The beneficial effects of combined grape pomace and omija fruit extracts on hyperglycemia, adiposity and hepatic steatosis in db/db mice: a comparison with major index compounds
This study investigated the effects of combined grape pomace and omija fruit extracts (GO) on diabetes-related metabolic changes in type 2 diabetic db/db mice. The effects of GO were compared with those of a resveratrol and schizandrin mixture (RS), which is a mixture of major components of GO. Mice...
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creator | Cho, Su-Jung Park, Hae-Jin Jung, Un Ju Kim, Hye-Jin Moon, Byoung Seok Choi, Myung-Sook |
description | This study investigated the effects of combined grape pomace and omija fruit extracts (GO) on diabetes-related metabolic changes in type 2 diabetic db/db mice. The effects of GO were compared with those of a resveratrol and schizandrin mixture (RS), which is a mixture of major components of GO. Mice were fed a normal diet with RS (0.005% resveratrol and 0.02% schizandrin in diet, w/w) or GO (0.3% grape pomace ethanol extract and 0.05% omija fruit ethanol extract in diet, w/w) for seven weeks. RS and GO not only lowered the levels of blood and plasma glucose, HbA1c, insulin and homeostasis model assessment of insulin resistance (HOMA-IR) with a simultaneous decrease in hepatic gluconeogenic enzymes activities and adiposity, but also improved preservation of the pancreatic β-cells. Plasma leptin and resistin levels were lower while the plasma adiponectin level was higher in the RS and GO groups than in the control group. Especially, GO increased hepatic glucokinase activity and gene expression and improved hepatic steatosis by elevating fatty acid oxidation compared to RS. These findings suggest that GO ameliorates hyperglycemia, adiposity and hepatic steatosis in type 2 diabetic mice. |
doi_str_mv | 10.3390/ijms151017778 |
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The effects of GO were compared with those of a resveratrol and schizandrin mixture (RS), which is a mixture of major components of GO. Mice were fed a normal diet with RS (0.005% resveratrol and 0.02% schizandrin in diet, w/w) or GO (0.3% grape pomace ethanol extract and 0.05% omija fruit ethanol extract in diet, w/w) for seven weeks. RS and GO not only lowered the levels of blood and plasma glucose, HbA1c, insulin and homeostasis model assessment of insulin resistance (HOMA-IR) with a simultaneous decrease in hepatic gluconeogenic enzymes activities and adiposity, but also improved preservation of the pancreatic β-cells. Plasma leptin and resistin levels were lower while the plasma adiponectin level was higher in the RS and GO groups than in the control group. Especially, GO increased hepatic glucokinase activity and gene expression and improved hepatic steatosis by elevating fatty acid oxidation compared to RS. These findings suggest that GO ameliorates hyperglycemia, adiposity and hepatic steatosis in type 2 diabetic mice.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms151017778</identifier><identifier>PMID: 25272231</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Adiponectin - blood ; Adiposity - drug effects ; Animals ; Biomarkers - blood ; Biomarkers - metabolism ; Blood Glucose - analysis ; Cyclooctanes - pharmacology ; Diabetes Mellitus, Experimental - metabolism ; Diabetes Mellitus, Experimental - pathology ; Fatty Liver - metabolism ; Fatty Liver - pathology ; Fruit - chemistry ; Fruit - metabolism ; Glycated Hemoglobin - analysis ; Hyperglycemia ; Hyperglycemia - metabolism ; Hyperglycemia - pathology ; Insulin - blood ; Leptin - blood ; Lignans - pharmacology ; Liver diseases ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Obese ; Obesity ; Plant Extracts - chemistry ; Plant Extracts - pharmacology ; Polycyclic Compounds - pharmacology ; Polyphenols ; Resistin - blood ; Resveratrol ; Rodents ; Schisandra - chemistry ; Schisandra - metabolism ; Stilbenes - pharmacology ; Vitis - chemistry ; Vitis - metabolism</subject><ispartof>International journal of molecular sciences, 2014-09, Vol.15 (10), p.17778-17789</ispartof><rights>Copyright MDPI AG 2014</rights><rights>2014 by the authors; licensee MDPI, Basel, Switzerland. