Effects of intravascular laser irradiation of blood in mitochondria dysfunction and oxidative stress in adults with chronic spinal cord injury

Photomedicine and Laser Surgery

Volumn 30, Issue 10, 2012, Pages 579-586

  Huang, Shih Fong ^a   Tsai, Yun An ^a   Wu, Shi Bei ^b   Wei, Yau Huei ^b,c   Tsai, Po Yi ^b   Chuang, Tien Yow ^b  

^a TAIPEI VETERANS GENERAL HOSPITAL   (Taiwan)

^b NATIONAL YANG MING UNIVERSITY   (Taiwan)

^c MACKAY MEDICAL COLLEGE   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIOXIDANT DEFENSE; ATP SYNTHESIS; CLINICAL EFFECTS; COPY NUMBER; HIGH-DENSITY LIPOPROTEINS; INTRA-GROUP; INTRAVASCULAR; LASER IRRADIATION OF BLOOD; LASER POWER; LOW DENSITY LIPOPROTEINS; MALONDIALDEHYDE; METABOLIC PATHWAYS; MITOCHONDRIAL DNA (MTDNA); MITOCHONDRIAL DYSFUNCTION; SPINAL CORD INJURIES (SCI); STATISTICAL DIFFERENCES; STUDY GROUPS; TOTAL ANTIOXIDANT CAPACITY; WHITE BLOOD CELLS;

ADENOSINETRIPHOSPHATE; ALDEHYDES; BLOOD; NUCLEIC ACIDS; OXIDATIVE STRESS; PATIENT REHABILITATION;

MITOCHONDRIA;

BIOLOGICAL MARKER;

ADULT; AGED; ANALYSIS OF VARIANCE; ARTICLE; BLOOD; CHI SQUARE DISTRIBUTION; CHRONIC DISEASE; COMPARATIVE STUDY; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENDOVASCULAR SURGERY; FEMALE; HUMAN; LOW LEVEL LASER THERAPY; MALE; METABOLISM; METHODOLOGY; MIDDLE AGED; NONPARAMETRIC TEST; OXIDATIVE STRESS; PROSPECTIVE STUDY; RADIATION EXPOSURE; RANDOMIZED CONTROLLED TRIAL; REFERENCE VALUE; RISK ASSESSMENT; SINGLE BLIND PROCEDURE; SPINAL CORD INJURY; TREATMENT OUTCOME;

ADULT; AGED; ANALYSIS OF VARIANCE; BIOLOGICAL MARKERS; BLOOD; CHI-SQUARE DISTRIBUTION; CHRONIC DISEASE; ENDOVASCULAR PROCEDURES; FEMALE; HUMANS; LASER THERAPY, LOW-LEVEL; MALE; MIDDLE AGED; MITOCHONDRIAL DISEASES; OXIDATIVE STRESS; PROSPECTIVE STUDIES; REFERENCE VALUES; RISK ASSESSMENT; SINGLE-BLIND METHOD; SPINAL CORD INJURIES; STATISTICS, NONPARAMETRIC; TREATMENT OUTCOME;

EID: 84867521654     PISSN: 15495418     EISSN: None     Source Type: Journal    
DOI: 10.1089/pho.2012.3228     Document Type: Article

References (37)

