Scholarly works in Veterinary Physiology Biochemistry & Pharmacology

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    Phytochkmical profiling antioxidant activities and essential oil, constituents of Androgkaphis Paniculata
    (Faculty of Veterinary Medicine, University of Ibadan, 2018) Adeoye, B. Q.; Akinrinde, A. S.; Oyagbemi, A. A.; Omobowale, T. O.; Afolayan, A. J.; Adedapo, A. A.
    Oxidative stress is involved in the pathogenesis of various diseases which lead to urgent- need to investigate new, safe and effective source of antioxidant agents. This research proposed to investigate in-vitro and phytochemical constituent of the plant Ancirographis paniculatei using phytochemical analysis, GC/MS, DPPH, ABTS, FRAP and NO. Phytochemica! analysis of Anclrographis paniculata revealed the presence of tannins, total fiavonoids, total phenol, total flavonols, and total proanthocyanidins. GC/MS analysis of essential oil of AP identified one major compound name benzencpropanoic acid clucked at 3.296 retention time and 0,74 area percentage. The ferric reducing potential of the extracts was concentration dependent and significantly different from that of rutin and vitamin E. The% inhibition ofABTS by the ethanol leaf extract o?A nclrographis paniculata was concentration dependent and compared favourably well with the rutin and vitamin E, in DPPH scavenging assays, the ICy50 value of the ethanol leaf extract of Andrographis paniculata was < 0.025 mg/ml, while IC50 of rutin and Vitamin E were < 0.025 mg/ml and 0.68mg/ml. Nitric oxide ICS, for extract is 1,05mg/ml, Vitamin E is 1.2 mg/ml, and rutin is < 0.025 mg/ml. The present study showed high level of radical scavenging activity by ethanol leaf .extract of Andrographis paniculata with higher antioxidant activities than Vitamin E but less than that of rutin. This show that Andrographis paniculata has antioxidant properties and the plant could be used in the prevention and treatment of diseases associated with oxidative stress.
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    Phytochemical composition and antioxidant activities of dianthus Thunbergii hooper and Hypoxis argentea harv ex baker: plants used for the management of diabetes mellitus in eastern cape, South Africa
    (Wolters Kluwer - Medknow, 2018) Akinrinde, A. S.; Afolayan, A. J.; Bradley, G.
    Background: Inhabitants of the Eastern Cape Province of South Africa use the roots of Dianthus thunbergii and corms of Hypoxis argentea to treat diabetes mellitus and other ailments. Objective: The objective of this study was to analyze the phytochemical composition and antioxidant activities of the aqueous and ethanol extracts of the roots and corms of two plants. Materials and Methods: Total phenolics, flavonoids, flavonols, proanthocyanidins, tannins, and alkaloids were determined by standard methods. The scavenging activities of the extracts against 1,1 diphenyl‑2‑picrylhydrazyl (DPPH), 2’‑azino‑bis (3‑ethylbenthiazoline‑6‑sulfonic acid (ABTS), nitric oxide (NO), hydrogen peroxide (H2O2), and their ferric‑reducing antioxidant potentials (FRAPs) were measured. Results: The ethanol extract of H. argentea had the highest content of phenolics (66.71 } 2.71 mg gallic acid equivalent/g) and tannins (1.18 } 0.07 mg TAE/g), while the ethanol extract of D. thunbergii gave higher contents of flavonoids and proanthocyanidins (62.21 } 1.75 mg Qe/g and 432.62 } 2.43 mg Ca/g, respectively). Flavonols were the most predominant in the aqueous extract of H. argentea (25.51 } 1.92 mg Qe/g). We observed a concentration‑dependent response in the ABTS‑ and H2O2‑scavenging activities and FRAP values of the extracts and standards (Vitamin C, butylated hydroxytoluene, and rutin). The ethanol extracts of both plants generally demonstrated better antioxidant activities against H2O2, NO, and ABTS while also possessing better reducing power than the aqueous extracts. The aqueous extract of D. thunbergii, however, showed the best DPPH scavenging activity. Conclusion: The higher content of phytochemicals and antioxidant capacity obtained for the ethanol extracts of D. thunbergii and H. argentea may prove to be valuable information in selecting suitable extraction solvents for the medicinal applications of both plants.
