Geraniol Attenuates Oxidative Stress and Apoptosis in the Liver and Kidney of Streptozotocin-Induced Diabetic Rats http://www.doi.org/10.26538/tjnpr/v6i10.20

Main Article Content

Tolulope A. Oyedeji
Holiness S. A. Olasore
Damilola O. Onadeko
Aisha I. Odunsi
Oluwatobiloba Fajemirokun
Eniola O. Oyedokun
Wisdom A. Idris

Abstract

Monoterpenes such as geraniol are known for their pharmacological properties. This study assessed geraniol’s antioxidant, and antiapoptotic potentials on diabetic rat liver and kidney. Male Wistar rats (24) were assigned into four groups of 6 rats per group. Diabetic rats (18) received a single dose of streptozotocin (STZ, 60 mg/kg) intraperitoneally. Animals were classified as control, STZ, STZ+GER (geraniol 200 mg/kg), and STZ+GLI (glibenclamide 5 mg/kg) groups. Treatment lasted 21 days. Blood glucose level was assessed using a glucometer. Superoxide dismutase (SOD), catalase (CAT), and glutathione (GSH) were assayed spectrophotometrically using standard commercial kits. Cytochrome c (Cyt c), caspase 9 (C9), and caspase 3 (C3) expressions in rat liver and kidney were assessed using commercial (ELISA) kits. The glucose level in the blood was elevated in the STZ group. Significant expressions of Cyt c, C9, and C3 and reduced SOD, CAT, and GSH levels were observed in rat liver and kidney of the STZ group. Treatment with geraniol significantly reduced blood glucose levels, Cyt c, C9, and C3 expressions relative to the STZ group. Similarly, antioxidant enzyme activities were significantly increased in the rat liver both in the STZ+GER and STZ+GLI groups. Thus, this study shows that geraniol has antidiabetic, antioxidant, and antiapoptotic effects on the liver and kidneys of streptozotocin-induced diabetic rats.

Downloads

Download data is not yet available.

Article Details

How to Cite
A. Oyedeji, T., S. A. Olasore, H., O. Onadeko, D., I. Odunsi, A., Fajemirokun, O., O. Oyedokun, E., & A. Idris, W. (2022). Geraniol Attenuates Oxidative Stress and Apoptosis in the Liver and Kidney of Streptozotocin-Induced Diabetic Rats: http://www.doi.org/10.26538/tjnpr/v6i10.20. Tropical Journal of Natural Product Research (TJNPR), 6(10), 1677-1681. https://tjnpr.org/index.php/home/article/view/1236
Section
Articles

How to Cite

A. Oyedeji, T., S. A. Olasore, H., O. Onadeko, D., I. Odunsi, A., Fajemirokun, O., O. Oyedokun, E., & A. Idris, W. (2022). Geraniol Attenuates Oxidative Stress and Apoptosis in the Liver and Kidney of Streptozotocin-Induced Diabetic Rats: http://www.doi.org/10.26538/tjnpr/v6i10.20. Tropical Journal of Natural Product Research (TJNPR), 6(10), 1677-1681. https://tjnpr.org/index.php/home/article/view/1236

References

Krijnen PAJ, Simsek S, Niessen HWN. Apoptosis in diabetes. Apoptosis. 2009; 14(12):1387-1388.

Giacco F and Brownlee M. Oxidative stress and diabetic complications. Circ Res. 2010; 107(9):1058 -1070.

Volpe CMO, Villar-Delfino PH, Dos Anjos PMF. Nogueira- Machado JA. Cellular death, reactive oxygen species (ROS), and diabetic complications. Cell Death Dis. 2018; 9(2):119.

Giri B, Dey S, Das T, Sarkar M, Banerjee J, Dash SK. Chronic hyperglycemia mediated physiological alteration and metabolic distortion leads to organ dysfunction, infection, cancer progression and other pathophysiological consequences: An update on glucose toxicity. Biomed. Pharmacother. 2018; 107:306-328.

Czajka A and Malik AN. Hyperglycemia induced damage to mitochondrial respiration in renal mesangial and tubular cells: implications for diabetic nephropathy. Redox Biol. 2016; 10:100-107.

Galvan DL, Mise K, Damesh FR. Mitochondrial regulation of diabetic kidney disease. Front Med (Lausanne). 2021; 8:745279.

Ramesh T. Oxidative stress and hepatocellular mitochondrial dysfunction attenuated by Asiatic acid in streptozotocin- induced diabetic rats. J King Saud Uni Sci. 2021; 33(3):101369.

Kwak S, Park KS, Lee K, Lee HK. Mitochondrial metabolism and diabetes. J Diab Invest. 2010; 1(5):161-169.

Sha W, Hu F, Bu S. Mitochondrial dysfunction and pancreatic β-cell failure (Review). Exp. Ther. Med. 2020; 20(6):266.

Webster KA. Mitochondrial membrane permeabilization and cell death during myocardial infarction: role of calcium and reactive oxygen species. Fut. Cardiol. 2012; 8(6):863–884.

Belosludtseva KN, Belosludtseva NV, Dubinin MV. Diabetes mellitus mitochondrial dysfunction and Ca2+-dependent permeability transition pore. Int J Mol Sci. 2020; 21(18): 6559.

Shakeri R., Kheirollahi A, Davoodi J. Apaf-1: Regulation and function in cell death. Biochim. 2017; 135:111-125.