1. Timofeyev, V.T., Poryadin, G.V., and Goloviznin, M.V. (2001). Laser irradiation as a potential pathogenetic method for immunocorrection for rheumatoid arthritis. Pathophy-siology 8, 35-40.
2. Arora, H., Pai. K.M., Maiya, A., Vidyasagar, M.S., and Ra-jeev, A. (2008). Efficacy of He-Ne laser in The prevention and treatment of radiotherapy-induced oral mucositis in oral cancer patients. Oral Surg. Oral Med. Pathol. Oral Radiol. Endod. 105, 180-186.
3. DerKacz, A., Protasiewicz, M., Poreba, R., Szuba, A., and Andrzejak, R. (2010). Usefulness of intravascular low power laser illumination in preventing restenosis after percutaneous coronary intervention. Am. J. Cardiol. 106(8), 1113-1117.
4. Weber, M.H., Fußgänger-May, T., and Wolf, T. (2007). The intravenous laser blood irradiation-introduction of a new therapy. Dt. Ztschr. F. Akup. 50, 12-23.
5. Karu, T.I., Pyatibrat, L.V., Kolyakov, S.F., and Afanasyeva, N.I. (2008). Absorption measurements of cell monolayers relevant to mechanisms of laser phototherapy: reduction or oxidation of cytochrome c oxidase under laser radiation at 632.8 nm. Photomed. Laser Surg. 26, 593-599.
6. Karu T.I. (2008). Mitochondrial signaling in mammalian cells activated by red and near-IR radiation. Photochem. Photo-biol. 84, 1091-1099.
7. Hu, W.P., Wang, J.J., Yu, C.L., Lan, C.C., Chen, G.S., and Yu, H.S. (2007). Helium-neon laser irradiation stimulates cell proliferation through photostimulatory effects in mitochondria. J. Invest. Dermatol. 127, 2048-2057.
8. Sroka, R., Schaffer, M., Fuchs, C., et al. (1999). Effects on The mitosis of normal and tumor cells induced by light treatment of different wavelengths. Lasers Surg. Med. 25, 263-271.
9. Fernández-Checa, J.C., Fernández, A., Morales, A., Marí, M., García-Ruiz, C., and Colell, A. (2010). Oxidative stress and altered mitochondrial function in neurodegenerative diseases: lessons from mouse models. CNS Neurol. Disord. Drug Targets 9, 439-454.
10. Hipkiss, A.R. (2010). Mitochondrial dysfunction, proteo-toxicity, and aging: causes or effects, and The possible impact of NAD+-controlled protein glycation. Adv. Clin. Chem. 50, 123-150.
11. Leduc, L., Levy, E., Bouity-Voubou, M., and Delvin, E. (2010). Fetal programming of atherosclerosis: possible role of The mitochondria. Eur. J. Obstet. Gynecol. Reprod. Biol. 149, 127-130.
12. Vaishnav, R.A., Singh, I.N., Miller, D.M., and Hall, E.D. (2010). Lipid Peroxidation-Derived Reactive Aldehydes Directly and Differentially Impair Spinal Cord and Brain Mitochondrial Function. J. Neurotrauma. 27, 1311-1320.
13. Frost, F., Roach, M.J., Kushner, I., and Schreiber, P. (2005). Inflammatory C-reactive protein and cytokine levels in asymptomatic people with chronic spinal cord injury. Arch. Phys. Med. Rehabil. 86, 312-317.
14. Rajan, S., McNeely, M.J., Hammond, M., Goldstein, B., and Weaver, F. (2010). Association between obesity and diabetes mellitus in veterans with spinal cord injuries and disorders. Am. J. Phys. Med. Rehabil. 89, 353-361.
15. Inskip, J., Plunet, W., Ramer, L., Ramsey, J.B., Yung, A., Kozlowski, P. Ramer, M., and Krassioukov, A. (2010). Car-diometabolic risk factors in experimental spinal cord injury. J. Neurotrauma. 27, 275-285.
16. Mokini, Z., Marcovecchio, M.L., and Chiarelli, F. (2010). Molecular pathology of oxidative stress in diabetic angiopathy: role of mitochondrial and cellular pathways. Diabetes Res. Clin. Pract. 87, 313-321.
17. Liang, H., Mojtahedi, M.C., Chen, D., and Braunschweig, C.L. (2008). Elevated C-reactive protein associated with decreased high-density lipoprotein cholesterol in men with spinal cord injury. Arch. Phys. Med. Rehabil. 89, 36-41.
18. Vaziri, N.D., Lee, Y.S., Lin, C.Y., Lin, V.W., and Sindu, R.K. (2004). NAD(P)H oxidase, superoxide dismutase, catalase, glutathione peroxidase and nitric oxide synthase expression in subacute spinal cord injury. Brain Res. 995, 76-83.
