The effect of lipoic acid on the content of SOD-1 and TNF-α in rat striated muscle

[1] Bolton CF. Neuromuscular manifestations of critical illness. Muscle Nerve. 2005; 32: 140–163. BoltonCF Neuromuscular manifestations of critical illness Muscle Nerve. 2005 32 140 163 10.1002/mus.2030415825186 Search in Google Scholar

[2] Valentine RJ, Jefferson MA, Kohut ML, Eo H. Imoxin attenuates LPS-induced inflammation and MuRF1 expression in mouse skeletal muscle. Physiol. Rep. 2018; 6: e13941. ValentineRJ JeffersonMA KohutML EoH Imoxin attenuates LPS-induced inflammation and MuRF1 expression in mouse skeletal muscle Physiol. Rep. 2018 6 e13941 10.14814/phy2.13941628689830548229 Search in Google Scholar

[3] Nedrebø T, Reed RK. Different serotypes of endotoxin (lipopolysaccha-ride) cause different increases in albumin extravasation in rats. Shock. 2002; 18: 138–141. NedrebøT ReedRK Different serotypes of endotoxin (lipopolysaccha-ride) cause different increases in albumin extravasation in rats Shock. 2002 18 138 141 10.1097/00024382-200208000-0000812166776 Search in Google Scholar

[4] Nemzek JA, Hugunin KM, Opp MR. Modeling sepsis in the laboratory: Merging sound science with animal well-being. Comp. Med. 2008; 58: 120–128. NemzekJA HuguninKM OppMR Modeling sepsis in the laboratory: Merging sound science with animal well-being Comp. Med. 2008 58 120 128 Search in Google Scholar

[5] Koyama S, Sato E, Nomura H, Kubo K, Miura M, Yamashita T, Nagai S, Izumi T. The potential of various lipopolysaccharides to release IL-8 and G-CSF. Am. J. Physiol. Lung Cell. Mol. Physiol. 2000; 278: L658–L666. KoyamaS SatoE NomuraH KuboK MiuraM YamashitaT NagaiS IzumiT The potential of various lipopolysaccharides to release IL-8 and G-CSF Am. J. Physiol. Lung Cell. Mol. Physiol. 2000 278 L658 L666 10.1152/ajplung.2000.278.4.L65810749742 Search in Google Scholar

[6] Lang CH, Frost RA, Jefferson LS, Kimball SR, Vary TC. Endotoxin-induced decrease in muscle protein synthesis is associated with changes in eIF2B, eIF4E, and IGF-I. Am. J. Physiol. Endocrinol. Metab. 2000; 278: E1133–E1143. LangCH FrostRA JeffersonLS KimballSR VaryTC Endotoxin-induced decrease in muscle protein synthesis is associated with changes in eIF2B, eIF4E, and IGF-I Am. J. Physiol. Endocrinol. Metab. 2000 278 E1133 E1143 10.1152/ajpendo.2000.278.6.E113310827017 Search in Google Scholar

[7] Roth J, De Souza GE. Fever induction pathways: Evidence from responses to systemic or local cytokine formation. Braz. J. Med. Biol. Res. 2001; 34: 301–314. RothJ De SouzaGE Fever induction pathways: Evidence from responses to systemic or local cytokine formation Braz. J. Med. Biol. Res. 2001 34 301 314 10.1590/S0100-879X2001000300003 Search in Google Scholar

[8] Sagy M, Al-Qaqaa Y, Kim P. Definitions and pathophysiology of sepsis. Curr. Probl. Pediatr. Adolesc. Health Care. 2013; 43: 260–263. SagyM Al-QaqaaY KimP Definitions and pathophysiology of sepsis Curr. Probl. Pediatr. Adolesc. Health Care. 2013 43 260 263 10.1016/j.cppeds.2013.10.00124295606 Search in Google Scholar

