Abstract
Introduction: Flavonoids are a class of polyphenols
that are widely available in plant being part of the
four main classes of polyphenols. They possess strong
antioxidant, anti-inflammatory and anti-cancer
properties. The effects of flavonoid on sodium
arsenite-induced hepatorenal toxicity was therefore
investigated.
Methods: Twenty-four adult (160 ± 20g) male Wistar
rats were randomly divided into four groups (A-D),
with six rats per group. Group A (negative control)
received distilled water; Group B received sodium
arsenite (SA) only; Group C received flavonoid
complex (FL) only and Group D initially received
flavonoid complex and later received sodium arsenite
every other day. SA was administered at 5mg/kg and
FL at 10mg/kg, all treatments were for fourteen days.
Results: Arsenic exposure resulted in significant
reduction (P<0.05) in in total protein, percentage body
and relative liver weights. Biochemical alterations in
ALT, AST, ALP activities, urea and creatinine levels
in the blood were significantly decreased.
Furthermore, a reduction in GSH level, GST and CAT
activities in the arsenic exposed group were also
significant. The LPO and NO levels were also
increased significantly. FL significantly restored the
hepatorenal parameters and promoted hepatocytes
and renal cells regeneration.
Conclusion: The present study indicates that
flavonoid complex is protective against hepatorenal
toxicities induced by sodium arsenite in Wistar rats.
References
Shalat, S.L., Walker, D.B., and Finnell, R.H.
Role of Arsenic as A Reproductive Toxin with
Particular Attention to Neural Tube Defects
J Toxicol. Environ. Health 1996; 48 253-
Owumi, S.E., Odunola, O.A., and Aliyu, M.
Co-administration of sodium arsenite and
ethanol: protection by aqueous extract of
Aframomumlongiscapum seeds
Pharmacognosy Research2012; 4 154–160
Odunola, O.A., Akinwumi, K.A., Ogunbiyi,
B., and Tugbobo, O. Interaction and
enhancement of the toxic effects of sodium
arsenite and lead acetate in wistar rats
African Journal ofBiomed Res 2007; 10
–65
Smith, A.H., Arroyo, A.P., and Mazumdar,
D.N. Arsenic-Induced Skin Lesions Among
Atacameno People in Northern Chile Despite
Good Nutrition and Centuries of Exposure.
Environ. Health Perspect 2000; 108 617–
Tseng, W.P. Effects and Dose Response
Relationships of Skin Cancer and Black Foot
Disease. Environ. Health Perspect. 1977;
109-119
USEPA, IRIS. (Integrated Risk Information
System) On Line Data Base Maintained in
Toxicology Data Network (TOXNET) By
the National Library of Medicine Bethesda
Maryland 1997; 180 20–30
IARC (International Agency for Research
on Cancer). Arsenic And Arsenic
Compounds, IARC Monographs on The
Evaluation of Carcinogenicity; Updating of
IARC Monographs. Lyon: IARC (Suppl.7)
; 100 1-42
Bhattacharya, P., Welch, A.H., Ahmed,
K.M., Jacks, G., and Naidu, R., 2004.
Arsenic in Ground Waters of Sedimentary.
Aquifers Appl Geoch 19 163-260
JO Teibo, MA Gbadegesin, AM Adegoke, OB Silifat, OA Odunola
Huang, C., Ke, Q., Costa, M., and Shi, X.
Molecular Mechanism of Arsenic
Carcinogenesis. Mol Cell Biochem 2004;
57- 66.
Janga YC, Somanna Y, Kim H. Source,
distribution, toxicity and remediation of
arsenic in the environment – A review. Int J
of Applied Env Sci2016;11:559–81.
Halliwell B, Whiteman M. Measuring
reactive species and oxidative damage in vivo
and in cell culture: how should you do it and
what do the results mean? Br J
Pharmacol2004;142:231–55.
J. B. Harborne (ED.) The flavonoids–
Advances in research since 1986 Chapman
& Hall, London, U.K. 1994, 676 pp. ISBN
-412-48070-0
Benavente García, O., Castillo, J., Marin,
F.R., Ortuño, A., and Del Río, J.A. Uses and
properties of citrus flavonoids. Journal of
Agricultural and Food Chem 1997; 45
-4515
Neolife Resource 2015. https://
newlifevitaminshop.com/products/flavonoidcomplex
Seyoum, A., Asres, K., El Fiky, F.K.
Structure radical scavenging activity
relationships of flavonoids. Phytochemistry
; 67 2058-2070
Chuarienthong, P., Lourith, N., and
Leelapornpisid, P. Clinical efficacy
comparison of anti wrinkle cosmetics
containing herbal flavonoids. International
Journal of Cosmetic Sci 2010; 32 99-106
Escamilla, C.O., Cuevas, E.Y., and Guevara,
J.Flavonoides y sus
accionesantioxidantesRevista de la
Facultad de Medicina. 2009; 52 73-75
Basu, A., Das, A.S., Majumder, M., and
Mukhopadhyay, R. Anti atherogenic roles of
dietary flavonoids chrysin, quercetin and
luteolin. Journal of Cardiovascular
Pharma. 2016; 68 89-96
Gbadegesin, M.A., Odunola, O.A.,
Akinwumi, K.A., Osifeso, O.O.
Comparative hepatotoxicity and
clastogenicity of sodium arsenite and three
petroleum products in experimental Swiss Albino
Mice: the modulatory effects of Aloe vera
gel. Food Chem Toxicol 2009; 47 2454–
Jain NC. Schalm’s Veterinary Hematology.
th ed. Philadelphia, USA: Lea and Febiger;
Fawcett JK, Scott JE. A rapid and precise
method for the determination of urea. J Clin
Pathol1960;13:156–59.
