The Treatment of Rhodiola Mimics Exercise to Resist High-Fat Diet-Induced Muscle Dysfunction via Sirtuin1-Dependent Mechanisms

Muscle dysfunction is a complication of high-fat diet (HFD)-induced obesity that could be prevented by exercise, but patients did not get enough therapeutic efficacy from exercise due to multiple reasons. To explore alternative or supplementary approaches to prevent or treat muscle dysfunction in in...

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Published inFrontiers in Pharmacology Vol. 12; p. 646489
Main Authors You, Baiyang, Dun, Yaoshan, Fu, Siqian, Qi, Dake, Zhang, Wenliang, Liu, Yuan, Qiu, Ling, Xie, Murong, Liu, Suixin
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Published Switzerland Frontiers Media SA 15.04.2021
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Abstract Muscle dysfunction is a complication of high-fat diet (HFD)-induced obesity that could be prevented by exercise, but patients did not get enough therapeutic efficacy from exercise due to multiple reasons. To explore alternative or supplementary approaches to prevent or treat muscle dysfunction in individuals with obesity, we investigated the effects of Rhodiola on muscle dysfunction as exercise pills. SIRT1 might suppress atrogenes expression and improve mitochondrial quality control, which could be a therapeutic target stimulated by exercise and Rhodiola, but further mechanisms remain unclear. We verified the lipid metabolism disorders and skeletal muscle dysfunction in HFD feeding mice. Moreover, exercise and Rhodiola were used to intervene mice with a HFD. Our results showed that exercise and Rhodiola prevented muscle atrophy and dysfunction in obese mice and activating the SIRT1 pathway, while atrogenes were suppressed and mitochondrial quality control was improved. EX-527, SIRT1 inhibitor, was used to validate the essential role of SIRT1 in salidroside benefit. Results of cell culture experiment showed that salidroside alleviated high palmitate-induced atrophy and mitochondrial quality control impairments, but these improvements of salidroside were inhibited by EX-527 in C2C12 myotubes. Overall, Rhodiola mimics exercise that activates SIRT1 signaling leading to improvement of HFD-induced muscle dysfunction.
AbstractList Muscle dysfunction is a complication of high-fat diet (HFD)-induced obesity that could be prevented by exercise, but patients did not get enough therapeutic efficacy from exercise due to multiple reasons. To explore alternative or supplementary approaches to prevent or treat muscle dysfunction in individuals with obesity, we investigated the effects of Rhodiola on muscle dysfunction as exercise pills. SIRT1 might suppress atrogenes expression and improve mitochondrial quality control, which could be a therapeutic target stimulated by exercise and Rhodiola, but further mechanisms remain unclear. We verified the lipid metabolism disorders and skeletal muscle dysfunction in HFD feeding mice. Moreover, exercise and Rhodiola were used to intervene mice with a HFD. Our results showed that exercise and Rhodiola prevented muscle atrophy and dysfunction in obese mice and activating the SIRT1 pathway, while atrogenes were suppressed and mitochondrial quality control was improved. EX-527, SIRT1 inhibitor, was used to validate the essential role of SIRT1 in salidroside benefit. Results of cell culture experiment showed that salidroside alleviated high palmitate-induced atrophy and mitochondrial quality control impairments, but these improvements of salidroside were inhibited by EX-527 in C2C12 myotubes. Overall, Rhodiola mimics exercise that activates SIRT1 signaling leading to improvement of HFD-induced muscle dysfunction.