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-7dcb8265d1e9bea80ebec3d11ea7fa32086c79a0e2d3fb42315553c2af07ea2e3</citedby><cites>FETCH-LOGICAL-c415t-7dcb8265d1e9bea80ebec3d11ea7fa32086c79a0e2d3fb42315553c2af07ea2e3</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/PMC4227189/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227189/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25272231$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cho, Su-Jung</creatorcontrib><creatorcontrib>Park, Hae-Jin</creatorcontrib><creatorcontrib>Jung, Un Ju</creatorcontrib><creatorcontrib>Kim, Hye-Jin</creatorcontrib><creatorcontrib>Moon, Byoung Seok</creatorcontrib><creatorcontrib>Choi, Myung-Sook</creatorcontrib><title>The beneficial effects of combined grape pomace and omija fruit extracts on hyperglycemia, adiposity and hepatic steatosis in db/db mice: a comparison with major index compounds</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>This study investigated the effects of combined grape pomace and omija fruit extracts (GO) on diabetes-related metabolic changes in type 2 diabetic db/db mice. The effects of GO were compared with those of a resveratrol and schizandrin mixture (RS), which is a mixture of major components of GO. Mice were fed a normal diet with RS (0.005% resveratrol and 0.02% schizandrin in diet, w/w) or GO (0.3% grape pomace ethanol extract and 0.05% omija fruit ethanol extract in diet, w/w) for seven weeks. RS and GO not only lowered the levels of blood and plasma glucose, HbA1c, insulin and homeostasis model assessment of insulin resistance (HOMA-IR) with a simultaneous decrease in hepatic gluconeogenic enzymes activities and adiposity, but also improved preservation of the pancreatic β-cells. Plasma leptin and resistin levels were lower while the plasma adiponectin level was higher in the RS and GO groups than in the control group. Especially, GO increased hepatic glucokinase activity and gene expression and improved hepatic steatosis by elevating fatty acid oxidation compared to RS. These findings suggest that GO ameliorates hyperglycemia, adiposity and hepatic steatosis in type 2 diabetic mice.</description><subject>Adiponectin - blood</subject><subject>Adiposity - drug effects</subject><subject>Animals</subject><subject>Biomarkers - blood</subject><subject>Biomarkers - metabolism</subject><subject>Blood Glucose - analysis</subject><subject>Cyclooctanes - pharmacology</subject><subject>Diabetes Mellitus, Experimental - metabolism</subject><subject>Diabetes Mellitus, Experimental - pathology</subject><subject>Fatty Liver - metabolism</subject><subject>Fatty Liver - pathology</subject><subject>Fruit - chemistry</subject><subject>Fruit - metabolism</subject><subject>Glycated Hemoglobin - analysis</subject><subject>Hyperglycemia</subject><subject>Hyperglycemia - metabolism</subject><subject>Hyperglycemia - pathology</subject><subject>Insulin - blood</subject><subject>Leptin - blood</subject><subject>Lignans - pharmacology</subject><subject>Liver diseases</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Obese</subject><subject>Obesity</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - pharmacology</subject><subject>Polycyclic Compounds - pharmacology</subject><subject>Polyphenols</subject><subject>Resistin - blood</subject><subject>Resveratrol</subject><subject>Rodents</subject><subject>Schisandra - chemistry</subject><subject>Schisandra - metabolism</subject><subject>Stilbenes - pharmacology</subject><subject>Vitis - chemistry</subject><subject>Vitis - metabolism</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkstu1TAQhiMEoqWwZIsssWFBqC9JnLBAQhU3qRKbso4m9vjEUWIH24Gex-IN8TktVcvKluebf-YfT1G8ZPSdEB09t9MSWc0ok1K2j4pTVnFeUtrIx_fuJ8WzGCdKueB197Q44TWXnAt2Wvy5GpEM6NBYZWEmaAyqFIk3RPllsA412QVYkax-AYUEnCZ-sRMQEzabCF6nAMcMR8b9imE37xUuFt4S0Hb10ab9MWnEFZJVJCaElJ8jsY7o4VwPZLEK3xM4VFwh2Jilfts0kgUmHzKm8foY85vT8XnxxMAc8cXteVb8-Pzp6uJrefn9y7eLj5elqlidSqnV0PKm1gy7AaGlOKASmjEEaUBw2jZKdkCRa2GGKg-jrmuhOBgqETiKs-LDje66DQtqhS4bnfs12AXCvvdg-4cRZ8d-53_1eeiStV0WeHMrEPzPDWPqFxsVzjM49FvsWd02tMvNHtDX_6GT34LL9nrW8KrjvBIHqryhVPAxBjR3zTDaH5ahf7AMmX9138Ed_e_3xV9LZLVM</recordid><startdate>20140930</startdate><enddate>20140930</enddate><creator>Cho, Su-Jung</creator><creator>Park, Hae-Jin</creator><creator>Jung, Un Ju</creator><creator>Kim, Hye-Jin</creator><creator>Moon, Byoung Seok</creator><creator>Choi, Myung-Sook</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</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>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140930</creationdate><title>The beneficial effects of combined grape pomace and omija fruit extracts on hyperglycemia, adiposity and hepatic steatosis in db/db mice: a comparison with major index compounds</title><author>Cho, Su-Jung ; Park, Hae-Jin ; Jung, Un Ju ; Kim, Hye-Jin ; Moon, Byoung Seok ; Choi, Myung-Sook</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-7dcb8265d1e9bea80ebec3d11ea7fa32086c79a0e2d3fb42315553c2af07ea2e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adiponectin - blood</topic><topic>Adiposity - drug effects</topic><topic>Animals</topic><topic>Biomarkers - blood</topic><topic>Biomarkers - metabolism</topic><topic>Blood Glucose - analysis</topic><topic>Cyclooctanes - pharmacology</topic><topic>Diabetes Mellitus, Experimental - metabolism</topic><topic>Diabetes Mellitus, Experimental - pathology</topic><topic>Fatty Liver - metabolism</topic><topic>Fatty Liver - pathology</topic><topic>Fruit - chemistry</topic><topic>Fruit - metabolism</topic><topic>Glycated Hemoglobin - analysis</topic><topic>Hyperglycemia</topic><topic>Hyperglycemia - metabolism</topic><topic>Hyperglycemia - pathology</topic><topic>Insulin - blood</topic><topic>Leptin - blood</topic><topic>Lignans - pharmacology</topic><topic>Liver diseases</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Obese</topic><topic>Obesity</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - pharmacology</topic><topic>Polycyclic Compounds - pharmacology</topic><topic>Polyphenols</topic><topic>Resistin - blood</topic><topic>Resveratrol</topic><topic>Rodents</topic><topic>Schisandra - chemistry</topic><topic>Schisandra - metabolism</topic><topic>Stilbenes - pharmacology</topic><topic>Vitis - chemistry</topic><topic>Vitis - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cho, Su-Jung</creatorcontrib><creatorcontrib>Park, Hae-Jin</creatorcontrib><creatorcontrib>Jung, Un Ju</creatorcontrib><creatorcontrib>Kim, Hye-Jin</creatorcontrib><creatorcontrib>Moon, Byoung Seok</creatorcontrib><creatorcontrib>Choi, Myung-Sook</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</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 Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cho, Su-Jung</au><au>Park, Hae-Jin</au><au>Jung, Un Ju</au><au>Kim, Hye-Jin</au><au>Moon, Byoung Seok</au><au>Choi, Myung-Sook</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The beneficial effects of combined grape pomace and omija fruit extracts on hyperglycemia, adiposity and hepatic steatosis in db/db mice: a comparison with major index compounds</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2014-09-30</date><risdate>2014</risdate><volume>15</volume><issue>10</issue><spage>17778</spage><epage>17789</epage><pages>17778-17789</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>This study investigated the effects of combined grape pomace and omija fruit extracts (GO) on diabetes-related metabolic changes in type 2 diabetic db/db mice. The effects of GO were compared with those of a resveratrol and schizandrin mixture (RS), which is a mixture of major components of GO. Mice were fed a normal diet with RS (0.005% resveratrol and 0.02% schizandrin in diet, w/w) or GO (0.3% grape pomace ethanol extract and 0.05% omija fruit ethanol extract in diet, w/w) for seven weeks. RS and GO not only lowered the levels of blood and plasma glucose, HbA1c, insulin and homeostasis model assessment of insulin resistance (HOMA-IR) with a simultaneous decrease in hepatic gluconeogenic enzymes activities and adiposity, but also improved preservation of the pancreatic β-cells. Plasma leptin and resistin levels were lower while the plasma adiponectin level was higher in the RS and GO groups than in the control group. Especially, GO increased hepatic glucokinase activity and gene expression and improved hepatic steatosis by elevating fatty acid oxidation compared to RS. These findings suggest that GO ameliorates hyperglycemia, adiposity and hepatic steatosis in type 2 diabetic mice.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>25272231</pmid><doi>10.3390/ijms151017778</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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source | MDPI - Multidisciplinary Digital Publishing Institute; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Adiponectin - blood Adiposity - drug effects Animals Biomarkers - blood Biomarkers - metabolism Blood Glucose - analysis Cyclooctanes - pharmacology Diabetes Mellitus, Experimental - metabolism Diabetes Mellitus, Experimental - pathology Fatty Liver - metabolism Fatty Liver - pathology Fruit - chemistry Fruit - metabolism Glycated Hemoglobin - analysis Hyperglycemia Hyperglycemia - metabolism Hyperglycemia - pathology Insulin - blood Leptin - blood Lignans - pharmacology Liver diseases Male Mice Mice, Inbred C57BL Mice, Obese Obesity Plant Extracts - chemistry Plant Extracts - pharmacology Polycyclic Compounds - pharmacology Polyphenols Resistin - blood Resveratrol Rodents Schisandra - chemistry Schisandra - metabolism Stilbenes - pharmacology Vitis - chemistry Vitis - metabolism |
title | The beneficial effects of combined grape pomace and omija fruit extracts on hyperglycemia, adiposity and hepatic steatosis in db/db mice: a comparison with major index compounds |
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