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<title>CYTOREMEDIATIVE POTENTIALS OF Vitellaria paradoxa (Gaertn. C.F) IN  ARSENIC-INDUCED TOXICITY IN WISTAR RAT, HARWICH FRUIT FLY AND  ITS ANTIPROLIFERATIVE ACTIVITY IN MCF-7 CELLS</title>
<link href="http://hdl.handle.net/123456789/1737" rel="alternate"/>
<subtitle/>
<id>http://hdl.handle.net/123456789/1737</id>
<updated>2026-04-21T01:57:53Z</updated>
<dc:date>2026-04-21T01:57:53Z</dc:date>
<entry>
<title>CYTOREMEDIATIVE POTENTIALS OF Vitellaria paradoxa (Gaertn. C.F) IN  ARSENIC-INDUCED TOXICITY IN WISTAR RAT, HARWICH FRUIT FLY AND  ITS ANTIPROLIFERATIVE ACTIVITY IN MCF-7 CELLS</title>
<link href="http://hdl.handle.net/123456789/1738" rel="alternate"/>
<author>
<name>OYIBO, AGHOGHO</name>
</author>
<id>http://hdl.handle.net/123456789/1738</id>
<updated>2024-04-18T09:17:04Z</updated>
<published>2021-11-01T00:00:00Z</published>
<summary type="text">CYTOREMEDIATIVE POTENTIALS OF Vitellaria paradoxa (Gaertn. C.F) IN  ARSENIC-INDUCED TOXICITY IN WISTAR RAT, HARWICH FRUIT FLY AND  ITS ANTIPROLIFERATIVE ACTIVITY IN MCF-7 CELLS
OYIBO, AGHOGHO
Arsenic, a class 1 carcinogen, is a major contaminant in drinking water globally. When &#13;
ingested by humans and animals, it contributes to tissue damage through the mechanisms &#13;
of oxidative stress and inflammation. Search is ongoing for plants with antioxidative and &#13;
anti-inflammatory properties that might ameliorate toxic effects of arsenic. Vitellaria &#13;
paradoxa (Vp) was reported to possess anti-oxidative and anti-inflammatory properties. &#13;
Therefore, cytoremediative potentials of Vp against Sodium arsenite (SA)-induced toxicity &#13;
in Wistar rats and fruit fly (Drosophila melanogaster), as well as its anti-proliferative action&#13;
on breast cancer cell line (MCF-7) were evaluated.&#13;
Leaves of Vp were obtained from Saki, Oyo State, authenticated at University of Ibadan &#13;
Herbarium (UIH-22624), air-dried and pulverised. Hydroethanol leaf extract of Vp was &#13;
obtained by maceration in 70% ethanol (ELVp), and fractionated by vacuum liquid &#13;
chromatography to obtain four fractions including Ethyl acetate Fraction (EAcF). Forty &#13;
male Wistar rats, divided into 8 groups (n=5), were administered distilled water 2mL/kg &#13;
(Control), Vitamin E (100 mg/kg), ELVp (100, 200 mg/kg), SA (2.5 mg/kg), SA + Vitamin &#13;
E, SA + ELVp (100, 200 mg/kg) orally for 14 days. Serum Alanine Aminotransferase &#13;
(ALT), Alkaline Phosphatase (ALP), creatinine, urea and malondialdehyde were &#13;
determined spectrophotometrically. Micronucleated Polychromatic Erythrocytes (mPCE), &#13;
liver and kidney histology and immunohistochemistry of proteins [(Nuclear Factor kappa B &#13;
(NF-κB), P53, B-Cell Lymphoma 2 (BCL-2)] were evaluated. Ameliorative role of EAcF &#13;
in SA-induced toxicity in D. melanogaster was evaluated by measuring longevity rate, &#13;
Nitric Oxide (NO), Hydrogen Peroxide (H2O2), Total Thiol (T-SH), reduced glutathione &#13;
(GSH) levels, catalase and glutathione S-transferase (GST) activities. Anti-proliferative &#13;
effects of EAcF on MCF-7 cells were determined by measuring viability, colony formation &#13;
and Reactive Oxygen Species (ROS) generation. Also, cell cycle was determined using flow &#13;
cytometer. Data were analysed using ANOVA at α0.05. &#13;
Co-treatment of SA with ELVp (100 mg/kg) significantly reduced serum ALT (68.73±0.50 &#13;
vs 89.67±8.78U/L), ALP (174.80±1.84 vs 450.20±69.47U/L), creatinine (1.32±0.00 vs &#13;
1.93±0.15mg/dL), urea (33.72±9.07 vs 75.14±1.13mg/dL), malondialdehyde (0.049±0.005 &#13;
viii&#13;
vs 0.067±0.012µmol/gprotein) and mPCEs (10.00±2.83 vs 16.00±2.00mPES/1000PCEs) &#13;
relative to SA. The ELVp (200 mg/kg) ameliorated SA-induced severe periportal and mild &#13;
peritubular inflammation of the liver and kidney of rats, respectively. The ELVp &#13;
ameliorated SA-induced increase in BCL-2 protein expression without significant effects &#13;
on NF-κB and P53 expression in both organs. The EAcF increased longevity of D. &#13;
melanogaster by 20.0% compared with control and ameliorated SA-induced elevation of &#13;
NO and H2O2 levels by 24.0% and 19.0%, respectively. Also, it ameliorated SA-induced &#13;
reduction of contents of T-SH by 88.0%, GSH by 253.0% and inhibition of catalase and &#13;
GST activities by 57.8% and 156.0% respectively. The EAcf showed anti-proliferative &#13;
activity, reduced ROS generation, induced Sub G0 cell death and arrest at G0/G1 phase in &#13;
MCF-7 cells. &#13;
Hydroethanol leaf extract and ethyl acetate fraction of Vitellaria paradoxa demonstrated &#13;
antihepatotoxic, antinephrotoxic and antioxidative properties against sodium arsenite induced toxicity in rat and Drosophila melanogaster. The anti-proliferative activity in MCF 7 cells was via inhibition of reactive oxygen species accumulation and G0/G1 cell cycle &#13;
arrest.
</summary>
<dc:date>2021-11-01T00:00:00Z</dc:date>
</entry>
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