scholarly works

Permanent URI for this collectionhttps://repository.ui.edu.ng/handle/123456789/585

Browse

Start date: 2011

Search Results

Now showing 1 - 10 of 25
  • No Thumbnail Available
    Item
    Changes in serum cytokine levels, hepatic and intestinal morphology in aflatoxin B1-induced injury: modulatory roles of melatonin and flavonoid-rich fractions from Chromolena odorata
    (Springer, 2015) Akinrinmade, F. J.; Akinrinde, A. S.; Amid, A.
    Aflatoxins are known to produce chronic carcinogenic, mutagenic, and teratogenic effects, as well as acute inflammatory effects, especially in the gastrointestinal tract. The potentials of the flavonoid-rich extract from Chromolena odorata (FCO) and melatonin (a standard anti-oxidant and anti-inflammatory agent) against aflatoxin B1 (AFB1)-induced alterations in pro-inflammatory cytokine levels and morphology of liver and small intestines were evaluated in this study. We utilized Wistar albino rats (200–230 g) randomly divided into five groups made up of group A, control rats; group B, rats given AFB1 (2.5 mg/kg, intraperitone al) twice on days 5 and 7; rats in groups C, D, and E were treated with melatonin (10 mg/kg, intraperitoneal) or oral doses of FCO1 (50 mg/kg) and FCO2 (100 mg/kg) for 7 days, respectively, along with AFB1 injection on days 5 and 7. Serum levels of interleukin 1 beta (IL-1β) and tumor necrosis factor alpha (TNF-α) were determined using commercial ELISA kits and histopathological evaluation of the liver, duodenum, and ileum were also carried out. We observed significant elevation (p < 0.05) in serum IL-1β correlating with hemorrhages and leucocytic and lymphocytic infiltration in the liver and intestines as evidences of an acute inflammatory response to AFB1 administration. All treatments yielded significant reduction (p < 0.05) in IL-1β levels, although TNF-α levels were not significantly altered in all rats that received AFB1, irrespective of the treatments. Melatonin and FCO2 produced considerable protection of hepatic tissues, although melatonin was not quite effective in protecting the intestinal lesions. Our findings suggest a modulation of cytokine expression that may, in part, be responsible for the abilities of C. odorata or melatonin in amelioration of hepatic and intestinal lesions associated with aflatoxin B1 injury.
  • No Thumbnail Available
    Item
    Changes in serum cytokine levels, hepatic and intestinal morphology in aflatoxin B1-induced injury: modulatory roles of melatonin and flavonoid-rich fractions from Chromolena odorata
    (Springer, 2015) Akinrinmade, F. J.; Akinrinde, A. S.; Amid, A.
    Aflatoxins are known to produce chronic carcinogenic, mutagenic, and teratogenic effects, as well as acute inflammatory effects, especially in the gastrointestinal tract. The potentials of the flavonoid-rich extract from Chromolena odorata (FCO) and melatonin (a standard anti-oxidant and anti-inflammatory agent) against aflatoxin B1 (AFB1)-induced alterations in pro-inflammatory cytokine levels and morphology of liver and small intestines were evaluated in this study. We utilized Wistar albino rats (200–230 g) randomly divided into five groups made up of group A, control rats; group B, rats given AFB1 (2.5 mg/kg, intraperitone al) twice on days 5 and 7; rats in groups C, D, and E were treated with melatonin (10 mg/kg, intraperitoneal) or oral doses of FCO1 (50 mg/kg) and FCO2 (100 mg/kg) for 7 days, respectively, along with AFB1 injection on days 5 and 7. Serum levels of interleukin 1 beta (IL-1β) and tumor necrosis factor alpha (TNF-α) were determined using commercial ELISA kits and histopathological evaluation of the liver, duodenum, and ileum were also carried out. We observed significant elevation (p < 0.05) in serum IL-1β correlating with hemorrhages and leucocytic and lymphocytic infiltration in the liver and intestines as evidences of an acute inflammatory response to AFB1 administration. All treatments yielded significant reduction (p < 0.05) in IL-1β levels, although TNF-α levels were not significantly altered in all rats that received AFB1, irrespective of the treatments. Melatonin and FCO2 produced considerable protection of hepatic tissues, although melatonin was not quite effective in protecting the intestinal lesions. Our findings suggest a modulation of cytokine expression that may, in part, be responsible for the abilities of C. odorata or melatonin in amelioration of hepatic and intestinal lesions associated with aflatoxin B1 injury.
