IN VITRO BIOMOLECULAR PROTECTIVE EFFECT OF CINNAMOMUM ZEYLANICUM BARK EXTRACTS AGAINST OXIDATIVE DAMAGE

Authors

  • Varalakshmi B. Department of Biochemistry, Shrimati Indira Gandhi College, Trichy, Tamil nadu, India
  • Vijaya Anand
  • Sampath Kumar

Keywords:

Lipid and DNA models, Lipid peroxidation, DNA damage, antioxidant activity, C zeylanicum bark

Abstract

Objective: Free radicals play an important role in the pathogenesis of many disorders by damaging important biomolecules such as lipids, proteins and DNA. Natural antioxidants are safer, cheaper and potential therapeutics to scavenge free radicals. Hence, this study was aimed to assess the biomolecular protective effect of Cinnamomum zeylanicum bark, a culinary spice, on the oxidant-treated membrane lipids and DNA in cell-free systems.

Methods: The total phenolics and flavonoid content of the bark were estimated. The extent of inhibition of lipid peroxidation (LPO) by aqueous, methanolic and chloroform extracts of bark was studied in vitro in three different membrane models such as goat RBC ghosts, goat liver homogenate, and goat liver slices which differ in architecture and lipid composition. The extent of inhibition of oxidant-induced DNA damage by the bark extracts was assessed in commercial DNA preparations such as pBR322, herring sperm, and calf thymus DNA.

Results: The total phenolic content was 153.33±23.09 mg of pyrocatechol equivalents/g, and flavonoid was 33.66±1.15 mg of catechin equivalents/g of powdered bark. All the three extracts exhibited a considerable inhibition of LPO in all the membrane systems, and most significant inhibition was exerted by methanolic extract on the RBC ghosts. All the three extracts were able to revert the oxidant-induced DNA damage, and more significant DNA protection was rendered by methanolic extract on calf thymus DNA.

Conclusion: The present study showed that C. zeylanicum bark is a nutraceutical rich in phenolic antioxidants that can protect biomolecules against oxidative stress.

Keywords: Lipid and DNA models, Lipid peroxidation (LPO), DNA damage, Antioxidant activity, C. zeylanicum bark

Downloads

Download data is not yet available.

References

Niki E. Do free radicals play a causal role in atherosclerosis? Low-density lipoprotein oxidation and vitamin E revisited. J Clin Biochem Nutr 2011;48:3–7.

Kohen R, Gati I. Skin low molecular weight antioxidants and their role in aging and in oxidative stress. Toxicol 2000;148:149–57.

Radha P, Padma PR. The free radical scavenging activity of Majorana hortensis leaves. Ancient Sci Life 2011;30:96-9.

Poulson HE, Prieme H, Loft S. Role of oxidative DNA damage in cancer initiation and promotion. Eur J Cancer Prev 1998;7:9–16.

Gulcin I, Mshvildadze V, Gepdiremen A, Elias R. Screening of antioxidant and antiradical activity of monodesmosides and crude extract from Leontice smirnowii tuber. Phytomedicine 2006;13:343-51.

Nargis Begum T, Muhammad Ilyas MH, Kalavathy S, Vijaya Anand A, Sampath Kumar P, Senthil R. Effects of ethanolic leaf extract of Azima tetracantha Lam. on ehrlich ascites carcinoma tumour bearing mice. Res J Med Sci 2009;4:351–4.

Gulcin I, Zubeyr H, Mahfuz E, Aboul-Enein HY. Radical scavenging and antioxidant activity of tannic acid. Arab J Chem 2010;3:43–53.

Matkowski A. Plant in vitro culture for the production of antioxidants a review. Biotechnol Adv 2008;26:548–60.

Matan N, Rimkeeree H, Mawson AJ, Chompreeda P, Haruthaithanasan V, Parker M. Antimicrobial activity of cinnamon and clove oils under modified atmosphere conditions. Int J Food Microbiol 2006;107:180–5.

Tung YT, Yen PL, Lin CY, Chang ST. Antiinflammatory activities of essential oils and their constituents from different provenances of indigenous cinnamon (Cinnamomum osmophloeum) leaves. Pharm Biol 2010;48:1130–6.

Kim SH, Hyun SH, Choung SY. Anti–diabetic effect of cinnamon extract on blood glucose in db/db mice. J Ethnopharmacol 2006;104:119–23.

