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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Evidence-based complementary and alternative medicine 2018-01, Vol.2018 (2018), p.1-8
Hauptverfasser: Bnouham, Mohamed, Aziz, Mohammed, Ziyyat, A., Mekhfi, H., Bouhrim, Mohamed, Bouknana, Saliha, Zahidi, Touda, Ouassou, Hayat, Legssyer, A.
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 &amp; Allied Health Database</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>ProQuest Psychology</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; 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