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    Phytochemical, analgesic, in-Vitro anti-oxidant and GC-MS analysis of Vernonia amygdalina leaves
    (Biomedical Communications Group, 2018) Adeoye, A. T.; Akinrinde, A. S.; Oyagbemi, A. A.; Omobowale, T. O.; Adedapo, A. D. A.; Ayodele, E. A.; Yakubu, M. A.; Adedapo, A. A.
    The powdered leaf of Vernonia amygdalina was subjected to phytochemical screening, and in vitro antioxidant studies. The volatile oil of the leaves of the plant was also screened to determine the constituents. Analgesic tests using acetic acid induced writhing and paw licking (formalin) test in mice were also carried out. The in vitro antioxidant assay used include FRAP, ABTS, DPPH, and NO assay and then compared these with standards (Vitamin E and Rutin). Results showed the presence of saponins and tannins strongly, while alkaloids, flavonoids, anthraquinones and terpenoids were present in little quantities. On the other hand however, cardiac glycosides were absent in the plant. In the FRAP assay method, the absorbance of Vernonia amygdalina was found to be dose dependent with the maximum absorbance of 0.641nm at 0.5mg/ml which was significantly higher than that of rutin (0.56nm) and lower than that of Vitamin E (0.77nm). The ABTS radical scavenging activity of Vernonia amygdalina showed a dose dependent increase in the inhibition of the ABTS radical scavenging activity (91.93, 95.42, 99.24, 99.34 and 99.53% at 0.025, 0.05, 0.1, 0.2 and 0.5mg/ml respectively). This was comparable to that of rutin. The extract and the reference antioxidant (Rutin and Vitamin E) promoted an inhibition of DPPH radical at all concentrations tested in this study. Vernonia amygdalina showed a relatively stable effect in inhibiting the DPPH radical at all doses tested reaching 74.76%, 69.11% and 86.90% for Vernonia amygdalina, Vitamin E and Rutin respectively at the highest concentration. Vernonia amygdalina showed a dose dependent increase in the inhibition of the nitric oxide radical. The major compounds obtained from the GC-MS analysis of the essential of Vernonia amygdalina in this study were caryophyllene oxide (23.48%), phytol (22.92%), 2-Pentadecanone, 6,10,14-trimethyl (12.98%), hexadecanoic acid ethyl ester (12.24%), Oxirane, heptadecyl (12.11%), benzaldehyde (4.97%), benzeneacetaldehyde (5.83%), and trans-beta-ionone (5.47%). The methanol leaf extract of Vernonia amygdalina inhibited the acetic acid induced writhing in a manner comparable with the standard drug used in this study. The paw licking (formalin) test produces a distinct biphasic response to pain stimulus and the extract caused a dose dependent decrease in the inhibition of pain in both phases of the formalin paw lick test.
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    Phytochemical, acute toxicity, analgesic, in vitro antioxidant studies and GC-MS investigation of Essential Oil of the Methanol Leaf Extract of Momordica charantia
    (Sciencedomain International, 2017) Ofuegbe, S. O.; Akinrinde, A. S.; Oyagbemi, A. A.; Omobowale, T. O.; Yakubu, M. A.; Adedapo, A. A.