Muscle dysfunction is a complication of high-fat diet (HFD)-induced obesity that could be prevented by exercise, but patients did not get enough therapeutic efficacy from exercise due to multiple reasons. To explore alternative or supplementary approaches to prevent or treat muscle dysfunction in individuals with obesity, we investigated the effects of Rhodiola on muscle dysfunction as exercise pills. SIRT1 might suppress atrogenes expression and improve mitochondrial quality control, which could be a therapeutic target stimulated by exercise and Rhodiola, but further mechanisms remain unclear. We verified the lipid metabolism disorders and skeletal muscle dysfunction in HFD feeding mice. Moreover, exercise and Rhodiola were used to intervene mice with a HFD. Our results showed that exercise and Rhodiola prevented muscle atrophy and dysfunction in obese mice and activating the SIRT1 pathway, while atrogenes were suppressed and mitochondrial quality control was improved. EX-527, SIRT1 inhibitor, was used to validate the essential role of SIRT1 in salidroside benefit. Results of cell culture experiment showed that salidroside alleviated high palmitate-induced atrophy and mitochondrial quality control impairments, but these improvements of salidroside were inhibited by EX-527 in C2C12 myotubes. Overall, Rhodiola mimics exercise that activates SIRT1 signaling leading to improvement of HFD-induced muscle dysfunction.Muscle dysfunction is a complication of high-fat diet (HFD)-induced obesity that could be prevented by exercise, but patients did not get enough therapeutic efficacy from exercise due to multiple reasons. To explore alternative or supplementary approaches to prevent or treat muscle dysfunction in individuals with obesity, we investigated the effects of Rhodiola on muscle dysfunction as exercise pills. SIRT1 might suppress atrogenes expression and improve mitochondrial quality control, which could be a therapeutic target stimulated by exercise and Rhodiola, but further mechanisms remain unclear. We verified the lipid metabolism disorders and skeletal muscle dysfunction in HFD feeding mice. Moreover, exercise and Rhodiola were used to intervene mice with a HFD. Our results showed that exercise and Rhodiola prevented muscle atrophy and dysfunction in obese mice and activating the SIRT1 pathway, while atrogenes were suppressed and mitochondrial quality control was improved. EX-527, SIRT1 inhibitor, was used to validate the essential role of SIRT1 in salidroside benefit. Results of cell culture experiment showed that salidroside alleviated high palmitate-induced atrophy and mitochondrial quality control impairments, but these improvements of salidroside were inhibited by EX-527 in C2C12 myotubes. Overall, Rhodiola mimics exercise that activates SIRT1 signaling leading to improvement of HFD-induced muscle dysfunction.
Author Dake Qi
Yaoshan Dun
Yuan Liu
Ling Qiu
Siqian Fu
Murong Xie
Suixin Liu
Wenliang Zhang
Baiyang You
AuthorAffiliation 1 Division of Cardiac Rehabilitation, Department of Physical Medicine and Rehabilitation, Xiangya Hospital of Central South University, Changsha , China
2 National Clinical Research Center for Geriatric Disorders, Xiangya Hospital of Central South University, Changsha , China
3 Division of Preventive Cardiology, Department of Cardiovascular Medicine, Mayo Clinic, Rochester , MN , United States
4 College of Pharmacy, University of Manitoba, Winnipeg , MB , Canada
AuthorAffiliation_xml – name: 1 Division of Cardiac Rehabilitation, Department of Physical Medicine and Rehabilitation, Xiangya Hospital of Central South University, Changsha , China
– name: 2 National Clinical Research Center for Geriatric Disorders, Xiangya Hospital of Central South University, Changsha , China
– name: 3 Division of Preventive Cardiology, Department of Cardiovascular Medicine, Mayo Clinic, Rochester , MN , United States
