Static magnetic field attenuates lipopolysaccharide-induced multiple organ failure: A histopathologic study in mice
Abstract Purpose: Previous studies demonstrated that static magnetic fields (SMF) were effective in down-regulating the expression of lipopolysaccharide (LPS)-induced inflammatory cytokines. The aim of this study was to provide histological evidence of SMF attenuating LPS-induced multiple organ fail...
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Published in | International journal of radiation biology Vol. 91; no. 2; pp. 135 - 141 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Informa Healthcare
01.02.2015
Taylor & Francis |
Subjects | |
Online Access | Get full text |
ISSN | 0955-3002 1362-3095 1362-3095 |
DOI | 10.3109/09553002.2015.959669 |
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Abstract | Abstract
Purpose: Previous studies demonstrated that static magnetic fields (SMF) were effective in down-regulating the expression of lipopolysaccharide (LPS)-induced inflammatory cytokines. The aim of this study was to provide histological evidence of SMF attenuating LPS-induced multiple organ failure (MOF).
Materials and methods: In this study, BALB/cByJNarl (5 weeks, weighing 20-25 g) mice were chosen as test subjects. The tested animals were challenged with 50 mg/kg LPS after they were exposed to a continuous SMF for 2 h. The survival rate and pathological changes in lungs, kidneys, and livers of the LPS- challenged mice were examined with and without SMF treatment. In addition, the effects of SMF exposure on body temperature control of the LPS-challenged mice were monitored.
Results: Our results showed that at 30 h the survival rate of LPS-challenged mice increased 3.6-fold (p < 0.05). In addition, 6 h after LPS injection, the average body temperature of SMF-exposed mice was 1.07°C lower than that of unexposed animals. Tissue biopsies demonstrated that SMF exposure reduced damage to the lungs, livers, and kidneys in the LPS-challenged mice.
Conclusions: SMF show potential as a viable prophylactic alternative for controlling LPS-induced MOF. |
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AbstractList | Purpose: Previous studies demonstrated that static magnetic fields (SMF) were effective in down-regulating the expression of lipopolysaccharide (LPS)-induced inflammatory cytokines. The aim of this study was to provide histological evidence of SMF attenuating LPS-induced multiple organ failure (MOF).
Materials and methods: In this study, BALB/cByJNarl (5 weeks, weighing 20-25 g) mice were chosen as test subjects. The tested animals were challenged with 50 mg/kg LPS after they were exposed to a continuous SMF for 2 h. The survival rate and pathological changes in lungs, kidneys, and livers of the LPS- challenged mice were examined with and without SMF treatment. In addition, the effects of SMF exposure on body temperature control of the LPS-challenged mice were monitored.
Results: Our results showed that at 30 h the survival rate of LPS-challenged mice increased 3.6-fold (p < 0.05). In addition, 6 h after LPS injection, the average body temperature of SMF-exposed mice was 1.07°C lower than that of unexposed animals. Tissue biopsies demonstrated that SMF exposure reduced damage to the lungs, livers, and kidneys in the LPS-challenged mice.
Conclusions: SMF show potential as a viable prophylactic alternative for controlling LPS-induced MOF. Previous studies demonstrated that static magnetic fields (SMF) were effective in down-regulating the expression of lipopolysaccharide (LPS)-induced inflammatory cytokines. The aim of this study was to provide histological evidence of SMF attenuating LPS-induced multiple organ failure (MOF). In this study, BALB/cByJNarl (5 weeks, weighing 20-25 g) mice were chosen as test subjects. The tested animals were challenged with 50 mg/kg LPS after they were exposed to a continuous SMF for 2 h. The survival rate and pathological changes in lungs, kidneys, and livers of the LPS- challenged mice were examined with and without SMF treatment. In addition, the effects of SMF exposure on body temperature control of the LPS-challenged