    Medicinal plants have bioactive compounds which play an important role in the healing of various diseases. They are the best sources for chemical ingredients, antimicrobial and antioxidant agents for cure of different diseases. Most medicinal plants possess pharmacological activities (anti-inflammatory, antidiabetic, antioxidant, antibacterial, antifungal etc.) due to the presence of these phytochemicals in them. In this study, we intend to conduct qualitative phytochemical screening and to quantitatively evaluate the total phenol, flavonols, tannins, proanthocyanidins and flavonoids contents of the plant, Mormodica charantia. The acute toxicity studies of the methanol leaf extract of M. charantia on mice was conducted to evaluate how safe the plant is in relation to dosage, and this is intended to establish the safety of the plant in mice with reference to OECD guidelines. Furthermore, the analgesic activity of the methanol leaf extract of M. charantia and the free radical scavenging activities of the plant in vitro were demonstrated using various standard procedures. We also intend to profile the major compounds present in the essential oil of the plant understudied using Gas Chromatography-Mass Spectrometry Analysis. Summarily, this study was aimed to investigate the phytochemical screening, acute toxicity, analgesic, in vitro antioxidant, as well as the chemical constituents in the essential oil of the methanol leaf extract of M. charantia.
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    Phytochemical, acute toxicity, analgesic, in vitro antioxidant studies and GC-MS investigation of Essential Oil of the Methanol Leaf Extract of Momordica charantia
    (Sciencedomain International, 2017) Ofuegbe, S. O.; Akinrinde, A. S.; Oyagbemi, A. A.; Omobowale, T. O.; Yakubu, M. A.; Adedapo, A. A.
    Medicinal plants have bioactive compounds which play an important role in the healing of various diseases. They are the best sources for chemical ingredients, antimicrobial and antioxidant agents for cure of different diseases. Most medicinal plants possess pharmacological activities (anti-inflammatory, antidiabetic, antioxidant, antibacterial, antifungal etc.) due to the presence of these phytochemicals in them. In this study, we intend to conduct qualitative phytochemical screening and to quantitatively evaluate the total phenol, flavonols, tannins, proanthocyanidins and flavonoids contents of the plant, Mormodica charantia. The acute toxicity studies of the methanol leaf extract of M. charantia on mice was conducted to evaluate how safe the plant is in relation to dosage, and this is intended to establish the safety of the plant in mice with reference to OECD guidelines. Furthermore, the analgesic activity of the methanol leaf extract of M. charantia and the free radical scavenging activities of the plant in vitro were demonstrated using various standard procedures. We also intend to profile the major compounds present in the essential oil of the plant understudied using Gas Chromatography-Mass Spectrometry Analysis. Summarily, this study was aimed to investigate the phytochemical screening, acute toxicity, analgesic, in vitro antioxidant, as well as the chemical constituents in the essential oil of the methanol leaf extract of M. charantia.
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    Effect of exposure and withdrawal on lead-induced toxicity and oxidative stress in cardiac tissues of rats
    (Informatics Publishing Limited, 2016) Omobowale, T. O.; Oyagbemi, A. A.; Akinrinde, A. S.; Ola-Davies, O. E.; Saba, A. B.; Olopade, J. O.; Adedapo, A. A.
    Lead poisoning continues to pose a serious health challenge and more significantly so in developing countries with ineffective waste disposal systems. Recent efforts at solving lead poisoning issues have seen entire towns being resettled from lead-contaminated areas. This study was designed to investigate whether withdrawal of lead exposure results in a resolution of toxic effects of lead in cardiac tissues. Adult male Wistar rats were exposed orally to lead acetate (PbA) at doses of 0.25, 0.5, and 1.0 mg/ml for 6-week duration, after which one-half was sacrificed and the remaining left for a further 6 weeks without lead treatment. Exposure of rats to PbA produced significant decline (P < 0.05) in the activities of antioxidant parameters, including superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione-S-transferase (GST), catalase (CAT), and reduced glutathione (GSH), whereas malondialdehyde (MDA) concentration was significantly elevated. Animals from the withdrawal period exhibited a similar pattern of alterations, with a significant (P < 0.05) reduction in GSH, GPx, and SOD and a significant elevation in MDA and H2O2 concentrations. However, GST activity was elevated, whereas CAT activity remained unaltered in the withdrawal period. The results of this study showed that cardiotoxicity indicated by induction of oxidative stress and reduction in antioxidant parameters failed to resolve upon withdrawal of lead exposure in male rats during the period of study.
