Insulin signaling pathway assessment by enhancing antioxidant activity due to morin using in vitro rat skeletal muscle L6 myotubes cells
Background Plant-derived phytochemicals such as flavonoids have been explored to be powerful antioxidants that protect against oxidative stress-related diseases. In the present study, Morin, a flavonoid compound was studied for its antioxidant and antidiabetic properties in relation to oxidative str...
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creator | Issac, Praveen Kumar Karan, Rupmanjari Guru, Ajay Pachaiappan, R. Arasu, Mariadhas Valan Al-Dhabi, Naif Abdullah Choi, Ki Choon Harikrishnan, Ramasamy Raj, Jesu Arockia |
description | Background
Plant-derived phytochemicals such as flavonoids have been explored to be powerful antioxidants that protect against oxidative stress-related diseases. In the present study, Morin, a flavonoid compound was studied for its antioxidant and antidiabetic properties in relation to oxidative stress in insulin resistant models conducted in rat skeletal muscle L6 cell line model.
Methods
Evaluation of antioxidant property of morin was assayed using in vitro methods such as cell viability by MTT assay, estimation of SOD and CAT activity and NO scavenging activity. The anti-oxidative nature of morin on L6 cell line was conducted by the DCF-DA fluorescent activity. Glucose uptake in morin treated L6 myotubes are accessed by 2-NBDG assay in the presence or absence of IRTK and PI3K inhibitors. Further glycogen content estimation due to the morin treatment in L6 myotubes was performed. Antioxidant and insulin signaling pathway gene expression was examined over RT-PCR analysis.
Results
Morin has a negligible cytotoxic effect at doses of 20, 40, 60, 80, and 100 µM concentration according to cell viability assay. Morin revealed that the levels of the antioxidant enzymes SOD and CAT in L6 myotubes had increased. When the cells were subjected to the nitro blue tetrazolium assay, morin lowered reactive oxygen species (ROS) formation at 60 µM concentration displaying 39% ROS generation in oxidative stress condition. Lesser NO activity and a drop in green fluorescence emission in the DCFDA assay, demonstrating its anti-oxidative nature by reducing ROS formation in vitro. Glucose uptake by the L6 myotube cells using 2-NBDG, and with IRTK and PI3K inhibitors (genistein and wortmannin) showed a significant increase in glucose uptake by the cells which shows the up regulated GLUT-4 movement from intracellular pool to the plasma membrane. Morin (60 µM) significantly enhanced the expression of antioxidant genes GPx, GST and GCS as well as insulin signalling genes IRTK, IRS-1, PI3K, GLUT-4, GSK-3β and GS in L6 myotubes treated cells.
Conclusion
Morin has the ability to act as an anti-oxidant by lowering ROS levels and demonstrating insulin mimetic activity by reversing insulin resistance associated with oxidative stress. |
doi_str_mv | 10.1007/s11033-021-06580-x |
format | Article |
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Plant-derived phytochemicals such as flavonoids have been explored to be powerful antioxidants that protect against oxidative stress-related diseases. In the present study, Morin, a flavonoid compound was studied for its antioxidant and antidiabetic properties in relation to oxidative stress in insulin resistant models conducted in rat skeletal muscle L6 cell line model.
Methods
Evaluation of antioxidant property of morin was assayed using in vitro methods such as cell viability by MTT assay, estimation of SOD and CAT activity and NO scavenging activity. The anti-oxidative nature of morin on L6 cell line was conducted by the DCF-DA fluorescent activity. Glucose uptake in morin treated L6 myotubes are accessed by 2-NBDG assay in the presence or absence of IRTK and PI3K inhibitors. Further glycogen content estimation due to the morin treatment in L6 myotubes was performed. Antioxidant and insulin signaling pathway gene expression was examined over RT-PCR analysis.