– name: 4 College of Pharmacy, University of Manitoba, Winnipeg , MB , Canada
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Cites_doi 10.1530/JOE-19-0393
10.3390/ijerph15102301
10.1016/j.cbpa.2008.01.019
10.1038/jcbfm.2015.27
10.1096/fj.10-177295
10.1039/c8fo01992d
10.1002/jcsm.12054
10.1155/2017/8024857
10.1016/j.coph.2012.02.010
10.2174/138161282035140911142118
10.1186/s12933-019-0907-0
10.1007/s13539-014-0134-1
10.1016/j.cger.2011.03.009
10.1519/JSC.0b013e31825d9799
10.1016/j.cmet.2012.04.022
10.1073/pnas.0607795103
10.2337/db14-0667
10.1016/j.phymed.2018.10.031
10.1038/s41380-019-0352-1
10.1074/jbc.M113.489716
10.3390/nu12051280
10.1023/b:bebm.0000020211.24779.15
10.3389/fphys.2019.00665
10.7150/ijms.53899
10.1016/j.mayocp.2019.04.033
10.1124/pr.110.003905
10.1111/jnc.13225
10.1038/s41422-018-0078-7
10.1016/j.lfs.2019.03.027
10.1139/h11-070
10.33594/000000282
10.1093/eurjhf/hfs048
10.1073/pnas.0630588100
10.1111/j.1474-9726.2012.00844.x
10.1016/j.cell.2006.11.013
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Keywords salidroside
rhodiola
SIRT1
atrogenes
mitochondrion
Language English
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This article was submitted to Ethnopharmacology, a section of the journal Frontiers in Pharmacology
Giuseppe Annunziata, University of Naples Federico II, Italy
Edited by: Takashi Sato, Tokyo University of Pharmacy and Life Sciences, Japan
Reviewed by: Suresh Kumar Mohankumar, Swansea University Medical School, United Kingdom
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References Xie (B35) 2019; 224
Lei (B20) 2020; 25
Gan (B11) 2018; 28
Mavros (B22) 2014; 5
Lee (B19) 2013; 288
Perry (B27) 2016; 22
Van De Weijer (B33) 2015; 64
Nisr (B25) 2020; 54
Barhwal (B3) 2015; 135
Cantó (B5) 2012; 15
Tonkin (B31) 2012; 12
Valero (B32) 2014; 20
Gurd (B12) 2011; 36
Dun (B9); 94
You (B37) 2020; 244
Abidov (B1) 2003; 136
Wu (B34) 2019; 10
Lagouge (B18) 2006; 127
Noreen (B26) 2013; 27
Momken (B24) 2011; 25
Chen (B6) 2016; 7
Jørgensen (B15) 2015; 35
Jiang (B14) 2021; 18
Milne (B23) 2008; 12
Conraads (B7) 2012; 14
Annunziata (B2) 2020; 12
Dun (B8) 2017; 2017
Pillard (B28) 2011; 27
Sandri (B29) 2006; 103
Listenberger (B21) 2003; 100
Tong (B30) 2019; 10
Joseph (B16) 2012; 11
Heo (B13) 2018; 15
Xue (B36) 2019; 54
Dun (B10); 18
Kelly (B17) 2001; 6
Cantó (B4) 2012; 64
References_xml – volume: 244
  start-page: 383
  year: 2020
  ident: B37
  article-title: Anti-insulin resistance effects of salidroside through mitochondrial quality control
  publication-title: J Endocrinol
  doi: 10.1530/JOE-19-0393
– volume: 15
  start-page: 2301
  year: 2018
  ident: B13
  article-title: Exercise Training Attenuates Obesity-Induced Skeletal Muscle Remodeling and Mitochondria-Mediated Apoptosis in the Skeletal Muscle
  publication-title: Ijerph
  doi: 10.3390/ijerph15102301
– volume: 12
  start-page: 11
  year: 2008
  ident: B23
  article-title: The Sirtuin family: therapeutic targets to treat diseases of aging
  publication-title: Current Opinion in Chemical Biology
  doi: 10.1016/j.cbpa.2008.01.019
– volume: 6
  start-page: 293
  year: 2001
  ident: B17
  article-title: Rhodiola rosea: a possible plant adaptogen
  publication-title: Altern Med Rev.
– volume: 35
  start-page: 943
  year: 2015
  ident: B15
  article-title: One-year high fat diet affects muscle-but not brain mitochondria
  publication-title: J Cereb Blood Flow Metab.
  doi: 10.1038/jcbfm.2015.27
– volume: 25
  start-page: 3646
  year: 2011
  ident: B24
  article-title: Resveratrol prevents the wasting disorders of mechanical unloading by acting as a physical exercise mimetic in the rat
  publication-title: FASEB j.
  doi: 10.1096/fj.10-177295
– volume: 10
  start-page: 1167
  year: 2019
  ident: B30
  article-title: α-Ionone attenuates high-fat diet-induced skeletal muscle wasting in mice via activation of cAMP signaling
  publication-title: Food Funct.
