Oxidative impairment of plasma and skeletal muscle sarcoplasmic reticulum in rats with adjuvant arthritis - effects of pyridoindole antioxidants
- PMID: 18987589
Oxidative impairment of plasma and skeletal muscle sarcoplasmic reticulum in rats with adjuvant arthritis - effects of pyridoindole antioxidants
Abstract
Objectives: To study possible oxidation of proteins and lipids in plasma and sarcoplasmic reticulum (SR) from skeletal muscles and to assess the effects of pyridoindole antioxidants in rats with adjuvant arthritis (AA) and to analyze modulation of Ca-ATPase activity from SR (SERCA).
Methods: SR was isolated by ultracentrifugation, protein carbonyls in plasma and SR were determined by ELISA. Lipid peroxidation was analyzed by TBARS determination and by mass spectrometry. ATPase activity of SERCA was measured by NADH-coupled enzyme assay. Tryptophan fluorescence was used to analyze conformational alterations.
Results: Increase of protein carbonyls and lipid peroxidation was observed in plasma of rats with adjuvant arthritis. Pyridoindole antioxidant stobadine and its methylated derivative SMe1 decreased protein carbonyl formation in plasma, effect of stobadine was significant. Lipid peroxidation of plasma was without any effect of pyridoindole derivatives. Neither protein oxidation nor lipid peroxidation was identified in SR from AA rats. SERCA activity from AA rats increased significantly, stobadine and SMe1 diminished enzyme activity. Ratio of tryptophan fluorescence intensity in SR of AA rats increased and was not influenced by antioxidants.
Conclusion: Plasma proteins and lipids were oxidatively injured in rats with AA; antioxidants exerted protection only with respect to proteins. In SR, SERCA activity was altered, apparently induced by its conformational changes, as supported by study of tryptophan fluorescence. Stobadine and SMe1 induced a decrease of SERCA activity, elevated in AA rats, but they did not affect conformational changes associated with tryptophan fluorescence.
Similar articles
-
Modulation of SERCA in the chronic phase of adjuvant arthritis as a possible adaptation mechanism of redox imbalance.Free Radic Res. 2009 Sep;43(9):852-64. doi: 10.1080/10715760903089708. Epub 2009 Jul 8. Free Radic Res. 2009. PMID: 19591012
-
Modulation of sarcoplasmic/endoplasmic reticulum Ca(2+)-ATPase activity and oxidative modification during the development of adjuvant arthritis.Arch Biochem Biophys. 2011 Jul;511(1-2):40-7. doi: 10.1016/j.abb.2011.04.011. Epub 2011 Apr 22. Arch Biochem Biophys. 2011. PMID: 21531199
-
Effect of some antioxidants on sarcoplasmic reticulum Ca2+-ATPase activity from rabbit skeletal muscle.Neuro Endocrinol Lett. 2006 Dec;27 Suppl 2:164-7. Neuro Endocrinol Lett. 2006. PMID: 17159806
-
A review of recent insights into the role of the sarcoplasmic reticulum and Ca entry in uterine smooth muscle.Eur J Obstet Gynecol Reprod Biol. 2009 May;144 Suppl 1:S11-9. doi: 10.1016/j.ejogrb.2009.02.010. Epub 2009 Mar 13. Eur J Obstet Gynecol Reprod Biol. 2009. PMID: 19285773 Review.
-
Nitric-oxide-induced vasodilatation: regulation by physiologic s-glutathiolation and pathologic oxidation of the sarcoplasmic endoplasmic reticulum calcium ATPase.Trends Cardiovasc Med. 2006 May;16(4):109-14. doi: 10.1016/j.tcm.2006.02.001. Trends Cardiovasc Med. 2006. PMID: 16713532 Review.
Cited by
-
Effect of Carnosine in Experimental Arthritis and on Primary Culture Chondrocytes.Oxid Med Cell Longev. 2016;2016:8470589. doi: 10.1155/2016/8470589. Epub 2016 Jan 17. Oxid Med Cell Longev. 2016. PMID: 26885252 Free PMC article.
-
Pharmacological influence on processes of adjuvant arthritis: Effect of the combination of an antioxidant active substance with methotrexate.Interdiscip Toxicol. 2012 Jun;5(2):84-91. doi: 10.2478/v10102-012-0015-4. Interdiscip Toxicol. 2012. PMID: 23118593 Free PMC article.
-
Utilization of adjuvant arthritis model for evaluation of new approaches in rheumatoid arthritis therapy focused on regulation of immune processes and oxidative stress.Interdiscip Toxicol. 2011 Mar;4(1):33-9. doi: 10.2478/v10102-011-0007-9. Interdiscip Toxicol. 2011. PMID: 21577282 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical
Research Materials