Results
Morin has a negligible cytotoxic effect at doses of 20, 40, 60, 80, and 100 µM concentration according to cell viability assay. Morin revealed that the levels of the antioxidant enzymes SOD and CAT in L6 myotubes had increased. When the cells were subjected to the nitro blue tetrazolium assay, morin lowered reactive oxygen species (ROS) formation at 60 µM concentration displaying 39% ROS generation in oxidative stress condition. Lesser NO activity and a drop in green fluorescence emission in the DCFDA assay, demonstrating its anti-oxidative nature by reducing ROS formation in vitro. Glucose uptake by the L6 myotube cells using 2-NBDG, and with IRTK and PI3K inhibitors (genistein and wortmannin) showed a significant increase in glucose uptake by the cells which shows the up regulated GLUT-4 movement from intracellular pool to the plasma membrane. Morin (60 µM) significantly enhanced the expression of antioxidant genes GPx, GST and GCS as well as insulin signalling genes IRTK, IRS-1, PI3K, GLUT-4, GSK-3β and GS in L6 myotubes treated cells.
Conclusion
Morin has the ability to act as an anti-oxidant by lowering ROS levels and demonstrating insulin mimetic activity by reversing insulin resistance associated with oxidative stress.</description><identifier>ISSN: 0301-4851</identifier><identifier>EISSN: 1573-4978</identifier><identifier>DOI: 10.1007/s11033-021-06580-x</identifier><identifier>PMID: 34302266</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>1-Phosphatidylinositol 3-kinase ; Animal Anatomy ; Animal Biochemistry ; Animal models ; Animals ; Antidiabetics ; Antioxidants ; Antioxidants - pharmacology ; Biomedical and Life Sciences ; Cell Line ; Cell Survival - drug effects ; Cell viability ; Cytotoxicity ; Diabetes mellitus ; Flavonoids ; Flavonoids - metabolism ; Flavonoids - pharmacology ; Gene expression ; Genistein ; Glucose ; Glucose - metabolism ; Glycogen ; Glycogen - metabolism ; Glycogen Synthase Kinase 3 beta - metabolism ; Histology ; Hypoglycemic Agents - pharmacology ; Insulin ; Insulin - metabolism ; Insulin receptor substrate 1 ; Insulin resistance ; Insulin Resistance - physiology ; Life Sciences ; Morphology ; Muscle Fibers, Skeletal - metabolism ; Muscle, Skeletal - metabolism ; Musculoskeletal system ; Myoblasts - metabolism ; Myotubes ; Original Article ; Oxidants ; Oxidative stress ; Oxidative Stress - drug effects ; Oxidative Stress - physiology ; Phosphatidylinositol 3-Kinases - metabolism ; Plant cells ; Plants ; Polymerase chain reaction ; Rats ; Reactive oxygen species ; Reactive Oxygen Species - metabolism ; Signal transduction ; Signal Transduction - drug effects ; Skeletal muscle ; Wortmannin</subject><ispartof>Molecular biology reports, 2021-08, Vol.48 (8), p.5857-5872</ispartof><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2021</rights><rights>2021. The Author(s), under exclusive licence to Springer Nature B.V.</rights><rights>The Author(s), under exclusive licence to Springer Nature B.V. 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-7c5456e99c28eb18f508e0a76f8a76a4b1f1c6bb8f2ae29298a22a900570694b3</citedby><cites>FETCH-LOGICAL-c441t-7c5456e99c28eb18f508e0a76f8a76a4b1f1c6bb8f2ae29298a22a900570694b3</cites><orcidid>0000-0001-5898-2121 ; 0000-0003-3007-8792 ; 0000-0002-2663-6328 ; 0000-0002-4807-758X ; 0000-0002-0240-7141 ; 0000-0002-8583-9352</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11033-021-06580-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11033-021-06580-x$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34302266$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Issac, Praveen Kumar</creatorcontrib><creatorcontrib>Karan, Rupmanjari</creatorcontrib><creatorcontrib>Guru, Ajay</creatorcontrib><creatorcontrib>Pachaiappan, R.</creatorcontrib><creatorcontrib>Arasu, Mariadhas Valan</creatorcontrib><creatorcontrib>Al-Dhabi, Naif Abdullah</creatorcontrib><creatorcontrib>Choi, Ki Choon</creatorcontrib><creatorcontrib>Harikrishnan, Ramasamy</creatorcontrib><creatorcontrib>Raj, Jesu Arockia</creatorcontrib><title>Insulin signaling pathway assessment by enhancing antioxidant activity due to morin using in vitro rat skeletal muscle L6 myotubes cells</title><title>Molecular biology reports</title><addtitle>Mol Biol Rep</addtitle><addtitle>Mol Biol Rep</addtitle><description>Background
Plant-derived phytochemicals such as flavonoids have been explored to be powerful antioxidants that protect against oxidative stress-related diseases. In the present study, Morin, a flavonoid compound was studied for its antioxidant and antidiabetic properties in relation to oxidative stress in insulin resistant models conducted in rat skeletal muscle L6 cell line model.