19. Azbill, R.D., Mu, X.J., Bruce-Keller, A.J., Mattson, M.P., and Springer, J.E. (1997). Impaired mitochondrial function, oxi-dative stress and altered antioxidant enzyme activities following traumatic spinal cord injury. Brain Res. 765, 283-290.
20. Jia, Z., Zhu, H., Li, J., Wang, X., Misra, H., and Li, Y. (2012). Oxidative stress in spinal cord injury and antioxidant-based intervention. Spinal Cord 50, 264-274.
21. Lee, H.C., Li, S.H., Lin, J.C., Wu, C.C., Yeh, D.C., and Wei, Y.H. (2004). Somatic mutations in The D-loop and decrease in The copy number of mitochondrial DNA in human hepato-cellular carcinoma. Mutat. Res. 547, 71-78.
22. Chen, C.T., Shih, Y.R., Kuo, T.K., Lee, O.K., and Wei, Y.H. (2008). Coordinated changes of mitochondrial biogenesis and antioxidant enzymes during osteogenic differentiation of human mesenchymal stem cells. Stem Cells 26, 960-968.
23. Chen, S.S., Wu, S.B., and Wei, Y.H. (2010). The difference in oxidative stress of The blood between using 5% glucose water and distilled water as The irrigant for BPH patients undergoing transurethral resection of The prostate. World J. Urol. 28, 33-37.
24. Li, X.Z., Li, M.X., and Wang, Y.F. (1998). He-Ne laser intravascular irradiation therapy in The treatment of 55 cases with acute cerebral infarction. Chin. J. Phys. Ther. 21, 17-19.
25. Huo, X.L., Zhang, Y.D., Di, Q., Wu, X.F., Fang, Q., and Hu, Z.R. (2000). Effect of The intravascular low level laser irradiation with different doses of different lasers on The blood biomarkers in patients with cerebral infarction. Chin. J. Laser Med. Surg. 9, 80-84.
26. Timofeyev, V.T., Poryadin, G.V., and Goloviznin M.V. (2001). Laser irradiation as a potential pathogenetic method for immunocorrection in rheumatoid arthritis. Pathophy-siology 8, 35-40.
27. Czernicki, J., Radziszewski, K., and Talar, J. (1994). Effect of laser biostimulation on leg blood flow in The course of arteriosclerosis. Pol. Tyg. Lek. 25, 363-365.
28. Andra, F. (2007). The effects of intravascular low level laser therapy in The scope of a redifferentiation therapy of malignant tumors. German Med. J. Oncol. 6, 1-5.
29. Tafur, J., and Mills, P.J. (2008). Low-intensity light therapy: exploring The role of redox mechanisms. Photomed. Laser Surg. 26, 323-328.
30. Arcari, D.P., Porto, V.B., Rodrigues, E.R.V., et al. (2011). Effect of mate tea (Ilex paraguariensis) supplementation on oxidative stress biomarkers and LDL oxidisability in normo-and hyperlipidaemic humans. J. Funct. Foods 3, 190-197.
31. Zhang, J., Xing, D., and Gao, X. (2008). Low-power laser irradiation activates Src tyrosine kinase through reactive oxygen species-mediated signaling pathway. J. Cell Physiol. 217, 518-528.
32. Van Raam, B.J., Sluiter, W., Wit, E., Roos, D., Verhoeven, A.J., and Kuijpers, T.W. (2008). Mitochondrial membrane potential in human neutrophils is maintained by complex III activity in The absence of supercomplex organization. PloS One 3, 1-12.
33. Galland, F., Duvillard, L., Petit, J.M., et al. (2006). Effect of insulin treatment on plasma oxidized LDL/LDL-cholesterol ratio in type 2 diabetic patients. Diabetes Metab. 32, 625-631.
34. Rezen, T., Roman, D., Pascussi, J.M., and Monostory, K. (2011). Interplay between cholesterol and drug metabolism. Biochim Biophys Acta 1814, 146-160.
35. Alving, C.R., and Wassef, N.M. (1999). Naturally occurring antibodies to cholesterol: A new theory of LDL cholesterol metabolism. Immunol. Today. 20(8), 362-366.
36. Link, J.J., Rohatgi, A., and De Lemos, J.A. (2007). HDL cholesterol:physiology, pathophysiology and management. Curr. Probl. Cardiol.32, 268-314.
37. Raveh, O., Pinchuk, I., Fainaru, M., and Lichtenberg, D. (2001). Kinetics of lipid peroxidation in mixtures of HDL and LDL mutual effects. Free Radic. Biol. Med. 31(11), 1486-1497.