Anti-fatigue effect of Myelophil in a chronic forced exercise mouse model

This study was performed to evaluate the anti-fatigue effects of Myelophil. ICR male mice (10 weeks old) were forced to run for 1 hour, 5 days/week for 4 weeks. Each running session was followed by administration of distilled water, Myelophil (50 or 100mg/kg), or ascorbic acid (100mg/kg) 1h later. E...

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Veröffentlicht in:European journal of pharmacology 2015-10, Vol.764, p.100-108
Hauptverfasser: Lee, Jin-Seok, Kim, Hyeong-Geug, Han, Jong-Min, Kim, Young-Ae, Son, Chang-Gue
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Kim, Hyeong-Geug
Han, Jong-Min
Kim, Young-Ae
Son, Chang-Gue
description This study was performed to evaluate the anti-fatigue effects of Myelophil. ICR male mice (10 weeks old) were forced to run for 1 hour, 5 days/week for 4 weeks. Each running session was followed by administration of distilled water, Myelophil (50 or 100mg/kg), or ascorbic acid (100mg/kg) 1h later. Equal proportions of Astragali Radix and Salviae Miltiorrhizae Radix were extracted using 30% ethanol, and formulated into Myelophil. To evaluate the anti-fatigue effects of Myelophil, exercise tolerance and forced swimming tests were conducted. Underlying mechanisms, including oxidant–antioxidant balance, inflammatory response, and energy metabolism, were investigated by analyzing skeletal muscle tissues and/or sera. Myelophil significantly increased exercise ability and latency times, and decreased the number of electric shocks and immobility time on exercise tolerance and forced swimming tests compared with control group. Myelophil also significantly ameliorated fatigue-induced alterations in oxidative stress biomarkers, antioxidant enzymes and antioxidant capacity, as measured by multiple assays, including enzyme activity assays and western blotting, as well as alterations in pro- and anti-inflammatory cytokines in skeletal muscle. Furthermore, Myelophil normalized alterations in energy metabolic markers in sera. These findings suggest that Myelophil reduces the effects of chronic fatigue, likely by attenuating oxidative and inflammatory responses and normalizing energy metabolism. Consequently, this study provides evidence for the clinical relevance of Myelophil. [Display omitted]
doi_str_mv 10.1016/j.ejphar.2015.06.055
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ICR male mice (10 weeks old) were forced to run for 1 hour, 5 days/week for 4 weeks. Each running session was followed by administration of distilled water, Myelophil (50 or 100mg/kg), or ascorbic acid (100mg/kg) 1h later. Equal proportions of Astragali Radix and Salviae Miltiorrhizae Radix were extracted using 30% ethanol, and formulated into Myelophil. To evaluate the anti-fatigue effects of Myelophil, exercise tolerance and forced swimming tests were conducted. Underlying mechanisms, including oxidant–antioxidant balance, inflammatory response, and energy metabolism, were investigated by analyzing skeletal muscle tissues and/or sera. Myelophil significantly increased exercise ability and latency times, and decreased the number of electric shocks and immobility time on exercise tolerance and forced swimming tests compared with control group. Myelophil also significantly ameliorated fatigue-induced alterations in oxidative stress biomarkers, antioxidant enzymes and antioxidant capacity, as measured by multiple assays, including enzyme activity assays and western blotting, as well as alterations in pro- and anti-inflammatory cytokines in skeletal muscle. Furthermore, Myelophil normalized alterations in energy metabolic markers in sera. These findings suggest that Myelophil reduces the effects of chronic fatigue, likely by attenuating oxidative and inflammatory responses and normalizing energy metabolism. Consequently, this study provides evidence for the clinical relevance of Myelophil. [Display omitted]</description><identifier>ISSN: 0014-2999</identifier><identifier>EISSN: 1879-0712</identifier><identifier>DOI: 10.1016/j.ejphar.2015.06.055</identifier><identifier>PMID: 26142828</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Antioxidant ; Blood Glucose - metabolism ; Blood Urea Nitrogen ; Chronic fatigue ; Chronic forced exercise ; Cytokines - metabolism ; Drugs, Chinese Herbal - pharmacology ; Energy Metabolism - drug effects ; L-Lactate Dehydrogenase - blood ; Lactic Acid - blood ; Lactic Acid - metabolism ; Male ; Malondialdehyde - metabolism ; Mice ; Mice, Inbred ICR ; Muscle Fatigue - drug effects ; Muscle, Skeletal - drug effects ; Muscle, Skeletal - metabolism ; Muscle, Skeletal - physiology ; Myelophil ; Nitric Oxide - metabolism ; Oxidative stress ; Physical Conditioning, Animal ; Reactive Oxygen Species - blood ; Reactive Oxygen Species - metabolism ; Swimming</subject><ispartof>European journal of pharmacology, 2015-10, Vol.764, p.100-108</ispartof><rights>2015 Elsevier B.V.