In Vitro Studies to Assess the α-Glucosidase Inhibitory Activity and Insulin Secretion Effect of Isorhamnetin 3-<i<O</i<-Glucoside and Quercetin 3-<i<O</i<-Glucoside Isolated from <i<Salicornia herbacea</i<
In this study, we examined the effect of ethanolic extract of <i<Salicornia herbacea</i< (ESH), isorhamnetin 3-<i<O</i<-glucoside (I3G), quercetin 3-<i<O</i<-glucoside (Q3G), quercetin, and isorhamnetin on α-glucosidase activity and glucose-stimulated insulin secr...
Ausführliche Beschreibung
Autor*in: |
Dahae Lee [verfasserIn] Jun Yeon Park [verfasserIn] Sanghyun Lee [verfasserIn] Ki Sung Kang [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2021 |
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Schlagwörter: |
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Übergeordnetes Werk: |
In: Processes - MDPI AG, 2013, 9(2021), 483, p 483 |
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Übergeordnetes Werk: |
volume:9 ; year:2021 ; number:483, p 483 |
Links: |
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DOI / URN: |
10.3390/pr9030483 |
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Katalog-ID: |
DOAJ024008419 |
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10.3390/pr9030483 doi (DE-627)DOAJ024008419 (DE-599)DOAJ8ff830a10285456e9c8db9e120c2c01d DE-627 ger DE-627 rakwb eng TP1-1185 QD1-999 Dahae Lee verfasserin aut In Vitro Studies to Assess the α-Glucosidase Inhibitory Activity and Insulin Secretion Effect of Isorhamnetin 3-<i<O</i<-Glucoside and Quercetin 3-<i<O</i<-Glucoside Isolated from <i<Salicornia herbacea</i< 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier In this study, we examined the effect of ethanolic extract of <i<Salicornia herbacea</i< (ESH), isorhamnetin 3-<i<O</i<-glucoside (I3G), quercetin 3-<i<O</i<-glucoside (Q3G), quercetin, and isorhamnetin on α-glucosidase activity and glucose-stimulated insulin secretion (GSIS) in insulin-secreting rat insulinoma (INS-1) cells. A portion of the ethyl acetate fraction of ESH was chromatographed on a silica gel by a gradient elution with chloroform and methanol to provide Q3G and I3G. ESH, Q3G, and quercetin inhibited α-glucosidase activity, and quercetin (IC<sub<50</sub< value was 29.47 ± 3.36 μM) inhibited the activity more effectively than Q3G. We further demonstrated that ESH, Q3G, quercetin, I3G, and isorhamnetin promote GSIS in INS-1 pancreatic β-cells without inducing cytotoxicity. Among them, I3G was the most effective in enhancing GSIS. I3G enhanced the phosphorylation of total extracellular signal-regulated kinase (ERK), insulin receptor substrate-2 (IRS-2), phosphatidylinositol 3-kinase (PI3K), Akt, and activated pancreatic and duodenal homeobox-1 (PDX-1), which are associated with insulin secretion and β-cell function. As components of ESH, Q3G has the potential to regulate blood glucose by inhibiting α-glucosidase activity, and I3G enhances the insulin secretion, but its bioavailability should be considered in determining biological importance. <i<Salicornia herbacea</i< α-Glucosidase Insulin ERK PI3K AKT Chemical technology Chemistry Jun Yeon Park verfasserin aut Sanghyun Lee verfasserin aut Ki Sung Kang verfasserin aut In Processes MDPI AG, 2013 9(2021), 483, p 483 (DE-627)750371439 (DE-600)2720994-5 22279717 nnns volume:9 year:2021 number:483, p 483 https://doi.org/10.3390/pr9030483 kostenfrei https://doaj.org/article/8ff830a10285456e9c8db9e120c2c01d kostenfrei https://www.mdpi.com/2227-9717/9/3/483 kostenfrei https://doaj.org/toc/2227-9717 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2021 483, p 483 |
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TP1-1185 QD1-999 In Vitro Studies to Assess the α-Glucosidase Inhibitory Activity and Insulin Secretion Effect of Isorhamnetin 3-<i<O</i<-Glucoside and Quercetin 3-<i<O</i<-Glucoside Isolated from <i<Salicornia herbacea</i< <i<Salicornia herbacea</i< α-Glucosidase Insulin ERK PI3K AKT |
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In Vitro Studies to Assess the α-Glucosidase Inhibitory Activity and Insulin Secretion Effect of Isorhamnetin 3-<i<O</i<-Glucoside and Quercetin 3-<i<O</i<-Glucoside Isolated from <i<Salicornia herbacea</i< |
