Mulberry leaf extract reduces the glycemic indexes of four common dietary carbohydrates

1-Deoxynojirimycin (DNJ), a component of mulberry leaf extract (MLE), reduces postprandial hyperglycemia by inhibiting intestinal a-glycosidase. The aim of this exploratory study was to investigate the effects of MLE on the glycemic indexes (GI) of common dietary carbohydrates. This single-center, r...

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Veröffentlicht in:Medicine (Baltimore) 2018-08, Vol.97 (34), p.e11996-e11996
Hauptverfasser: Wang, Ruihua, Li, Yanfen, Mu, Wei, Li, Ziqiang, Sun, Jinxia, Wang, Baohe, Zhong, Zhong, Luo, Xiuzhen, Xie, Chen, Huang, Yuhong
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container_end_page e11996
container_issue 34
container_start_page e11996
container_title Medicine (Baltimore)
container_volume 97
creator Wang, Ruihua
Li, Yanfen
Mu, Wei
Li, Ziqiang
Sun, Jinxia
Wang, Baohe
Zhong, Zhong
Luo, Xiuzhen
Xie, Chen
Huang, Yuhong
description 1-Deoxynojirimycin (DNJ), a component of mulberry leaf extract (MLE), reduces postprandial hyperglycemia by inhibiting intestinal a-glycosidase. The aim of this exploratory study was to investigate the effects of MLE on the glycemic indexes (GI) of common dietary carbohydrates. This single-center, randomized, open-label, 7-cycle self-controlled crossover study enrolled 15 healthy volunteers at the National Drug Clinical Trial Institution, Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine (June 2014 to December 2014). The participants were randomized to receive glucose (3 occasions), glucose+MLE, sucrose+MLE, maltose+MLE, and maltodextrin+MLE orally during 7 visits (every 3 days). Blood glucose level was tested at 15 minutes before and at 15, 30, 45, 60, 90, and 120 minutes after carbohydrate intake. The GI of each carbohydrate relative to glucose (GI = 100) was calculated using the incremental area under the curve method. Safety was assessed at each visit. All participants completed the protocol. After carbohydrate ingestion, blood glucose level peaked at 30 minutes (glucose, glucose+MLE, sucrose+MLE, and maltose+MLE) or 45 minutes (maltodextrin+MLE) before returning to preprandial levels at 120 minutes. At 30 minutes, the change in blood glucose level was lower for sucrose+MLE, maltose+MLE, and maltodextrin+MLE than for glucose or glucose+MLE (P 
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The aim of this exploratory study was to investigate the effects of MLE on the glycemic indexes (GI) of common dietary carbohydrates. This single-center, randomized, open-label, 7-cycle self-controlled crossover study enrolled 15 healthy volunteers at the National Drug Clinical Trial Institution, Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine (June 2014 to December 2014). The participants were randomized to receive glucose (3 occasions), glucose+MLE, sucrose+MLE, maltose+MLE, and maltodextrin+MLE orally during 7 visits (every 3 days). Blood glucose level was tested at 15 minutes before and at 15, 30, 45, 60, 90, and 120 minutes after carbohydrate intake. The GI of each carbohydrate relative to glucose (GI = 100) was calculated using the incremental area under the curve method. Safety was assessed at each visit. All participants completed the protocol. After carbohydrate ingestion, blood glucose level peaked at 30 minutes (glucose, glucose+MLE, sucrose+MLE, and maltose+MLE) or 45 minutes (maltodextrin+MLE) before returning to preprandial levels at 120 minutes. At 30 minutes, the change in blood glucose level was lower for sucrose+MLE, maltose+MLE, and maltodextrin+MLE than for glucose or glucose+MLE (P &lt; .05). GI was lowest for sucrose+MLE (43.22 ± 17.47) and maltose+MLE (49.23 ± 22.39), intermediate for maltodextrin+MLE (75.90 ± 26.01), and higher for glucose+MLE (91.88 ± 27.24). MLE reduced the GIs for maltose, sucrose, maltodextrin, and glucose by 53.11%, 33.51%, 31.00%, and 8.12%, respectively. MLE was well tolerated. Coconsumption of MLE with sucrose, maltose, or maltodextrin can reduce the GI values of these carbohydrates. Chinese Clinical Trial Registry Platform, no. ChiCTR-IPR-15006484. Registered on May 28, 2015.</description><identifier>ISSN: 0025-7974</identifier><identifier>EISSN: 1536-5964</identifier><identifier>DOI: 10.1097/MD.0000000000011996</identifier><identifier>PMID: 30142838</identifier><language>eng</language><publisher>United States: The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved</publisher><subject>Adult ; Blood Glucose - drug effects ; Clinical Trial/Experimental Study ; Cross-Over Studies ; Dietary Carbohydrates - administration &amp; dosage ; Female ; Glucose - administration &amp; dosage ; Glycemic Index - drug effects ; Humans ; Hyperglycemia - blood ; Hyperglycemia - drug therapy ; Hypoglycemic Agents - pharmacology ; Male ; Maltose - administration &amp; dosage ; Morus - chemistry ; Plant Extracts - pharmacology ; Plant Leaves - chemistry ; Polysaccharides - administration &amp; dosage ; Postprandial Period ; Sucrose - administration &amp; dosage ; Young Adult</subject><ispartof>Medicine (Baltimore), 2018-08, Vol.97 (34), p.e11996-e11996</ispartof><rights>The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved.