Browsing by Author "Gbadamosi, I. T."

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Antiplasmodial potential of garcinia kola (HECKEL) stembark extract in albino mice
(Federal University of Agriculture, Abeokuta (FUNAAB), 2019) Gbadamosi, I. T.; Adeyi, A. O.; Braimoh, M. O.
Garcinia kola stem bark forms part of recipes used traditionally for the treatment of malaria. In view of the prevalence of malaria in Nigeria, this study investigated the phytochemical, mineral and proximate components, as well as antiplasmodial activity and toxicological effect of Garcinia kola stem bark extract against Plasmodium berghei infected mice. The plant sample was screened for phytochemical, mineral and proximate components using standard laboratory techniques. Thirty five mice were divided into seven groups of five mice each. Malaria was induced in all the groups intraperitoneally with 0.2 mL of infected blood containing about 107 of P. berghei parasitized red blood cells, except group 6 (extract only) and group 7 (normal control). Group 1 received 100 mg/kg bodyweight of the extract orally. Group 2 received 200 mg/kg of the extract. Group 3 received 300 mg/kg of the extract. Group 4 received 5 mg/kg of chloroquine. Group 5 (induced but untreated control). The haematology, liver function enzymes and histopathology of the liver were carried out using standard protocols. The plant was rich in alkaloids, iron and fibre. The extract treated groups (1-3) showed significant decrease (p≤0.05) in parasitemia level after seven days of treatment. There was no significant difference in AST, ALT, ALP, bilirubin and GGT activities in all the extract treated groups compared to the control. No pathological changes were evident in histopathology of all the groups treated with various concentration of the extract. The result obtained from this study confirmed the antiplasmodial activity of methanol extract of G. kola stem bark. The highest inhibition of P. berghie parasite was observed at dose 300 mg/kg comparable to chloroquine, with no hepatoxicity which confirmed the safety of G. kola. The phytochemicals and nutritional components could be responsible for the observed antiplasmodial activity of the plant.
Antiplasmodial potential of garcinia kola (HECKEL) stembark extract in albino mice
(Federal University of Agriculture, Abeokuta (FUNAAB), 2019) Gbadamosi, I. T.; Adeyi, A. O.; Braimoh, M. O.
Garcinia kola stem bark forms part of recipes used traditionally for the treatment of malaria. In view of the prevalence of malaria in Nigeria, this study investigated the phytochemical, mineral and proximate components, as well as antiplasmodial activity and toxicological effect of Garcinia kola stem bark extract against Plasmodium berghei infected mice. The plant sample was screened for phytochemical, mineral and proximate components using standard laboratory techniques. Thirty five mice were divided into seven groups of five mice each. Malaria was induced in all the groups intraperitoneally with 0.2 mL of infected blood containing about 107 of P. berghei parasitized red blood cells, except group 6 (extract only) and group 7 (normal control). Group 1 received 100 mg/kg bodyweight of the extract orally. Group 2 received 200 mg/kg of the extract. Group 3 received 300 mg/kg of the extract. Group 4 received 5 mg/kg of chloroquine. Group 5 (induced but untreated control). The haematology, liver function enzymes and histopathology of the liver were carried out using standard protocols. The plant was rich in alkaloids, iron and fibre. The extract treated groups (1-3) showed significant decrease (p≤0.05) in parasitemia level after seven days of treatment. There was no significant difference in AST, ALT, ALP, bilirubin and GGT activities in all the extract treated groups compared to the control. No pathological changes were evident in histopathology of all the groups treated with various concentration of the extract. The result obtained from this study confirmed the antiplasmodial activity of methanol extract of G. kola stem bark. The highest inhibition of P. berghie parasite was observed at dose 300 mg/kg comparable to chloroquine, with no hepatoxicity which confirmed the safety of G. kola. The phytochemicals and nutritional components could be responsible for the observed antiplasmodial activity of the plant.