mice were monitored. Our results showed that at 30 h the survival rate of LPS-challenged mice increased 3.6-fold (p < 0.05). In addition, 6 h after LPS injection, the average body temperature of SMF-exposed mice was 1.07°C lower than that of unexposed animals. Tissue biopsies demonstrated that SMF exposure reduced damage to the lungs, livers, and kidneys in the LPS-challenged mice. SMF show potential as a viable prophylactic alternative for controlling LPS-induced MOF. Previous studies demonstrated that static magnetic fields (SMF) were effective in down-regulating the expression of lipopolysaccharide (LPS)-induced inflammatory cytokines. The aim of this study was to provide histological evidence of SMF attenuating LPS-induced multiple organ failure (MOF).PURPOSEPrevious studies demonstrated that static magnetic fields (SMF) were effective in down-regulating the expression of lipopolysaccharide (LPS)-induced inflammatory cytokines. The aim of this study was to provide histological evidence of SMF attenuating LPS-induced multiple organ failure (MOF).In this study, BALB/cByJNarl (5 weeks, weighing 20-25 g) mice were chosen as test subjects. The tested animals were challenged with 50 mg/kg LPS after they were exposed to a continuous SMF for 2 h. The survival rate and pathological changes in lungs, kidneys, and livers of the LPS- challenged mice were examined with and without SMF treatment. In addition, the effects of SMF exposure on body temperature control of the LPS-challenged mice were monitored.MATERIALS AND METHODSIn this study, BALB/cByJNarl (5 weeks, weighing 20-25 g) mice were chosen as test subjects. The tested animals were challenged with 50 mg/kg LPS after they were exposed to a continuous SMF for 2 h. The survival rate and pathological changes in lungs, kidneys, and livers of the LPS- challenged mice were examined with and without SMF treatment. In addition, the effects of SMF exposure on body temperature control of the LPS-challenged mice were monitored.Our results showed that at 30 h the survival rate of LPS-challenged mice increased 3.6-fold (p < 0.05). In addition, 6 h after LPS injection, the average body temperature of SMF-exposed mice was 1.07°C lower than that of unexposed animals. Tissue biopsies demonstrated that SMF exposure reduced damage to the lungs, livers, and kidneys in the LPS-challenged mice.RESULTSOur results showed that at 30 h the survival rate of LPS-challenged mice increased 3.6-fold (p < 0.05). In addition, 6 h after LPS injection, the average body temperature of SMF-exposed mice was 1.07°C lower than that of unexposed animals. Tissue biopsies demonstrated that SMF exposure reduced damage to the lungs, livers, and kidneys in the LPS-challenged mice.SMF show potential as a viable prophylactic alternative for controlling LPS-induced MOF.CONCLUSIONSSMF show potential as a viable prophylactic alternative for controlling LPS-induced MOF. Abstract Purpose: Previous studies demonstrated that static magnetic fields (SMF) were effective in down-regulating the expression of lipopolysaccharide (LPS)-induced inflammatory cytokines. The aim of this study was to provide histological evidence of SMF attenuating LPS-induced multiple organ failure (MOF). Materials and methods: In this study, BALB/cByJNarl (5 weeks, weighing 20-25 g) mice were chosen as test subjects. The tested animals were challenged with 50 mg/kg LPS after they were exposed to a continuous SMF for 2 h. The survival rate and pathological changes in lungs, kidneys, and livers of the LPS- challenged mice were examined with and without SMF treatment. In addition, the effects of SMF exposure on body temperature control of the LPS-challenged mice were monitored. Results: Our results showed that at 30 h the survival rate of LPS-challenged mice increased 3.6-fold (p < 0.05). In addition, 6 h after LPS injection, the average body temperature of SMF-exposed mice was 1.07°C lower than that of unexposed animals. Tissue biopsies demonstrated that SMF exposure reduced damage to the lungs, livers, and kidneys in the LPS-challenged mice. Conclusions: SMF show potential as a viable prophylactic alternative for controlling LPS-induced MOF. |