</rights><rights>Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5660-3c887471b5e51faa5688d78674a72756657d70edfa412bc53a271e2ee0add7233</citedby><cites>FETCH-LOGICAL-c5660-3c887471b5e51faa5688d78674a72756657d70edfa412bc53a271e2ee0add7233</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6113008/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6113008/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30142838$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Ruihua</creatorcontrib><creatorcontrib>Li, Yanfen</creatorcontrib><creatorcontrib>Mu, Wei</creatorcontrib><creatorcontrib>Li, Ziqiang</creatorcontrib><creatorcontrib>Sun, Jinxia</creatorcontrib><creatorcontrib>Wang, Baohe</creatorcontrib><creatorcontrib>Zhong, Zhong</creatorcontrib><creatorcontrib>Luo, Xiuzhen</creatorcontrib><creatorcontrib>Xie, Chen</creatorcontrib><creatorcontrib>Huang, Yuhong</creatorcontrib><title>Mulberry leaf extract reduces the glycemic indexes of four common dietary carbohydrates</title><title>Medicine (Baltimore)</title><addtitle>Medicine (Baltimore)</addtitle><description>1-Deoxynojirimycin (DNJ), a component of mulberry leaf extract (MLE), reduces postprandial hyperglycemia by inhibiting intestinal a-glycosidase. The aim of this exploratory study was to investigate the effects of MLE on the glycemic indexes (GI) of common dietary carbohydrates. This single-center, randomized, open-label, 7-cycle self-controlled crossover study enrolled 15 healthy volunteers at the National Drug Clinical Trial Institution, Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine (June 2014 to December 2014). The participants were randomized to receive glucose (3 occasions), glucose+MLE, sucrose+MLE, maltose+MLE, and maltodextrin+MLE orally during 7 visits (every 3 days). Blood glucose level was tested at 15 minutes before and at 15, 30, 45, 60, 90, and 120 minutes after carbohydrate intake. The GI of each carbohydrate relative to glucose (GI = 100) was calculated using the incremental area under the curve method. Safety was assessed at each visit. All participants completed the protocol. After carbohydrate ingestion, blood glucose level peaked at 30 minutes (glucose, glucose+MLE, sucrose+MLE, and maltose+MLE) or 45 minutes (maltodextrin+MLE) before returning to preprandial levels at 120 minutes. At 30 minutes, the change in blood glucose level was lower for sucrose+MLE, maltose+MLE, and maltodextrin+MLE than for glucose or glucose+MLE (P &lt; .05). GI was lowest for sucrose+MLE (43.22 ± 17.47) and maltose+MLE (49.23 ± 22.39), intermediate for maltodextrin+MLE (75.90 ± 26.01), and higher for glucose+MLE (91.88 ± 27.24). MLE reduced the GIs for maltose, sucrose, maltodextrin, and glucose by 53.11%, 33.51%, 31.00%, and 8.12%, respectively. MLE was well tolerated. Coconsumption of MLE with sucrose, maltose, or maltodextrin can reduce the GI values of these carbohydrates. Chinese Clinical Trial Registry Platform, no. ChiCTR-IPR-15006484. 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The aim of this exploratory study was to investigate the effects of MLE on the glycemic indexes (GI) of common dietary carbohydrates. This single-center, randomized, open-label, 7-cycle self-controlled crossover study enrolled 15 healthy volunteers at the National Drug Clinical Trial Institution, Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine (June 2014 to December 2014). The participants were randomized to receive glucose (3 occasions), glucose+MLE, sucrose+MLE, maltose+MLE, and maltodextrin+MLE orally during 7 visits (every 3 days). Blood glucose level was tested at 15 minutes before and at 15, 30, 45, 60, 90, and 120 minutes after carbohydrate intake. The GI of each carbohydrate relative to glucose (GI = 100) was calculated using the incremental area under the curve method. Safety was assessed at each visit. All participants completed the protocol. After carbohydrate ingestion, blood glucose level peaked at 30 minutes (glucose, glucose+MLE, sucrose+MLE, and maltose+MLE) or 45 minutes (maltodextrin+MLE) before returning to preprandial levels at 120 minutes. At 30 minutes, the change in blood glucose level was lower for sucrose+MLE, maltose+MLE, and maltodextrin+MLE than for glucose or glucose+MLE (P &lt; .05). GI was lowest for sucrose+MLE (43.22 ± 17.47) and maltose+MLE (49.23 ± 22.39), intermediate for maltodextrin+MLE (75.90 ± 26.01), and higher for glucose+MLE (91.88 ± 27.24). MLE reduced the GIs for maltose, sucrose, maltodextrin, and glucose by 53.11%, 33.51%, 31.00%, and 8.12%, respectively. MLE was well tolerated. Coconsumption of MLE with sucrose, maltose, or maltodextrin can reduce the GI values of these carbohydrates. Chinese Clinical Trial Registry Platform, no. ChiCTR-IPR-15006484. Registered on May 28, 2015.</abstract><cop>United States</cop><pub>The Authors. Published by Wolters Kluwer Health, Inc. All rights reserved</pub><pmid>30142838</pmid><doi>10.1097/MD.0000000000011996</doi><oa>free_for_read</oa></addata></record>
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subjects Adult
Blood Glucose - drug effects
Clinical Trial/Experimental Study
Cross-Over Studies
Dietary Carbohydrates - administration & dosage
Female
Glucose - administration & dosage
Glycemic Index - drug effects
Humans
Hyperglycemia - blood
Hyperglycemia - drug therapy
Hypoglycemic Agents - pharmacology
Male
Maltose - administration & dosage
Morus - chemistry
Plant Extracts - pharmacology
Plant Leaves - chemistry
Polysaccharides - administration & dosage
Postprandial Period
Sucrose - administration & dosage
Young Adult
title Mulberry leaf extract reduces the glycemic indexes of four common dietary carbohydrates
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