  doi: 10.1039/c8fo01992d
– volume: 7
  start-page: 225
  year: 2016
  ident: B6
  article-title: Salidroside alleviates cachexia symptoms in mouse models of cancer cachexia via activating mTOR signalling
  publication-title: Journal of Cachexia, Sarcopenia and Muscle
  doi: 10.1002/jcsm.12054
– volume: 2017
  start-page: 1
  year: 2017
  ident: B8
  article-title: Exercise Combined withRhodiola sacraSupplementation Improves Exercise Capacity and Ameliorates Exhaustive Exercise-Induced Muscle Damage through Enhancement of Mitochondrial Quality Control
  publication-title: Oxidative Medicine and Cellular Longevity
  doi: 10.1155/2017/8024857
– volume: 12
  start-page: 372
  year: 2012
  ident: B31
  article-title: SIRT1 signaling as potential modulator of skeletal muscle diseases
  publication-title: Current Opinion in Pharmacology
  doi: 10.1016/j.coph.2012.02.010
– volume: 20
  start-page: 5507
  year: 2014
  ident: B32
  article-title: Editorial (Thematic Issue: Mitochondrial Biogenesis: Pharmacological Approaches)
  publication-title: Cpd
  doi: 10.2174/138161282035140911142118
– volume: 18
  start-page: 104
  ident: B10
  article-title: High-intensity interval training improves metabolic syndrome and body composition in outpatient cardiac rehabilitation patients with myocardial infarction
  publication-title: Cardiovasc Diabetol
  doi: 10.1186/s12933-019-0907-0
– volume: 5
  start-page: 111
  year: 2014
  ident: B22
  article-title: Reductions in C-reactive protein in older adults with type 2 diabetes are related to improvements in body composition following a randomized controlled trial of resistance training
  publication-title: J Cachexia Sarcopenia Muscle
  doi: 10.1007/s13539-014-0134-1
– volume: 27
  start-page: 449
  year: 2011
  ident: B28
  article-title: Physical activity and sarcopenia
  publication-title: Clinics in Geriatric Medicine
  doi: 10.1016/j.cger.2011.03.009
– volume: 27
  start-page: 839
  year: 2013
  ident: B26
  article-title: The effects of an acute dose of Rhodiola rosea on endurance exercise performance
  publication-title: J Strength Cond Res.
  doi: 10.1519/JSC.0b013e31825d9799
– volume: 15
  start-page: 838
  year: 2012
  ident: B5
  article-title: The NAD+ Precursor Nicotinamide Riboside Enhances Oxidative Metabolism and Protects against High-Fat Diet-Induced Obesity
  publication-title: Cell Metabolism
  doi: 10.1016/j.cmet.2012.04.022
– volume: 103
  start-page: 16260
  year: 2006
  ident: B29
  article-title: PGC-1 protects skeletal muscle from atrophy by suppressing FoxO3 action and atrophy-specific gene transcription
  publication-title: Proceedings of the National Academy of Sciences
  doi: 10.1073/pnas.0607795103
– volume: 64
  start-page: 1193
  year: 2015
  ident: B33
  article-title: Evidence for a Direct Effect of the NAD+Precursor Acipimox on Muscle Mitochondrial Function in Humans
  publication-title: Diabetes
  doi: 10.2337/db14-0667
– volume: 54
  start-page: 240
  year: 2019
  ident: B36
  article-title: Salidroside stimulates the Sirt1/PGC-1α axis and ameliorates diabetic nephropathy in mice
  publication-title: Phytomedicine
  doi: 10.1016/j.phymed.2018.10.031
– volume: 25
  start-page: 1094
  year: 2020
  ident: B20
  article-title: SIRT1 in forebrain excitatory neurons produces sexually dimorphic effects on depression-related behaviors and modulates neuronal excitability and synaptic transmission in the medial prefrontal cortex
  publication-title: Mol Psychiatry
  doi: 10.1038/s41380-019-0352-1
– volume: 288
  start-page: 30515
  year: 2013
  ident: B19
  article-title: SIRT1 protein, by blocking the activities of transcription factors FoxO1 and FoxO3, inhibits muscle atrophy and promotes muscle growth
  publication-title: Journal of Biological Chemistry
  doi: 10.1074/jbc.M113.489716
– volume: 12
  start-page: 1280
  year: 2020
  ident: B2
  article-title: Grape Polyphenols Ameliorate Muscle Decline Reducing Oxidative Stress and Oxidative Damage in Aged Rats
  publication-title: Nutrients
  doi: 10.3390/nu12051280
– volume: 136
  start-page: 585
  year: 2003
  ident: B1
  article-title: Effect of extracts from Rhodiola rosea and Rhodiola crenulata (Crassulaceae) roots on ATP content in mitochondria of skeletal muscles
  publication-title: Bulletin of Experimental Biology and Medicine
  doi: 10.1023/b:bebm.0000020211.24779.15
– volume: 10
  start-page: 665
  year: 2019
  ident: B34
  article-title: Salidroside Attenuates Denervation-Induced Skeletal Muscle Atrophy Through Negative Regulation of Pro-inflammatory Cytokine
  publication-title: Front. Physiol.