Lu J, Zhang K, Nam S, Anderson RA, Jove R, Wen W. Novel angiogenesis inhibitory activity in cinnamon extract blocks VEGFR2 kinase and downstream signaling. Carcinogenesis 2010;31:481–8.

Mallick CP, Singh MB. Plant enzymology and plant histoenzymology, New Delhi: Kalyani Publishers; 1980. p. 286.

Cameron GR, Mitton RF, Allan JW. Measurement of flavonoids in plant sample. Lancet 1943;2:179.

Dodge JT, Mitchel C, Hanghan V. The preparation and chemical characteristics of hemoglobin free erythrocytes. Arch Biochem Biophys 1963;100:119-30.

Sumathi S, Padma PR. A comparative study on the inhibition of lipid peroxidation by Withania somnifera in different membrane models. Int J Plant Sci 2009;4:75-8.

Okhawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 1979;95:351-8.

Nichans WG, Samuelson B. Formation of malondialdehyde from phospholipids achidonate during microsomal lipid peroxidation. Eur J Biochem 1968;6:126-30.

Guha G, Rajkumar V, Mathew L, Kumar RA. The antioxidant and DNA protection potential of Indian tribal medicinal plants. Turk J Biol 2011;35:233-42.

Aeschlach R, Loliger J, Scott BC, Mureia A, Butter J, Halliwell B, et al. Antioxidant actions of thymol, carvacrol, 6-gingerol, zingerone and hydroxyl tyrosol. Food Chem Toxicol 1994;32:31-6.

El-Baroty GS, Abd El-Baky HH, Farag RS, Saleh MA. Characterization of antioxidant and antimicrobial compounds of cinnamon and ginger essential oils. Afr J Biochem Res 2010;4:167-74.

Jayaprakasha GK, Ohnishi-Kameyama M, Ono H, Yoshida M, Jaganmohan Rao L. Phenolic constituents in the fruits of Cinnamomum zeylanicum and their antioxidant activity. J Agric Food Chem 2006;54:1672-9.

Rice-Evans CA, Miller NJ, Paganga G. Structure–antioxidant activity relationships of flavonoids and phenolic acids. Free Radical Biol Med 1996;20:933-56.

Jayaprakasha GK, Negi PS, Jena BS, Mohan Rao LJ. Antioxidant and antimutagenic activities of Cinnamomumzeylanicum fruit extract. J Food Compos Anal 2007;20:330–6.

Seeram NP, Aviram M, Zhang Y, Henning SM, Feng L, Dreher M, et al. Comparison of antioxidant potency of commonly consumed polyphenol-rich beverages in the United States. J Agric Food Chem 2008;56:1415–22.

Liu LK, Lee HJ, Shih YW, Chyau CC, Wang CJ. Mulberry anthocyanin extracts inhibit LDL oxidation and macrophage-derived foam cell formation induced by oxidative LDL. J Food Sci 2008;73:113–21.

Fuhrman B, Volkova N, Coleman R, Aviram M. Grape powder polyphenols attenuate atherosclerosis development in apolipoprotein E deficient (E0) mice and reduce macrophage atherogenicity. J Nutr 2005;135:722–8.

Sumathi S, Padma PR, Radha P, Priyadharsini N, Padma N. Radical scavenging activity of different extracts of Withania somnifera leaves. Int J Plant Sci 2009;4:477-81.

Sreelatha S, Padma PR. Antioxidant activity and total phenolic content of Moringaoleifera leaves in two stages of maturity. Plant Foods Hum Nutr 2009;64:303–11.

Guha G, Rajkumar V, Ashok Kumar R, Mathew L. Antioxidant activity of lawsoniainermis extracts inhibits chromium (VI)-Induced cellular and DNA toxicity. J Evidence-Based Complementary Altern Med 2011. Doi:10.1093/ecam/nep205. [Article in Press].

Published

01-07-2016

How to Cite

B., V., V. Anand, and S. Kumar. “IN VITRO BIOMOLECULAR PROTECTIVE EFFECT OF CINNAMOMUM ZEYLANICUM BARK EXTRACTS AGAINST OXIDATIVE DAMAGE”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 8, no. 7, July 2016, pp. 369-72, https://journals.innovareacademics.in/index.php/ijpps/article/view/12205.

Issue

Section

Original Article(s)