  • No Thumbnail Available
    Item
    Gallic acid protects against cyclophosphamide-induced toxicity in testis and epididymis of rats
    (Blackwell Verlag GmbH, 2015) Oyagbemi, A. A.; Omobowale, T. O.; Saba, A. B.; Adedara, I. A.; Olowu, E. R.; Akinrinde, A. S.; Dada, R. O.
    The protective role of gallic acid (GA) on reproductive toxicity induced by cyclophosphamide (CPA), an antineoplastic drug, was investigated in male Wistar rats. Sixty rats were grouped into 10 rats per group. Group 1 (control) received distilled water. Rats in groups 2 and 3 received GA alone at 60 and 120 mg kg 1 for 14 consecutive days, respectively. Group 4 received a single intraperitoneal dose of CPA at 200 mg kg 1 on day 1. Groups 5 and 6 received a single dose of CPA (200 mg kg 1 ) intraperitoneally on day 1 followed by treatment with GA at 60 and 120 mg kg 1 for 14 consecutive days, respectively. In testes and epididymis of the treated rats, CPA administration resulted in significant elevation (P < 0.05) in malondialdehyde (MDA), nitrite and hydrogen peroxide levels. There was a significant decrease in the activities of superoxide dismutase and glutathione-S-transferase. Furthermore, there were significant reductions in plasma luteinising hormone (LH), follicle stimulation hormone (FSH) and testosterone levels, which were accompanied by significant decrease in sperm motility and viability in CPA-treated rats. Histological examination revealed marked testicular and epididymal atrophy in CPA alone trea ted rats and these aberrations were reversed by GA. In conclusion, GA has capacity to protect against reproductive toxicity induced by cyclophosphamide.
  • No Thumbnail Available
    Item
    Evidence of attenuation of intestinal ischemia–reperfusion injury following pre-treatment with methanolic extracts from Chromolena odorata in rats
    (Natural Health Product Research Society of Canada, 2015) Akinrinmade, J. F.; Akinrinde, S. A.; Odejobi, A.; Oyagbemi, A. A.
    Background: Chromolena odorata is a tropical species of flowering shrub in the family Asteraceae, leaves of it have been reported to be widely used as herbal remedy for the treatment of various ailments. It is particularly reported to be useful in the healing of wounds. Methods: We investigated the possibility of amelioration of intestinal ischemia–reperfusion (IR) injury in rats trea ted with methanolic extract of C. odorata (MECO). Wistar albino rats were divided randomly into five groups of six animals each as control, IR-treated, IR þ 200 mg/kg MECO, IR þ 400 mg/kg MECO, and IR þ 200 mg/kg vita min C. Pre-treatment with MECO or vitamin C was for 7 days. Results: The contents of hydrogen peroxide (H2O2) and malondialdehyde (MDA) were significantly reduced by MECO and vitamin C, while there were significant enhancements of the activities of superoxide dismutase (SOD), glutathione peroxidase (GPX), catalase (CAT), as well as the content of reduced glutathione (GSH) in pre-treated rats compared to IR-treated rats. Glutathione S-transferase (GST) activity was not significantly affected in all the groups. Histopathological examination of small intestinal mucosa revealed significant attenuation of intestinal pathology in animals pre-treated with MECO, while IR injury produced severe villi erosion, necrosis, and inflammatory cell infiltrations. Conclusions: The present study highlights the antioxi dant activities of MECO and its ability to inhibit inflammatory cell infiltration as mechanisms involved in its protection against IR injury in the intestine of rats, an effect that was largely comparable to that of vitamin C.
  • No Thumbnail Available
    Item
    Evidence of attenuation of intestinal ischemia–reperfusion injury following pre-treatment with methanolic extracts from Chromolena odorata in rats
    (Natural Health Product Research Society of Canada, 2015) Akinrinmade, J. F.; Akinrinde, S. A.; Odejobi, A.; Oyagbemi, A. A.
