Inhibition of α-Glucosidase, Intestinal Glucose Absorption, and Antidiabetic Properties by Caralluma europaea
Many medicinal plants around the world are used for therapeutic purposes against several diseases, including diabetes mellitus. Due to their composition of natural substances that are effective and do not represent side effects for users, unlike synthetic drugs, in this study, we investigated the in...
Gespeichert in:
Veröffentlicht in: | Evidence-based complementary and alternative medicine 2018-01, Vol.2018 (2018), p.1-8 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 8 |
---|---|
container_issue | 2018 |
container_start_page | 1 |
container_title | Evidence-based complementary and alternative medicine |
container_volume | 2018 |
creator | Bnouham, Mohamed Aziz, Mohammed Ziyyat, A. Mekhfi, H. Bouhrim, Mohamed Bouknana, Saliha Zahidi, Touda Ouassou, Hayat Legssyer, A. |
description | Many medicinal plants around the world are used for therapeutic purposes against several diseases, including diabetes mellitus. Due to their composition of natural substances that are effective and do not represent side effects for users, unlike synthetic drugs, in this study, we investigated the inhibitory effect of Caralluma europaea (CE) on α-glucosidase activity in vitro; then the kinetics of the enzyme were studied with increasing concentrations of sucrose in order to determine the inhibition type of the enzyme. In addition, this effect of Caralluma europaea (CE) was confirmed in vivo using rats as an experimental animal model. Among the five fractions of CE, only the ethyl acetate fraction of C. europaea (EACe) induced a significant inhibition of α-glucosidase and its inhibition mode was competitive. The in vivo studies were conducted on mice and rats using glucose and sucrose as a substrate, respectively, to determine the oral glucose tolerance test (OGTT). The results obtained showed that the EACe and the aqueous extract of C. europaea (AECe) have significantly reduced the postprandial hyperglycemia after sucrose and glucose loading in normal and diabetic rats. AECe, also, significantly decreased intestinal glucose absorption, in situ. The results obtained showed that Caralluma europaea has a significant antihyperglycemic activity, which could be due to the inhibition of α-glucosidase activity and enteric absorption of glucose. |
doi_str_mv | 10.1155/2018/9589472 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6136516</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2111153940</sourcerecordid><originalsourceid>FETCH-LOGICAL-c471t-ae7b85b1a695a05cda43228d3527a5d63f04d5006f26f7688d39764d26714d6d3</originalsourceid><addsrcrecordid>eNqNkc1q3DAUhUVoaH7aXdZFkE0h40aS9WNvAsPQpAOBdtFCd-LakjsKHmkq2Q15rLxInykyM520WVUbCZ1Ph6N7EDqj5AOlQlwyQqvLWlQ1V-wAHVPFacFZVb3an9X3I3SS0h0hrFZKvUZHJWGZYPUx8ku_co0bXPA4dPj3Y3HTj21IzkCyM7z0g02D89Dj7b3F8yaFuJkezDB4g-d-cMZBYwfX4i8xbGwcnE24ecALiND34xqwHbMAFt6gww76ZN_u9lP07frj18Wn4vbzzXIxvy1aruhQgFVNJRoKshZARGuAlzmxKQVTIIwsO8KNIER2THZKVlmpleSGSUW5kaY8RVdb383YrK1prR9yFL2Jbg3xQQdw-l_Fu5X-EX5pSUspqMwG73cGMfwc8wz02qXW9j14G8akGc1LlDUnGT1_gd6FMeaRTRShjOZiJmq2pdoYUoq224ehRE9F6qlIvSsy4-_-_sAe_tNcBi62wMp5A_fuP-1sZmwHzzQVsmaifAKcsbDU</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2101214720</pqid></control><display><type>article</type><title>Inhibition of α-Glucosidase, Intestinal Glucose Absorption, and Antidiabetic Properties by Caralluma europaea</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central Open Access</source><source>Wiley Online Library Open Access</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Bnouham, Mohamed ; Aziz, Mohammed ; Ziyyat, A. ; Mekhfi, H. ; Bouhrim, Mohamed ; Bouknana, Saliha ; Zahidi, Touda ; Ouassou, Hayat ; Legssyer, A.