Ozone oxidative post-conditioning reduces oxidative protein damage in patients with disc hernia

被引:34
作者
Leon Fernandez, Olga Sonia [1 ]
Pantoja, Marelis [1 ]
Diaz Soto, Maria Teresa [1 ]
Dranguet, Jaqueline [2 ]
Garcia Insua, Martina [3 ]
Viebhan-Hansler, Renata [4 ]
Menendez Cepero, Silvia [5 ]
Calunga Fernandez, Jose L. [5 ]
机构
[1] Univ Havana, Dept Pharmacol Toxicol, Inst Pharm & Food Sci, Havana 10400, Cuba
[2] Univ Havana, Ctr Studies Res & Biol Evaluat CEIEB IFAL, Havana 10400, Cuba
[3] Inst Angiol & Vasc Surg, Havana, Cuba
[4] J Hansler GmbH, Iffezheim, Germany
[5] Ozone Res Ctr, Havana, Cuba
关键词
Disc hernia; Oxidative protein damage; Ozone; INTERVERTEBRAL DISC; LIPID-PEROXIDATION; IN-VITRO; PROTECTION; PRODUCTS; MEDIATORS; ISCHEMIA; TISSUE; ALPHA; CELLS;
D O I
10.1179/1743132811Y.0000000060
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Introduction/objectives: Although inflammation in disc hernia (DH) has been recognized and it is a well-known process mediated by loss of the cellular redox balance, only a few studies about the impact of chronic oxidative stress on this neurological disorder have been made. Ozone therapy has been widely used with clinical efficacy in DH. This work aimed at characterizing the systemic redox status of patients with low back pain and neck pain as well as studying if ozone oxidative post-conditioning modified the pathological oxidative stress and protected against oxidative protein damage and if there is any relationship between oxidative changes and pain in both DH. Methods: Redox status of 33 patients with diagnosis of DH by computerized axial tomography, nuclear magnetic resonance, and clinical evaluations was studied. Ozone was administered by paravertebral way. After ozone treatment, plasmatic levels of antioxidant/pro-oxidant markers, pain, and life quality disability parameters were evaluated. Results: One hundred percent of patients showed a severe oxidative stress. Major changes in superoxide dismutase activity, total hydroperoxides, advanced oxidation protein products, fructolysine content, and malondialdehyde were observed. After ozone oxidative post-conditioning, there was a re-establishment of patients' cellular redox balance as well as a decrease in pain in both DH. A relationship between indicators of oxidative protein damage and pain was demonstrated. Conclusions: Ozone therapy protected against oxidation of proteins and reduced the pain. Relationship between markers of oxidative protein damage, disability parameters, and pain suggests the role of oxidative stress in the pathological processes involved in DH.
引用
收藏
页码:59 / 67
页数:9
相关论文
共 36 条
[1]
Similar protective effect of ischaemic and ozone oxidative preconditionings in liver ischaemia/reperfusion injury [J].
Ajamieh, H ;
Merino, N ;
Candelario-Jalil, E ;
Menéndez, S ;
Martinez-Sanchez, G ;
Re, L ;
Giuliani, A ;
Leon, OS .
PHARMACOLOGICAL RESEARCH, 2002, 45 (04) :333-339
[2]
Role of protein synthesis in the protection conferred by ozone-oxidative-preconditioning in hepatic ischaemia/reperfusion [J].
Ajamieh, HH ;
Berlanga, J ;
Merino, N ;
Sánchez, GM ;
Carmona, AM ;
Cepero, SM ;
Giuliani, A ;
Re, L ;
León, OS .
TRANSPLANT INTERNATIONAL, 2005, 18 (05) :604-612
[3]
Ischemic and ozone oxidative preconditioning in the protection against hepatic ischemic-reperfusion injury [J].
Ajamieh, HH ;
Menéndez, S ;
Merino, N ;
Martínez-Sánchez, G ;
Re, L ;
León, OS .
OZONE-SCIENCE & ENGINEERING, 2003, 25 (03) :241-250
[4]
Effects of ozone oxidative preconditioning on nitric oxide generation and cellular redox balance in a rat model of hepatic ischaemia-reperfusion [J].
Ajamieh, HH ;
Menéndez, S ;
Martínez-Sánchez, G ;
Candelario-Jalil, E ;
Re, L ;
Giuliani, A ;
Fernández, OSL .
LIVER INTERNATIONAL, 2004, 24 (01) :55-62
[5]
Al-Dalain SM, 2001, PHARMACOL RES, V44, P391
[6]
Relevance of in vitro and in vivo models for intervertebral disc degeneration [J].
An, HS ;
Masuda, K .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2006, 88A :88-94
[7]
*BIOCH INF, 1987, REV BIOCH REF SOURC, P15
[8]
SPARC, a matricellular protein that functions in cellular differentiation and tissue response to injury [J].
Bradshaw, AD ;
Sage, EH .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (09) :1049-1054
[9]
Oxidative preconditioning affords protection against carbon tetrachloride-induced glycogen depletion and oxidative stress in rats [J].
Candelario-Jalil, E ;
Mohammed-Al-Dalain, S ;
Fernández, OSL ;
Menéndez, S ;
Pérez-Davison, G ;
Merino, N ;
Sam, S ;
Ajamieh, HH .
JOURNAL OF APPLIED TOXICOLOGY, 2001, 21 (04) :297-301
[10]
Involvement of hydrogen peroxide in collagen cross-linking by high glucose in vitro and in vivo [J].
Elgawish, A ;
Glomb, M ;
Friedlander, M ;
Monnier, VM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (22) :12964-12971