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    Effect of exposure and withdrawal on lead-induced toxicity and oxidative stress in cardiac tissues of rats
    (Informatics Publishing Limited, 2016) Omobowale, T. O.; Oyagbemi, A. A.; Akinrinde, A. S.; Ola-Davies, O. E.; Saba, A. B.; Olopade, J. O.; Adedapo, A. A.
    Lead poisoning continues to pose a serious health challenge and more significantly so in developing countries with ineffective waste disposal systems. Recent efforts at solving lead poisoning issues have seen entire towns being resettled from lead-contaminated areas. This study was designed to investigate whether withdrawal of lead exposure results in a resolution of toxic effects of lead in cardiac tissues. Adult male Wistar rats were exposed orally to lead acetate (PbA) at doses of 0.25, 0.5, and 1.0 mg/ml for 6-week duration, after which one-half was sacrificed and the remaining left for a further 6 weeks without lead treatment. Exposure of rats to PbA produced significant decline (P < 0.05) in the activities of antioxidant parameters, including superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione-S-transferase (GST), catalase (CAT), and reduced glutathione (GSH), whereas malondialdehyde (MDA) concentration was significantly elevated. Animals from the withdrawal period exhibited a similar pattern of alterations, with a significant (P < 0.05) reduction in GSH, GPx, and SOD and a significant elevation in MDA and H2O2 concentrations. However, GST activity was elevated, whereas CAT activity remained unaltered in the withdrawal period. The results of this study showed that cardiotoxicity indicated by induction of oxidative stress and reduction in antioxidant parameters failed to resolve upon withdrawal of lead exposure in male rats during the period of study.
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    Cobalt chloride-induced hepatic and intestinal damage in rats: protection by ethyl acetate and chloroform fractions of Ocimum gratissimum
    (Informatics Publishing Limited, 2016) Akinrinde, A. S.; Oyagbemi, A. A.; Omobowale, T. O.; Nwozuzu, V. C.
    Cobalt chloride is known to produce symptoms of diarrhea, vomiting and other gastrointestinal disturbances. We investigated the potential roles of the ethyl acetate and chloroform fractions of Ocimum gratissimum (OG), traditionally used to treat diarrhea and other gastrointestinal disorders in protection against cobalt chloride (CoCl2)-induced liver and intestinal damage. Wistar albino rats were given CoCl2 (350 ppm) in drinking water for 7 days, alone or concurrently with either fractions of OG at 100 and 200mg/kg each. Gallic acid (120 mg/kg) was administered to a group of rats as a standard flavonoid. Biochemical indices of oxidative stress, antioxidant enzyme activities, the levels of pro-inflammatory cytokines (Interleukin 1β; IL-1β and Tumor necrosis factor, TNF-α) were evaluated and the histological appearance of the liver and intestinal mucosa was investigated. CoCl2 produced significant elevations (p<0.05) in hydrogen peroxide (H2O2), malondialdehyde (MDA), IL-1β, alanine transaminase (ALT), aspartate transaminase (AST) and alkaline phosphatase (ALP). This was accompanied with significant reductions (p<0.05) in reduced glutathione (GSH), glutathione peroxidase (GPX) and glutathione S-transferase (GST) activities. Liver sections of rats exposed to CoCl2 had poor architecture and areas of necrosis with several dead hepatocytes, while some appeared with hyperchromic nuclei. Intestinal mucosa showed significant loss of absorptive epithelial cells with CoCl2 exposure. Treatment with the fractions from OG produced reduction in H2O2, MDA and IL-1β levels; reduced serum activities of ALT, AST and ALP; restoration of GSH levels and improved activities of GPX and GST. The fractions significantly preserved the hepatic and intestinal architecture.Our results indicate that the fractions of OG exhibited considerable hepatic and intestinal protection by reduction in levels of oxidants and pro-inflammatory cytokines, enhancement of antioxidant enzyme activities and preservation of tissue integrity and might thus be very useful agents in protecting the liver and intestines during concurrent exposure to Cobalt chloride.
