Browsing by Author "Ojetola, Abodunrin"

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    Changes in Antioxidants Status, Atherogenic Index and Cardiovascular Variables after Prolonged Doses of D-ribose-L-cysteine in Male Wistar Rats Abodunrin
    (Elsevier, 2021-02-10) Ojetola, Abodunrin
    D-ribose-L-cysteine (DRLC) acts as a rate limiting substrate for the synthesis of glutathione (GSH). GSH deficiency has been linked to oxidative stress, hypertension and cardiovascular diseases. There are limited findings on the effects of DRLC in the physiologic state. This study was therefore designed to investigate cardiovascular effects of different doses of DRLC in normal Wistar rats. Fifteen male Wistar rats were assigned into 3 groups (n ¼ 5). Group 1 was administered orally with 10 mg/kg distilled water (Control). Groups 2 and 3 were administered orally with DRLC 125 mg/kg and 250 mg/kg respectively daily for 8 weeks, respectively. Animals were weighed; blood pressure and heart rate measured using rat tail cuff method. They were euthanized, blood collected and organs harvested. Serum C-reactive protein (CRP) was determined through ELISA. Gamma glutamyl transferase (GGT), heart GSH, glutathione peroxidase (GPx), total thiol and lipid profile and were assessed through spectrophotometry. Data were expressed as mean ? SEM and compared by ANOVA at P < 0.05. DRLC 250 significantly increased total thiol, GSH and GPx in heart tissues but decreased GGT, atherogenic index and CRP in normal male Wistar rats compared to DRLC 125 and control. DRLC supplementation in normal male Wistar rats may sustain cardio functions and decrease atherogenicity.
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    D-Ribose-L-Cysteine Prevents Oxidative Stress and Cardiometabolic Syndrome in High Fructose High Fat Diet Fed Rats
    (Elsevier, 2021-08-13) Ojetola, Abodunrin
    Cardiometabolic syndrome has been linked with dietary modification. Therefore, we investigated the effects of D-ribose-L-cysteine (DRLC) in rats fed with high fructose high fat (HFHF) diet. Twenty rats (n = 5), divided into 4 groups were concurrently exposed to HFHF and/or DRLC (250 mg/kg, p.o) during the 8 weeks study. The result showed that compared to control group, HFHF group had significant impairment in lipid and glucose homeo- stasis, increased cardiac xanthine oxidase, systolic blood pressure, heart rate, %body weight change and fluid intake. Also, there were significant reductions in HDL-C, cardiac (GPX, NO&GGT), feed intake and relative heart weight in the latter, relative to the former. However, there were no significant differences in most of the observed physical and biochemical changes in HFHF + DRLC group compared to control. DRLC alone did not disrupt the level of biomarkers. Conclusively, DRLC prevented the manifestation of oxidative stress and cardiometabolic syndrome in HFHF-diet fed rats.
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    Orange Peel extract Corrected Lipid Dysmetabolism and Pro- inflammation, but not Deranged Antioxidant and Hormonal Status in Orchidectomised Rats
    (Journal of African Association of Physiological Sciences, 2020-07-10) Ojetola, Abodunrin
    Background: Testosterone is a metabolic hormone; therefore, its absence would affect food metabolism, and subsequently a wide array of associated endogenous processes, including oxidative and inflammatory events. Contrarily, orange peel is known to be rich in flavonoids, which have strong antioxidant and anti-inflammatory properties, asides from their modulatory roles on lipolysis and lipogenesis. Hence, we investigated the effects of ethanolic extract of orange peel (EEOP) on antioxidant, inflammatory, and lipid and reproductive hormonal profiles in experimental animal. Methods: The rats were divided into four groups (N=10), which included: Control (Sham orchidectomised) (group 1); Orchidectomised (Orchid) (group 2); Orchidectomised + Low dose of orange peel (Orchid + LDOP) (group 3); and Orchidectomised + High dose of orange peel (Orchid + HDOP) (group 4). EEOP was administered at a low and high dose of 200 and 600 mg/kg BW, p.o. respectively; however, normal saline (vehicle) was administered at 1 ml/kg BW, p.o. to groups 1 and 2 throughout the four weeks duration of the experiment. Results: Castration was accompanied by dsylipidaemia, without alteration of oxidative, inflammatory, and reproductive hormonal status. Although EEOP reversed alterations in lipid metabolism back to the baseline, it neither showed significant effects on oxidative markers (SOD, catalase, total antioxidant capacity and malondialdehyde) nor reproductive hormone (testosterone, FSH and LH) profile, even though it significantly reduced uric acid. The effects of EEOP were not dose-graded, except in the MDA result, which was significantly higher in group 3, relative to group 4. Conclusion: EEOP corrected lipid dysmetabolism and pro- inflammation, but not deranged antioxidant and hormonal status in a dose-independent manner in orchidectomised rats.