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Protective effect of Scutellaria species on AAPH-induced oxidative damage in human erythrocyte

  • Sasidharan Salini , Menon Kunnathully Divya , Thomas Chubicka , Nair Meera , Devanand P. Fulzele , Achuthan C. Ragavamenon and Thekkekara Devassy Babu EMAIL logo
Published/Copyright: December 15, 2015

Abstract

Background:Scutellaria baicalensis is a well-known plant in traditional Chinese medicine. Recently, several Scutellaria species with therapeutic potential have been recognized worldwide. Scutellaria colebrookiana and Scutellaria violacea, native to the Western Ghats of India, are reported to possess free radical scavenging efficacy. At present, the protective effect of these Scutellaria spp. against 2,2′ azobis (2-amidinopropane) hydrochloride (AAPH)-induced oxidative damage in human erythrocytes has been analyzed.

Methods: Oxidative stress in erythrocyte was induced by AAPH. The inhibition of hemolysis, membrane lipid peroxidation, and protein damage by chloroform extracts of Scutellaria spp. was assessed biochemically. Phytochemicals of the extracts were analyzed by Fourier transform infrared spectrophotometer (FTIR).

Results: Approximately 95% of erythrocytes were lysed by AAPH over 3 h of incubation. Significant reduction in hemolysis was observed by the extracts, and the IC50 values were 18.3 and 23.5 μg/mL for S. colebrookiana and S. violacea, respectively. Both the extracts were found to inhibit AAPH-induced lipid peroxidation in ghost membrane with IC50 92±2.8 and 70±5.6 μg/mL. In the analysis of the membrane proteins using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), the AAPH-induced degradation of actin was found reduced by both the extracts. The FTIR spectrum revealed the presence of polyphenols, carboxylic acids, alkanes, and aromatic compounds in extracts. In quantitative analysis, the total polyphenolic content estimated was 380±0.23 and 203.7±1.4 mg of gallic acid equivalent per gram extract of S. colebrookiana and S. violacea.

Conclusions: Results indicate that S. colebrookiana and S. violacea are capable of protecting erythrocytes from oxidative damage. This cytoprotective effect of the extract is possibly by its antioxidant property.


Corresponding author: Dr. Thekkekara Devassy Babu, Department of Biochemistry, Amala Cancer Research Centre, Amala Nagar PO, Thrissur 680 555, Kerala, India, Phone: +91-487-2304190, E-mail:

Acknowledgments

The authors are grateful to the Board of Research in Nuclear Sciences (BRNS), Department of Atomic Energy (DAE), Government of India (Grant/Award Number: ‘2013/35/11/BRNS/25 dt. 01/04/2013’), for providing the financial support for this work.

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Authors’ conflict of interest disclosure: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

  3. Research funding: None declared.

  4. Employment or leadership: None declared.

  5. Honorarium: None declared.

References

1. Beris H. Antioxidant effects: a basis of drug selection. Drugs 1991;42:569–605.10.2165/00003495-199142040-00003Search in Google Scholar

2. Yerra R, Senthil GP, Gupta M, Mazumdar UK. Studies on in vitro antioxidant activities of methanol extract of Mucnna pruriens (Fabaceae) seeds. Eur Bull Drug Res 2005;13:31.Search in Google Scholar

3. Miki M, Tamai H, Mino M, Yamamoto Y, Niki E. Free radical chain oxidation of rat red blood cells by molecular oxygen and its inhibition by α-tocopherol. Arch Biochem Biophys 1987;258:373–80.10.1016/0003-9861(87)90358-4Search in Google Scholar

4. Niki E, Yamamoto Y, Komuro E, Sato K. Membrane damage due to lipid oxidation. Am J Cin Nuir 1991;53:20lS–5S.10.1093/ajcn/53.1.201SSearch in Google Scholar

5. Fridovich S, Porter N. Oxidation of arachidonic acid in micelles by superoxide and hydrogen peroxide. J Biol Chem 1981;256:260–5.10.1016/S0021-9258(19)70128-8Search in Google Scholar

6. Repetto M, Semprine J, Boveris A. Lipid peroxidation: chemical mechanism, biological implications and analytical determination. In: Catala A, editor. Lipid peroxidation. New Delhi: Intech, 2012:1–28.10.5772/45943Search in Google Scholar

7. Chance B, Sies H, Boveris A. Hydroperoxide metabolism in mammalian organs. Physiol Rev 1979;59:527–605.10.1152/physrev.1979.59.3.527Search in Google Scholar

8. Halliwell B, Gutteridge JM. Oxygen toxicity, oxygen radicals, transition metals and disease. Biochem J 1984;218:1–14.10.1042/bj2190001Search in Google Scholar

9. Temple MJ. Antioxidants and disease: more questions than answers. Nutr Res 2000;20:449–59.10.1016/S0271-5317(00)00138-XSearch in Google Scholar

10. Katiyar SK, Afaq F, Perez A, Mukhtar H. Green tea polyphenol (3)-epigallocatechin-3-gallate treatment of human skin inhibits ultraviolet radiation-induced oxidative stress. Carcinogenesis 2001;22:287–94.10.1093/carcin/22.2.287Search in Google Scholar

