Protective effect of Rhus coriaria fruit extracts against hydrogen peroxide-induced oxidative stress in muscle progenitors and zebrafish embryos

Oxidative stress is involved in normal and pathological functioning of skeletal muscle. Protection of myoblasts from oxidative stress may improve muscle contraction and delay aging. Here we studied the effect of sumac fruit extract on human myoblasts and zebrafish embryos in conditions of hydrogen p...

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Published inPeerJ (San Francisco, CA) Vol. 5; p. e4144
Main Authors Najjar, Fadia, Rizk, Francine, Carnac, Gilles, Nassar, Rim, Jabak, Sara, Sobolev, Anatoly Petrovich, Bou Saada, Yara, El Sabban, Marwan, Hamade, Aline
Format Journal Article
LanguageEnglish
Published United States PeerJ. Ltd 12.12.2017
PeerJ, Inc
PeerJ
PeerJ Inc
Subjects
Acetic acid
Aging
Analysis
Antioxidants
Atrophy
Biology
Catalase
Cell adhesion
Cell Biology
Cell cycle
Cyclin-dependent kinases
Danio rerio
Embryonic development
Embryos
Ethanol
Ethyl acetate
Flow cytometry
Free radicals
Gallic acid
Gene expression
Gene flow
Hydrogen peroxide
Life Sciences
Metabolism
Muscle contraction
Musculoskeletal system
Myoblast (LHCN-M2)
Myoblasts
NMR
Nuclear magnetic resonance
Nutrition research
Oxidative stress
Physiological aspects
Physiology
Properties
Rhus coriaria
Rodents
Skeletal muscle
Stem cells
Studies
Sumac Rhus coriaria extract
Superoxide dismutase
Translational Medicine
Zebrafish
Zebrafish embryos
Antioxidants
Aging
Zebrafish embryos
NMR
Sumac Rhus coriaria extract
Myoblast (LHCN-M2)
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Abstract Oxidative stress is involved in normal and pathological functioning of skeletal muscle. Protection of myoblasts from oxidative stress may improve muscle contraction and delay aging. Here we studied the effect of sumac fruit extract on human myoblasts and zebrafish embryos in conditions of hydrogen peroxide-induced oxidative stress. Crude ethanolic 70% extract (CE) and its fractions was obtained from sumac fruits. The composition of sumac ethyl acetate EtOAc fraction was studied by H NMR. The viability of human myoblasts treated with CE and the EtOAc fraction was determined by trypan blue exclusion test. Oxidative stress, cell cycle and adhesion were analyzed by flow cytometry and microscopy. Gene expression was analyzed by qPCR. The EtOAc fraction (IC 2.57 µg/mL) had the highest antioxidant activity and exhibited the best protective effect against hydrogen peroxide-induced oxidative stress. It also restored cell adhesion. This effect was mediated by superoxide dismutase 2 and catalase. Pre-treatment of zebrafish embryos with low concentrations of the EtOAc fraction protected them from hydrogen peroxide-induced death . H NMR analysis revealed the presence of gallic acid in this fraction. extracts inhibited or slowed down the progress of skeletal muscle atrophy by decreasing oxidative stress via superoxide dismutase 2 and catalase-dependent mechanisms.
AbstractList Background and Purpose Oxidative stress is involved in normal and pathological functioning of skeletal muscle. Protection of myoblasts from oxidative stress may improve muscle contraction and delay aging. Here we studied the effect of R. coriaria sumac fruit extract on human myoblasts and zebrafish embryos in conditions of hydrogen peroxide-induced oxidative stress. Study Design and Methods Crude ethanolic 70% extract (CE) and its fractions was obtained from sumac fruits. The composition of sumac ethyl acetate EtOAc fraction was studied by .sup.1 H NMR. The viability of human myoblasts treated with CE and the EtOAc fraction was determined by trypan blue exclusion test. Oxidative stress, cell cycle and adhesion were analyzed by flow cytometry and microscopy. Gene expression was analyzed by qPCR. Results The EtOAc fraction (IC.sub.50 2.57 [micro]g/mL) had the highest antioxidant activity and exhibited the best protective effect against hydrogen peroxide-induced oxidative stress. It also restored cell adhesion. This effect was mediated by superoxide dismutase 2 and catalase. Pre-treatment of zebrafish embryos with low concentrations of the EtOAc fraction protected them from hydrogen peroxide-induced death in vivo. .sup.1 H NMR analysis revealed the presence of gallic acid in this fraction. Conclusion Rhus coriaria extracts inhibited or slowed down the progress of skeletal muscle atrophy by decreasing oxidative stress via superoxide dismutase 2 and catalase-dependent mechanisms.