Imam K. Management and treatment of diabetes mellitus. Adv Exp Med Biol. 2012; 771:356–380.

Marin-Penalver JJ, Martin-Timon I, Sevillano-Collantes C, Canizo-Gomez J. Update on the treatment of type 2 diabetes mellitus. World J Dia. 2016; 7(17):354-395.

Kooti W, Farokhipour M, Asadzadeh Z, Ashtary-Larku D, Asadi-Samani M. The role of medicinal plants in the treatment of diabetes: a systematic review. Elect Phys. 2016; 8(1):1832- 1842.

Ojo OO, Adeoye AO, Ojowu J, Olorunsogo OO. Inhibition of liver mitochondrial membrane permeability transition pore opening by quercetin and vitamin E in streptozotocin-induced diabetic rats. Biochem. Biophys. Res. Commun. 2018; 504:460- 469.

Tran N, Pham B, Le L. Bioactive compounds in anti-diabetic plants: From herbal medicine to modern drug discovery. Biol (Basel). 2020; 9(9): 252, doi: 10.3390/biology9090252 252.

Khalivulla SI, Mohammed A, Mallikarjuna K. Novel phytochemical constituents and their potential to manage diabetes. Curr Pharm Des. 2021; 27(6):775-788.

Medicherla K, Sahu BD, Kuncha, M, Kumar JM, Sudhakar G, Sistla R. Oral administration of geraniol ameliorates acute experimental murine colitis by inhibiting pro-inflammatory cytokines and NF-kappa B signaling. Food Funct. 2015; 6:2984-2995.

Klobucar M, Grbcic P, Pavelic SK, Jonjic N, Visentin S, Sedic M. Acid ceramidase inhibition sensitizes human colon cancer cells to oxaliplatin through downregulation of transglutaminase 2 and beta 1 integrin/FAK-mediated signaling. Biochem Biophys Res Commun. 2018; 503:843-848.

Khan AQ, Khan R, Qamar W, Lateef A, Rehman MU, Tahir M, Ali F, Hamiza OO, Hasan SK, Suttana S. Geraniol attenuates 12-O-tetradecanoyl phorbol-13-acetate (TPA)-induced oxidative stress and inflammation and inflammation in mouse skin: possible role of p38 MAP kinase and NF-kappa B. Exp. Mol. Pathol. 2013; 94:419-429.

Rekha KR and Selvakumar GP. Gene expression regulation of Bcl-2, Bax and cytochrome C by geraniol on chronic MPTP/probenecid induced C57BL/6 mice model by Parkinson’s disease. Chem Biol Interact. 2014; 217:57-66.

Babukumar S, Vinothkumar V, Sankarnarayanan C, Srinivasan S. Geraniol, a natural monoterpene, ameliorates hyperglycemia by attenuating the key enzymes of carbohydrate metabolism in streptozotocin-induced diabetic rats. Pharm. Biol. 2017; 55(1):1442–1449.

Marklund S and Marklund G. Involvement of the superoxide anion radical in the autooxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur J Biochem. 1974; 47(3):469-74.

Goth L. A simple method for determination of serum catalase activity and revision of reference range. Cli Chim Act. 1991; 196:143-152.

Hadman MH and Abed HN. Data supporting the spectrophotometric method for the estimation of catalase activity. Data Brief. 2015; 6:194-199.

Ellman GL. Tissue sulfhydryl groups. Arch Biochem Biophys. 1959; 82:70-77.

Alam MM, Meerza D, Naseem I. Protective effect of quercetin on hyperglycemia, oxidative stress, and DNA damage in alloxan-induced type 2 diabetic mice. Life Sci. 2014; 109(1):8- 14.

Eskandari N, Bahramikia S, Mohammadi A, Taati M, Jafarabad SS. Geraniol ameliorated serum lipid profile and improved antioxidant defense system in pancreas, liver and heart tissues of alloxan-induced diabetic rats. Biologia. 2022; 77:241-248.

Mahmoud NM, Elshazly SM, Rezq S. Geraniol protects against cyclosporine A-induced renal injury in rats: Role of Wnt/β- catenin and PPARy signaling pathways. Life Sci. 2022; 291:120259.

Grassmann J. Terpenoids as plant antioxidants. Vitam. Horm. 2005; 72:505–535.

Erejuwa OO, Sulaiman SA, Abdul Wahab MS, Salam SLN, Md Salleh M, Gurtu S. Antioxidant protective effect of glibenclamide and metformin in combination with honey in pancreas of streptozotocin-induced diabetic rats. Int J Mol Sci. 2010; 11(5):2056-2066.

Cai L, Li W, Wang G, Guo L, Jiang Y, Kang YJ. Hyperglycemia-induced apoptosis in mouse myocardium: mitochondrial cytochrome C – mediated caspase – 3 activation pathway. Diabetes. 2002; 51(6):1938-48

Peng J, Li X, Zhang D, Chen J, Su Y, Smith S, B, Dong Z. Hyperglycemia, p53, and mitochondrial pathway of apoptosis are involved in the susceptibility of diabetic models to ischemic acute kidney injury. Kidney Int. 2015; 87(1):137-50.

Gorlach A, Bertram K, Huderova S, Krizanova O. Calcium and ROS: A mutual interplay. Redox Biol. 2015; 6:260–271.