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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Veröffentlicht in:Molecular biology reports 2021-08, Vol.48 (8), p.5857-5872
Hauptverfasser: Issac, Praveen Kumar, Karan, Rupmanjari, Guru, Ajay, Pachaiappan, R., Arasu, Mariadhas Valan, Al-Dhabi, Naif Abdullah, Choi, Ki Choon, Harikrishnan, Ramasamy, Raj, Jesu Arockia
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container_end_page 5872
container_issue 8
container_start_page 5857
container_title Molecular biology reports
container_volume 48
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
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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. 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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. 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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 &amp; 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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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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
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