    Background: Chromolena odorata is a tropical species of flowering shrub in the family Asteraceae, leaves of it have been reported to be widely used as herbal remedy for the treatment of various ailments. It is particularly reported to be useful in the healing of wounds. Methods: We investigated the possibility of amelioration of intestinal ischemia–reperfusion (IR) injury in rats trea ted with methanolic extract of C. odorata (MECO). Wistar albino rats were divided randomly into five groups of six animals each as control, IR-treated, IR þ 200 mg/kg MECO, IR þ 400 mg/kg MECO, and IR þ 200 mg/kg vita min C. Pre-treatment with MECO or vitamin C was for 7 days. Results: The contents of hydrogen peroxide (H2O2) and malondialdehyde (MDA) were significantly reduced by MECO and vitamin C, while there were significant enhancements of the activities of superoxide dismutase (SOD), glutathione peroxidase (GPX), catalase (CAT), as well as the content of reduced glutathione (GSH) in pre-treated rats compared to IR-treated rats. Glutathione S-transferase (GST) activity was not significantly affected in all the groups. Histopathological examination of small intestinal mucosa revealed significant attenuation of intestinal pathology in animals pre-treated with MECO, while IR injury produced severe villi erosion, necrosis, and inflammatory cell infiltrations. Conclusions: The present study highlights the antioxi dant activities of MECO and its ability to inhibit inflammatory cell infiltration as mechanisms involved in its protection against IR injury in the intestine of rats, an effect that was largely comparable to that of vitamin C.
  • No Thumbnail Available
    Item
    Lack of reversal of oxidative damage in renal tissues of Lead Acetate-Treated rats
    (Wiley Periodicals, Inc., 2014) Oyagbemi, A. A.; Omobowale, T. O.; Akinrinde, A. S.; Saba, A. B.; Ogunpolu, B. S.; Daramola, O.
    Removal of lead from the environment of man or otherwise, the movement of man from lead-contaminated areas has been employed as a means of abatement of the toxic effects of lead. Whether toxic effects in already-exposed individuals subside after lead withdrawal remains unanswered. To understand the reversibility of nephrotoxicity induced by lead acetate, male Wistar rats were orally exposed to 0.25, 0.5, and 1.0 mg/mL of lead acetate for 6 weeks. Activities of glutathione-s-transferase, catalase (CAT), superoxide dismutase (SOD) and the concentrations of hydrogen peroxide (H2O2), and malondialdehyde increased significantly (p < 0.05) in a dose dependent manner, whereas reduced glutathione (GSH) level and glutathione peroxidase activity were significantly reduced. The pattern of alterations in most of the oxidative stress and antioxidant parameters remained similar in rats from the withdrawal period, although CAT and SOD activities reduced, in contrast to their elevation during the exposure period. Serum creatinine levels were significantly elevated in both exposure and withdrawal experiments whereas serum blood urea nitrogen levels were not significantly different from the control in both exposure and withdrawal periods. The histological damage observed include multifocal areas of inflammation, disseminated tubular necrosis, and fatty infiltration of the kidney tubules both at exposure and withdrawal periods. The results suggest that lead acetate-induced nephrotoxicity by induction of oxidative stress and disruption of anti-oxidant. The aforementioned alterations were not reversed in the rats left to recover within the time course of study.
  • Thumbnail Image
    Item
    Gastrointestinal protective efficacy of Kolaviron (a bi‑flavonoid from Garcinia kola) following a single administration of sodium arsenite in rats: Biochemical and histopathological studies
    (Wolters Kluver, 2015) Akinrinde, A. S.; Olowu, E.; Oyagbemi, A. A.; Omobowale, O. T.
