Browsing by Author "Mamman M"
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Item A controlled study to investigate anti-diarrhoeal effect of the stem-bark fractions of Terminalia avicennioides in laboratory animal models(2017) Suleiman MM; Oyelowo BB; Abubakar A; Mamman M; Bello KDDue to the shortcomings associated with modern synthetic antidiarrhoeal drugs, it is important to find newer, safer and cheaper antidiarrhoeal agents from natural sources. The study was conducted to evaluate the anti-diarrhoeal activity of the fractions of the stem-bark of Terminalia avicennioides in laboratory animal models. The effect of different concentrations (1.0×10−3, 2.0×10−3, 4.0×10−3 and 8.0×10−3mg/mL) of the aqueous methanol (AMF), ethyl acetate (EAF) and hexane (HXF) fractions of T. avicennioides were tested against spontaneous and acetylcholine-induced contractions of rabbit jejunum as well as on histamine-induced contraction of guinea pig ileum. Similarly, the effects of the AMF on gastro-intestinal transit time, castor oil-induced diarrhoea and castor oil-induced enteropooling were evaluated. The AMF, EAF and HXF at concentrations of 1.0×10−3, 2.0×10−3, 4.0×10−3 and 8.0×10−3mg/mL attenuated the contractile effects of both the spontaneous and acetylcholine-induced contractions of rabbit jejunum and that of histamine-induced contraction of guinea pig ileum in a concentration-dependent manner. The AMF at doses of 200, 300 and 500mg/kg produced significant (p<0.05) reductions in gastrointestinal transit time of charcoal and incidence of castor oil-induced diarrhoea in mice relative to the untreated control. Similarly, at doses of 300 and 500mg/kg, AMF significantly (p<0.05) reduced the weight and volume of intestinal fluid in the treated mice when compared to the untreated animals. The results of this study showed that the stem-bark of T. avicennioides possesses spasmolytic effect and could be a potential antidiarrhoeal agent. However, detailed pharmacological trials are required to justify the clinical use of the plant for treating diarrhoea.Item Antitrypanosomal properties of Anogeissus leiocarpa extracts and their inhibitory effect on trypanosome alternative oxidase(2022) Tauheed AM; Mamman M; Ahmed A; Suleiman MM; Balogun EOBackground African trypanosomiasis is a protozoan disease with huge socio-economic burden to sub-Saharan African exceeding US$4.6 annual loss. To mitigate the incidence of trypanosomal drug resistance, efforts are geared towards discovery of molecules, especially from natural products, with potential to inhibit important molecular target (trypanosome alternative oxidase, TAO) in trypanosomes that are critical to their survival. Method Crude methanol extract of Anogeissus leiocarpa was subjected to in vitro bioassay-guided antitrypanosomal assay to identify the most active extract with trypanocidal activity. The most active extract was run on a column chromatography yielding five fractions, F1-F5. The fractions were assayed for inhibitory effect on TAO. The most promising TAO inhibitor was subjected to antitrypanosomal evaluation by trypanosome count, drug incubation infectivity test (DIIT) and in vivo studies. Gas chromatography-mass spectrometry (GC-MS) was used to identify and quantify phytochemical constituents of the potential TAO-inhibiting fraction. Results Ethyl acetate extract (EtOAc) significantly (p<0.05) produced trypanocidal effect and was the most active extract. Of the five fractions, only F4 significantly (p<0.05) inhibited TAO compared to the control. F4 completely immobilised the trypanosomes up to 0.5 µg/µl, yielding an EC50 of 0.024 µg/µl compared to the 0.502 µg/µl of diminazene aceturate positive control group. The DIIT showed that F4 was significantly (p<0.05) potent up to 0.1 µg/µl. F4 significantly (p<0.05) suppressed parasite multiplication in systemic circulation of the treated rats and significantly (p<0.05) maintained high PCV when compared to the 5% DMSO group. Furthermore, F4 significantly (p<0.05) lowered serum concentrations of malondialdehyde. Phytoconstituents identified by the GC-MS include tetradecene; cetene; 3-(benzylthio) acrylic acid, methyl ester; 1-octadecene; 9-heptadecanone; hexadecanoic acid, methyl ester; dibutyl phthalate; eicosene; octadecenoic acid, methyl ester; oleic acid; 2-methyl-Z,Z-3,13-octadecadienol; 1-docosene; 3-phenylthiane, s-oxide; phenol, 3-methyl; phthalic acid, di(2-propylpentyl) ester and 1,4-benzenedicarboxylic acid, bis (2-ethylhexyl) ester. Conclusion F4 from EtOAc contains six carbohydrates (9.58%), two free fatty acids (6.48%), five fatty acid esters (27.73%), two aromatic compounds (50.63%) and one organosulphide (5.61%). It inhibited TAO and demonstrated antitrypanosomal effects.Item In vitro assay and in vivo effect of artemisinin in Trypanosoma brucei brucei-infected Wistar rats(2021) Jolayemi KO; Mamman M; Sani D; Okoronkwo MO; Usman A; Udechukwu CC; Oyetunde JSBackground Control of the trypanosomosis has been targeted towards vector control or by the use of antitrypanosomal drugs such as diminazene aceturate and isometamidium with reports of toxicity and relapse following treatment. Hence, the need for continuous research for a safe, efficacious and less toxic drug. In previous studies, artemisinin