CHEMO-PROTECTIVE EFFECT ON HEPATO-RENAL TOXCICITY AND CYTOTOXIC ACTIVITY OF LIPOIDAL MATTER OF ATRIPLEX LINDLEYI MOQ

Authors

  • AZZA A. MATLOUB Pharmacognosy Dept., National Research Centre, 12622, Egypt.
  • MANAL A. HAMED Therapeutic Chemistry Dept., National Research Centre 12622, Egypt.
  • SAHAR S. M. EL-SOUDA Chemistry of Natural Compounds Dept., National Research Center, 12622, Egypt.

Keywords:

Atriplex lindleyi, Petroleum ether extract, Oleanane skeleton, Fatty acids, Hepato-renal and cytotoxic activity

Abstract

Objective: Bromobenzene (BB) is frequently encountered in table-ready foods as contaminant residues. Therefore, the present study is designed to evaluate the petroleum ether extract of Atriplex lindleyi to attenuate the hepato-renal injury induced by BB exposure and study its cytotoxic activity against different human cell line as well as to describe the chemical composition of the petroleum ether extract.

Methods: The phytochemical study of petroleum ether extract was implemented using both GC/MS and column chromatography analysis. The isolated compounds were identified using different spectroscopic analysis.

Hepato-renal assay, rats were intraperitonealy injected bromobenzene at a dose 460 mg/kg BW. The petroleum ether extract as well as Hepaticum were administrated orally twice a week for three consecutive weeks with a dose 150 & 100 mg/kg body weight, respectively. Liver marker enzymes, liver function indices and kidney function tests were estimated.

The cytotoxic activity of, petroleum ether extract was assessed by the mitochondrial dependent reduction of MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide).

Results: Forty two compounds as well as sixteen fatty acids were identified in unsaponifiable and saponifiable fractions, respectively. Unsaponifiable fraction constituted of hydrocarbons (73.39% of total unsaponifiable matter), alcoholic (0.88%) and steroidal compounds (2.22%). Furthermore, column chromatography of petroleum ether extract afforded nonsterol tritrepenoids; olean-12-en-3,11-dione (1), β-amyrenone (2), erythrodiol I (3), Lupeol (4) as well as sterol triterpenoids; cholesterol (5) and mixture of β-sitosterol and stigmasterol (6). Compounds 1, 3 and 5 are first reported from Atriplex lindleyi. In addition, GC/MS analysis of the main fraction isolated from column chromatography revealed phytol as a major component.

Drastic changes were observed after BB intoxication in liver function parameters; kidney disorder indices and certain oxidative stress markers. Treatment with petroleum ether extract improved all biochemical parameters under investigation as well as the histopathology of liver and kidney. Petroleum ether extract showed growth inhibition of HepG2 and MCF7 human cells by 44.8 and 29.9%, respectively at 100 µg/ml.

Conclusion: The petroleum ether extract of A. lindleyi contains bioactive compounds exhibiting hepato-renal protection and cytotoxic activity.

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References

Asilbekova DT, Tursunkhodzhaeva FM, Gazizov FYu. Lipids from Atriplex dimorphostegia leaves. J Chem Nat Compd 2008;44 (6):764.

Omar AA, Sarg TM, Mansour ES, Abdel-Salam NM. Isolation of oleanolic and echinocystic acid from Atriplex nummularia. J Fitoterapia 1984;55(1):59.

Siddiqui BS, Ahmed S, Ghiasuddin, Khan MA. Triterpenoids of Atriplex stocksii. J Phytochemistry 1994;37:1123-5.

Tawfik WA, AbdelMohsen MM, Radwan HM, Habib AA, Yeramian MA. Phytochemical and biological investigations of Atriplex semibacata R. BR. Growing in Egypt. AJTCAM 2011;8(4):435-43.

Shaker HK, Dockendorff K, Seifert K. Triterpenoid saponins from Atriplex semibaccata. J Z Naturforsch [C] 2003;58 (7-8):485-9.

Jabrane P, Ben Jannet H, Miyamoto T, Tanaka C, Mirjolet J-F, Duchamp O. Glaucasides A-C, three saikosaponins from Atriplex glauca L. var. ifiniensis (Caball) Maire. J Mag Reson Chem 2011;49:83-9.

Al-Jaber NA, Mujahid TG, Al-Hazimi HMG. Secondary metabolites of Chenopodiaceace species. J Chem Soc Pak 1992;14 (1):76-83.

Emam SS. Bioactive constituents of Atriplex halimus plant. J Nat Prod 2011;4:25-41.

Mohammed R, El-Hawary SS, Abo-youssef AM. Biological investigation of some wild Aizoaceace and Chenopediaceae species growing in Egypt. J Nat Prod 2012;5:193-206.

Alicata ML, Amato G, Bonanno A, Giambalvo D, Leto G. In vivo digestibility and nutritive value of Atriplex halimus alone and mixed wheat straw. J Agr Sci 2002;139:139-42.