Methods
Evaluation of antioxidant property of morin was assayed using in vitro methods such as cell viability by MTT assay, estimation of SOD and CAT activity and NO scavenging activity. The anti-oxidative nature of morin on L6 cell line was conducted by the DCF-DA fluorescent activity. Glucose uptake in morin treated L6 myotubes are accessed by 2-NBDG assay in the presence or absence of IRTK and PI3K inhibitors. Further glycogen content estimation due to the morin treatment in L6 myotubes was performed. Antioxidant and insulin signaling pathway gene expression was examined over RT-PCR analysis.
Results
Morin has a negligible cytotoxic effect at doses of 20, 40, 60, 80, and 100 µM concentration according to cell viability assay. Morin revealed that the levels of the antioxidant enzymes SOD and CAT in L6 myotubes had increased. When the cells were subjected to the nitro blue tetrazolium assay, morin lowered reactive oxygen species (ROS) formation at 60 µM concentration displaying 39% ROS generation in oxidative stress condition. Lesser NO activity and a drop in green fluorescence emission in the DCFDA assay, demonstrating its anti-oxidative nature by reducing ROS formation in vitro. Glucose uptake by the L6 myotube cells using 2-NBDG, and with IRTK and PI3K inhibitors (genistein and wortmannin) showed a significant increase in glucose uptake by the cells which shows the up regulated GLUT-4 movement from intracellular pool to the plasma membrane. Morin (60 µM) significantly enhanced the expression of antioxidant genes GPx, GST and GCS as well as insulin signalling genes IRTK, IRS-1, PI3K, GLUT-4, GSK-3β and GS in L6 myotubes treated cells.
Conclusion
Morin has the ability to act as an anti-oxidant by lowering ROS levels and demonstrating insulin mimetic activity by reversing insulin resistance associated with oxidative stress.</description><subject>1-Phosphatidylinositol 3-kinase</subject><subject>Animal Anatomy</subject><subject>Animal Biochemistry</subject><subject>Animal models</subject><subject>Animals</subject><subject>Antidiabetics</subject><subject>Antioxidants</subject><subject>Antioxidants - pharmacology</subject><subject>Biomedical and Life Sciences</subject><subject>Cell Line</subject><subject>Cell Survival - drug effects</subject><subject>Cell viability</subject><subject>Cytotoxicity</subject><subject>Diabetes mellitus</subject><subject>Flavonoids</subject><subject>Flavonoids - metabolism</subject><subject>Flavonoids - pharmacology</subject><subject>Gene expression</subject><subject>Genistein</subject><subject>Glucose</subject><subject>Glucose - metabolism</subject><subject>Glycogen</subject><subject>Glycogen - metabolism</subject><subject>Glycogen Synthase Kinase 3 beta - metabolism</subject><subject>Histology</subject><subject>Hypoglycemic Agents - pharmacology</subject><subject>Insulin</subject><subject>Insulin - metabolism</subject><subject>Insulin receptor substrate 1</subject><subject>Insulin resistance</subject><subject>Insulin Resistance - physiology</subject><subject>Life Sciences</subject><subject>Morphology</subject><subject>Muscle Fibers, Skeletal - metabolism</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Musculoskeletal system</subject><subject>Myoblasts - metabolism</subject><subject>Myotubes</subject><subject>Original Article</subject><subject>Oxidants</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Oxidative