AMELIORATION OF GENTAMICIN-INDUCED NEPHROTOXICITY USING ESSENTIAL OIL EXTRACT FROM Otostegia fruticosa LEAVES IN ALBINO RATS

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Published: 2020-09-07

Page: 90-106


HUDA ABDEL RAHMAN OWYED AL-JUMAYI *

Nutrition and Food Science, Faculty of Science, Taif University, Kingdom of Saudi Arabia

*Author to whom correspondence should be addressed.


Abstract

Nephrotoxicity is an injury to the kidney it associated with impaired kidney function may be due to oxygen free radicals produced by drugs, chemical, and non-infectious agents. Therefore, the aim of this study was to evaluate Otostegia fruticosa (O. fruticosa) leaves for fractionation of flavonoids compounds and phenolic acids using HPLC and also the determination of essential oil using GC-MS. Acute and sub-acute oral toxicity was determined from the O. fruticosa leaves extract in mice. Moreover, the biological experiment was performed to assess the ameliorative effect of essential oil extract from O. fruticosa leaves at doses of 50, 100 and 200 mg/kg b.wt on gentamicin-induced nephrotoxicity in rats.

The results revealed that the O. fruticosa leaves extract was the highest containt of flavonoids as hispertin, kampferol, narengin, rutin, apigenin, rosmarinic and quercetrin. Total phenolic compounds were showed that the vanillic, pyrogallol, salycilic and catechein acids were the highest amounted in O. fruticosa leaves extract. The essential oils from O. fruticosa leaves extract as 2,5Dimethyl-p-cymene, 2-Allyl-4-methyl phenol, Apiol and Isolongipholene were the highest followed by Isocalamendiol, β-Caryophyllene, Limonene, γ-terpineol, α-Copaene, β-citronellol, Pulegone and α-Himachalene, respectively.

The acute toxicity experiment demonstrated that the essential oils from O. fruticosa leaves extract had no significant toxic effect in rats after administered at doses until 5000 mg/kg b.wt and sub-acute toxicity test confirmed that the O. fruticosa leaves the safety of the extract at the given dose.

The effect of essential oils from O. fruticosa leaves on antioxidant enzymes including GPx, SOD and CAT in rats suffering kidney damage groups, the results showed that the control positive group exhibited a significant decrease and the highest in the control negative group for antioxidant enzymes activity and also the different rat groups were fed administered orally essential oil extract from O. fruticosa increased gradually for antioxidant enzymes activity. In addition, essential oil of O. fruticosa leaves improved the kidney functions and some levels in the different nephrotoxicity rats groups. These results were confirmed by histological examination of the kidney this study concluded that the essential oil from O. fruticosa leaves extract protect the kidney from gentamicin-induced nephrotoxicity and thus substantiate the beneficial effects attributed traditionally to this plant.

Keywords: Gentamicin, nephrotoxicity, O. fruticosa leaves, flavonoids, antioxidant


How to Cite

AL-JUMAYI, H. A. R. O. (2020). AMELIORATION OF GENTAMICIN-INDUCED NEPHROTOXICITY USING ESSENTIAL OIL EXTRACT FROM Otostegia fruticosa LEAVES IN ALBINO RATS. PLANT CELL BIOTECHNOLOGY AND MOLECULAR BIOLOGY, 21(37-38), 90–106. Retrieved from https://ikprress.org/index.php/PCBMB/article/view/5416

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References

Shsrms S, Thokchom R. A review on endangered medicinal plants of India and their conservation. J. Crop Weed. 2014;10:205–218.

Das S, Roy A, Das PK. Ethnomedicinal uses of plants for wound healing in Khargone district, MP: A survey over Nimari communities. Res. J. Pharmacol. Pharmacodyn. 2014;6:21–29.

Sebald O. Otostegia Benth. In: Hadberg I, Kelbessa E, Edward S, Demissew S, Persson E, Editors. Flora of Ethiopia and Eritrea from Gentianaceae to Cyclocheilaceae, vol. 5. Addis Ababa & Uppsala: National Herbarium, Addis Ababa University. 2006;538.

Khan S, Syed F. Bioactive constituents from genus Otostegia. SARJ of Physical Sci. 2013;1:15-25.

Mothana RA, Al-Musayeib NM, Al-Ajmi MF, Cos P, Maes L. Evaluation of the In vitro antiplasmodial, antileishmanial and antitrypanosomal activity of medicinal plants used in Saudi and Yemeni traditional medicine. Evidence-Based Complementary and Alternative Medicine. 2014;1-8.

Scalbert A, Williamson G. Dietary intake and bioavailability of polyphenols. Journal of Nutrition. 2000;130:2073S–2085S.

Tungmunnithum D, Thongboonyou A, Pholboon A, Yangsabai A. Flavonoids and other phenolic compounds from medicinal plants for pharmaceutical and medical aspects: An overview. Medicines. 2018;5(93):2-16.

Edris AE. Pharmaceutical and therapeutic potentials of essential oils and their individual volatile constituents: A review. Phytotherapy Research. 2007;21(4):308-323.