Reitman S, Frankel S. A colorimetric method
for the determination of serum glutamic
oxalacetic and glutamic pyruvic
transaminases. Am J Clin
Pathol1957;28:56–3.
Rec GS. Determination of alkaline
phosphatase. Z. Clin. Chem1972;10:281–91.
Claiborne A. Catalase activity. In: Greenwald
RA, editor. Handbook of methods for oxygen
radical research. Boca Raton (FL);
:283–84.
Misra HP, Fridovich I. The role of supeoxide
anion in the autooxidation of epinephrine and
a simple assay for superoxide dismutase. J
Biol Chem. 1972;247:3170–175.
Habig WH, Pabst MJ, Jacoby WB.
Glutathione S-transferases: the first
enzymatic step in mercapturic acid
formation. J Biol Chem1974;249:7130–139.
Rotruck JT, Pope AL, Ganther HE, et al.
Selenium: biochemical role as a component
of glutathione peroxidase.
Science1973;179:588–90.
Beutler E, Duran O, Kelly BM. Improved
method for the determination of blood
glutathione. J Lab Clin Med1963;61:882–
Adam-Vizi V, Seregi A. Receptor
independent stimulatory effect of
noradrenaline on Na, K-ATPase in rat brain
homogenate. Role of lipid peroxidation.
BiochemPharmacol1982;31: 2231–236.
Trush MA, Enger PA, Kensler TW.
Myeloperoxidase as a biomarker of skin
irritation and inflammation. Food Chem
Toxicol1994;34:143–47.
Green LC, Wagner DA, Glogowski J, et al.
Analysis of nitrate, nitrite and (15N) nitrate
in biological fluids. Anal
Biochem1982;126:131–38.
Mahomoodally, M.F., Gurib-Fakim A., and
Subratty, A.H. Antimicrobial activities and
phytochemical profiles of endemic medicinal
plants of Mauritius. Pharma. Biol. 2005; 43
–242
Pandey, A.K. Anti-staphylococcal activity of
a pan-tropical aggressive and obnoxious
Flavonoid complex protect against hepatorenal toxicity 263
weed Pariheniumhisterophorus: an in
vitro study. National Academy Science
Letters 2007; 30 383–386
Teibo, J.O., Ayinde, K.S., Olaoba, O.T.,
Adelusi, T.I., Teibo, T.K.A., Bamikunle,
M.V., Jimoh, Y.A., et al. Functional foods’
bioactive components and their
chemoprevention mechanism in cervical,
breast, and liver cancers: A systematic
review. FFHD 2021; 11 559-585
Fowler, B.A., Woods, J.S., Schiller, C.M.
Ultrastructural and biochemical effects of
prolonged oral arsenic exposure on liver
mitochondria of rats. Environ Health
Perspect 1977; 19 197 204
Chattopadhyay, S., Ghosh, S., Debnath, J.,
Ghosh, D. Protection of sodium arsenite
induced ovarian toxicity by coadministration
of L ascorbate (Vitamin C) in mature wistar
strain rat. Arch Environ ContamToxicol
; 41 83 89
Das, N.K., Sengupta, S.R.Arsenicosis:
Diagnosis and treatment. Indian J Dermatol
VenereolLeprol 2008; 74 571 581
Ali, B.H., Ben Ismail T.H., Basheer, A.A.
Sex related differences in the susceptibility
of rat to gentamicin nephrotoxicity: Influence
of gonadectomy and hormonal replacement
therapy. Indian J Pharmacol 2001;33 369
Gbadegesin, M.A., Teibo, J.O., Adegoke,
A.M., Olajire, G., Odunola, O.A. D-RiboseL-Cysteine protects against sodium arseniteinduced hepato-nephrotoxicity in rats.
African Health Science (Submitted).
Ramanathan, K., Balakumar, B.S.,
Panneerselvam. C., 2002. Effects of
ascorbic acid rat hepatocytes. Toxicol In
Vitro 12 699–704
Nam T. G. Lipid peroxidation and its
toxicological implications. Toxicological
research, 2011; 27(1), 1–6. https://doi.org/
5487/TR.2011.27.1.001
Sharma, A., Sharma, M.K., and Kumar, M.
Modulatory role of Emblica officinalis fruit
extract against arsenic induced oxidative
stress in Swiss albino mice. ChemicoBiological Interactions 2009;180 20-30
Olaniyan, O.T., Kunle-alabi, O.T., and Raji,
Y. Original article Protective effects of
methanol extract of Plukenetia conophora
seeds reproductive function of male Wistar
rats treated with cadmium chloride. JBRA
Assit. Reprod. 2018; 22 289–300
Gupta, R., Flora, S.J. Protective value of
Aloe vera against some toxic effects of
arsenic in rats. Phytother Res 2005;19 23
Abbasi, E., Nassiri-Asl, M., Shafeei, M. and
Sheikhi, M. Neuroprotective Effects of
Vitexin, a Flavonoid, on PentylenetetrazoleInduced Seizure in Rats. Chemical Biology
& Drug Design, 2012; 80: 274-278.
Krylova, S.G., Afanas’eva, O.G., Zibareva,
L.N. et al. Evaluation of the
Gastroprotective Effect of the Flavonoid
Complex from Lychnischalcedonica L. on
the Models of Experimental
Ulcerogenesis. Bull Exp Biol Med 2021;171,
–217.
Omer Coskun, Mehmet Kanter, Ahmet
Korkmaz, Sukru Oter, Quercetin, a flavonoid
antioxidant, prevents and protects
streptozotocin-induced oxidative stress and
â-cell damage in rat pancreas,
Pharmacological Research, Volume 51,
Issue 2, 2005, Pages 117-123.