Ateya AM, El-Shafae AM, El-Shazly AM, Hemdan DE. Antihepatotoxic, anti-inflammatory, antimicrobial activities and chemical constituents of Atriplex inflata. J Bull Fac Pharm Cairo Univ 2005;43(2):265-72.

Boughalleb N, Trabelsi L, Harzallah-Skhiri F. Antifungal activity from polar and non-polar extracts of some Chenopodiaceae wild species growing in Tunisia. J Nat Prod Res 2009;23 (11):988-97.

Ben Sassi A, Harzallah-Skhiri F, Bourgougnon N, Aouni M. Antiviral activity of some Tunisian medicinal plants against Herpes simplex virus type 1. J Nat Prod Res 2008;22:53-65.

Heikes DL, Jensen SR, Fleming-Jones ME. Purge and trap extraction with GC–MS determination of volatile organic compounds in table-ready foods. J Agric Food Chem 1995;43:2869-75.

El-Sharaky AS, Newairy AA, Kamel MA, Eweda SM. Protective effect of ginger extract against bromobenzene-induced hepatotoxicity in male rats. J Food Chem Toxicol 2009;47(7):1584-90.

Swift ML. Analysis of molluscan sterols:Colorimetric methods. J Lipids 1984;19(8):625-30.

Matloub AA, Awad NE Phycochemistry of some Sargassum species and their cytotoxicity and antimicrobial activities. Egypt Pharm J 2012;11:99-108.

Mass Spectrometry Data Centre Eight Peaks Index of Mass Spectra. 2nd ed, AWRE:Aldermaston, Reading;1974.

Jennings W, Shibamoto T. Qualitative analysis of flavor and fragrance volatiles by glass capillary gas chromatography. New York:Academic Press;1980.

Adams RP. Identification of essential oils by ion trap mass spectroscopy. San Diego:Academic Press;1989.

Adams RP. Identification of essential oil components by gas chromatography/ mass spectroscopy. Allured Publishing Corp:Carol Stream, IL, USA;1995.

Wiley (Wiley Institute, USA) and NIST (National Institute of Technology, USA).

Harborne JB. Phytochemical Methods:A Guide to Modern Techniques of Plant Analysis. 3rd ed. London:Chapman and Hall;1998.

Li CS, Yu HW, Li GY, Zhang GL. Chemical constituents from the roots of Dysoxylum densiflorum. CJ NM 2010;8 (4):270-3.

Zhang XT, Zhang LH, Wang Y, Li Y, Wang YS, Ye WC. Chemical constituents from Thalictrum fortunei. CJNM 2009;7 (4):293-6.

Kamboj A, Saluja AK. Isolation of stigmasterol and β-sitosterol from petroleum ether extract of aerial parts of Ageratum conyzoides (Asteraceae). Int J Pharm Pharm Sci 2011;3:94-6.

Said O, Fulder S, Khalil K, Azaizeh H, Kassis E, Saad B. Maintaining a physiological blood glucose level with ‘Glucolevel’, a combination of four anti-diabetes plants used in the traditional arab herbal medicine. J Evid Based Complement Altern Med 2008;5(4):421-28.

Rice ME, Shelton E. Comparison of the reduction of two tetrazolium salts with succinoxidase activity of tissue homogenates. J Nat Cancer Inst 1957;18:117-25.

Babson AL, Babson SR. Kinetic colorimetric measurement of serum lactate dehydrogenase activity. J Clin Chem 1973;19:766-9.

Wattiaux R, De Duve C. Release of bound hydrolase by means of Triton X-100. Biochem J 1956;63:606-8.

Swanson MA. Glucose –6-phosphatase from liver. In:Methods in Enzymology, vol. 2. New York:Academic press;1955. p. 541-3.

Bodansiky O, Schwartz MK. Comparative effects of L-histidine on the activities of 5-nucleotidase and alkaline phosphatase. J Biol Chem 1963;238:3420-27.

Gella FJ, Olivella T, Cruz PM, Arenas J, Moreno R, Durban R, et al. A simple procedure for routine determination of aspartate aminotransferase and alanine aminotransferase with pyridoxal phosphate. J Clin Chem Acta 1985;153:241-7.

Rosalki SB, Foo AY, Burlina A. Multicenter evaluation of iso-ALP test kit for measurement of bone alkaline phosphatase activity in serum and plasma. J Clin Chem 1993;39:648-52.

Szasz G. A kinetic photometric method for serum γ-glutamyl transpeptidase. J Clin Chem 1969;15:124-36.

Bartels H, Bohmer M. Eine mikromethode zur kreatininbestimmung. J Clin Chem Acta 1971;32:81-5.

Tabacco A, Meiattini F, Moda E, Tarli P. Simplified enzymic colorimetric serum urea determination. J Clin Chem 1979;25:336-7.

Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. J Anal Biochem 1976;72:248-54.

