Inhibitory Activities of Medicinal Mushrooms on Alpha-Amylase and Alpha-Glucosidase Related To Type 2 Diabetes

dc.contributor.author Deveci, Ebru
dc.contributor.author Çayan, Fatih
dc.contributor.author Çayan, Gülsen Tel
dc.contributor.author Duru, Mehmet Emin
dc.date.accessioned 2021-12-13T10:26:45Z
dc.date.available 2021-12-13T10:26:45Z
dc.date.issued 2021
dc.description.abstract Mushrooms have been used as a primary source of medicines since ancient times due to the presence of bioactive compounds. Enzyme inhibition is an important field of pharmaceutical research that provides insight into the discovery of a large variety of drugs that are useful in treating many diseases. The inhibitory activities of the hexane and methanol extracts of twenty-four medicinal mushrooms on alpha-amylase and alpha-glucosidase enzymes related to type 2 diabetes were evaluated in this study. Among all studied mushroom extracts, C. rutilus hexane extract (IC50: 0.05 +/- 0.01 mg/mL) demonstrated the highest inhibitory activity on alpha-amylase while P. ostreatus hexane (IC50: 0.10 +/- 0.01 mg/mL) showed the highest inhibitory activity on alpha-glucosidase. The hexane extracts of C. rutilus (98.81 +/- 0.01 %), G. adspersum (96.96 +/- 0.47 %), G. sepiarium (96.89 +/- 1.01 %), and S. granulatus (97.74 +/- 0.27 %) displayed higher inhibitory activity on alpha-amylase enzyme than acarbose at 1.00 mg/mL concentration. Also, the hexane extracts of P. ostreatus (IC50: 0.10 +/- 0.01 mg/mL), M. procera (IC50: 0.11 +/- 0.01 mg/mL), P. schweinitzii (IC50: 0.14 +/- 0.01 mg/mL), L. gentianeus (IC50: 0.22 +/- 0.02 mg/mL), P. pini (IC50: 0.22 +/- 0.03 mg/mL) and the methanol extracts of T. pubescens (IC50: 0.12 +/- 0.02 mg/mL) and G. adspersum (IC50: 0.20 +/- 0.04 mg/mL) showed higher inhibitory activity on alpha-glucosidase enzyme than acarbose (IC50: 0.37 +/- 0.01 mg/mL). This study with the reported results supported the use of mushrooms in the pharmaceutical industries as natural antidiabetic agents through key enzyme inhibition. (C) 2020 SAAB. Published by Elsevier B.V. All rights reserved. en_US
dc.identifier.doi 10.1016/j.sajb.2020.09.039
dc.identifier.issn 0254-6299
dc.identifier.issn 1727-9321
dc.identifier.scopus 2-s2.0-85092897899
dc.identifier.uri https://doi.org/10.1016/j.sajb.2020.09.039
dc.identifier.uri https://hdl.handle.net/20.500.13091/452
dc.language.iso en en_US
dc.publisher ELSEVIER en_US
dc.relation.ispartof SOUTH AFRICAN JOURNAL OF BOTANY en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Type 2 Diabetes en_US
dc.subject Alpha-Amylase en_US
dc.subject Alpha-Glucosidase en_US
dc.subject Mushrooms en_US
dc.subject Extract en_US
dc.subject Antidiabetic Properties en_US
dc.subject Antioxidant en_US
dc.subject Peptides en_US
dc.title Inhibitory Activities of Medicinal Mushrooms on Alpha-Amylase and Alpha-Glucosidase Related To Type 2 Diabetes en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Tel-Cayan, Gulsen/0000-0002-1916-7391
gdc.author.scopusid 56089358000
gdc.author.scopusid 56005323200
gdc.author.scopusid 57194732739
gdc.author.scopusid 12789661400
gdc.author.wosid DURU, Mehmet Emin/ABA-2426-2021
gdc.bip.impulseclass C3
gdc.bip.influenceclass C4
gdc.bip.popularityclass C3
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department Fakülteler, Mühendislik ve Doğa Bilimleri Fakültesi, Kimya Mühendisliği Bölümü en_US
gdc.description.endpage 23 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.startpage 19 en_US
gdc.description.volume 137 en_US
gdc.description.wosquality Q2
gdc.identifier.openalex W3093941399
gdc.identifier.wos WOS:000644371800003
gdc.index.type WoS
gdc.index.type Scopus
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gdc.oaire.sciencefields 0106 biological sciences
gdc.oaire.sciencefields 0301 basic medicine
gdc.oaire.sciencefields 03 medical and health sciences
gdc.oaire.sciencefields 01 natural sciences
gdc.openalex.collaboration National
gdc.openalex.fwci 5.59032667
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gdc.opencitations.count 36
gdc.plumx.crossrefcites 36
gdc.plumx.mendeley 81
gdc.plumx.scopuscites 56
gdc.scopus.citedcount 56
gdc.virtual.author Deveci, Ebru
gdc.wos.citedcount 46
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