</creator><contributor>Harris, Cory S. ; Cory S Harris</contributor><creatorcontrib>Bnouham, Mohamed ; Aziz, Mohammed ; Ziyyat, A. ; Mekhfi, H. ; Bouhrim, Mohamed ; Bouknana, Saliha ; Zahidi, Touda ; Ouassou, Hayat ; Legssyer, A. ; Harris, Cory S. ; Cory S Harris</creatorcontrib><description>Many medicinal plants around the world are used for therapeutic purposes against several diseases, including diabetes mellitus. Due to their composition of natural substances that are effective and do not represent side effects for users, unlike synthetic drugs, in this study, we investigated the inhibitory effect of Caralluma europaea (CE) on α-glucosidase activity in vitro; then the kinetics of the enzyme were studied with increasing concentrations of sucrose in order to determine the inhibition type of the enzyme. In addition, this effect of Caralluma europaea (CE) was confirmed in vivo using rats as an experimental animal model. Among the five fractions of CE, only the ethyl acetate fraction of C. europaea (EACe) induced a significant inhibition of α-glucosidase and its inhibition mode was competitive. The in vivo studies were conducted on mice and rats using glucose and sucrose as a substrate, respectively, to determine the oral glucose tolerance test (OGTT). The results obtained showed that the EACe and the aqueous extract of C. europaea (AECe) have significantly reduced the postprandial hyperglycemia after sucrose and glucose loading in normal and diabetic rats. AECe, also, significantly decreased intestinal glucose absorption, in situ. The results obtained showed that Caralluma europaea has a significant antihyperglycemic activity, which could be due to the inhibition of α-glucosidase activity and enteric absorption of glucose.</description><identifier>ISSN: 1741-427X</identifier><identifier>EISSN: 1741-4288</identifier><identifier>DOI: 10.1155/2018/9589472</identifier><identifier>PMID: 30228829</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Absorption ; Acetic acid ; Antidiabetics ; Chemical compounds ; Chloride ; Chronic illnesses ; Diabetes ; Diabetes mellitus ; Ethyl acetate ; Glucose ; Glucose tolerance ; Glucosidase ; Herbal medicine ; Hyperglycemia ; Inhibition ; Insulin resistance ; Intestine ; Kinetics ; Medicinal plants ; Metabolism ; Pharmaceuticals ; Pharmacy ; Rats ; Side effects ; Sucrose ; Sugar ; Therapeutic applications ; α-Glucosidase</subject><ispartof>Evidence-based complementary and alternative medicine, 2018-01, Vol.2018 (2018), p.1-8</ispartof><rights>Copyright © 2018 Hayat Ouassou et al.</rights><rights>Copyright © 2018 Hayat Ouassou et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2018 Hayat Ouassou et al. 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-ae7b85b1a695a05cda43228d3527a5d63f04d5006f26f7688d39764d26714d6d3</citedby><cites>FETCH-LOGICAL-c471t-ae7b85b1a695a05cda43228d3527a5d63f04d5006f26f7688d39764d26714d6d3</cites><orcidid>0000-0001-6384-2537 ; 0000-0002-3006-2523 ; 0000-0003-1295-9588 ; 0000-0001-9473-1290</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6136516/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6136516/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30228829$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Harris, Cory S.</contributor><contributor>Cory S Harris</contributor><creatorcontrib>Bnouham, Mohamed</creatorcontrib><creatorcontrib>Aziz, Mohammed</creatorcontrib><creatorcontrib>Ziyyat, A.</creatorcontrib><creatorcontrib>Mekhfi, H.</creatorcontrib><creatorcontrib>Bouhrim, Mohamed</creatorcontrib><creatorcontrib>Bouknana, Saliha</creatorcontrib><creatorcontrib>Zahidi, Touda</creatorcontrib><creatorcontrib>Ouassou, Hayat</creatorcontrib><creatorcontrib>Legssyer, A.</creatorcontrib><title>Inhibition of α-Glucosidase, Intestinal Glucose Absorption, and Antidiabetic Properties by Caralluma europaea</title><title>Evidence-based complementary and alternative medicine</title><addtitle>Evid Based Complement Alternat Med</addtitle><description>Many medicinal plants around the world are used for therapeutic purposes against several diseases, including diabetes mellitus. Due to their composition of natural substances that are effective and do not represent side effects for users, unlike synthetic drugs, in this study, we investigated the inhibitory effect of Caralluma europaea (CE) on α-glucosidase activity in vitro; then the kinetics of the enzyme were studied with increasing concentrations of sucrose in order to determine the inhibition type of the enzyme. In addition, this effect of Caralluma europaea (CE) was confirmed in vivo using rats as an experimental animal model. Among the five fractions of CE, only the ethyl acetate fraction of C. europaea (EACe) induced a significant inhibition of α-glucosidase and its inhibition mode was competitive. The in vivo studies were conducted on mice and rats using glucose and sucrose as a substrate, respectively, to determine the oral glucose tolerance test (OGTT). The results obtained showed that the EACe and the aqueous extract of C. europaea (AECe) have significantly reduced the postprandial hyperglycemia after sucrose and glucose loading in normal and diabetic rats. AECe, also, significantly decreased intestinal glucose absorption, in situ. The results obtained showed that Caralluma europaea has a significant antihyperglycemic activity, which could be due to the inhibition of α-glucosidase activity and enteric absorption of glucose.