[9] Langhans C, Weber-Carstens S, Schmidt F, Hamati J, Kny M, Zhu X, Wollersheim T, Koch S, Krebs M, Schulz H, et al. Inflammation-induced acute phase response in skeletal muscle and critical illness myopathy. PLoS. One. 2014; 9: e92048. LanghansC Weber-CarstensS SchmidtF HamatiJ KnyM ZhuX WollersheimT KochS KrebsM SchulzH Inflammation-induced acute phase response in skeletal muscle and critical illness myopathy PLoS. One. 2014 9 e92048 10.1371/journal.pone.0092048396129724651840 Search in Google Scholar

[10] Morgan MJ, Liu ZG. Crosstalk of reactive oxygen species and NF-κB signaling. Cell Res. 2011; 21: 103–115. MorganMJ LiuZG Crosstalk of reactive oxygen species and NF-κB signaling Cell Res. 2011 21 103 115 10.1038/cr.2010.178319340021187859 Search in Google Scholar

[11] Chen Y, Zhou Z, Min W. Mitochondria, oxidative stress and innate immunity. Front Physiol. 2018; 9: 1487. ChenY ZhouZ MinW Mitochondria, oxidative stress and innate immunity Front Physiol. 2018 9 1487 10.3389/fphys.2018.01487620091630405440 Search in Google Scholar

[12] Kuwahara H, Horie S, Ishikawa S, Tsuda C, Kawakami S, Noda Y, Kaneko T, Tahara S, Tachibana T, Okabe M, et al. Oxidative stress in skeletal muscle causes severe disturbance of exercise activity without muscle atrophy. Free. Radic. Biol. Med. 2010; 48: 1252–1262. KuwaharaH HorieS IshikawaS TsudaC KawakamiS NodaY KanekoT TaharaS TachibanaT OkabeM Oxidative stress in skeletal muscle causes severe disturbance of exercise activity without muscle atrophy Free. Radic. Biol. Med. 2010 48 1252 1262 10.1016/j.freeradbiomed.2010.02.01120156551 Search in Google Scholar

[13] Maestraggi Q, Lebas B, Clere-Jehl R, Ludes PO, Chamaraux-Tran TN, Schneider F, Diemunsch P, Geny B, Pottecher J. Skeletal muscle and lymphocyte mitochondrial dysfunctions in septic shock trigger ICU-acquired weakness and sepsis-induced immunoparalysis. Biomed. Res. Int. 2017; 2017: 7897325. MaestraggiQ LebasB Clere-JehlR LudesPO Chamaraux-TranTN SchneiderF DiemunschP GenyB PottecherJ Skeletal muscle and lymphocyte mitochondrial dysfunctions in septic shock trigger ICU-acquired weakness and sepsis-induced immunoparalysis Biomed. Res. Int. 2017 2017 7897325 10.1155/2017/7897325544726828589148 Search in Google Scholar

[14] Muller FL, Song W, Jang YC, Liu Y, Sabia M, Richardson A, Van Remmen H. Denervation-induced skeletal muscle atrophy is associated with increased mitochondrial ROS production. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2007; 293: R1159–R1168. MullerFL SongW JangYC LiuY SabiaM RichardsonA Van RemmenH Denervation-induced skeletal muscle atrophy is associated with increased mitochondrial ROS production Am. J. Physiol. Regul. Integr. Comp. Physiol. 2007 293 R1159 R1168 10.1152/ajpregu.00767.200617584954 Search in Google Scholar

[15] Meyer M, Pahl HL, Baeuerle PA. Regulation of the transcription factors NF-κB and AP-1 by redox changes. Chem. Biol. Interact. 1994; 91: 91–100. MeyerM PahlHL BaeuerlePA Regulation of the transcription factors NF-κB and AP-1 by redox changes Chem. Biol. Interact. 1994 91 91 100 10.1016/0009-2797(94)90029-98194138 Search in Google Scholar

[16] Sundaram K, Panneerselvam K. Oxidative stress and DNA single strand breaks in skeletal muscle of aged rats: Role of carnitine and lipoic acid. Biogerontology. 2006; 7: 111–118. SundaramK PanneerselvamK Oxidative stress and DNA single strand breaks in skeletal muscle of aged rats: Role of carnitine and lipoic acid Biogerontology. 2006 7 111 118 10.1007/s10522-006-0002-216802114 Search in Google Scholar

