Drug Res (Stuttg) 2018; 68(02): 104-112
DOI: 10.1055/s-0043-119070
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

Telferia Occidentalis and Vitamin C Attenuate Phenylhydrazine-Induced Haemolytic Anaemia and Associated Cardio-renal Dysfunctions via Inhibition of Oxidative Stress and Proapoptotic -Protein (Bax) Expressions

Temitayo Olabisi Ajibade
1   Department of Veterinary Physiology and Biochemistry, Faculty of Veterinary Medicine, University of Ibadan, Nigeria
,
Ademola Adetokunbo Oyagbemi
1   Department of Veterinary Physiology and Biochemistry, Faculty of Veterinary Medicine, University of Ibadan, Nigeria
,
Temidayo Olutayo Omobowale
2   Department of Veterinary Medicine, Faculty of veterinary Medicine, University of Ibadan, Nigeria
,
Ebunoluwa Rachael Asenuga
3   Department of Veterinary Physiology and Biochemistry, Faculty of veterinary Medicine, University of Benin, Nigeria
,
Adebowale Bernard Saba
4   Department of Veterinary Pharmacology and Toxicology, Faculty of veterinary Medicine, University of Ibadan, Nigeria
› Author Affiliations
Further Information

Publication History

received 15 April 2017

accepted 21 August 2017

Publication Date:
19 September 2017 (online)

Abstract

Background The study investigated the modulatory roles of the aqueous leaf extract of Telferia occidentalis, a traditional haematinic, and vitamin C on cardiovascular dysfunction associated with subchronic Phenylhydrazine exposure.

Methods Fifty adult male rats were randomly selected and divided into one of five groups of ten animals each: Control; 40 mgkg−1 Phenylhydrazine (PHZ); PHZ with 100 mgkg−1 T.occidentalis; PHZ with 200 mgkg−1 T.occidentalis; and PHZ with 100 mgkg−1 vitamin C.

Results Oral exposure of rats to PHZ, without T. occidentalis or vitamin C treatment, resulted in a significant (p<0.05) decrease in the haematological parameters, but increased the blood pressure parameters of rats However, treatment with vitamin C and T. occidentalis leaf extract significantly (p<0.05) ameliorated the aforementioned PHZ-induced alterations of rats haemogram, and blood pressure. Biochemical analysis revealed significant (p<0.05) reduction in the activities of superoxide dismutase and catalase of untreated PHZ-exposed rats, but the levels of malondialdehyde, hydrogen peroxide and myeloperoxidase of the rats were significantly (p<0.05) increased compared with those of the extract treated rats. Immunohistochemical analysis revealed a greater expression of Bax-protein in the cardiac and renal tissues of the untreated PHZ exposed rats, compared with the extract and vitamin C treated groups.

Conclusions The mitigation of oxidative stress and inhibition of Bax-protein expression are probable mechanisms of action of T. occidentalis in the amelioration of haemolytic anaemia, and its use as adjunct medication in the management of some diseases is justifiable