  doi: 10.3389/fphys.2019.00665
– volume: 18
  start-page: 1680
  year: 2021
  ident: B14
  article-title: Exercise combined with trimetazidine improves anti-fatal stress capacity through enhancing autophagy and heat shock protein 70 of myocardium in mice
  publication-title: Int. J. Med. Sci.
  doi: 10.7150/ijms.53899
– volume: 94
  start-page: 1718
  ident: B9
  article-title: High-Intensity Interval Training in Cardiac Rehabilitation: Impact on Fat Mass in Patients With Myocardial Infarction
  publication-title: Mayo Clinic Proceedings
  doi: 10.1016/j.mayocp.2019.04.033
– volume: 64
  start-page: 166
  year: 2012
  ident: B4
  article-title: Targeting Sirtuin 1 to Improve Metabolism: All You Need Is NAD+?
  publication-title: Pharmacol Rev.
  doi: 10.1124/pr.110.003905
– volume: 135
  start-page: 332
  year: 2015
  ident: B3
  article-title: Insulin receptor A and Sirtuin 1 synergistically improve learning and spatial memory following chronic salidroside treatment during hypoxia
  publication-title: J. Neurochem.
  doi: 10.1111/jnc.13225
– volume: 28
  start-page: 969
  year: 2018
  ident: B11
  article-title: Skeletal muscle mitochondrial remodeling in exercise and diseases
  publication-title: Cell Res.
  doi: 10.1038/s41422-018-0078-7
– volume: 224
  start-page: 157
  year: 2019
  ident: B35
  article-title: Trimetazidine combined with exercise improves exercise capacity and anti-fatal stress ability through enhancing mitochondrial quality control
  publication-title: Life Sciences
  doi: 10.1016/j.lfs.2019.03.027
– volume: 36
  start-page: 589
  year: 2011
  ident: B12
  article-title: Deacetylation of PGC-1α by SIRT1: importance for skeletal muscle function and exercise-induced mitochondrial biogenesis
  publication-title: Appl. Physiol. Nutr. Metab.
  doi: 10.1139/h11-070
– volume: 54
  start-page: 975
  year: 2020
  ident: B25
  article-title: Mono- and Polyunsaturated Fatty Acids Counter Palmitate-Induced Mitochondrial Dysfunction in Rat Skeletal Muscle Cells
  publication-title: Cell Physiol Biochem.
  doi: 10.33594/000000282
– volume: 14
  start-page: 451
  year: 2012
  ident: B7
  article-title: Adherence of heart failure patients to exercise: barriers and possible solutions
  publication-title: European Journal of Heart Failure
  doi: 10.1093/eurjhf/hfs048
– volume: 100
  start-page: 3077
  year: 2003
  ident: B21
  article-title: Triglyceride accumulation protects against fatty acid-induced lipotoxicity
  publication-title: Proceedings of the National Academy of Sciences
  doi: 10.1073/pnas.0630588100
– volume: 22
  start-page: 94
  year: 2016
  ident: B27
  article-title: Muscle atrophy in patients with Type 2 Diabetes Mellitus: roles of inflammatory pathways, physical activity and exercise
  publication-title: Exerc Immunol Rev.
– volume: 11
  start-page: 801
  year: 2012
  ident: B16
  article-title: The impact of aging on mitochondrial function and biogenesis pathways in skeletal muscle of sedentary high- and low-functioning elderly individuals
  publication-title: Aging Cell
  doi: 10.1111/j.1474-9726.2012.00844.x
– volume: 127
  start-page: 1109
  year: 2006
  ident: B18
  article-title: Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1α
  publication-title: Cell
  doi: 10.1016/j.cell.2006.11.013
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Snippet Muscle dysfunction is a complication of high-fat diet (HFD)-induced obesity that could be prevented by exercise, but patients did not get enough therapeutic...
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SubjectTerms atrogenes
mitochondrion
Pharmacology
rhodiola
RM1-950
salidroside
SIRT1
Therapeutics. Pharmacology
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Title The Treatment of Rhodiola Mimics Exercise to Resist High-Fat Diet-Induced Muscle Dysfunction via Sirtuin1-Dependent Mechanisms
URI https://cir.nii.ac.jp/crid/1871428068021126400
https://www.ncbi.nlm.nih.gov/pubmed/33935745
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https://pubmed.ncbi.nlm.nih.gov/PMC8082455
https://doaj.org/article/25e8457f18c14f51a893e6042066b2e0
Volume 12
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