[17] Thoma A, Lightfoot AP. NF-kB and inflammatory cytokine signaling: Role in skeletal muscle atrophy. Adv. Exp. Med. Biol. 2018; 1088: 267–279. ThomaA LightfootAP NF-kB and inflammatory cytokine signaling: Role in skeletal muscle atrophy Adv. Exp. Med. Biol. 2018 1088 267 279 10.1007/978-981-13-1435-3_1230390256 Search in Google Scholar

[18] Zhang Q, Pi J, Woods CG, Andersen ME. A systems biology perspective on Nrf2-mediated antioxidant response. Toxicol. Appl. Pharmacol. 2010; 244: 84–97. ZhangQ PiJ WoodsCG AndersenME A systems biology perspective on Nrf2-mediated antioxidant response Toxicol. Appl. Pharmacol. 2010 244 84 97 10.1016/j.taap.2009.08.018283775719716833 Search in Google Scholar

[19] Seifar F, Khalili M, Khaledyan H., Moghadam SA, Izadi A, Azimi A, Shakouri SK. α-Lipoic acid, functional fatty acid, as a novel therapeutic alternative for central nervous system diseases: A review. Nutr. Neurosci. 2019; 22: 306–316. SeifarF KhaliliM KhaledyanH. MoghadamSA IzadiA AzimiA ShakouriSK α-Lipoic acid, functional fatty acid, as a novel therapeutic alternative for central nervous system diseases: A review Nutr. Neurosci. 2019 22 306 316 10.1080/1028415X.2017.138675529185388 Search in Google Scholar

[20] Malińska D, Winiarska K. Kwas liponowy - charakterystyka i zastosowanie w terapii. Postep Hig. Med. Dosw. 2005; 59: 535–543. MalińskaD WiniarskaK Kwas liponowy - charakterystyka i zastosowanie w terapii Postep Hig. Med. Dosw. 2005 59 535 543 Search in Google Scholar

[21] Caldow MK, Ham DJ, Chee A, Trieu J, Naim T, Stapleton DI, Swiderski KG, Lynch GS, Koopman R. Muscle-specific deletion of SOCS3 does not reduce the anabolic response to leucine in a mouse model of acute inflammation. Cytokine. 2017; 96: 274–278. CaldowMK HamDJ CheeA TrieuJ NaimT StapletonDI SwiderskiKG LynchGS KoopmanR Muscle-specific deletion of SOCS3 does not reduce the anabolic response to leucine in a mouse model of acute inflammation Cytokine. 2017 96 274 278 10.1016/j.cyto.2017.05.01628554144 Search in Google Scholar

[22] Li YP, Atkins CM, Sweatt JD, Reid MB. Mitochondria mediate tumor necrosis factor-α/NF-κB signaling in skeletal muscle myotubes. Antoxid. Redox. Signal. 1999; 1: 97–104. LiYP AtkinsCM SweattJD ReidMB Mitochondria mediate tumor necrosis factor-α/NF-κB signaling in skeletal muscle myotubes Antoxid. Redox. Signal. 1999 1 97 104 10.1089/ars.1999.1.1-9711225736 Search in Google Scholar

[23] Supinski GS, Alimov AP, Wang L, Song XH, Callahan LA. Neutral sphingomyelinase 2 is required for cytokine-induced skeletal muscle calpain activation. Am. J. Physiol. Lung Cell. Mol. Physiol. 2015; 309: L614–L624. SupinskiGS AlimovAP WangL SongXH CallahanLA Neutral sphingomyelinase 2 is required for cytokine-induced skeletal muscle calpain activation Am. J. Physiol. Lung Cell. Mol. Physiol. 2015 309 L614 L624 10.1152/ajplung.00141.2015457241726138644 Search in Google Scholar

[24] Linke A, Adams V, Schulze PC, Erbs S, Gielen S, Fiehn E, Möbius-Winkler S, Schubert A, Schuler G, Hambrecht R. Antioxidative effects of exercise training in patients with chronic heart failure: Increase in radical scavenger enzyme activity in skeletal muscle. Circulation. 2005; 111: 1763–1770. LinkeA AdamsV SchulzePC ErbsS GielenS FiehnE Möbius-WinklerS SchubertA SchulerG HambrechtR Antioxidative effects of exercise training in patients with chronic heart failure: Increase in radical scavenger enzyme activity in skeletal muscle Circulation. 2005 111 1763 1770 10.1161/01.CIR.0000165503.08661.E515809365 Search in Google Scholar

