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1.
IBRO Rep ; 9: 164-182, 2020 Dec.
Article in English | MEDLINE | ID: mdl-32803016

ABSTRACT

Vanadium, a transition series metal released during some industrial activities, induces oxidative stress and lipid peroxidation. Ameliorative effect of a pure compound from the methanolic extract of Moringa oleifera leaves, code-named MIMO2, in 14-day old mice administered with vanadium (as sodium metavanadate 3 mg/kg) for 2 weeks was assessed. Results from body weight monitoring, muscular strength, and open field showed slight reduction in body weight and locomotion deficit in vanadium-exposed mice, ameliorated with MIMO2 co-administration. Degeneration of the Purkinje cell layer and neuronal death in the hippocampal CA1 region were observed in vanadium-exposed mice and both appeared significantly reduced with MIMO2 co-administration. Demyelination involving the midline of the corpus callosum, somatosensory and retrosplenial cortices was also reduced with MIMO2. Microglia activation and astrogliosis observed through immunohistochemistry were also alleviated. Immunohistochemistry for myelin, axons and oligodendrocyte lineage cells were also carried out and showed that in vanadium-treated mice brains, oligodendrocyte progenitor cells increased NG2 immunolabelling with hypertrophy and bushy, ramified appearance of their processes. MIMO2 displayed ameliorative and antioxidative effects in vanadium-induced neurotoxicity in experimental murine species. This is likely the first time MIMO2 is being used in vivo in an animal model.

2.
Niger J Physiol Sci ; 35(2): 217-219, 2020 Dec 31.
Article in English | MEDLINE | ID: mdl-34009195

ABSTRACT

Bats and human biological structures are believed to be similar in terms of phylogeny, reproductive biology, and early development. Adequate knowledge of placental morphology will have important implications for research and in comparative anatomy. This report is a part of on-going studies on the African fruit bat species and is a case report from an incidental discovery of the foetus and placenta in an African fruit bat (Epomops franqueti) captured for research.


Subject(s)
Chiroptera , Animals , Female , Fetus , Humans , Placenta , Pregnancy
3.
J Basic Clin Physiol Pharmacol ; 29(1): 29-35, 2018 Jan 26.
Article in English | MEDLINE | ID: mdl-29283882

ABSTRACT

BACKGROUND: Elevation of phosphodiesterase-5 (PDE5) activity converts cyclic guanosine monophosphate (cGMP) to 5'-GMP, a mechanism that could be associated with drug-mediated hepatotoxicity. This study investigated whether selective inhibition of PDE5 by sildenafil could offer protection against hepatotoxicity induced by carbon tetrachloride (CCl4). METHODS: CCl4 (0.5 mL/kg) was administered intraperitoneally to induce hepatotoxicity. The control group received normal saline. Sildenafil (5 mg, 10 mg, and 20 mg/kg, p.o.) was administered to CCl4-treated rats. RESULTS: CCl4 significantly increased the serum levels of gamma glutamyl transferase (γ-GT), alkaline phosphatase (ALP), aspartate aminotransferase (AST), and alanine aminotransferase (ALT) and reduced total protein (TP) (p<0.05). Pretreatment with sildenafil moderately reduced ALP, AST, and ALT activities with modest increase in TP level. CCl4-induced changes in the antioxidant status of the liver were significantly improved by sildenafil, especially at the lowest dose of 5 mg/kg by elevating the levels of reduced glutathione (GSH), glutathione peroxidase (GPx), catalase (CAT), superoxide dismutase (SOD), and glutathione-S-transferase (GST) and preventing lipid peroxidation (p<0.05). Sildenafil did not significantly alter the total cholesterol and triglyceride levels. However, high-density lipoprotein (HDL) level was significantly increased by sildenafil (p<0.05). CONCLUSIONS: The results from this study suggest that sildenafil, when used at low doses, may be a useful pharmacological protective agent against CCl4-induced hepatotoxicity.


Subject(s)
Carbon Tetrachloride/adverse effects , Chemical and Drug Induced Liver Injury/drug therapy , Cyclic Nucleotide Phosphodiesterases, Type 5/metabolism , Liver/drug effects , Phosphodiesterase 5 Inhibitors/pharmacology , Protective Agents/pharmacology , Sildenafil Citrate/pharmacology , Alanine Transaminase/metabolism , Alkaline Phosphatase/metabolism , Animals , Antioxidants/metabolism , Aspartate Aminotransferases/metabolism , Catalase/metabolism , Chemical and Drug Induced Liver Injury/metabolism , Glutathione/metabolism , Lipid Peroxidation/drug effects , Liver/metabolism , Male , Oxidative Stress/drug effects , Rats , Rats, Wistar , Superoxide Dismutase/metabolism , gamma-Glutamyltransferase/metabolism
4.
Int J Biol Macromol ; 79: 226-34, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25940525

