Browsing by Author "Akinyele, Akinsola"
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Item EFFECTS OF WHOLE CANNABIS SATIVA INGESTION ON BEHAVIOURAL PATTERNS AND OXIDATIVE STRESS IN MICE BRAIN TISSUES(Animal Research International, 2019-04-12) Akinola, Olugbenga; Olumoh-Abdul, Hidayah Ayodeji; Oyewole, L. Aboyeji; Owolodun, O. Abibat; Egboro, D. Efe; Abdulkadir, B. Fatima; Iyenmoana, Ese; Yakub, Y. Olatunji; Akinyele, Akinsola; Ogbeche, O.ElizabethThe unregulated habitual use of whole Cannabis sativa remains a challenge for the potential medical usefulness of the plant. As a psychoactive substance with different physiological properties, the onset and extent of its effects are often a factor of the mode of consumption. This study evaluated the neuro-behavioural effects of daily oral ingestion of C. sativa and its modulatory changes in oxidative stress parameters in mice brain tissues. Twenty-five male Swiss albino mice were separated into 5 groups of 5 animals each. Cannabis-diet were prepared from whole dried cannabis and standard mice feed. Groups I – IV, were fed with 40, 20, 10 and 1 % cannabis-diet ad libitum for 14 days, while group V animals were fed the standard mice diet ad libitum for 14 days and served as control. Neuro-behavioural activities were assessed by observing animals rearing, grooming, ambulation, head dipping and freezing times. The brain oxidative stress parameters were assayed to determine the effect of cannabis oral consumption on activity in mice brain. The animals fed with cannabis-diet displayed significantly reduced anxiety but statistically insignificant locomotory function, exploratory tendencies and neophilia, in a quantity dependent manner relative to the controls. Cannabis demonstrated both antioxidant and oxidative stress tendencies. Ingestion of whole cannabis plants may not adversely influence neuro-behavioural patterns in animals. A trade-off between oxidative stress induction and brain tissue injury repair mechanisms may have been elicited by different constituents of Cannabis. Thus, oral ingestion of cannabis may not readily cause changes in neuro-behavioural patterns.Item Irvingia gabonensis Seed Extract: An Effective Attenuator of Doxorubicin-Mediated Cardiotoxicity in Wistar Rats(Hindawi publishers, 2020) Olorundare, Olufunke; Adeneye, Adejuwon; Akinyele, Akinsola; Kolo, Philip; Agede, Olalekan; Soyemi, SundayCardiotoxicity as an off-target effect of doxorubicin therapy is a major limiting factor for its clinical use as a choice cytotoxic agent. Seeds of Irvingia gabonensis have been reported to possess both nutritional and medicinal values which include antidiabetic, weight losing, antihyperlipidemic, and antioxidative effects. Protective effects of Irvingia gabonensis ethanol seed extract (IGESE) was investigated in doxorubicin (DOX)-mediated cardiotoxicity induced with single intraperitoneal injection of 15 mg/kg of DOX following the oral pretreatments of Wistar rats with 100-400 mg/kg/day of IGESE for 10 days, using serum cardiac enzyme markers (cardiac troponin I (cTI) and lactate dehydrogenase (LDH)), cardiac tissue oxidative stress markers (catalase (CAT), malonyldialdehyde (MDA), superoxide dismutase (SOD), glutathione-S-transferase (GST), glutathione peroxidase (GSH-Px), and reduced glutathione (GSH)), and cardiac histopathology endpoints. In addition, both qualitative and quantitative analyses to determine IGESE’s secondary metabolites profile and its in vitro antioxidant activities were also conducted. Results revealed that serum cTnI and LDH were significantly elevated by the DOX treatment. Similarly, activities of tissue SOD, CAT, GST, and GSH levels were profoundly reduced, while GPx activity and MDA levels were profoundly increased by DOX treatment. These biochemical changes were associated with microthrombi formation in the DOX-treated cardiac tissues on histological examination. However, oral pretreatments with 100-400 mg/kg/day of IGESE dissolved in 5% DMSO in distilled water significantly attenuated increases in the serum cTnI and LDH, prevented significant alterations in the serum lipid profile and the tissue activities and levels of oxidative stress markers while improving cardiovascular disease risk indices and DOX-induced histopathological lesions. The in vitro antioxidant studies showed IGESE to have good antioxidant profile and contained 56 major secondary metabolites prominent among which are γ-sitosterol, Phytol, neophytadiene, stigmasterol, vitamin E, hexadecanoic acid and its ethyl ester, Phytyl palmitate, campesterol, lupeol, and squalene. Overall, both the in vitro and in vivo findings indicate that IGESE may be a promising prophylactic cardioprotective agent against DOX-induced cardiotoxicity, at least in part mediated via IGESE’s antioxidant and free radical scavenging and antithrombotic mechanisms.