</rights><rights>Copyright © 2015 Elsevier B.V. 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ICR male mice (10 weeks old) were forced to run for 1 hour, 5 days/week for 4 weeks. Each running session was followed by administration of distilled water, Myelophil (50 or 100mg/kg), or ascorbic acid (100mg/kg) 1h later. Equal proportions of Astragali Radix and Salviae Miltiorrhizae Radix were extracted using 30% ethanol, and formulated into Myelophil. To evaluate the anti-fatigue effects of Myelophil, exercise tolerance and forced swimming tests were conducted. Underlying mechanisms, including oxidant–antioxidant balance, inflammatory response, and energy metabolism, were investigated by analyzing skeletal muscle tissues and/or sera. Myelophil significantly increased exercise ability and latency times, and decreased the number of electric shocks and immobility time on exercise tolerance and forced swimming tests compared with control group. Myelophil also significantly ameliorated fatigue-induced alterations in oxidative stress biomarkers, antioxidant enzymes and antioxidant capacity, as measured by multiple assays, including enzyme activity assays and western blotting, as well as alterations in pro- and anti-inflammatory cytokines in skeletal muscle. Furthermore, Myelophil normalized alterations in energy metabolic markers in sera. These findings suggest that Myelophil reduces the effects of chronic fatigue, likely by attenuating oxidative and inflammatory responses and normalizing energy metabolism. Consequently, this study provides evidence for the clinical relevance of Myelophil. [Display omitted]</description><subject>Animals</subject><subject>Antioxidant</subject><subject>Blood Glucose - metabolism</subject><subject>Blood Urea Nitrogen</subject><subject>Chronic fatigue</subject><subject>Chronic forced exercise</subject><subject>Cytokines - metabolism</subject><subject>Drugs, Chinese Herbal - pharmacology</subject><subject>Energy Metabolism - drug effects</subject><subject>L-Lactate Dehydrogenase - blood</subject><subject>Lactic Acid - blood</subject><subject>Lactic Acid - metabolism</subject><subject>Male</subject><subject>Malondialdehyde - metabolism</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>Muscle Fatigue - drug effects</subject><subject>Muscle, Skeletal - drug effects</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Muscle, Skeletal - physiology</subject><subject>Myelophil</subject><subject>Nitric Oxide - metabolism</subject><subject>Oxidative stress</subject><subject>Physical Conditioning, Animal</subject><subject>Reactive Oxygen Species - blood</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Swimming</subject><issn>0014-2999</issn><issn>1879-0712</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kD1PwzAQhi0EoqXwDxDyyJJwdhI7WZCqii-piAVmK7bP1FWaFDtF9N-T0sLIcrc87308hFwySBkwcbNMcble1CHlwIoURApFcUTGrJRVApLxYzIGYHnCq6oakbMYlwBQVLw4JSMuWM5LXo7J07TtfeLq3r9vkKJzaHraOfq8xaZbL3xDfUtrahaha72hrgsGLcUvDMZHpKtu81MtNufkxNVNxItDn5C3-7vX2WMyf3l4mk3nickE7xNhAITN0AnjtM5tzkSOoKEsbSW1qIFhYWRR8ky7jLOCaSOZ1bkW1mRS1tmEXO_nrkP3scHYq5WPBpumbnG4RjHJWZZLUWUDmu9RE7oYAzq1Dn5Vh61ioHYS1VLtJaqdRAVCDRKH2NVhw0av0P6Ffq0NwO0ewOHPT49BReOxHcz4MPhTtvP_b_gGqMiEeQ</recordid><startdate>20151005</startdate><enddate>20151005</enddate><creator>Lee, Jin-Seok</creator><creator>Kim, Hyeong-Geug</creator><creator>Han, Jong-Min</creator><creator>Kim, Young-Ae</creator><creator>Son, Chang-Gue</creator><general>Elsevier 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>7X8</scope></search><sort><creationdate>20151005</creationdate><title>Anti-fatigue effect of Myelophil in a chronic forced exercise mouse model</title><author>Lee, Jin-Seok ; 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subjects Animals
Antioxidant
Blood Glucose - metabolism
Blood Urea Nitrogen
Chronic fatigue
Chronic forced exercise
Cytokines - metabolism
Drugs, Chinese Herbal - pharmacology
Energy Metabolism - drug effects
L-Lactate Dehydrogenase - blood
Lactic Acid - blood
Lactic Acid - metabolism
Male
Malondialdehyde - metabolism
Mice
Mice, Inbred ICR
Muscle Fatigue - drug effects
Muscle, Skeletal - drug effects
Muscle, Skeletal - metabolism
Muscle, Skeletal - physiology
Myelophil
Nitric Oxide - metabolism
Oxidative stress
Physical Conditioning, Animal
Reactive Oxygen Species - blood
Reactive Oxygen Species - metabolism
Swimming
title Anti-fatigue effect of Myelophil in a chronic forced exercise mouse model
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