Treatment with coenzyme Q10, omega-3-polyunsaturated fatty acids and their combination improved bioenergetics and levels of coenzyme Q9 and Q10 in skeletal muscle mitochondria in experimental model of arthritis
Jazyk angličtina Země Česko Médium print-electronic
Typ dokumentu hodnotící studie, časopisecké články
PubMed
34505525
PubMed Central
PMC8820522
DOI
10.33549/physiolres.934664
PII: 934664
Knihovny.cz E-zdroje
- MeSH
- antioxidancia metabolismus MeSH
- artritida experimentální krev dietoterapie MeSH
- C-reaktivní protein metabolismus MeSH
- chemokin CCL2 krev MeSH
- krysa rodu Rattus MeSH
- omega-3 mastné kyseliny terapeutické užití MeSH
- potkani inbrední LEW MeSH
- potravní doplňky MeSH
- revmatoidní artritida krev dietoterapie MeSH
- svalové mitochondrie metabolismus MeSH
- ubichinon analogy a deriváty metabolismus terapeutické užití MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- hodnotící studie MeSH
- Názvy látek
- antioxidancia MeSH
- C-reaktivní protein MeSH
- chemokin CCL2 MeSH
- coenzyme Q10 MeSH Prohlížeč
- omega-3 mastné kyseliny MeSH
- ubichinon MeSH
- ubiquinone 9 MeSH Prohlížeč
Rheumatoid arthritis (RA) and its animal model adjuvant arthritis (AA) are inflammatory diseases characterized by chronic inflammation, systemic oxidative stress and disturbed mitochondrial bioenergetics of skeletal muscle. The present study aimed to evaluate the effects of coenzyme Q10 - CoQ10 (100 mg/kg b.w.), omega-3-polyunsaturated fatty acids - omega-3-PUFA (400 mg/kg b.w.) and their combined treatment in AA on impaired skeletal muscle mitochondrial bioenergetics, inflammation and changes in levels CoQ9 and CoQ10 in plasma. Markers of inflammation (C-reactive protein, monocyte-chemotactic protein-1), antioxidant capacity of plasma, respiratory chain parameters of skeletal muscle mitochondria and concentrations of CoQ9 and CoQ10 in plasma and in muscle tissue were estimated. Treatment of the arthritic rats with CoQ10, omega-3-PUFA alone and in combination partially reduced markers of inflammation and increased antioxidant capacity of plasma, significantly increased concentrations of coenzyme Q in mitochondria and improved mitochondrial function in the skeletal muscle. Combined treatment has similar effect on the mitochondrial function as monotherapies; however, it has affected inflammation and antioxidant status more intensively than monotherapies. Long-term supplementary administration of coenzyme Q10 and omega-3-PUFA and especially their combination is able to restore the impaired mitochondrial bioenergetics and antioxidant status in AA.