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In Vitro Studies to Assess the α-Glucosidase Inhibitory Activity and Insulin Secretion Effect of Isorhamnetin 3-<i<O</i<-Glucoside and Quercetin 3-<i<O</i<-Glucoside Isolated from <i<Salicornia herbacea</i< |
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in vitro studies to assess the α-glucosidase inhibitory activity and insulin secretion effect of isorhamnetin 3-<i<o</i<-glucoside and quercetin 3-<i<o</i<-glucoside isolated from <i<salicornia herbacea</i< |
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In Vitro Studies to Assess the α-Glucosidase Inhibitory Activity and Insulin Secretion Effect of Isorhamnetin 3-<i<O</i<-Glucoside and Quercetin 3-<i<O</i<-Glucoside Isolated from <i<Salicornia herbacea</i< |
abstract |
In this study, we examined the effect of ethanolic extract of <i<Salicornia herbacea</i< (ESH), isorhamnetin 3-<i<O</i<-glucoside (I3G), quercetin 3-<i<O</i<-glucoside (Q3G), quercetin, and isorhamnetin on α-glucosidase activity and glucose-stimulated insulin secretion (GSIS) in insulin-secreting rat insulinoma (INS-1) cells. A portion of the ethyl acetate fraction of ESH was chromatographed on a silica gel by a gradient elution with chloroform and methanol to provide Q3G and I3G. ESH, Q3G, and quercetin inhibited α-glucosidase activity, and quercetin (IC<sub<50</sub< value was 29.47 ± 3.36 μM) inhibited the activity more effectively than Q3G. We further demonstrated that ESH, Q3G, quercetin, I3G, and isorhamnetin promote GSIS in INS-1 pancreatic β-cells without inducing cytotoxicity. Among them, I3G was the most effective in enhancing GSIS. I3G enhanced the phosphorylation of total extracellular signal-regulated kinase (ERK), insulin receptor substrate-2 (IRS-2), phosphatidylinositol 3-kinase (PI3K), Akt, and activated pancreatic and duodenal homeobox-1 (PDX-1), which are associated with insulin secretion and β-cell function. As components of ESH, Q3G has the potential to regulate blood glucose by inhibiting α-glucosidase activity, and I3G enhances the insulin secretion, but its bioavailability should be considered in determining biological importance. |
abstractGer |
In this study, we examined the effect of ethanolic extract of <i<Salicornia herbacea</i< (ESH), isorhamnetin 3-<i<O</i<-glucoside (I3G), quercetin 3-<i<O</i<-glucoside (Q3G), quercetin, and isorhamnetin on α-glucosidase activity and glucose-stimulated insulin secretion (GSIS) in insulin-secreting rat insulinoma (INS-1) cells. A portion of the ethyl acetate fraction of ESH was chromatographed on a silica gel by a gradient elution with chloroform and methanol to provide Q3G and I3G. ESH, Q3G, and quercetin inhibited α-glucosidase activity, and quercetin (IC<sub<50</sub< value was 29.47 ± 3.36 μM) inhibited the activity more effectively than Q3G. We further demonstrated that ESH, Q3G, quercetin, I3G, and isorhamnetin promote GSIS in INS-1 pancreatic β-cells without inducing cytotoxicity. Among them, I3G was the most effective in enhancing GSIS. I3G enhanced the phosphorylation of total extracellular signal-regulated kinase (ERK), insulin receptor substrate-2 (IRS-2), phosphatidylinositol 3-kinase (PI3K), Akt, and activated pancreatic and duodenal homeobox-1 (PDX-1), which are associated with insulin secretion and β-cell function. As components of ESH, Q3G has the potential to regulate blood glucose by inhibiting α-glucosidase activity, and I3G enhances the insulin secretion, but its bioavailability should be considered in determining biological importance. |
abstract_unstemmed |