Ali NAA, Alhamzy EH, Chhetric BK, Dosokyc NS, Setzerc WN. Chemical composition, antimicrobial and cytotoxic activities of the essential oil of Otostegia fruticosa subsp. schimperi from yemen. Natural Product Communications. 2017;12(6):969-972.

Al-Musayeib M, Abbas A, Ahmad S, Mossa S, El- Feraly S. Labdanediterpenes from Otostegia fruticosa. Phytochemistry. 2000;54:771-776.

Dennen P, Douglas IS, Anderson R. Acute kidney injury in the intensive care unit: An update and primer for the intensivist. Crit Care Med. 2010;38:261–275.

Uchino S, Kellum JA, Bellomo R. Acute renal failure in critically ill patients: A multinational, multicenter study. JAMA. 2005;294:813–818.

Yaklin KM. Acute kidney injury: An overview of pathophysiology and treatments. Nephrol Nurs J. 2011;38:13–18.

Zuo Y, Chen H, Deng Y. Simultaneous determination of catechins caffeine and gallic acids in green, oolong, black and purer teas using HPLC with a photodiode array detector. Talanta. 2002;57:307-316.

Goupy P, Hugues M, Biovin P, Amiot MJ. Antioxidant composition and activity of barley (Hordeum vulgare) and malt extracts and of isolated phenolic compounds. J. Sci. Food Agric. 1999;79:1625-1634.

Adams RP. Identification of essential oil components by gas chromatography/ mass spectroscopy. Carol Stream, IL: Allured Publishing Corporation (2nd Edn). Sarker D, Latif Z, Gray A, (Eds). Humana Press: Totowa. 1995;269–273.

Sadeghi H, Zarezade V, Sadeghi H, Akbartabar Toori M, Jafari Barmak M, Azizi A, Ghavamizadeh M, Mostafazadeh M. Anti-inflammatory activity of Stachys pilifera Benth. Iran Red Crescent Med J. 2014;16:9.

Kumar D, Bhat ZA, Shah MY. Effect of successive extracts of Stachys tibetica Vatke (Lamiaceae) in anxiety. Orient Pharm Exp Med. 2012;12:247-253.

Pell JD, Gee JM, Wortley GM, Johnson IT. Both dietary corn oil and guar gum stimulate intestinal crypt cell proliferation in rats, by independent but potentially synergistic mechanisms. J. Nutr. 1992;122:2447–2456.

Farombi OE, Ekott M. Cureuminatteruates gentamicin induced renal oxidative damage in rats. Food and Chem. Toxic. 2006;44:1443-1448.

Aebi ME. Catalase. In: Bergmeyer J, Grabl BM, (Eds) Methods of enzymatic analysis vol. III. Enzymes oxidoreductases, 3rd Ed. Weinheim: Verlag-Chemie. 1995;273-286.

Janknegt PJ, Rijstenbil JW, van de Poll WH, Gechev TS, Buma AG. A comparison of quantitative and qualitative superoxide dismutase assays for application to low temperature microalgae. J. Photochem. Photobiol. B Biol. 2007;87:218-226.

Paglia DE, Valentine WE. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J. Lab. Clin. Med. 1967;1:158-169.

Bowers LD, Wong ET. Kinetic serum creatinine assays. II. A critical evaluation and review. Clin. Chem. 1980;26:555-561.

Burtis AC, Ashwood. Tietz Textbook of Clinical Chemistry. 3rd Ed. AACCW. B. Sounders Co. London; 1999.

Jelikić-Stankov M, Djurdjević P, Stankov D. Determination of uric acid in human serum by an enzymatic method using N-methyl-N-(4-aminophenyl)-3-methoxyaniline reagent. J. Serb. Chem. Soc. 2003;68(8–9):691–698.

Doku GN, Gadzekpo VPY. Simultaneous determination of lithium, sodium and potassium in blood serum by flame photometric flow-injection analysis. Elsevier. 1996;43(5):735–739.

Wang Y, Han T, Xue LM, Han P, Zhang QY, Huang BK. Hepatotoxicity of kaurene glycosides from Xanthium strumarium L. fruits in mice. Pharmazie. 2011;66:445–449.

SAS. Statistical analysis system. SAS User’s Statistics SAS Institute Inc. Editors, Cary, NC; 2004.

Zahoor M, Shafiq S, Ullah H, Sadiq A, Ullah F. Isolation of quercetin and mandelic acid from Aesculus indica fruit and their biological activities. BMC Biochem. 2018;19:5.