Stress - physiology</subject><subject>Phosphatidylinositol 3-Kinases - metabolism</subject><subject>Plant cells</subject><subject>Plants</subject><subject>Polymerase chain reaction</subject><subject>Rats</subject><subject>Reactive oxygen species</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Signal transduction</subject><subject>Signal Transduction - drug effects</subject><subject>Skeletal muscle</subject><subject>Wortmannin</subject><issn>0301-4851</issn><issn>1573-4978</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kc9u1DAQxi1ERZfCC3BAlrj0Ejr-FztHVEGptBIXOEdOdrJNSZzF49DNG_DYOGwBiQOXmZG-33y25mPslYC3AsBekRCgVAFSFFAaB8XxCdsIY1WhK-uesg0oEIV2Rpyz50T3AKCFNc_YudIKpCzLDftxG2ge-sCp3wefhz0_-HT34BfuiZBoxJB4s3AMdz60q-5D6qdjv8ud-zb13_u08N2MPE18nGL2mmnl8pClOPHoE6evOGDyAx9nagfk25KPy5TmBom3OAz0gp11fiB8-dgv2JcP7z9ffyy2n25ur99ti1ZrkQrbGm1KrKpWOmyE6ww4BG_LzuXidSM60ZZN4zrpUVaycl5KXwEYC2WlG3XBLk--hzh9m5FSPfa0_sAHnGaqpTFGCC1dldE3_6D30xzzlVbKWquNUpApeaLaOBFF7OpD7Ecfl1pAveZUn3Kqc071r5zqY156_Wg9NyPu_qz8DiYD6gRQlsIe49-3_2P7EyUOoDE</recordid><startdate>20210801</startdate><enddate>20210801</enddate><creator>Issac, Praveen Kumar</creator><creator>Karan, Rupmanjari</creator><creator>Guru, Ajay</creator><creator>Pachaiappan, R.</creator><creator>Arasu, Mariadhas Valan</creator><creator>Al-Dhabi, Naif Abdullah</creator><creator>Choi, Ki Choon</creator><creator>Harikrishnan, Ramasamy</creator><creator>Raj, Jesu Arockia</creator><general>Springer Netherlands</general><general>Springer Nature B.V</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>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5898-2121</orcidid><orcidid>https://orcid.org/0000-0003-3007-8792</orcidid><orcidid>https://orcid.org/0000-0002-2663-6328</orcidid><orcidid>https://orcid.org/0000-0002-4807-758X</orcidid><orcidid>https://orcid.org/0000-0002-0240-7141</orcidid><orcidid>https://orcid.org/0000-0002-8583-9352</orcidid></search><sort><creationdate>20210801</creationdate><title>Insulin signaling pathway assessment by enhancing antioxidant activity due to morin using in vitro rat skeletal muscle L6 myotubes cells</title><author>Issac, Praveen Kumar ; Karan, Rupmanjari ; Guru, Ajay ; Pachaiappan, R. ; Arasu, Mariadhas Valan ; Al-Dhabi, Naif Abdullah ; Choi, Ki Choon ; Harikrishnan, Ramasamy ; Raj, Jesu Arockia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-7c5456e99c28eb18f508e0a76f8a76a4b1f1c6bb8f2ae29298a22a900570694b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>1-Phosphatidylinositol 3-kinase</topic><topic>Animal Anatomy</topic><topic>Animal Biochemistry</topic><topic>Animal models</topic><topic>Animals</topic><topic>Antidiabetics</topic><topic>Antioxidants</topic><topic>Antioxidants - pharmacology</topic><topic>Biomedical and Life Sciences</topic><topic>Cell Line</topic><topic>Cell Survival - drug effects</topic><topic>Cell viability</topic><topic>Cytotoxicity</topic><topic>Diabetes mellitus</topic><topic>Flavonoids</topic><topic>Flavonoids - metabolism</topic><topic>Flavonoids - pharmacology</topic><topic>Gene expression</topic><topic>Genistein</topic><topic>Glucose</topic><topic>Glucose - metabolism</topic><topic>Glycogen</topic><topic>Glycogen - metabolism</topic><topic>Glycogen Synthase Kinase 3 beta - metabolism</topic><topic>Histology</topic><topic>Hypoglycemic Agents - pharmacology</topic><topic>Insulin</topic><topic>Insulin - metabolism</topic><topic>Insulin receptor substrate 1</topic><topic>Insulin resistance</topic><topic>Insulin Resistance - physiology</topic><topic>Life Sciences</topic><topic>Morphology</topic><topic>Muscle Fibers, Skeletal - metabolism</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Musculoskeletal system</topic><topic>Myoblasts - metabolism</topic><topic>Myotubes</topic><topic>Original Article</topic><topic>Oxidants</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Oxidative Stress - physiology</topic><topic>Phosphatidylinositol 3-Kinases - metabolism</topic><topic>Plant cells</topic><topic>Plants</topic><topic>Polymerase chain reaction</topic><topic>Rats</topic><topic>Reactive oxygen species</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Signal transduction</topic><topic>Signal Transduction - drug effects</topic><topic>Skeletal muscle</topic><topic>Wortmannin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Issac, Praveen Kumar</creatorcontrib><creatorcontrib>Karan, Rupmanjari</creatorcontrib><creatorcontrib>Guru, Ajay</creatorcontrib><creatorcontrib>Pachaiappan, R.</creatorcontrib><creatorcontrib>Arasu, Mariadhas Valan</creatorcontrib><creatorcontrib>Al-Dhabi, Naif Abdullah</creatorcontrib><creatorcontrib>Choi, Ki Choon</creatorcontrib><creatorcontrib>Harikrishnan, Ramasamy</creatorcontrib><creatorcontrib>Raj, Jesu Arockia</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>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</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>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular biology reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Issac, Praveen Kumar</au><au>Karan, Rupmanjari</au><au>Guru, Ajay</au><au>Pachaiappan, R.</au><au>Arasu, Mariadhas Valan</au><au>Al-Dhabi, Naif Abdullah</au><au>Choi, Ki Choon</au><au>Harikrishnan, Ramasamy</au><au>Raj, Jesu Arockia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insulin signaling pathway assessment by enhancing antioxidant activity due to morin using in vitro rat skeletal muscle L6 myotubes cells</atitle><jtitle>Molecular biology reports</jtitle><stitle>Mol Biol Rep</stitle><addtitle>Mol Biol Rep</addtitle><date>2021-08-01</date><risdate>2021</risdate><volume>48</volume><issue>8</issue><spage>5857</spage><epage>5872</epage><pages>5857-5872</pages><issn>0301-4851</issn><eissn>1573-4978</eissn><abstract>Background
Plant-derived phytochemicals such as flavonoids have been explored to be powerful antioxidants that protect against oxidative stress-related diseases. In the present study, Morin, a flavonoid compound was studied for its antioxidant and antidiabetic properties in relation to oxidative stress in insulin resistant models conducted in rat skeletal muscle L6 cell line model.
Methods
Evaluation of antioxidant property of morin was assayed using in vitro methods such as cell viability by MTT assay, estimation of SOD and CAT activity and NO scavenging activity. The anti-oxidative nature of morin on L6 cell line was conducted by the DCF-DA fluorescent activity. Glucose uptake in morin treated L6 myotubes are accessed by 2-NBDG assay in the presence or absence of IRTK and PI3K inhibitors. Further glycogen content estimation due to the morin treatment in L6 myotubes was performed. Antioxidant and insulin signaling pathway gene expression was examined over RT-PCR analysis.