 
  • References

  • 1 Ferrali M, Signorini C, Ciccoli L. et al. Iron release and membrane damage in erythrocytes exposed to oxidizing agents, phenylhydrazine, divicine and isouramil. Biochem J 1992; 285: 295-301
  • 2 Fibach E, Rachmilewitz E. The role of oxidative stress in hemolytic anemia. Curr Mol Med 2008; 8 (07) 609-619
  • 3 Akoroda MO. Ethnobotany of Telfairia occidentalis (Curcurbitacae) among Igbos of Nigeria. Econo Bota 1990; 44: 29-39
  • 4 Gbile ZO. Ethnobotany, Taxonomy and conservation of medicinal plants. In: Sofowora A. ed. The State of Medicinal Plants Research in Nigeria. Nigeria: University of Ibadan Press; 1986: 13-29
  • 5 Alada ARA. The haematological effect of Telferia occidentalis diet preparation. Afr J Biomed Res 2000; 3: 185-186
  • 6 Atabo S, James DB, Mamman A. et al. Bio-content of Telferia occidentalis and their effect on methemoglobin formation in sickled erythrocytes. Asian Pac J Trop Med 2014; 7: 262-266
  • 7 Evans WC. Trease and Evans’ pharmacognosy. 15th ed. India: Saunders, Elsevier; 2002: 221-336
  • 8 Misra HP, Fridovich I. The role of superoxide anoin in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem 1972; 217: 3170-3175
  • 9 Oyagbemi AA, Omobowale TO, Akinrinde AS. Lack of reversal of oxidative damage in renal tissues of lead acetate-treated rats. Environ Toxicol 2015; 30 (11) 1235-1243
  • 10 Varshney R, Kale RK. Effect of calmodulin antagonists on radiation induced lipid peroxidation in microsomes. Int J Biol 1990; 158: 73-741
  • 11 Wolff SF. Ferrous ion oxidation in the presence of ferric ion indicator xylenol orange for measurement of hydrogen peroxides. Methods Enzymol 1994; 233: 182-189
  • 12 Gornal AG, Bardawill JC, David MM. Determination of serum proteins by means of Biuret reaction. J Biol Chem 1949; 177: 751-766
  • 13 Xia Y, Zweier JL. Measurement of myeloperoxidase in leukocyte-containing tissues. Anal Biochem 1997; 245 (01) 93-96
  • 14 Sinha KA. Colorimetric assay of catalase. Anal Biochem. 1971; 47: 389-394
  • 15 Drury RA, Wallington EA, Cancerson R. Carlton’s histopathological techniques. 4th ed. London: Oxford University Press; 1976
  • 16 Todorich B, Zhang X, Connor JR. H-ferritin is the major source of iron for oligodendrocytes. Glia 2011; 59: 927-935
  • 17 Ramos AJ, Hernandez E. In vitro aflatoxin adsorption by means of a montmorillonite silicate. A study of adsorption isotherms. Anim Feed Sci Technol 1996; 62: 263-269
  • 18 Pande K, Anil KM, Akansha J. et al. Molecular mechanism of phenylhydrazineinduced haematotoxicity: A review. Ame J Phytomed Clin Therapeut 2014; 2: 390-394
  • 19 Ibrahim IH, Sallam SM, Omar H. et al. Oxidative hemolysis of erythrocytes induced by various vitamins. Int J Biomed Sci 2006; 2 (03) 295-298
  • 20 Jeney V, Balla J, Yachie A. et al. Pro-oxidant and cytotoxic effects of circulating heme. Blood 2002; 100: 879-887
  • 21 Balla J, Balla G, Jeney V. et al. Ferriporphyrins and endothelium: a 2-edged sword promotion of oxidation and induction of cytoprotectants. Blood 2000; 95: 3442-3450
  • 22 Koury MJ, Price JO, Hicks GG. Apoptosis in megaloblastic anemia occurs during DNA synthesis by a p53-independent, nucleoside-reversible mechanism. Blood 2000; 96 (09) 3249-3255
  • 23 Salman TM, Olayaki LA, Oyeyemi WA. Aqueous extract of Telfairia occidentalis leaves reduces blood sugar and increases haematological and reproductive indices in male rats. Afr J Biotech 2008; 7 (14) 2299-2303
  • 24 Osuntoki AA, Sanusi AO. Telfairia occidentalis extract stabilizes human erythrocyte membranes. Nig Q J Hosp Med 2007; 17: 116-119
  • 25 Kawaguchi Y, Mizuta T, Takahashi K. et al. High-dose vitamins E and C supplementation prevents ribavirin-induced haemolytic anaemia in patients with chronic hepatitis C. Hepatol Res 2007; 37 (05) 317-324
  • 26 Claro LM, Leobart MSS, Comar SR. et al. Effect of vitamins C and E on oxidative processes in human erythrocytes. Cell Bioch Funct 2006; 24: 531-535
  • 27 Oboh G, Akindahunsi AA. Changes in the ascorbic acid, total phenol content and antioxidant activity of some sun dried green leafy vegetables in Nigeria. Nutr Health 2004; 18: 29-36
  • 28 Li PF, Maasch C, Haller H. et al. Requirement for protein kinase C in reactive oxygen species–induced apoptosis of vascular smooth muscle cells. Circulation 1999; 100: 967-973
  • 29 Fukai T, Ushio-Fukai M. Superoxide dismutases: Role in redox signaling, vascular function, and diseases. Antioxid Redox Signal 2011; 15: 1583-1606
  • 30 Lacy F, Kailasam MT, O’Connor DT. et al. Plasma hydrogen peroxide production in human essential hypertension: Role of heredity, gender, and ethnicity. Hypertension 2000; 36: 878-884
  • 31 Song J, Li J, Qiao J. et al PKD prevents h2o2-induced apoptosis via NF-κB AND p38 MAPK. Biochem Biophys Res Commun 2009; 378 (03) 610-614
  • 32 Intengan HD, Ernesto LS. Vascular remodeling in hypertension: Roles of apoptosis, inflammation, and fibrosis. Hypertension 2001; 38: 581-587
  • 33 Cotelle N. (2001). Role of flavonoids in oxidative stress. Curr Top Med Chem 2001; 1 (06) 569-590
  • 34 Ramón R, Hernán P, Walter P. et al. (2008). Decrease in oxidative stress through supplementation of vitamins C and E is associated with a reduction in blood pressure in patients with essential hypertension. Clin Sci 2008; 114 (10) 625-634
  • 35 Klebanoff SJ. Myeloperoxidase: Friend and foe. Leukoc Biol 2005; 77: 598-625
  • 36 Nicholls SJ, Hazen SL. Myeloperoxidase and cardiovascular disease. Arterioscl Thromb Vasc Bio 2005; 25: 1102-1111