Clofibrate, a peroxisome proliferator-activated receptor-alpha (PPARα) agonist, and its molecular mechanisms of action against sodium fluoride-induced toxicity
(Springer Nature, 2021) Oyagbemi, A. A.; Adejumobi, O. A.; Jarikre, T. A.; Ajani, S. O.; Asenuga, E. R.; Gbadamosi, I. T.; Adedapo, A. D. A.; Aro, A. O.; Ogunpolu, B. S.; Hassan, F. O.; Falayi, O. O.; Ogunmiluyi, I. O.; Omobowale, T. O.; Arojojoye, O. A.; Ola-Davies, O. E.; Saba, A. B.; Adedapo, A. A.; Emikpe, B. O.; Oyeyemi, M. O.; Nkadimeng, S. M.; McGaw, L. J.; Kayoka-Kabongo, P. N.; Oguntibeju, O. O.; Yakubu, M. A.
Sodium fluoride (NaF) is one of the neglected environmental pollutants. It is ubiquitously found in the soil, water, and environment. Interestingly, fluoride has been extensively utilized for prevention of dental caries and tartar formation, and may be added to mouthwash, mouth rinse, and toothpastes. This study is aimed at mitigating fluoride-induced hypertension and nephrotoxicity with clofibrate, a peroxisome proliferator–activated receptor-alpha (PPARα) agonist. For this study, forty male Wistar rats were used and randomly grouped into ten rats per group, control, sodium fluoride (NaF; 300 ppm) only, NaF plus clofibrate (250 mg/kg) and NaF plus lisinopril (10 mg/kg), respectively, for 7 days. The administration of NaF was by drinking water ad libitum, while clofibrate and lisinopril were administered by oral gavage. Administration of NaF induced hypertension, and was accompanied with exaggerated oxidative stress; depletion of antioxidant defence system; reduced nitric oxide production; increased systolic, diastolic and mean arterial pressure; activation of angiotensin-converting enzyme activity and nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB); and testicular apoptosis. Treatment of rats with clofibrate reduced oxidative stress, improved antioxidant status, lowered high blood pressure through the inhibition of angiotensin-converting enzyme activity, mineralocorticoid receptor over-activation, and abrogated testicular apoptosis. Taken together, clofibrate could offer exceptional therapeutic benefit in mitigating toxicity associated with sodium fluoride.
Potential health benefits of zinc supplementation for the management of the COVID-19 pandemic
(Wiley, 2020) Oyagbemi, A. A.; Ajibade, T. O.; Aboua, Y. G.; Gbadamosi, I. T.; Adedapo, A. D. A.; Aro, A. O.; Adejumobi, O. A.; Thamahane-Katengua, E.; Omobowale, T. O.; Falayi, O. O.; Oyagbemi, T. O.; Ogunpolu, B. S.; Hassan, F. O.; Ogunmiluyi, I. O.; Ola-Davies, O. E.; Saba, A. B.; Adedapo, A. A.; Nkadimeng, S. M.; McGaw, L. J.; Kayoka-Kabongo, P. N.; Oguntibeju, O. O.; Yakubu, M. A.
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the etiological agent for the Coronavirus Disease 2019 (COVID-19). The COVID-19 pandemic has created unimaginable and unprecedented global health crisis. Since the outbreak of COVID-19, millions of dollars have been spent, hospitalization overstretched with increasing morbidity and mortality. All these have resulted in unprecedented global economic catastrophe. Several drugs and vaccines are currently being evaluated, tested, and administered in the frantic efforts to stem the dire consequences of COVID-19 with varying degrees of successes. Zinc possesses potential health benefits against COVID-19 pandemic by improving immune response, minimizing infection and inflammation, preventing lung injury, inhibiting viral replication through the interference of the viral genome transcription, protein translation, attachment, and host infectivity. However, this review focuses on the various mechanisms of action of zinc and its supplementation as adjuvant for vaccines an effective therapeutic regimen in the management of the ravaging COVID-19 pandemic.