Kumar S, Pandey AK. Chemistry and biological activities of flavonoids: An overview. Sci. World J. 2013;162750. [CrossRef] [PubMed]

Repo-Carrasco-Valencia R, Hellström JK, Pihlava JM, Mattila PH. Flavonoids and other phenolic compounds in Andean indigenous grains: Quinoa (Chenopodium quinoa), kañiwa (Chenopodium pallidicaule) and kiwicha (Amaranthus caudatus). Food Chem. 2010;120:128–133. [CrossRef]

Han X, Gao S, Cheng Y, Sun Y, Liu W, Tang L, Ren D. Protective effect of naringenin-7-O-glucoside against oxidative stress induced by doxorubicin in H9c2 cardiomyocytes. Biosci. Trends. 2012;6:19–25. [CrossRef] [PubMed]

Syama HP, Arya AD, Dhanya R, Nisha P, Sundaresan A, Jacob E, Jayamurthy P. Quantification of phenolics in Syzygium cumini seed and their modulatory role on tertiary butyl-hydrogen peroxide-induced oxidative stress in H9c2 cell lines and key enzymes in cardioprotection. J. Food Sci. Technol. 2017;54:2115– 2125.

Javidnia K, Miri R, Soltani M, Khosravi A. Chemical constituents of the essential oil of Otostegia michauxii Briq. from Iran. J Essential Oil Res. 2010;22:1-2.

Ahmad U, Kahn A, Farooq U, Kousar F, Khan S, Nawaz A, Abbasi A, Choudhary I. Three new cholinesterase inhibiting cis clerodane diterpenoids from Otostegia limbata. Chem Pharm Bull. 2005;53:378-381.

Ahmad U, Kahn A, Farooq U, Kousar F, Khan S, Hussain J. Two new trans- clerodane diterpenoids from Otostegia limbata. J Asian Nat Prod Res. 2007;9:91-95.

Farooq U, Khan A, Ahmad U, Khan S, Kousar F, Arshad S. Two new rare class tetra cyclic diterpenoids from Otostegia limbata. Chem Pharm Bull. 2007;55:471-473.

Dewick PM. Medicinal natural products: A biosynthetic approach (2nd Edn). John Wiley and Sons Ltd: Cichester. 2002;220.

Jones P, Kinghorn D. Extraction of plant secondary metabolites. In: Methods in Bio-technology Natural Products Isolation; 2006.

Suresh DR, Annam V, Pratibha K, Prasad BVM. Total antioxidant capacity ±a novel early bio-chemical marker of oxidative stress in HIV infected individuals. J Biomed Sci. 2009;16:61-64.

Zarei A, Vaezi G, Malekirad AA, Abdollahi M. Effects of ethanol extract of Salvia hydrangea on hepatic and renal functions of streptozotocin-induced diabetic rats. AJP. 2015;5(2):138-147.

Di Giulio RT, Washburn PC, Wenning RJ, Winston GW, Jewell CS. Biochemical responses in aquatic animals: A review of determinants of oxidative stress. Environ. Toxicol. Chem. 1989;8:1103-1123.

Miao L, St. Clair DK. Regulation of superoxide dismutase genes: Implications in diseases. Free Radic Biol Med. 2009;47(4):344–356.

Pietta PG. Flavonoids as antioxidants. J Nat Prod. 2000;63:1035-1042.

Refaat J, Desoukey SY, Ramadan MA, Kamel MS, Han J, Isoda H. Comparative polyphenol contents, free radical scavenging properties and effects on adipogenesis of Chorisia chodatii and Chorisia speciosa. JHD. 2015;5:193-207.

Wolf G, Ziyadeh FN. Cellular and molecular mechanisms of proteinuria in diabetic nephropathy. Nephron Physiol. 2007;106:26–31.

Zare T, Mokhtari M, Mohammadi J. The effect of hydroalcoholic extracts of Prangos ferulacea on blood factors of kidney and liver functions in diabetic male wistar rats. Journal of Fasa University of Medical Sciences. 2012;2:174-180.

Wang J, Liu H, Li N, Zhang Q, Zhang H. The protective effect of Fucoidan in rats with streptozotocin-induced diabetic nephropathy. Mar. Drugs. 2014;12:3292-3306.

Gil N, Goldberg R, Neuman T, Garsen M, Zcharia E, Rubinstein AM, van Kuppevelt T, Meirovitz A, Pisano C, Li JP. Heparanase is essential for the development of diabetic nephropathy in mice. Diabetes. 2012;61:208–216.

Ash SR, Singh B, Lavin PT, Stavros F, Rasmussen HS. A phase 2 study on the treatment of hyperkalemia in patients with chronic kidney disease suggests that the selective potassium trap, ZS-9, is safe and efficient. Kidney Int. 2015;88(2):404–11.

Ruiz-Gutierrez V, Stiefel P, Villar J, García-Donas MA, Acosta D, Carneado J. Cell membrane fatty acid composition in type 1 (insulin-dependent) diabetic patients: relationship with sodium transport abnormalities and metabolic control. Diabetologia. 1993;36(9):850-856.

Fila M, Brideau G, Morla L, Cheval L, Deschênes G, Doucet A. Inhibition of K+ secretion in the distal nephron in the nephrotic syndrome: Possible role of albuminuria. J. Physiol. 2011;589(14): 3417.

Reungjui S, Roncal CA, Sato W, Glushakova OY, Croker BP, Suga S. Hypokalemic nephropathy is associated with impaired angiogenesis. J Am SocNephrol. 2008;19(1):125–34.