11. Manach C, Regerat F, Texier O, Agullo G, Demigne C, Remesy C. Bioavailability, metabolism and physiological impact of 4-oxo flavonoids. Nutr Res 1996;16:517–44.10.1016/0271-5317(96)00032-2Search in Google Scholar

12. Shang X, He X, He X, Li M, Zhang R, Fan P, et al. The genus Scutellaria an ethnopharmacological and phytochemical review. J Ethnopharmacol 2010;128:279–313.10.1016/j.jep.2010.01.006Search in Google Scholar PubMed

13. Salini S, Chubicka T, Sasidharan N, Sindhu ER, Babu TD. Cytotoxic and antioxidant properties of selected Scutellaria species from the Western Ghats of Peninsular India. Pharm Biol 2013;51:152–9.10.3109/13880209.2012.715170Search in Google Scholar

14. Jimenez I, Garrido A, Bannach R, Gotteland M, Speisky H. Protective effects of boldine against free radical-induced erythrocyte lysis. Phytother Res 2000;14:339–43.10.1002/1099-1573(200008)14:5<339::AID-PTR585>3.0.CO;2-TSearch in Google Scholar

15. McDonald S, Prenzler PD, Autolovich M, Robards K. Phenolic content and antioxidant activity of olive extracts. Food Chem 2001;73:73–84.10.1016/S0308-8146(00)00288-0Search in Google Scholar

16. Chang C, Yang M, Wen H, Chern J. Estimation of total flavonoid content in propolis by two complementary colorimetric methods. J Food Drug Anal 2002;10:178–82.10.38212/2224-6614.2748Search in Google Scholar

17. Fairbanks G, Steck TL, Wallach DF. Electrophoretic analysis of the major polypeptide of the human erythrocyte membrane. Biochemistry 1971;10:2606–17.10.1021/bi00789a030Search in Google Scholar

18. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem 1951;193:265–75.10.1016/S0021-9258(19)52451-6Search in Google Scholar

19. Stocks J, Dormandy TL. The autoxidation of human red cell lipids induced by hydrogen peroxide. Br J Haemat 1972;20:95–111.10.1111/j.1365-2141.1971.tb00790.xSearch in Google Scholar

20. Chevion M, Berenshtein E, Stadtman ER. Human studies related to protein oxidation: protein carbonyl content as a marker of damage. Free Radic Res 2000;33:S99–108.Search in Google Scholar

21. Ajila CM, Rao PU. Protection against hydrogen peroxide induced oxidative damage in rat erythrocytes by Mangifera indica L. peel extract. Food Chem Toxicol 2008;46:303–9.10.1016/j.fct.2007.08.024Search in Google Scholar

22. Snyder LM, Fortier NL, Trainor J, Jacobs J, Leb L, Lubin B, et al. Effect of hydrogen peroxide exposure on normal human erythrocyte deformability, morphology, surface characteristics and spectrin-hemoglobin crosslinking. J Clin Invest 1985;76:1971–7.10.1172/JCI112196Search in Google Scholar

23. Flynn TP, Allen DW, Johnson GJ, White JG. Oxidant damage of the lipids and proteins of the erythrocyte membranes in unstable hemoglobin disease. Evidence for the role of lipid peroxidation. J Clin Invest 1983;71:1215–23.10.1172/JCI110870Search in Google Scholar

24. Yamamoto Y, Niki E, Eguchi J, Kamiya Y, Shimasaki H. Oxidation of biological membranes and its inhibition. Free radical chain oxidation of erythrocyte ghost membranes by oxygen. Biochim Biophys Acta 1985;819:29–36.10.1016/0005-2736(85)90192-0Search in Google Scholar

25. Sato Y, Kanazawa S, Sato K, Suzuki Y. Mechanism of free radical-induced hemolysis of human erythrocytes: II. Hemolysis by lipid-soluble radical initiator. Biol Pharm Bull 1998;21:250–6.10.1248/bpb.21.250Search in Google Scholar

26. Yen GC, Duh PD, Tsai CL. Relationship between antioxidant activity and maturity of peanut hulls. J Agric Food Chem 1993;41:67–70.10.1021/jf00025a015Search in Google Scholar

27. Bravo L. Polyphenols: chemistry, dietary sources, metabolism and nutritional significance. Nutr Rev 1998;56:317–33.10.1111/j.1753-4887.1998.tb01670.xSearch in Google Scholar

28. Li-Weber M. New therapeutic aspects of flavones: the anticancer properties of Scutellaria and its main active constituents wogonin, baicalein and baicalin. Cancer Treat Rev 2009;35:57–68.10.1016/j.ctrv.2008.09.005Search in Google Scholar

29. Gao Z, Huang K, Yang X, Xu H. Free radical scavenging and antioxidant activities of flavonoids extracted from the radix of Scutellaria baicalensis Georgi. Biochim Biophys Acta 1999;1472:643–50.10.1016/S0304-4165(99)00152-XSearch in Google Scholar

30. Zhu QY, Huang Y, Tsang D, Chen ZY. Regeneration of α-tocopherol in human LDL by green tea catechins. J Agric Food Chem 1999;47:2020–5.10.1021/jf9809941Search in Google Scholar PubMed

Received: 2015-7-8
Accepted: 2015-10-24
Published Online: 2015-12-15
Published in Print: 2016-6-1

©2016 by De Gruyter

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