Zobrazit více v PubMed
ABDOLLAHZAD H, AGHDASHI MA, ASGHARI JAFARABADI M, ALIPOUR B. Effects of coenzyme Q10 supplementation on inflammatory cytokines (TNF-α, IL-6) and oxidative stress in rheumatoid arthritis patients: A randomized controlled trial. Arch Med Res. 2015;46:527–533. doi: 10.1016/j.arcmed.2015.08.006. PubMed DOI
BALOGH E, VEALE DJ, McGARRY T, ORR C, SZEKANECZ Z, NG CT, FEARON U, BINIECKA M. Oxidative stress impairs energy metabolism in primary cells and synovial tissue of patients with rheumatoid arthritis. Arthritis Res Ther. 2018;20:95. doi: 10.1186/s13075-018-1592-1. PubMed DOI PMC
BAUEROVA K, KUCHARSKA J, MIHALOVA D, NAVAROVA J, GVOZDJAKOVA A, SUMBALOVA Z. Effect of coenzyme Q (10) supplementation in the rat model of adjuvant arthritis. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2005;149:501–503. doi: 10.5507/bp.2005.090. PubMed DOI
BAUEROVA K, PAULOVICOVA E, MIHALOVA D, DRAFI F, STROSOVA M, MASCIA C, BIASI F, ROVENSKY J, KUCHARSKA J, GVOZDJAKOVA A, PONIST S. Combined methotrexate and coenzyme Q10 therapy in adjuvant-induced arthritis evaluated using parameters of inflammation and oxidative stress. Acta Biochemica Polonica. 2010;57:347–354. doi: 10.18388/abp.2010_2415. PubMed DOI
CRANE FL, NAVAS P. The diversity of coenzyme Q function. Mol Aspects Med. 1997;18:1–6. doi: 10.1016/S0098-2997(97)00016-2. PubMed DOI
De PALMA L, CHILLEMI C, ALBANELLI S, RAPALI S, BERTONI-FREDDARI C. Muscle involvement in rheumatoid arthritis: an ultrastructural study. Ultrastruct Pathol. 2000;24:151–156. doi: 10.1080/01913120050132886. PubMed DOI
ESTABROOK RW. Mitochondrial respiratory control and the polarographic measurement of ADP:O ratios. In: ESTABROOK RW, PULLMAN ME, editors. Methods in Enzymology. Academic Press; New York and London: 1967. pp. 41–47. DOI
GIORDANO E, VISIOLI F. Long-chain omega 3 fatty acids: Molecular bases of potential antioxidant actions. Prostaglandins Leukot Essent Fatty Acids. 2014;90:1–4. doi: 10.1016/j.plefa.2013.11.002. PubMed DOI
GIOXARI A, KALIORA AC, MARANTIDOU F, PANAGIOTAKOS DP. Intake of ω-3 polyunsaturated fatty acids in patient with rheumatoid arthritis: A systemic review and meta-analysis. Nutrition. 2018;45:114–124. doi: 10.1016/j.nut.2017.06.023. PubMed DOI
GVOZDJAKOVA A. Mitochondrial physiology. In: GVOZDJAKOVA A, editor. Mitochondrial Medicine. Springer Science + Business Media; Germany: 2008. pp. 1–16. DOI
KHANNA S, TRIPATHY A, PADHAN P, GUPTA B. Unravelling mitochondrial dysfunction in rheumatoid arthritis patients. Can J Biotech. 2017;1:95. doi: 10.24870/cjb.2017-a82. DOI
KOHUTIAR M, ECKHARDT A, MIKŠÍK I, ŠANTOROVÁ P, WILHELM J. Proteomic analysis of peroxynitrite-induced protein nitration in isolated beef heart mitochondria. Physiol Res. 2018;67:239–250. doi: 10.33549/10.33549/physiolres.933608. PubMed DOI
KOVES TR, NOLAND RC, BATES AL, HENES ST, MUOIO DM, CORTRIGHT RN. Subsarcolemmal and intermyofibrillar mitochondria play distinct roles in regulating skeletal muscle fatty acid metabolism. Am J Physiol Cell Physiol. 2005;288:C1074–C1082. doi: 10.1152/ajpcell.00391.2004. PubMed DOI