[25] Appell HJ, Duarte JA, Soares JM. Supplementation of vitamin E may attenuate skeletal muscle immobilization atrophy. Int. J. Sports Med. 1997; 18: 157–160. AppellHJ DuarteJA SoaresJM Supplementation of vitamin E may attenuate skeletal muscle immobilization atrophy Int. J. Sports Med. 1997 18 157 160 10.1055/s-2007-9726129187967 Search in Google Scholar

[26] Bianca RD, Wayman NS, McDonald MC, Pinto A, Sharpe MA, Cuzzocrea S, Chatterjee PK, Thiemermann C. Superoxide dismutase mimetic with catalase activity, EUK-134, attenuates the multiple organ injury and dysfunction caused by endotoxin in the rat. Med. Sci. Monit. 2002; 8: BR1–BR7. BiancaRD WaymanNS McDonaldMC PintoA SharpeMA CuzzocreaS ChatterjeePK ThiemermannC Superoxide dismutase mimetic with catalase activity, EUK-134, attenuates the multiple organ injury and dysfunction caused by endotoxin in the rat Med. Sci. Monit. 2002 8 BR1 BR7 Search in Google Scholar

[27] Kozakowska M, Pietraszak-Gremplewicz K, Jozkowicz A, Jozkowicz A, Dulak J. The role of oxidative stress in skeletal muscle injury and regeneration: Focus and antioxidant enzymes. J. Muscle Res. Cell Motil. 2015; 36: 377–393. KozakowskaM Pietraszak-GremplewiczK JozkowiczA JozkowiczA DulakJ The role of oxidative stress in skeletal muscle injury and regeneration: Focus and antioxidant enzymes J. Muscle Res. Cell Motil. 2015 36 377 393 10.1007/s10974-015-9438-9476291726728750 Search in Google Scholar

[28] Min W, Bin ZW, Quan ZB, Hui ZJ, Sheng FG. The signal transduction pathway of PKC/NF-κB/c-fos may be involved in the influence of high glucose on the cardiomyocytes of neonatal rats. Cardiovasc. Diabetol. 2009; 8: 8. MinW BinZW QuanZB HuiZJ ShengFG The signal transduction pathway of PKC/NF-κB/c-fos may be involved in the influence of high glucose on the cardiomyocytes of neonatal rats Cardiovasc. Diabetol. 2009 8 8 10.1186/1475-2840-8-8265244219210763 Search in Google Scholar

[29] Devasagayam TP, Tilak JC, Boloor KK, Sane KS, Ghaskadbi SS, Lele RD. Free radicals and antioxidants in human health: Current status and future prospects. J. Assoc. Physicians India. 2004; 52: 794–804. DevasagayamTP TilakJC BoloorKK SaneKS GhaskadbiSS LeleRD Free radicals and antioxidants in human health: Current status and future prospects J. Assoc. Physicians India. 2004 52 794 804 Search in Google Scholar

[30] Savikj M, Kostovski E, Lundell LS, Iversen PO, Massart J, Widegren U. Altered oxidative stress and antioxidant defence in skeletal muscle during the first year following spinal cord injury. Physiol. Rep. 2019; 7: e14218. SavikjM KostovskiE LundellLS IversenPO MassartJ WidegrenU Altered oxidative stress and antioxidant defence in skeletal muscle during the first year following spinal cord injury Physiol. Rep. 2019 7 e14218 10.14814/phy2.14218671223631456346 Search in Google Scholar

[31] Bhowmick S, D’Mello V, Caruso D, Abdul-Muneer PM. Traumatic brain injury-induced downregulation of Nrf2 activates inflammatory response and atopic cell death. J. Mol. Med. 2019; 97: 1627–1641. BhowmickS D’MelloV CarusoD Abdul-MuneerPM Traumatic brain injury-induced downregulation of Nrf2 activates inflammatory response and atopic cell death J. Mol. Med. 2019 97 1627 1641 10.1007/s00109-019-01851-431758217 Search in Google Scholar