has shown antitrypanosomal effects against Trypanosoma brucei rhodesiense and also against Trypanosoma brucei brucei (T. b. brucei) in vitro. This period of drug repurposing has led to scientists searching for ways of utilising artemisinin because of its reported multifunctionality and ability to mediate several targets that are important for different diseases. Purpose To evaluate the in vivo effects of artemisinin against T. b. brucei following the in vitro assay. Methods Previously to perform the in vivo assays, the in vitro effects of artemisinin on the T. b. brucei trypomastigotes growth were assessed. The in vivo effects were tested on Wistar rats at doses 5 mg/kg and 10 mg/kg, respectively. All Wistar rats were euthanised at the end of the experiment; kidney, lung, liver and brain samples were harvested and processed for histopathological examination. Results Complete cessation (p < 0.001) of trypanosomal motility in vitro by 2 and 20 µg/µl artemisinin between 10 to 60 min was observed when compared to the controls. Artemisinin showed an IC50 value of 0.42 µg/µl while the positive control drug diminazene aceturate displayed a lower activity with IC50 of 2.99 µg/µl. Level of parasitaemia and survival rate showed significant differences (p < 0.05) in treated groups compared to group II (Infected and untreated). Mean packed cell volume, haemoglobin concentration, mean corpuscular volume and mean corpuscular haemoglobin concentration decreased significantly (p < 0.05) in all infected groups and returned to almost pre-infection values following treatment. Histopathological evaluation showed artemisinin to prevent the distortion of normal architecture of the selected organs. Conclusions In vitro, artemisinin produced a complete inhibition of T. b. brucei motility at 2 and 20 µg/µl. In vivo, artemisinin at 5 and 10 mg/kg prevented histoarchitecture damage of selected organs and caused an elevated haematological profile.Item Research Note: Evaluation of acute oral toxicity of povidone-iodine in cockerels using the up-and-down procedure(2021) Sani D; Abdu PA; Mamman M; Jolayemi KO; Yusuf PO; Andamin ADPovidone-iodine (Polidine) is a synthetic broad-spectrum antiseptic and being applied topically to treat wounds and prevent their infection. It is however used by poultry farmers, field veterinarians, and other animal health workers with the claim that it is effective for treatment of infectious bursal disease when administered orally. Hence, an acute oral toxicity study was conducted to ascertain its safety profile. Ten cockerel chicks were randomly selected and divided into 2 groups of 5 chicks per group. One group served as the negative control, whereas the other group was administered povidone-iodine at a dose of 2,000 mg/kg of BW orally. The blood sample was collected at the end of the study to determine changes in hematological and biochemical parameters. In addition, vital organs were also harvested and preserved for histopathological examinations. The result showed that the median lethal dose (LD50) of the povidone-iodine is higher than 2,000 mg/kg of BW in cockerels. There were no significant changes in the hematological parameters measured. Biochemical evaluation (renal and liver function test) showed an increase in aspartate aminotransferase, alanine aminotransferase, and alkaline phosphatase levels after administration of povidone-iodine. The study indicated that the LD50 of povidone-iodine is higher than 2,000 mg/kg of BW of cockerels, and there were increases in urinary and liver enzymes at this dose.Item Toxicological evaluation of repeated administration of povidone iodine in cockerels(2022) Sani D; Abdu PA; Mamman M; Jolayemi KOPovidone-iodine (Polidine®) is a synthetic broad-spectrum antiseptic being applied topically to treat wounds and prevent their infection. It has been however reported with the assertions that it is effective in the treatment of infectious bursa disease (IBD) when administered orally by practicing Veterinarians and other poultry handlers. Acute kidney injury has been reported also with povidone iodine ingestion. Hence, in this study, graded dose administration was conducted to ascertain its safety profile. Forty chicks were obtained from a poultry hatchery in Ibadan, Oyo State. They were randomly divided into four (4) groups of ten chicks each. Group I served as negative control, groups II, III and IV were administered Polidine® at 1 mL/50 L, 1 mL/25 L, and 1 mL/10 L of water respectively for 7 days. Blood samples were collected on Days 3 and 7 post administration for determination of haematological and biochemical parameters. Liver and Kidney tissues were harvested following termination of the experiment and processed for histopathological examination. Results revealed no significant (p > 0.05) effect in the haematological and biochemical parameters of cockerels treated with Povidone iodine at 1 mL/50 and 25 L of water. On histopathological examination no lesion was also observed in the liver and kidney tissues of groups I, II and III (normal control, 1 mL/50 and 25 L respectively) when compared to group IV (1 mL PI /50 L of water) where lesions were recorded. Hence, this study has shown the relative safety of povidone iodine at different doses in cockerels.