Author | Lai, Wei-Yi Lin, Che-Tong Fong, Tsorng-Harn Wang, Hsin-Ta Huang, Haw-Ming Huang, Yu-Chih Chang, Wei-Jen |
Author_xml | – sequence: 1 givenname: Wei-Yi surname: Lai fullname: Lai, Wei-Yi email: hhm@tmu.edu.tw, hhm@tmu.edu.tw organization: School of Dentistry, College of Oral Medicine, Taipei Medical University – sequence: 2 givenname: Yu-Chih surname: Huang fullname: Huang, Yu-Chih email: hhm@tmu.edu.tw, hhm@tmu.edu.tw organization: School of Dentistry, College of Oral Medicine, Taipei Medical University – sequence: 3 givenname: Wei-Jen surname: Chang fullname: Chang, Wei-Jen email: hhm@tmu.edu.tw, hhm@tmu.edu.tw organization: School of Dentistry, College of Oral Medicine, Taipei Medical University – sequence: 4 givenname: Hsin-Ta surname: Wang fullname: Wang, Hsin-Ta email: hhm@tmu.edu.tw, hhm@tmu.edu.tw organization: School of Organic and Polymeric, National Taipei University of Technology – sequence: 5 givenname: Tsorng-Harn surname: Fong fullname: Fong, Tsorng-Harn email: hhm@tmu.edu.tw, hhm@tmu.edu.tw organization: Department of Anatomy, School of Medicine, College of Medicine, Taipei Medical University – sequence: 6 givenname: Che-Tong surname: Lin fullname: Lin, Che-Tong email: hhm@tmu.edu.tw, hhm@tmu.edu.tw organization: School of Dentistry, College of Oral Medicine, Taipei Medical University – sequence: 7 givenname: Haw-Ming surname: Huang fullname: Huang, Haw-Ming email: hhm@tmu.edu.tw, hhm@tmu.edu.tw organization: Graduate Institute of Biomedical Materials and Tissue Engineering, College of Oral Medicine, Taipei Medical University |
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Cites_doi | 10.1136/bmj.327.7421.974 10.1080/09553000801902158 10.1016/j.pbiomolbio.2004.09.001 10.1016/S0749-0704(05)70113-5 10.1371/journal.pone.0072374 10.1097/01.shk.0000145937.70085.89 10.1152/ajpregu.00274.2006 10.1080/09553000902993908 10.1007/s00383-003-1123-1 10.1159/000356644 10.1007/s00134-005-2701-6 10.1016/j.etap.2006.09.001 10.1097/00003246-199506000-00008 10.1023/A:1024141128546 10.1016/S0167-5699(97)01103-1 10.1160/TH03-03-0182 10.3390/ijms140715017 10.1152/ajpregu.00370.2005 10.1002/ar.20646 10.1080/095530099140384 10.2478/v10001-010-0041-4 10.1186/1757-7241-22-16 10.1086/500836 10.1002/bem.10071 10.1007/s11605-007-0144-9 10.1155/2013/602987 10.1016/S1473-3099(02)00226-8 10.1097/00003246-200011000-00027 10.1016/j.jevs.2010.12.004 10.1080/15368370600925342 10.3109/15368378.2013.794734 10.1007/s00134-004-2234-4 10.1016/j.etap.2010.09.010 10.1097/01.shk.0000092268.01859.0d 10.1016/j.rvsc.2007.01.008 10.1177/000348940611500506 |
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References_xml | – volume: 327 start-page: 974 year: 2003 ident: CIT0036 publication-title: BMJ doi: 10.1136/bmj.327.7421.974 – volume: 5 start-page: 57 year: 2006 ident: CIT0008 publication-title: J Cell Mol Biol – ident: CIT0021 doi: 10.1080/09553000801902158 – volume: 87 start-page: 225 year: 2005 ident: CIT0031 publication-title: Prog Biophys Mol Biol doi: 10.1016/j.pbiomolbio.2004.09.001 – volume: 16 start-page: 337 year: 2000 ident: CIT0005 publication-title: Crit Care Clin doi: 10.1016/S0749-0704(05)70113-5 – volume: 8 start-page: e72374 year: 2013 ident: CIT0039 publication-title: PLoS ONE doi: 10.1371/journal.pone.0072374 – volume: 23 start-page: 88 year: 2005 ident: CIT0020 publication-title: Shock doi: 10.1097/01.shk.0000145937.70085.89 – volume-title: Environmental health criteria 232 – static fields year: 2006 ident: CIT0042 – volume: 292 start-page: 1667 year: 2007 ident: CIT0004 publication-title: Am J Physiol Regul Integr Comp Physiol doi: 10.1152/ajpregu.00274.2006 – ident: CIT0022 doi: 10.1080/09553000902993908 – volume: 20 start-page: 263 year: 2004 ident: CIT0006 publication-title: Pediatr Surg Int doi: 10.1007/s00383-003-1123-1 – volume: 32 start-page: 1878 year: 2013 ident: CIT0012 publication-title: Cell Physiol Biochem doi: 10.1159/000356644 – volume: 31 start-page: 1262 year: 2005 ident: CIT0026 publication-title: Intensive Care Med doi: 10.1007/s00134-005-2701-6 – volume: 23 start-page: 193 year: 2007 ident: CIT0002 publication-title: Environ Toxicol Pharmacol