</description><subject>Absorption</subject><subject>Acetic acid</subject><subject>Antidiabetics</subject><subject>Chemical compounds</subject><subject>Chloride</subject><subject>Chronic illnesses</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Ethyl acetate</subject><subject>Glucose</subject><subject>Glucose tolerance</subject><subject>Glucosidase</subject><subject>Herbal medicine</subject><subject>Hyperglycemia</subject><subject>Inhibition</subject><subject>Insulin resistance</subject><subject>Intestine</subject><subject>Kinetics</subject><subject>Medicinal plants</subject><subject>Metabolism</subject><subject>Pharmaceuticals</subject><subject>Pharmacy</subject><subject>Rats</subject><subject>Side effects</subject><subject>Sucrose</subject><subject>Sugar</subject><subject>Therapeutic applications</subject><subject>α-Glucosidase</subject><issn>1741-427X</issn><issn>1741-4288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNkc1q3DAUhUVoaH7aXdZFkE0h40aS9WNvAsPQpAOBdtFCd-LakjsKHmkq2Q15rLxInykyM520WVUbCZ1Ph6N7EDqj5AOlQlwyQqvLWlQ1V-wAHVPFacFZVb3an9X3I3SS0h0hrFZKvUZHJWGZYPUx8ku_co0bXPA4dPj3Y3HTj21IzkCyM7z0g02D89Dj7b3F8yaFuJkezDB4g-d-cMZBYwfX4i8xbGwcnE24ecALiND34xqwHbMAFt6gww76ZN_u9lP07frj18Wn4vbzzXIxvy1aruhQgFVNJRoKshZARGuAlzmxKQVTIIwsO8KNIER2THZKVlmpleSGSUW5kaY8RVdb383YrK1prR9yFL2Jbg3xQQdw-l_Fu5X-EX5pSUspqMwG73cGMfwc8wz02qXW9j14G8akGc1LlDUnGT1_gd6FMeaRTRShjOZiJmq2pdoYUoq224ehRE9F6qlIvSsy4-_-_sAe_tNcBi62wMp5A_fuP-1sZmwHzzQVsmaifAKcsbDU</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Bnouham, Mohamed</creator><creator>Aziz, Mohammed</creator><creator>Ziyyat, A.</creator><creator>Mekhfi, H.</creator><creator>Bouhrim, Mohamed</creator><creator>Bouknana, Saliha</creator><creator>Zahidi, Touda</creator><creator>Ouassou, Hayat</creator><creator>Legssyer, A.</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88G</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</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>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M2M</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6384-2537</orcidid><orcidid>https://orcid.org/0000-0002-3006-2523</orcidid><orcidid>https://orcid.org/0000-0003-1295-9588</orcidid><orcidid>https://orcid.org/0000-0001-9473-1290</orcidid></search><sort><creationdate>20180101</creationdate><title>Inhibition of α-Glucosidase, Intestinal Glucose Absorption, and Antidiabetic Properties by Caralluma europaea</title><author>Bnouham, Mohamed ; Aziz, Mohammed ; Ziyyat, A. ; Mekhfi, H. ; Bouhrim, Mohamed ; Bouknana, Saliha ; Zahidi, Touda ; Ouassou, Hayat ; Legssyer, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c471t-ae7b85b1a695a05cda43228d3527a5d63f04d5006f26f7688d39764d26714d6d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Absorption</topic><topic>Acetic acid</topic><topic>Antidiabetics</topic><topic>Chemical compounds</topic><topic>Chloride</topic><topic>Chronic illnesses</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Ethyl acetate</topic><topic>Glucose</topic><topic>Glucose tolerance</topic><topic>Glucosidase</topic><topic>Herbal medicine</topic><topic>Hyperglycemia</topic><topic>Inhibition</topic><topic>Insulin resistance</topic><topic>Intestine</topic><topic>Kinetics</topic><topic>Medicinal plants</topic><topic>Metabolism</topic><topic>Pharmaceuticals</topic><topic>Pharmacy</topic><topic>Rats</topic><topic>Side effects</topic><topic>Sucrose</topic><topic>Sugar</topic><topic>Therapeutic applications</topic><topic>α-Glucosidase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bnouham, Mohamed</creatorcontrib><creatorcontrib>Aziz, Mohammed</creatorcontrib><creatorcontrib>Ziyyat, A.</creatorcontrib><creatorcontrib>Mekhfi, H.</creatorcontrib><creatorcontrib>Bouhrim, Mohamed</creatorcontrib><creatorcontrib>Bouknana, Saliha</creatorcontrib><creatorcontrib>Zahidi, Touda</creatorcontrib><creatorcontrib>Ouassou, Hayat</creatorcontrib><creatorcontrib>Legssyer, A.