Results
Morin has a negligible cytotoxic effect at doses of 20, 40, 60, 80, and 100 µM concentration according to cell viability assay. Morin revealed that the levels of the antioxidant enzymes SOD and CAT in L6 myotubes had increased. When the cells were subjected to the nitro blue tetrazolium assay, morin lowered reactive oxygen species (ROS) formation at 60 µM concentration displaying 39% ROS generation in oxidative stress condition. Lesser NO activity and a drop in green fluorescence emission in the DCFDA assay, demonstrating its anti-oxidative nature by reducing ROS formation in vitro. Glucose uptake by the L6 myotube cells using 2-NBDG, and with IRTK and PI3K inhibitors (genistein and wortmannin) showed a significant increase in glucose uptake by the cells which shows the up regulated GLUT-4 movement from intracellular pool to the plasma membrane. Morin (60 µM) significantly enhanced the expression of antioxidant genes GPx, GST and GCS as well as insulin signalling genes IRTK, IRS-1, PI3K, GLUT-4, GSK-3β and GS in L6 myotubes treated cells.
Conclusion
Morin has the ability to act as an anti-oxidant by lowering ROS levels and demonstrating insulin mimetic activity by reversing insulin resistance associated with oxidative stress.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>34302266</pmid><doi>10.1007/s11033-021-06580-x</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0001-5898-2121</orcidid><orcidid>https://orcid.org/0000-0003-3007-8792</orcidid><orcidid>https://orcid.org/0000-0002-2663-6328</orcidid><orcidid>https://orcid.org/0000-0002-4807-758X</orcidid><orcidid>https://orcid.org/0000-0002-0240-7141</orcidid><orcidid>https://orcid.org/0000-0002-8583-9352</orcidid></addata></record> |
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recordid | cdi_proquest_miscellaneous_2555114289 |
source | MEDLINE; SpringerLink Journals - AutoHoldings |
subjects | 1-Phosphatidylinositol 3-kinase Animal Anatomy Animal Biochemistry Animal models Animals Antidiabetics Antioxidants Antioxidants - pharmacology Biomedical and Life Sciences Cell Line Cell Survival - drug effects Cell viability Cytotoxicity Diabetes mellitus Flavonoids Flavonoids - metabolism Flavonoids - pharmacology Gene expression Genistein Glucose Glucose - metabolism Glycogen Glycogen - metabolism Glycogen Synthase Kinase 3 beta - metabolism Histology Hypoglycemic Agents - pharmacology Insulin Insulin - metabolism Insulin receptor substrate 1 Insulin resistance Insulin Resistance - physiology Life Sciences Morphology Muscle Fibers, Skeletal - metabolism Muscle, Skeletal - metabolism Musculoskeletal system Myoblasts - metabolism Myotubes Original Article Oxidants Oxidative stress Oxidative Stress - drug effects Oxidative Stress - physiology Phosphatidylinositol 3-Kinases - metabolism Plant cells Plants Polymerase chain reaction Rats Reactive oxygen species Reactive Oxygen Species - metabolism Signal transduction Signal Transduction - drug effects Skeletal muscle Wortmannin |
title | Insulin signaling pathway assessment by enhancing antioxidant activity due to morin using in vitro rat skeletal muscle L6 myotubes cells |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T23%3A04%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Insulin%20signaling%20pathway%20assessment%20by%20enhancing%20antioxidant%20activity%20due%20to%20morin%20using%20in%20vitro%20rat%20skeletal%20muscle%20L6%20myotubes%20cells&rft.jtitle=Molecular%20biology%20reports&rft.au=Issac,%20Praveen%20Kumar&rft.date=2021-08-01&rft.volume=48&rft.issue=8&rft.spage=5857&rft.epage=5872&rft.pages=5857-5872&rft.issn=0301-4851&rft.eissn=1573-4978&rft_id=info:doi/10.1007/s11033-021-06580-x&rft_dat=%3Cproquest_cross%3E2577745330%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2577745330&rft_id=info:pmid/34302266&rfr_iscdi=true |