KUCHARSKA J, BRAUNOVA Z, ULICNA O, ZLATOS L, GVOZDJAKOVA A. Deficit of coenzyme Q in heart and liver mitochondria of rats with streptozotocin-induced diabetes. Physiol Res. 2000;49:411–418. PubMed
LALIA AZ, DASARI S, ROBINSON MM, ABID H, MORSE DM, KLAUS KA, LANZA IR. Influence of omega-3 fatty acids on skeletal muscle protein metabolism and mitochondrial bioenergetics in older adults. Aging (Albany NY) 2017;9:1096–1129. doi: 10.18632/aging.101210. PubMed DOI PMC
LANG JK, GOHIL K, PACKER L. Simultaneous determination of tocopherols, ubiquinols, and ubiquinones in blood, plasma, tissue homogenates, and subcellular fractions. Anal Biochem. 1986;157:106–116. doi: 10.1016/0003-2697(86)90203-4. PubMed DOI
LEE J, HONG YS, JEONG JH, YANG EJ, JHUN JY, PARK MK, JUNG YO, MIN JK, KIM HY, PARK SH, CHO ML. Coenzyme Q10 ameliorates pain and cartilage degradation in a rat model of osteoarthritis by regulating nitric oxide and inflammatory cytokines. PLoS One. 2013;8:e69362. doi: 10.1371/journal.pone.0069362. PubMed DOI PMC
LI X, GUO Y, HUANG S, HE M, LIU Q, CHEN W, LIU M, XU D, HE P. Coenzyme Q10 prevents the interleukin-1 beta induced inflammatory response via inhibition of MAPK signaling pathways in rat articular chondrocytes. Drug Dev Res. 2017;78:403–410. doi: 10.1002/ddr.21412. PubMed DOI
LOPEZ-ARMADA MJ, RIVEIRO-NAVEIRA RR, VAAMONDE-GARCIA C, VALCARCEL-ARES MN. Mitochondrial dysfunction and the inflammatory response. Mitochondrion. 2013;13:106–118. doi: 10.1016/j.mito.2013.01.003. PubMed DOI
LORENTE-CEBRIAN S, COSTA AG, NAVAS-CARRETERO S, ZABALA M, LAIGLESIA LM, MARTINEZ JA, MORENO-ALIAGA MJ. An update on the role of omega-3 fatty acids on inflammatory and degenerative diseases. J Physiol Biochem. 2015;71:341–349. doi: 10.1007/s13105-015-0395-y. PubMed DOI
LOWRY DH, ROSENBROUGH NY, FARR AL, RANDALL RJ. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951;193:265–276. doi: 10.1016/S0021-9258(19)52451-6. PubMed DOI
MIRO O, PEDROL E, CASADEMONT J, GARCIA-CARRASCO M, SANMARTI R, CEBRIAN M, GRAN JM. Muscle involvement in rheumatoid arthritis: clinicopathological study of 21 symptomatic cases. Semin Arthritis Rheum. 1996;25:421–428. doi: 10.1016/S0049-0172(96)80007-2. PubMed DOI
MITCHEL P. The vital protonmotive role of coenzyme Q. In: FOLKERS K, LITTARRU GP, YAMAGAMI T, editors. Biomedical and Clinical Aspects of Coenzyme Q. Vol. 6. Amsterdam: Elsevier Science Publishers BV; 1991. pp. 3–10.
MOSCA F, FATTORINI D, BOMPADRE S, LITTARRU GP. Assay of coenzyme Q10 in plasma by a single dilution step. Anal Biochem. 2002;305:49–54. doi: 10.1006/abio.2002.5653. PubMed DOI
NAVARINI L, AFELTRA A, GALLO AFFLITO G, MARGIOTTA DPE. Polyunsaturated fatty acids: any role in rheumatoid arthritis. Lipids Health Dis. 2017;16:197. doi: 10.1186/s12944-017-0586-3. PubMed DOI PMC
NORDSTROM DC, HONKANEN VE, NASU Y, ANTILA E, FRIMAN C, KONTTINEN YT. Alpha-linolenic acid in the treatment of rheumatoid arthritis. A double-blind, placebo-controlled and randomized study: flaxseed vs. safflower seed. Rheumatol Int. 1995;14:231–234. doi: 10.1007/BF00262088. PubMed DOI
