Browsing by Author "Olajide, O.J."

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    Exposure to varied cage-size habitats alters pain sensitivity and inflammation-related biomarkers.
    (Elsevier, 2020) Oyewole, A. L.; Oyafemi, K. O.; Badmus, K. S. J. O.; Omoleye, K. S.; Abubakar, M. F.; Adeniyi-Raheem, O.; Amedu, A.; Lawal, D. L.; Ijiyode, A. O.; Yussuf, A. O.; Ishola, S. S.; Sulaimon, F. A.; Alli-Oluwafuyi, A.O.; Nafiu, A.B.; Akinola, O.; Olajide, O.J.; Amin, A.; Abdulmajeed, W.I.; Michael, O.S.; Adeyanju, O.A.; Ogunjimi, G.L.
    Background: Nature and size of rodent cages vary from one laboratory or country to another. Little is however known about the physiological implications of exposure to diverse cage sizes in animal-based experiments. Method: Here, two groups of male Swiss mice (Control group – Cage stationed, and Test group – Cage migrated) were used for this study. The cage-migrated mice were exposed daily to various cage sizes used across labora tories in Nigeria while the cage-stationed mice exposed daily to different but the same cage size and shape. At the end of the 30 days exposure, top-rated paradigms were used to profile changes in physiological behaviours, and this was followed by evaluation of histological and biochemical metrics. Results: The study showed a significant (p < 0.05) decrease in blood glucose levels (at 60 and 120 min of oral glucose tolerance test) in the cage-migrated mice compared to cage-stationed mice. Strikingly, peripheral oxi dative stress (plasma malondialdehyde) and pain sensitivity (formalin test, hot-and-cold plate test, and von Frey test) decreased significantly in cage-migrated mice compared to cage-stationed animals. Also, the pro-in flammation mediators (IL-6 and NF-κB) increased significantly in cage-migrated mice compared to cage-sta tioned mice. However, emotion-linked behaviours, neurotransmitters (serotonin, noradrenaline and GABA), brain and plasma electrolytes were not significantly difference in cage-migrated animals compared to cage stationed mice. Conclusion: Taken together, these results suggest that varied size cage-to-cage exposure of experimental mice could affect targeted behavioural and biomolecular parameters of pain and inflammation, thus diminishing research reproducibility, precipitating false negative/positive results and leading to poor translational outcomes.
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    Kolaviron ameliorates histomorphological changes associated with Cuprizone-induced CerebellarDamage
    (2017) Omotoso, G.O.; Olajide, O.J.; Gbadamosi, I.T.; Suleiman, F.A.; Oladimeji, J.O
    Cuprizone is a copper chelator and a drug of choice in studing demyelination/remyelination in the central nervous system. This study assessed the effect of Kolaviron, on cuprizone-induced damage to the cerebellum of Wistar rat. Twenty-four adult male Wistar rats were grouped into 5: Group A received 0.5 ml of normal saline for 6 weeks; Group B received 0.5 ml of corn oil for 6 weeks; Group C was treated with 0.2% of cuprizone for 3 weeks followed by treatment with 200 mg/kg of Kolaviron for another 3 weeks; Group D received 200 mg/kg Kolaviron for 3 weeks followed by 0.2% cuprizone from another 3 weeks; while Group E received 0.2% cuprizone for 6 weeks. Meanwhile, 0.5 ml of corn oil was used as a vehicle for Kolaviron. The body and brain weight of the rats showed significant decrease in all treated groups when compared to the control groups. Histological demonstration showed varying degrees of architectural distortions, including depletion of Nissl bodies, disruption of cortical cell layers and depletion of myelin, which were more pronounced in the cerebellar cortex of cuprizone-treated rats. Kolaviron offered mild cytoprotection to the cerebellar histomorphology of cuprizone-treated rats. Further studies would ascertain the effectiveness of Kolaviron in mitigating cerebellar lesions in well-established demyelination.