In this study, we examined the effect of ethanolic extract of <i<Salicornia herbacea</i< (ESH), isorhamnetin 3-<i<O</i<-glucoside (I3G), quercetin 3-<i<O</i<-glucoside (Q3G), quercetin, and isorhamnetin on α-glucosidase activity and glucose-stimulated insulin secretion (GSIS) in insulin-secreting rat insulinoma (INS-1) cells. A portion of the ethyl acetate fraction of ESH was chromatographed on a silica gel by a gradient elution with chloroform and methanol to provide Q3G and I3G. ESH, Q3G, and quercetin inhibited α-glucosidase activity, and quercetin (IC<sub<50</sub< value was 29.47 ± 3.36 μM) inhibited the activity more effectively than Q3G. We further demonstrated that ESH, Q3G, quercetin, I3G, and isorhamnetin promote GSIS in INS-1 pancreatic β-cells without inducing cytotoxicity. Among them, I3G was the most effective in enhancing GSIS. I3G enhanced the phosphorylation of total extracellular signal-regulated kinase (ERK), insulin receptor substrate-2 (IRS-2), phosphatidylinositol 3-kinase (PI3K), Akt, and activated pancreatic and duodenal homeobox-1 (PDX-1), which are associated with insulin secretion and β-cell function. As components of ESH, Q3G has the potential to regulate blood glucose by inhibiting α-glucosidase activity, and I3G enhances the insulin secretion, but its bioavailability should be considered in determining biological importance. |
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In Vitro Studies to Assess the α-Glucosidase Inhibitory Activity and Insulin Secretion Effect of Isorhamnetin 3-<i<O</i<-Glucoside and Quercetin 3-<i<O</i<-Glucoside Isolated from <i<Salicornia herbacea</i< |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">DOAJ024008419</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230307072023.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">230226s2021 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.3390/pr9030483</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)DOAJ024008419</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)DOAJ8ff830a10285456e9c8db9e120c2c01d</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">TP1-1185</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">QD1-999</subfield></datafield><datafield tag="100" ind1="0" ind2=" "><subfield code="a">Dahae Lee</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">In Vitro Studies to Assess the α-Glucosidase Inhibitory Activity and Insulin Secretion Effect of Isorhamnetin 3-<i<O</i<-Glucoside and Quercetin 3-<i<O</i<-Glucoside Isolated from <i<Salicornia herbacea</i<</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2021</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">In this study, we examined the effect of ethanolic extract of <i<Salicornia herbacea</i< (ESH), isorhamnetin 3-<i<O</i<-glucoside (I3G), quercetin 3-<i<O</i<-glucoside (Q3G), quercetin, and isorhamnetin on α-glucosidase activity and glucose-stimulated insulin secretion (GSIS) in insulin-secreting rat insulinoma (INS-1) cells. A portion of the ethyl acetate fraction of ESH was chromatographed on a silica gel by a gradient elution with chloroform and methanol to provide Q3G and I3G. ESH, Q3G, and quercetin inhibited α-glucosidase activity, and quercetin (IC<sub<50</sub< value was 29.47 ± 3.36 μM) inhibited the activity more effectively than Q3G. We further demonstrated that ESH, Q3G, quercetin, I3G, and isorhamnetin promote GSIS in INS-1 pancreatic β-cells without inducing cytotoxicity. Among them, I3G was the most effective in enhancing GSIS. I3G enhanced the phosphorylation of total extracellular signal-regulated kinase (ERK), insulin receptor substrate-2 (IRS-2), phosphatidylinositol 3-kinase (PI3K), Akt, and activated pancreatic and duodenal homeobox-1 (PDX-1), which are associated with insulin secretion and β-cell function. As components of ESH, Q3G has the potential to regulate blood glucose by inhibiting α-glucosidase activity, and I3G enhances the insulin secretion, but its bioavailability should be considered in determining biological importance.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a"><i<Salicornia herbacea</i<</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">α-Glucosidase</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Insulin</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">ERK</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">PI3K</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">AKT</subfield></datafield><datafield tag="653" ind1=" " ind2="0"><subfield code="a">Chemical technology</subfield></datafield><datafield tag="653" ind1=" " ind2="0"><subfield code="a">Chemistry</subfield></datafield><datafield 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