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    Alterations in blood pressure, antioxidant status and caspase 8expression in cobalt chloride-induced cardio-renal dysfunction arereversed by Ocimum gratissimum and gallic acid in Wistar rats
    (Elsevier B.V., 2016) Akinrinde, A. S.; Oyagbemi, A. A.; Omobowale, T. O.; Asenuga, E. R.; Ajibade, T. O.
    The protective abilities of the chloroform extract of Ocimum gratissimum (COG) and gallic acid againstcobalt chloride (CoCl2) − induced cardiac and renal toxicity were evaluated. Rats were exposed to CoCl2(350 ppm) for 7 days, either alone, or in combination with COG (100 and 200 mg/kg) or gallic acid(120 mg/kg). CoCl2given alone, caused significant increases (p < 0.05) in oxidative stress parameters(hydrogen peroxide, H2O2and malondialdehyde, MDA) and increased expression of the apoptotic initia-tor caspase 8 in the heart and kidneys. There was significant reduction (p < 0.05) in reduced glutathione(GSH) in cardiac and renal tissues; reduction in superoxide dismutase (SOD) activity in the kidneys andadaptive increases in Glutathione S-transferase (GST) and catalase (CAT). CoCl2also produced signifi-cant reduction (p < 0.05) in systolic (SBP), diastolic (DBP) and mean arterial (MAP) blood pressures. OralCOG and gallic acid treatment significantly reduced (p < 0.05) the levels of H2O2and MDA; with reducedexpression of caspase 8 and restoration of GSH levels, GPx, SOD and CAT activities, howbeit, to varyingdegrees in the heart and kidneys. COG (200 mg/kg) was most effective in restoring the blood pressures inthe rats to near control levels. CoCl2-induced histopathological lesions including myocardial infarctionand inflammation and renal tubular necrosis and inflammation were effectively ameliorated by the treat-ments administered. This study provides evidence for the protective roles of O. gratissimum and gallicacid by modulation of CoCl2-induced alterations in blood pressure, antioxidant status and pro-apoptoticcaspase 8 in Wistar rats.
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    Gallic acid ameliorates Cyclophosphamide-Induced neurotoxicity in Wistar rats Through Free radical scavenging activity and improvement in antioxidant defense system
    (Taylor & Francis, 2016) Oyagbemi, A. A.; Omobowale, T. O.; Saba, A. B.; Olowu, E. R.; Dada, R. O.; Akinrinde, A. S.
    Cyclophosphamide (CPA) is a widely used anticancer chemotherapeutic agent and its toxicity has been associated with its toxic metabolites phosphormide mustard. Therefore, the ameliorative effect of Gallic acid against neurotoxicity was examined in this study. Sixty rats were grouped into 10 rats per group. Group 1 received saline orally.Group 2 received CPA at 100 mg/kg single dose intraperitoneally on day 1. Groups 3 and 4were treated with Gallic acid (GA) at 60 and 120 mg/kg body weight only for 10 days and also received a single dose of CPA (100 mg/kg) intraperitoneally on day 1, respectively. Rats in groups 5 and 6 receivedGAat 60 and 120 mg/kg body weight only for 10 days. Groups 3, 4, 5, and 6 received GA orally. The cerebellar and cerebral malondialdehyde (MDA) contents and hydrogen peroxide generation were significantly (p < .05) elevated. The cerebellar and cerebral catalase (CAT), superoxide dismutase and glutathione-S-transferase (GST) activities were significantly (p < .05) reduced in CPA treated group. The activity of glutathione peroxidase (GPx) was significantly increased in rats that were treatment with CPA. Also, nitrite content was significantly elevated in the brain of rats that received the toxic dose of CPA. All these findings suggest that treatment with GA (60 and 120 mg/kg) ameliorated the neurotoxicity induced by CPA via reduction of oxidative stress and increase in antioxidant defense system. Combining all, chemotherapeutic agents with structure/function similar to GA could be of potential benefit to the pharmaceutical industries as an adjuvant in chemotherapy with little or no side effects.