BACKGROUND AND PURPOSEOxidative stress is involved in normal and pathological functioning of skeletal muscle. Protection of myoblasts from oxidative stress may improve muscle contraction and delay aging. Here we studied the effect of R. coriaria sumac fruit extract on human myoblasts and zebrafish embryos in conditions of hydrogen peroxide-induced oxidative stress. STUDY DESIGN AND METHODSCrude ethanolic 70% extract (CE) and its fractions was obtained from sumac fruits. The composition of sumac ethyl acetate EtOAc fraction was studied by 1H NMR. The viability of human myoblasts treated with CE and the EtOAc fraction was determined by trypan blue exclusion test. Oxidative stress, cell cycle and adhesion were analyzed by flow cytometry and microscopy. Gene expression was analyzed by qPCR. RESULTSThe EtOAc fraction (IC50 2.57 µg/mL) had the highest antioxidant activity and exhibited the best protective effect against hydrogen peroxide-induced oxidative stress. It also restored cell adhesion. This effect was mediated by superoxide dismutase 2 and catalase. Pre-treatment of zebrafish embryos with low concentrations of the EtOAc fraction protected them from hydrogen peroxide-induced death in vivo. 1H NMR analysis revealed the presence of gallic acid in this fraction. CONCLUSIONRhus coriaria extracts inhibited or slowed down the progress of skeletal muscle atrophy by decreasing oxidative stress via superoxide dismutase 2 and catalase-dependent mechanisms.
Oxidative stress is involved in normal and pathological functioning of skeletal muscle. Protection of myoblasts from oxidative stress may improve muscle contraction and delay aging. Here we studied the effect of sumac fruit extract on human myoblasts and zebrafish embryos in conditions of hydrogen peroxide-induced oxidative stress. Crude ethanolic 70% extract (CE) and its fractions was obtained from sumac fruits. The composition of sumac ethyl acetate EtOAc fraction was studied by H NMR. The viability of human myoblasts treated with CE and the EtOAc fraction was determined by trypan blue exclusion test. Oxidative stress, cell cycle and adhesion were analyzed by flow cytometry and microscopy. Gene expression was analyzed by qPCR. The EtOAc fraction (IC 2.57 µg/mL) had the highest antioxidant activity and exhibited the best protective effect against hydrogen peroxide-induced oxidative stress. It also restored cell adhesion. This effect was mediated by superoxide dismutase 2 and catalase. Pre-treatment of zebrafish embryos with low concentrations of the EtOAc fraction protected them from hydrogen peroxide-induced death . H NMR analysis revealed the presence of gallic acid in this fraction. extracts inhibited or slowed down the progress of skeletal muscle atrophy by decreasing oxidative stress via superoxide dismutase 2 and catalase-dependent mechanisms.
Oxidative stress is involved in normal and pathological functioning of skeletal muscle. Protection of myoblasts from oxidative stress may improve muscle contraction and delay aging. Here we studied the effect of R. coriaria sumac fruit extract on human myoblasts and zebrafish embryos in conditions of hydrogen peroxide-induced oxidative stress.
Background and Purpose Oxidative stress is involved in normal and pathological functioning of skeletal muscle. Protection of myoblasts from oxidative stress may improve muscle contraction and delay aging. Here we studied the effect of R. coriaria sumac fruit extract on human myoblasts and zebrafish embryos in conditions of hydrogen peroxide-induced oxidative stress. Study Design and Methods Crude ethanolic 70% extract (CE) and its fractions was obtained from sumac fruits. The composition of sumac ethyl acetate EtOAc fraction was studied by 1H NMR. The viability of human myoblasts treated with CE and the EtOAc fraction was determined by trypan blue exclusion test. Oxidative stress, cell cycle and adhesion were analyzed by flow cytometry and microscopy. Gene expression was analyzed by qPCR. Results The EtOAc fraction (IC50 2.57 µg/mL) had the highest antioxidant activity and exhibited the best protective effect against hydrogen peroxide-induced oxidative stress. It also restored cell adhesion. This effect was mediated by superoxide dismutase 2 and catalase. Pre-treatment of zebrafish embryos with low concentrations of the EtOAc fraction protected them from hydrogen peroxide-induced death in vivo. 1H NMR analysis revealed the presence of gallic acid in this fraction. Conclusion Rhus coriaria extracts inhibited or slowed down the progress of skeletal muscle atrophy by decreasing oxidative stress via superoxide dismutase 2 and catalase-dependent mechanisms.