[32] Yin F, Sancheti H, Cadenas E. Mitochondrial thiols in the regulation of cell death pathways. Antioxid. Redox. Signal. 2012; 17: 1714–1727. YinF SanchetiH CadenasE Mitochondrial thiols in the regulation of cell death pathways Antioxid. Redox. Signal. 2012 17 1714 1727 10.1089/ars.2012.4639347418422530585 Search in Google Scholar

[33] Qin Z, Reszka KJ, Fukai T, Weintraub NL. Extracellular superoxide dismutase (ecSOD) in vascular biology: An update on exogenous gene transfer and endogenous regulators of ecSOD. Transl. Res. 2008; 151: 68–78. QinZ ReszkaKJ FukaiT WeintraubNL Extracellular superoxide dismutase (ecSOD) in vascular biology: An update on exogenous gene transfer and endogenous regulators of ecSOD Transl. Res. 2008 151 68 78 10.1016/j.trsl.2007.10.003423048618201674 Search in Google Scholar

[34] Gorąca A, Huk-Kolega H, Piechota A, Kleniewska P, Ciejka E, Skibska B. Lipoic acid-biological activity and therapeutic potential. Pharmaco.l Rep. 2011; 63: 849–858. GorącaA Huk-KolegaH PiechotaA KleniewskaP CiejkaE SkibskaB Lipoic acid-biological activity and therapeutic potential Pharmaco.l Rep. 2011 63 849 858 10.1016/S1734-1140(11)70600-4 Search in Google Scholar

[35] Packer L, Roy S, Sen CK. α-Lipoic acid: A metabolic antioxidant and potential redox modulator of transcription. Adv. Pharmacol. 1997; 38: 79–101. PackerL RoyS SenCK α-Lipoic acid: A metabolic antioxidant and potential redox modulator of transcription Adv. Pharmacol. 1997 38 79 101 10.1016/S1054-3589(08)60980-1 Search in Google Scholar

[36] Camiolo G, Tibullo D, Giallongo C, Romano A, Parrinello NL, Musumeci G, Di Rosa M, Vicario N, Brundo MV, Amenta F, et al. α-Lipoic acid reduces iron-induced toxicity and oxidative stress in a model of iron overload. Int. J. Mol. Sci. 2019; 20: 609. CamioloG TibulloD GiallongoC RomanoA ParrinelloNL MusumeciG Di RosaM VicarioN BrundoMV AmentaF α-Lipoic acid reduces iron-induced toxicity and oxidative stress in a model of iron overload Int. J. Mol. Sci. 2019 20 609 10.3390/ijms20030609638729830708965 Search in Google Scholar

[37] Fei M, Xie Q, Zou Y, He R, Zhang Y, Wang J, Bo L, Li J, Deng X. Alpha-lipoic acid protects mice against concanavalin A-induced hepatitis by modulating cytokine secretion and reducing reactive oxygen species generation. Int. Immunopharmacol. 2016; 35: 53–60. FeiM XieQ ZouY HeR ZhangY WangJ BoL LiJ DengX Alpha-lipoic acid protects mice against concanavalin A-induced hepatitis by modulating cytokine secretion and reducing reactive oxygen species generation Int. Immunopharmacol. 2016 35 53 60 10.1016/j.intimp.2016.03.02327018751 Search in Google Scholar

[38] Haleagrahara N, Jackie T, Chakravarthi S, Kulur AB. Protective effect of alpha-lipoic acid against lead acetate-induced oxidative stress in the bone marrow of rats. Int. J. Pharmacol. 2011; 7: 217–227. HaleagraharaN JackieT ChakravarthiS KulurAB Protective effect of alpha-lipoic acid against lead acetate-induced oxidative stress in the bone marrow of rats Int. J. Pharmacol. 2011 7 217 227 10.3923/ijp.2011.217.227 Search in Google Scholar