    Background: Arsenic intoxication is known to produce symptoms including diarrhea and vomiting, which are indications of gastrointestinal dysfunction. Objective: We investigated whether Kolaviron (KV) administration protected against sodium arsenite (NaAsO2)-induced damage to gastric and intestinal epithelium in rats. Materials and Methods: Control rats (Group I) were given a daily oral dose of corn oil. Rats in other groups were given a single dose of NaAsO2 (100 mg/kg; intraperitoneal) alone (Group II) or after pretreatment for 7 days with KV at 100 mg/kg (Group III) and 200 mg/kg (Group IV). Rats were sacrificed afterward and portions of the stomach, small intestine and colon were processed for histopathological examination. Hydrogen peroxide, reduced glutathione, malondialdehyde (MDA) concentrations as well as activities of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPX), glutathione S transferase (GST) and myeloperoxidase (MPO) were measured in the remaining portions of the different gastrointestinal tract (GIT) segments. Results: NaAsO2 caused significant increases (P < 0.05) in MDA levels and MPO activity, with significant reductions (P < 0.05) in GST, GPX, CAT and SOD activities in the stomach and intestines. KV significantly reversed the changes (P < 0.05) in a largely dose-dependent manner. The different segments had marked inflammatory cellular infiltration, with hyperplasia of the crypts, which occurred to much lesser degrees with KV administration. Conclusion: The present findings showed that KV might be a potent product for mitigating NaAsO2 toxicity in the GIT.
  • Thumbnail Image
    Item
    Saponins – A ubiquitous phytochemical: A review of its biochemical, physiological and pharmacological effects
    (Studium Press LLC, 2014) Soetan, K. O.; Ajibade, T. O.; Akinrinde, A. S.
    Saponins are ubiquitous phytochemicals widely reported to be present in many species of plants and animals. Some saponin containing plants, mainly legumes, have been used as animal feed, but others are toxic. In this review, the biochemical, physiological and pharmacological effects of saponins in humans and animals have been highlighted. Physiological and biochemical effects examined include the effects on biological membranes, gastrointestinal absorption, blood and liver cholesterol, enzymes and general body metabolism, reproductive, antioxidant and free-radical scavenging effect, smooth muscle activity and effects on ruminant digestion. Pharmacological effects of saponins such as anti-inflammatory, diuretic, hypoglycaemic, antidiabetic, antiulcer and anti-ageing effects are also examined. From the literature reviewed, it can be concluded that saponins, in general, are toxic when administered intravenously but possess a lot of therapeutic potentials especially as cytotoxic agents.
  • Thumbnail Image
    Item
    Clinical biochemistry as a prognostic tool in the management of the critically-ill patient
    (Nigerian Veterinary Medical Association, 2014) Akinrinmade, J. F.; Akinrinde, A. S.
  • Thumbnail Image
    Item
    Comparative studies on the proximate composition, mineral and anti-nutritional factors in the seeds and leaves of African locust bean (Parkia biglobosa)
    (Valahia University Press, 2014) Soetan, K. O.; Akinrinde, A. S.; Adisa, S. B.
    The seeds and leaves of African Locust Bean (Parkia biglobosa) were evaluated for their proximate analysis, minerals and anti-nutritional factors. Atomic absorption spectrometry was used in the determination of the levels of Ca, Mg,K, Na, Mn, Fe, Cu and Zn. Anti-nutritional Factors (ANFs), including Trypsin inhibitor, oxalates, phytates, tannins, saponins, hydrocyanic acid were also determined using appropriate techniques. The result showed that the seeds of P.biglobosa had significantly higher (p<0.05)crude protein (33.50%), crude fat (49.20%) and %dry matter (95.20%) contents compared to the leaves having crude protein(18.40%), crude fat (8.11%) and %dry matter (88.80%), while the leaves had significantly higher (p<0.05) contents of ash (13.60%), crude fibre(18.90%) and moisture (11.20%) as against the seeds havingash (4.81%), crude fibre (4.66%)and moisture (4.89%). The mineral content of the analyzed samples showed that the seeds were richer in Ca (0.703%), Mg (0.356%), K (0.211%), Na (86.729ppm), Mn (54.811ppm), Fe (69.828ppm), Cu (9.766ppm) and Zn (12.156ppm), while the leaves recorded higher Phosphorus level (79.833ppm) than the seeds. For the ANFs, the seeds recorded higher levels of trypsin inhibitor (0.059+0.01),haemagglutinating units (46.00+0.07) and tannins (0.51+0.00) than the leaves, while the leaves recorded higher levels of oxalates (0.97+0.00), phytates (2.16+0.03), saponins (1.24+0.00) and hydrogen cyanide (87.9+0.56)than the seeds. The overall results are suggestive of higher nutritional quality of the seeds than the leaves due to higher mineral contents and lower presence of some anti-nutritional factors.