Moron MS, Depierre JW, Mannervik B. Level of glutathione, glutathione reductase and glutathone-S-transferase activities in rat lung and liver. J Biochim Biophys Acta 1979;582:67-78.

Buege JA, Aust SD. Microsomal lipid peroxidation. J Meth Enzymol 1978;52:302-10.

Nishikimi M, Rae NA, Yagi K. The occurrence of superoxide anion in the action of reduced phenazine methosulphate and molecular oxygen. J Biochem Biophys Res Commun 1972;46:849-53.

Suzuki H, Suzuki K. Rat hypoplastic kidney (hpk/hpk) induces renal anemia, hyperparathyroidism, and osteodystrophy at the end stage of renal failure. J Vet Med Sci 1998;60:1051-8.

Mosmann T. Rapid colorimetric assays for cellular growth and survival:Application to proliferation and cytotoxicity assays. J Immunol Method 1983;65:55-63.

Thabrew MI, Hughes RD, McFarlane IG. Screening of hepatoprotective plant components using a HepG2 cell cytotoxicity assay. J Pharm Pharmacol 1997;49:1132-5.

Budzikiewich H, Wilson JM, Djerassi C. Mass spectrometry in structural and stereochemical problems XXXII. Pentacyclic triterpene. J Am Chem Soc 1963;85:3688-99.

Xiao Y, Guo-liang W, Fu-jun G. Studies on triterpenoid constituents isolated from the roots of Sabia schumanniana. J Acta Bot Sin 1994;36(2):153-8.

Hu HJ, Wang KW, Wu B, Sun CR, Pan YJ. Chemical shift assignments of two oleanane triterpenes from Euonymus hederaceus. J Zhejiang Univ Sci B 2005;6(8):719-21.

Branco A, Pinto AC, Filho RB. Chemical constituents from Vellozia graminifolia (Velloziaceae). J Ann Braz Acad Sci 2004;76(3):505-18.

Río JCD, Marques G, Rodríguez IM, Gutiérrez A. Chemical composition of lipophilic extractives from jute (Corchorus capsularis) fibers used for manufacturing of high-quality paper pulps. J Ind Crop Prod 2009;30:241-9.

Hashem FA, Sengab AE, Shabana MH, Khaled S. Antioxidant activity of Mayodendron igneum Kurz and the cytotoxicity of the isolated terpenoids. J Med Act Plant 2012;1:88-97.

Aktar F, Abdul Kaisar M, Hamidul Kabir ANM, Hasan C, Rashid MA. Phytochemical and Biological investigations of Ixora arbotea Roxb. DUJPS 2009;8(2):161-6.

Prakash CVS, Prakash I. Isolation and structural characterization of Lupane triterpenes from Polypodium vulgare. J RPS 2012;1:23-7.

Mansour HH, Hafez HF, Fahmy NM. Silymarin modulates cisplatin-induced oxidative stress and hepatotoxicity in rats. J Biochem Mol Biol 2006;39:656-61.

Wang BH, Zuzel KA, Rahman K, Billington D. Treatment with aged garlic extract protects against bromobenzene toxicity to precision cut rat liver slices. J Toxicology 1999;132:215-25.

Capua CJ, Hopson NP, Stewart CMM, Johnston GR, O’Neill KL, Schaalje GB et al. Cytotoxicity of Atriplex confertifolia. J Tox 2010;Article ID 976548, 7 pages. doi.org/ 10.1155/ 2010/ 976548.

Donaldson JR, M.S. thesis, BYU, Provo, Utah, USA in Capua CJ, et al. A new approach:comparing ethnobotany and chemical ecology approaches in the search for medicinal plants. J Cytotoxicity of Atriplex Confertifolia 2010 [Ref 55].

Salt TA, Adler JH. Diversity of sterol composition in the family Chenopodiaceae. J Lipids 1985;20:594-601.

Xu S, Patterson GW, Lusby WR, Schmid KM, Salt TA. The distribution and phylogenetic significance of desmethylsterols in Chenopodium and Atriplex:Coexistence of Δ7 -and Δ5-sterols. J Lipids 1990;25:61-4.

Tashima S, Kanazawa A, Yoshioka M, Kitahara K. Hypocholesterolemic effect of 24-methylene cholesterol and 7-cholestrol in rat. J Steroid Biochem 1974;5:69-72.

Gallo MBC, Sarachine MJ. Biological activities of lupeol. Int J Biomed Pharm Sci 2009;3:46-66.

Published

31-08-2014

How to Cite

MATLOUB, A. A., M. A. HAMED, and S. S. M. EL-SOUDA. “CHEMO-PROTECTIVE EFFECT ON HEPATO-RENAL TOXCICITY AND CYTOTOXIC ACTIVITY OF LIPOIDAL MATTER OF ATRIPLEX LINDLEYI MOQ”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 6, no. 8, Aug. 2014, pp. 187-96, https://journals.innovareacademics.in/index.php/ijpps/article/view/1485.

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