PALMER JW, TANDLER B, HOPPEL CL. Biochemical properties of subsarcolemmal and interfibrillar mitochondria isolated from rat cardiac muscle. J Biol Chem. 1977;252:8731–8739. doi: 10.1016/S0021-9258(19)75283-1. PubMed DOI
PHULL AR, NASIR B, HAQ IU, KIM SJ. Oxidative stress, consequences and ROS mediated cellular signalling in rheumatoid arthritis. Chem Biol Interactions. 2018;281:121–136. doi: 10.1016/j.cbi.2017.12.024. PubMed DOI
REMANS PH, SONT JK, WAGENAAR LW, WOUTERS-WESSELING W, ZUIJDERDUIN WM, JONGMA A, BREEDVELD FC, Van LAAR JM. Nutrient supplementation with polyunsaturated fatty acids and micronutrients in rheumatoid arthritis: clinical and biochemical effects. Eur J Clin Nutr. 2004;58:839–845. doi: 10.1038/sj.ejcn.1601883. PubMed DOI
ROUSLIN W, MILLARD RW. Canine myocardial ischemia: Defect in mitochondrial electron transfer complex I. J Mol Cell Cardiol. 1980;12:639–645. doi: 10.1016/0022-2828(80)90021-8. PubMed DOI
SLOVAK L, SVIK K, MIHALOVA D, TOTH J, CZIGLE S, PASKOVA L, BILKA F, BAUEROVA K. Ferulaldehyde improves the effect of methotrexate in experimental arthritis. Molecules. 2017;22:1911. doi: 10.3390/molecules22111911. PubMed DOI PMC
SULLIVAN EM, PENNINGTON ER, GREEN WD, BECK MA, BROWN DA, SHAIKH SR. Mechanisms by which dietary fatty acids regulate mitochondrial structure-function in health and disease. Adv Nutr. 2018;9:247–262. doi: 10.1093/advances/nmy007. PubMed DOI PMC
SUMBALOVA Z, KUCHARSKA J, KASPAROVA S, MLYNARIK V, BYSTRICKY P, BOZEK P, ULICNA O, VANCOVA O, SINGH RB, GVOZDJAKOVA A. Brain energy metabolism in experimental chronic diabetes: effect of long-term administration of coenzyme Q10 and ω-3 polyunsaturated fatty acids. Biologia. 2005;60:105–108.
TAWFIK MK. Combination of coenzyme Q10 with methotrexate suppresses Freund’s complete adjuvant-induced synovial inflammation with reduced hepatotoxicity in rats: Effect on oxidative stress and inflammation. Int Immunopharmacol. 2015;24:80–87. doi: 10.1016/j.intimp.2014.11.018. PubMed DOI
TSIKLAURI L, DRÁFI F, PONIŠT S, SLOVÁK L, CHRASTINA M, ŠVÍK K, KEMOKLIDZE Z, KEMERTELIDZE E, BAUEROVÁ K. Study of anti-inflammatory activity of Fatsiphloginum™ (Fatsia japonica) and a new purified triterpene-rich extract of saponins (PS-551) in experimental model of arthritis. Physiol Res. 2019;68(Suppl 1):S75–S85. doi: 10.33549/physiolres.934328. PubMed DOI
UDHAYA LAVINYA B, BARDHAN I, EVAN PRINCE S. Efficacy of coenzyme Q10 in inhibiting monosodium urate crystal-induced inflammation in rats. Eur J Pharmacol. 2016;791:589–594. doi: 10.1016/j.ejphar.2016.09.036. PubMed DOI
Van der WOUDE D, Van der HELM-Van MIL AHM. Update of the epidemiology, risk factors, and disease outcomes of rheumatoid arthritis. Best Pract Res Clin Rheumatol. 2018;32:174–187. doi: 10.1016/j.berh.2018.10.005. PubMed DOI
ZHANG J, SONG S, CAO W, LU J, WANG X, WANG G, WANG Z, CHEN X. Autophagy and mitochondrial dysfunction in adjuvant-arthritis rats’ treatment with resveratrol. Sci Rep. 2016;6:32928. doi: 10.1038/srep32928. PubMed DOI PMC
ZOFKOVA I, NEMCIKOVA P. Osteoporosis complicating some inborn or acquired diseases. Physiol Res. 2018;67(Suppl 3):S441–S454. doi: 10.33549/physiolres.934027. PubMed DOI