[39] Zhao L, Liu Z, Jia H, Feng Z, Liu J, Li X. Lipoamide acts as an indirect antioxidant by simultaneously stimulating mitochondrial biogenesis and phase II antioxidant enzyme systems in ARPE-19 Cells. PLoS. One. 2015; 10: e0128502. ZhaoL LiuZ JiaH FengZ LiuJ LiX Lipoamide acts as an indirect antioxidant by simultaneously stimulating mitochondrial biogenesis and phase II antioxidant enzyme systems in ARPE-19 Cells PLoS. One. 2015 10 e0128502 10.1371/journal.pone.0128502445264426030919 Search in Google Scholar

[40] Shen HH, Lam KK, Cheng PY, Kung CW, Chen SY, Lin PC, Chung MT, Lee YM. Alpha-lipoic acid prevents endotoxic shock and multiple organ dysfunction syndrome induced by endotoxemia in rats. Shock. 2015; 43: 405–411. ShenHH LamKK ChengPY KungCW ChenSY LinPC ChungMT LeeYM Alpha-lipoic acid prevents endotoxic shock and multiple organ dysfunction syndrome induced by endotoxemia in rats Shock. 2015 43 405 411 10.1097/SHK.000000000000029525514429 Search in Google Scholar

[41] Cadirci E, Altunkaynak BZ, Halici Z, Odabasoglu F, Uyanik MH, Gundogdu C, Suleyman H, Halici M, Albayrak M, Unal B. Alpha-lipoic acid as a potential target for the treatment of lung injury caused by cecal ligation and puncture-induced sepsis model in rats. Shock. 2010; 33: 479–484. CadirciE AltunkaynakBZ HaliciZ OdabasogluF UyanikMH GundogduC SuleymanH HaliciM AlbayrakM UnalB Alpha-lipoic acid as a potential target for the treatment of lung injury caused by cecal ligation and puncture-induced sepsis model in rats Shock. 2010 33 479 484 10.1097/SHK.0b013e3181c3cf0e19823117 Search in Google Scholar

[42] Tian YF, He CT, Chen YT, Hsieh PS. Lipoic acid suppresses portal endotoxemia-induced steatohepatitis and pancreatic inflammation in rats. World. J. Gastroenterol. 2013; 19: 2761–2771. TianYF HeCT ChenYT HsiehPS Lipoic acid suppresses portal endotoxemia-induced steatohepatitis and pancreatic inflammation in rats World. J. Gastroenterol. 2013 19 2761 2771 10.3748/wjg.v19.i18.2761365315023687413 Search in Google Scholar

[43] Goraca A, Piechota A, Huk-Kolega H. Effect of alpha-lipoic acid on LPS-induced oxidative stress in the heart. J. Physiol. Pharmacol. 2009; 60: 61–68. GoracaA PiechotaA Huk-KolegaH Effect of alpha-lipoic acid on LPS-induced oxidative stress in the heart J. Physiol. Pharmacol. 2009 60 61 68 Search in Google Scholar

[44] Kurhaluk N, Szarmach A, Zaitseva OV, Sliuta A, Kyriienko S, Winklewski PJ. Effects of melatonin on low-dose lipopolysaccharide-induced oxidative stress in mouse liver, muscle, and kidney. Can. J. Physiol. Pharmacol. 2018; 96: 1153–1160. KurhalukN SzarmachA ZaitsevaOV SliutaA KyriienkoS WinklewskiPJ Effects of melatonin on low-dose lipopolysaccharide-induced oxidative stress in mouse liver, muscle, and kidney Can. J. Physiol. Pharmacol. 2018 96 1153 1160 10.1139/cjpp-2018-001130086243 Search in Google Scholar

[45] Steckert AV, de Castro AA, Quevedo J, Dal-Pizzol F. Sepsis in the central nervous system and antioxidant strategies with N-acetylcysteine, vitamins and statins. Curr. Neurovasc. Res. 2014; 11: 83–90. SteckertAV de CastroAA QuevedoJ Dal-PizzolF Sepsis in the central nervous system and antioxidant strategies with N-acetylcysteine, vitamins and statins Curr. Neurovasc. Res. 2014 11 83 90 10.2174/156720261066613121111101224329483 Search in Google Scholar