doi: 10.1016/j.etap.2006.09.001 – ident: CIT0030 doi: 10.1097/00003246-199506000-00008 – volume: 248 start-page: 35 year: 2003 ident: CIT0038 publication-title: Molec Cellular Biochem doi: 10.1023/A:1024141128546 – ident: CIT0035 doi: 10.1016/S0167-5699(97)01103-1 – volume: 91 start-page: 213 year: 2004 ident: CIT0011 publication-title: Thromb Haemost doi: 10.1160/TH03-03-0182 – volume: 7 start-page: 39 year: 2013 ident: CIT0025 publication-title: Afr J Biochem Res – volume: 14 start-page: 15017 year: 2013 ident: CIT0019 publication-title: Int J Mol Sci doi: 10.3390/ijms140715017 – volume: 289 start-page: 1244 year: 2005 ident: CIT0028 publication-title: Am J Physiol Regul Integr Comp Physiol doi: 10.1152/ajpregu.00370.2005 – volume: 291 start-page: 714 year: 2008 ident: CIT0034 publication-title: Anat Rec doi: 10.1002/ar.20646 – ident: CIT0029 doi: 10.1080/095530099140384 – volume: 23 start-page: 377 year: 2010 ident: CIT0027 publication-title: Int J Occup Med Environ Health doi: 10.2478/v10001-010-0041-4 – volume: 22 start-page: 16 year: 2014 ident: CIT0003 publication-title: Scand J Trauma Resusc Emerg Med doi: 10.1186/1757-7241-22-16 – volume: 193 start-page: 941 year: 2006 ident: CIT0013 publication-title: J Infect Dis doi: 10.1086/500836 – ident: CIT0001 doi: 10.1002/bem.10071 – volume: 11 start-page: 719 year: 2007 ident: CIT0017 publication-title: J Gastrointest Surg doi: 10.1007/s11605-007-0144-9 – volume: 2013 start-page: 1 year: 2013 ident: CIT0015 publication-title: Biomed Res Int doi: 10.1155/2013/602987 – volume: 2 start-page: 171 year: 2002 ident: CIT0016 publication-title: Lancet Infect Dis doi: 10.1016/S1473-3099(02)00226-8 – volume: 48 start-page: 28 year: 2006 ident: CIT0024 publication-title: Ann Emerg Med – volume: 28 start-page: 3697 year: 2000 ident: CIT0037 publication-title: Crit Care Med doi: 10.1097/00003246-200011000-00027 – volume: 31 start-page: 63 year: 2011 ident: CIT0018 publication-title: J Equine Vet Sci doi: 10.1016/j.jevs.2010.12.004 – ident: CIT0023 doi: 10.1080/15368370600925342 – volume: 33 start-page: 132 year: 2014 ident: CIT0033 publication-title: Electromagn Biol Med doi: 10.3109/15368378.2013.794734 – volume: 270 start-page: 927 year: 1996 ident: CIT0041 publication-title: Am J Physiol – volume: 216 start-page: 117 year: 1992 ident: CIT0009 publication-title: Pathophysiology and potential future therapy. Ann Surg – volume: 30 start-page: 1974 year: 2004 ident: CIT0010 publication-title: Intensive Care Med doi: 10.1007/s00134-004-2234-4 – volume: 31 start-page: 100 year: 2011 ident: CIT0014 publication-title: Environ Toxicol Pharmacol doi: 10.1016/j.etap.2010.09.010 – volume: 20 start-page: 402 year: 2003 ident: CIT0040 publication-title: Shock doi: 10.1097/01.shk.0000092268.01859.0d – volume: 83 start-page: 376 year: 2007 ident: CIT0032 publication-title: Res Vet Sci doi: 10.1016/j.rvsc.2007.01.008 – volume: 115 start-page: 350 year: 2006 ident: CIT0007 publication-title: Ann Otol Rhinol Laryngol doi: 10.1177/000348940611500506 |
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Purpose: Previous studies demonstrated that static magnetic fields (SMF) were effective in down-regulating the expression of lipopolysaccharide... Purpose: Previous studies demonstrated that static magnetic fields (SMF) were effective in down-regulating the expression of lipopolysaccharide (LPS)-induced... Previous studies demonstrated that static magnetic fields (SMF) were effective in down-regulating the expression of lipopolysaccharide (LPS)-induced... |
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SubjectTerms | Animals histopathology Kidney Cortex - drug effects Kidney Cortex - pathology lipopolysaccharide Lipopolysaccharides - adverse effects Liver - drug effects Liver - pathology Magnetic Fields Male Mice Mice, Inbred BALB C multiple organ failure Multiple Organ Failure - chemically induced Multiple Organ Failure - pathology Multiple Organ Failure - therapy Static magnetic field |
Title | Static magnetic field attenuates lipopolysaccharide-induced multiple organ failure: A histopathologic study in mice |
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