</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest Psychology</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content 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>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Evidence-based complementary and alternative medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bnouham, Mohamed</au><au>Aziz, Mohammed</au><au>Ziyyat, A.</au><au>Mekhfi, H.</au><au>Bouhrim, Mohamed</au><au>Bouknana, Saliha</au><au>Zahidi, Touda</au><au>Ouassou, Hayat</au><au>Legssyer, A.</au><au>Harris, Cory S.</au><au>Cory S Harris</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibition of α-Glucosidase, Intestinal Glucose Absorption, and Antidiabetic Properties by Caralluma europaea</atitle><jtitle>Evidence-based complementary and alternative medicine</jtitle><addtitle>Evid Based Complement Alternat Med</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>2018</volume><issue>2018</issue><spage>1</spage><epage>8</epage><pages>1-8</pages><issn>1741-427X</issn><eissn>1741-4288</eissn><abstract>Many medicinal plants around the world are used for therapeutic purposes against several diseases, including diabetes mellitus. Due to their composition of natural substances that are effective and do not represent side effects for users, unlike synthetic drugs, in this study, we investigated the inhibitory effect of Caralluma europaea (CE) on α-glucosidase activity in vitro; then the kinetics of the enzyme were studied with increasing concentrations of sucrose in order to determine the inhibition type of the enzyme. In addition, this effect of Caralluma europaea (CE) was confirmed in vivo using rats as an experimental animal model. Among the five fractions of CE, only the ethyl acetate fraction of C. europaea (EACe) induced a significant inhibition of α-glucosidase and its inhibition mode was competitive. The in vivo studies were conducted on mice and rats using glucose and sucrose as a substrate, respectively, to determine the oral glucose tolerance test (OGTT). The results obtained showed that the EACe and the aqueous extract of C. europaea (AECe) have significantly reduced the postprandial hyperglycemia after sucrose and glucose loading in normal and diabetic rats. AECe, also, significantly decreased intestinal glucose absorption, in situ. The results obtained showed that Caralluma europaea has a significant antihyperglycemic activity, which could be due to the inhibition of α-glucosidase activity and enteric absorption of glucose.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>30228829</pmid><doi>10.1155/2018/9589472</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-6384-2537</orcidid><orcidid>https://orcid.org/0000-0002-3006-2523</orcidid><orcidid>https://orcid.org/0000-0003-1295-9588</orcidid><orcidid>https://orcid.org/0000-0001-9473-1290</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1741-427X |
ispartof | Evidence-based complementary and alternative medicine, 2018-01, Vol.2018 (2018), p.1-8 |
issn | 1741-427X 1741-4288 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6136516 |
source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; Wiley Online Library Open Access; PubMed Central; Alma/SFX Local Collection |
subjects | Absorption Acetic acid Antidiabetics Chemical compounds Chloride Chronic illnesses Diabetes Diabetes mellitus Ethyl acetate Glucose Glucose tolerance Glucosidase Herbal medicine Hyperglycemia Inhibition Insulin resistance Intestine Kinetics Medicinal plants Metabolism Pharmaceuticals Pharmacy Rats Side effects Sucrose Sugar Therapeutic applications α-Glucosidase |
title | Inhibition of α-Glucosidase, Intestinal Glucose Absorption, and Antidiabetic Properties by Caralluma europaea |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T18%3A50%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Inhibition%20of%20%CE%B1-Glucosidase,%20Intestinal%20Glucose%20Absorption,%20and%20Antidiabetic%20Properties%20by%20Caralluma%20europaea&rft.jtitle=Evidence-based%20complementary%20and%20alternative%20medicine&rft.au=Bnouham,%20Mohamed&rft.date=2018-01-01&rft.volume=2018&rft.issue=2018&rft.spage=1&rft.epage=8&rft.pages=1-8&rft.issn=1741-427X&rft.eissn=1741-4288&rft_id=info:doi/10.1155/2018/9589472&rft_dat=%3Cproquest_pubme%3E2111153940%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2101214720&rft_id=info:pmid/30228829&rfr_iscdi=true |