ABSTRACT

Cissus gum has been employed as polymer with sodium alginate in the formulation of diclofenac microbeads and the in vivo mucoprotective properties of the polymer in anti-inflammatory therapy assessed in rats with carrageenan-induced paw edema in comparison to diclofenac powder and commercial diclofenac tablet. A full 2(3) factorial experimental design has been used to investigate the influence of concentration of cissus gum (X1); concentration of calcium acetate (X2) and stirring speed (X3) on properties of the microbeads. Optimized small discrete microbeads with size of 1.22±0.10 mm, entrapment efficiency of 84.6% and t80 of 15.2±3.5 h were obtained at ratio of cissus gum:alginate (1:1), low concentration of calcium acetate (5% w/v) and high stirring speed (400 rpm). In vivo studies showed that the ranking of percent inhibition of inflammation after 3h was diclofenac powder>commercial tablet=cissus>alginate. Histological damage score and parietal cell density were lower while crypt depth and mucosal width were significantly higher (p<0.05) in the groups administered with the diclofenac microbeads than those administered with diclofenac powder and commercial tablet, suggesting the mucoprotective property of the gum. Thus, cissus gum could be suitable as polymer in the formulation of non-steroidal anti-inflammatory drugs ensuring sustained release while reducing gastric side effects.


Subject(s)
Alginates/chemistry , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Diclofenac/pharmacology , Edema/drug therapy , Microspheres , Plant Gums/chemistry , Acetates/chemistry , Animals , Anti-Inflammatory Agents, Non-Steroidal/chemistry , Calcium Compounds/chemistry , Carrageenan , Delayed-Action Preparations , Diclofenac/chemistry , Drug Compounding , Drug Liberation , Edema/chemically induced , Edema/pathology , Factor Analysis, Statistical , Glucuronic Acid/chemistry , Hexuronic Acids/chemistry , Hindlimb , Kinetics , Male , Particle Size , Rats , Stomach/drug effects
5.
Drug Chem Toxicol ; 35(4): 371-80, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22288905

ABSTRACT

In this study, the morphological and biochemical susceptibility of the rat brain to vanadium, in the form of sodium metavanadate, and the comparative ameliorative effect of Garcinia kola and kolaviron (G. kola extract), was examined. Brain regions examined were the cerebrum, cerebellum, hippocampus and the olfactory bulb. We showed that vanadium administration caused cellular vacuolation, congestion, and Purkinje cell degeneration and a marked reduction in myelin tracts. Biochemical tests revealed increased lipid peroxidation induced by vanadium, which was ameliorated with the administration of G. kola and kolaviron. Vanadium administration caused an increase in thiobarbituric acid-reactive substances (TBARS) in the cerebrum and hippocampus, whereas the administration of kolaviron resulted in a reduction of the TBARS level by 65.7 and 80%, respectively, in the regions aforementioned. Also, the administration of kolaviron resulted in an increased activity of superoxide dismutase (61.24%) in all brain regions assessed, when compared with the group administered vanadium alone. Results obtained from this study led to the conclusion that kolaviron reduces vanadium-induced oxidative stress in the brain.


Subject(s)
Flavonoids/pharmacology , Garcinia kola/chemistry , Neuroprotective Agents/pharmacology , Plant Extracts/pharmacology , Vanadium/toxicity , Animals , Antidotes/isolation & purification , Antidotes/pharmacology , Brain/drug effects , Brain/pathology , Flavonoids/isolation & purification , Lipid Peroxidation/drug effects , Male , Neuroprotective Agents/isolation & purification , Neurotoxicity Syndromes/drug therapy , Neurotoxicity Syndromes/etiology , Oxidative Stress/drug effects , Rats , Rats, Wistar , Superoxide Dismutase/metabolism , Thiobarbituric Acid Reactive Substances/metabolism , Vanadates/administration & dosage , Vanadates/toxicity
6.
Ital J Anat Embryol ; 115(3): 241-4, 2010.
Article in English | MEDLINE | ID: mdl-21287980

ABSTRACT

The report of the occurrence of additional renal arteries in domestic animals is rare in the literature. We report a case of an additional renal artery in the left kidney found in a Red Sokoto goat cadaver. The additional renal artery originated from the abdominal aorta 3.80 cm cranial to the origin of the main renal artery. The additional renal artery was relatively long, being 6.30 cm from its origin to the cranial pole region of the kidney where it supplied the kidney. This to the best of our knowledge is the first report in the literature indexed in the Medline of an additional renal artery in a goat.


Subject(s)
Goats/abnormalities , Kidney/blood supply , Renal Artery/abnormalities , Animals , Aorta/abnormalities , Aorta/physiology , Dissection/methods , Functional Laterality/physiology , Goats/physiology , Kidney/physiology , Male , Nigeria , Renal Artery/physiology , Renal Circulation/physiology
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