au>Shin, Marley J</au><au>Heimuli, Micah S</au><au>Kim, Iris J</au><au>D'Agostino, Dominic P</au><au>Johnson, Richard J</au><au>Koutnik, Andrew P</au><au>Bellissimo, Nick</au><au>Diamond, David M</au><au>Norwitz, Nicholas G</au><au>Arroyo, Juan A</au><au>Reynolds, Paul R</au><au>Bikman, Benjamin T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Metabolic and Endocrine Effects of a 12-Week Allulose-Rich Diet</atitle><jtitle>Nutrients</jtitle><addtitle>Nutrients</addtitle><date>2024-06-10</date><risdate>2024</risdate><volume>16</volume><issue>12</issue><spage>1821</spage><pages>1821-</pages><issn>2072-6643</issn><eissn>2072-6643</eissn><abstract>The global rise in type 2 diabetes (T2D) and obesity necessitates innovative dietary interventions. This study investigates the effects of allulose, a rare sugar shown to reduce blood glucose, in a rat model of diet-induced obesity and T2D. Over 12 weeks, we hypothesized that allulose supplementation would improve body weight, insulin sensitivity, and glycemic control. Our results showed that allulose mitigated the adverse effects of high-fat, high-sugar diets, including reduced body weight gain and improved insulin resistance. The allulose group exhibited lower food consumption and increased levels of glucagon-like peptide-1 (GLP-1), enhancing glucose regulation and appetite control. Additionally, allulose prevented liver triglyceride accumulation and promoted mitochondrial uncoupling in adipose tissue. These findings suggest that allulose supplementation can improve metabolic health markers, making it a promising dietary component for managing obesity and T2D. 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subjects | adipose tissue Adipose Tissue - metabolism animal models Animals appetite blood glucose Blood Glucose - metabolism body weight changes Diabetes Diabetes Mellitus, Type 2 - metabolism Diabetes Mellitus, Type 2 - prevention & control Diet Diet, High-Fat - adverse effects Disease Models, Animal disease prevention food composition food consumption Fructose - administration & dosage glucagon-like peptide 1 Glucagon-Like Peptide 1 - blood Glucagon-Like Peptide 1 - metabolism Glucose glycemic control Health aspects Insulin Insulin Resistance Laboratory animals Liver Liver - metabolism Male Metabolism mitochondria noninsulin-dependent diabetes mellitus Obesity Obesity - metabolism Physiological aspects Proteins psicose Rats Rats, Sprague-Dawley Respiration Rodents Sucrose triacylglycerols Triglycerides - blood Weight control Weight Gain |
title | The Metabolic and Endocrine Effects of a 12-Week Allulose-Rich Diet |
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