Oxidative stress is involved in normal and pathological functioning of skeletal muscle. Protection of myoblasts from oxidative stress may improve muscle contraction and delay aging. Here we studied the effect of R. coriaria sumac fruit extract on human myoblasts and zebrafish embryos in conditions of hydrogen peroxide-induced oxidative stress. Crude ethanolic 70% extract (CE) and its fractions was obtained from sumac fruits. The composition of sumac ethyl acetate EtOAc fraction was studied by .sup.1 H NMR. The viability of human myoblasts treated with CE and the EtOAc fraction was determined by trypan blue exclusion test. Oxidative stress, cell cycle and adhesion were analyzed by flow cytometry and microscopy. Gene expression was analyzed by qPCR. The EtOAc fraction (IC.sub.50 2.57 [micro]g/mL) had the highest antioxidant activity and exhibited the best protective effect against hydrogen peroxide-induced oxidative stress. It also restored cell adhesion. This effect was mediated by superoxide dismutase 2 and catalase. Pre-treatment of zebrafish embryos with low concentrations of the EtOAc fraction protected them from hydrogen peroxide-induced death in vivo. .sup.1 H NMR analysis revealed the presence of gallic acid in this fraction. Rhus coriaria extracts inhibited or slowed down the progress of skeletal muscle atrophy by decreasing oxidative stress via superoxide dismutase 2 and catalase-dependent mechanisms.
ArticleNumber e4144
Audience Academic
Author Hamade, Aline
Rizk, Francine
Najjar, Fadia
Nassar, Rim
Jabak, Sara
Carnac, Gilles
Sobolev, Anatoly Petrovich
Bou Saada, Yara
El Sabban, Marwan
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  givenname: Anatoly Petrovich
  surname: Sobolev
  fullname: Sobolev, Anatoly Petrovich
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  givenname: Yara
  surname: Bou Saada
  fullname: Bou Saada, Yara
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  givenname: Marwan
  surname: El Sabban
  fullname: El Sabban, Marwan
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Keywords Antioxidants
Aging
Zebrafish embryos
NMR
Sumac Rhus coriaria extract
Myoblast (LHCN-M2)
Language English
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SSID ssj0000826083
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Snippet Oxidative stress is involved in normal and pathological functioning of skeletal muscle. Protection of myoblasts from oxidative stress may improve muscle...
Background and Purpose Oxidative stress is involved in normal and pathological functioning of skeletal muscle. Protection of myoblasts from oxidative stress...
BACKGROUND AND PURPOSEOxidative stress is involved in normal and pathological functioning of skeletal muscle. Protection of myoblasts from oxidative stress may...
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StartPage e4144
SubjectTerms Acetic acid
Aging
Analysis
Antioxidants
Atrophy
Biology
Catalase
Cell adhesion
Cell Biology
Cell cycle
Cyclin-dependent kinases
Danio rerio
Embryonic development
Embryos
Ethanol
Ethyl acetate
Flow cytometry
Free radicals
Gallic acid
Gene expression
Gene flow
Hydrogen peroxide
Life Sciences
Metabolism
Muscle contraction
Musculoskeletal system
Myoblast (LHCN-M2)
Myoblasts
NMR
Nuclear magnetic resonance
Nutrition research
Oxidative stress
Physiological aspects
Physiology
Properties
Rhus coriaria
Rodents
Skeletal muscle
Stem cells
Studies
Sumac Rhus coriaria extract
Superoxide dismutase
Translational Medicine
Zebrafish
Zebrafish embryos
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Title Protective effect of Rhus coriaria fruit extracts against hydrogen peroxide-induced oxidative stress in muscle progenitors and zebrafish embryos
URI https://www.ncbi.nlm.nih.gov/pubmed/29250470
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