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1.
Niger J Physiol Sci ; 31(1): 93-9, 2016 Aug 30.
Article in English | MEDLINE | ID: mdl-27574770

ABSTRACT

Buchholzia coriacea, taken by elderly, has phytochemicals that have neuro-active metabolites, and the folkloredocumented its use in neuro-behavioral despairs. Previous study in our laboratory shows that methanol extracts of Buchholziacoriacea (MEBC) seeds possess antidepressant-like potentials in laboratory rodents. This present study was conducted toinvestigate the probable mechanism(s) of action by which MEBC potentiates its effects using laboratory rodents.Involvements of serotonergic, cholinergic and adrenergic systems were studied using Forced Swimming Test (FST) and TailSuspension Test (TST) models of behavioral despair. Antagonists which including: Prazosin, an alpha-1-adrenergic receptorblocker (62.5 µg/kg, i.p.), metergoline, a 5HT2 receptor blocker (4 mg/kg, i.p.) and atropine, a -muscarinic cholinergicreceptor blocker (1mg/kg i.p.) were administered before effective dose of MEBC (50mg/kg). Also, the hippocampi of theanimals were studied for changes in neuronal density using Nissl Staining. Our findings showed that mobility was reversedin animals pre-treated with atropine, prazosin, and metergoline significantly (P˂0.05), showing a possible involvement ofthe corresponding systems. However, there was a significant reduction in immobility time (P<0.001) during FST afterchronic administration of the MEBC. The hippocampus showed no significant changes (P<0.05) in neuronal density. Inconclusion, MEBC probably potentiates its antidepressant-like potentials via the cholinergic, adrenergic and partly byserotonergic systems.


Subject(s)
Antidepressive Agents/pharmacology , Biogenic Monoamines/antagonists & inhibitors , Capparaceae , Hippocampus/cytology , Muscarinic Antagonists/pharmacology , Plant Extracts/pharmacology , Adrenergic Antagonists/pharmacology , Animals , Antidepressive Agents/isolation & purification , Female , Hippocampus/drug effects , Mice , Neurons/drug effects , Plant Extracts/isolation & purification , Seeds , Serotonin Antagonists/pharmacology
2.
Afr J Med Med Sci ; 44(3): 251-9, 2015 Sep.
Article in English | MEDLINE | ID: mdl-27280238

ABSTRACT

BACKGROUND: Nevirapine is a very potent antiretroviral drug frequently used in the management of Human Immunodeficiency Virus (HIV). Opportunistic pathologies in HIV/AIDS patients include gastric ulcer and gastrointestinal haemorrhage. Hence, the impact of nevirapine on induced gastric ulcer was studied using Wistar rats. METHODS: Anti-ulcer activity of nevirapine was evaluated using cold restraint stress-induced, ethanol-induced and pylorus ligation-induced gastric ulcer models for acute ulceration; and acetic acid-induced ulcer model for the chronic ulceration in Wistar rats. RESULTS: Nevirapine (9 mg/kg, 18 mg/kg and 36 mg/kg) showed significant (P < 0.05) reduction in ulcer severity score and ulcer index as compared to the control in the models,.with corresponding increase in percentage inhibition. Histopathological studies showed that nevirapine has a positive effect on the healing of gastric ulcer in the groups treated with the nevirapine compared with the control. The induced ulcers healed up in all the groups administered with nevirapine compared to what was found in the omeprazole group where manifestations of ulcer like inflammatory cells infiltration is still present. CONCLUSION: Nevirapine may possess highly therapeutic effect in the treatment and prevention of gastrointestinal complications that might come with the presence of HIV virus in patients.


Subject(s)
Nevirapine/pharmacology , Reverse Transcriptase Inhibitors/pharmacology , Stomach Ulcer/drug therapy , Animals , Models, Animal , Rats, Wistar
3.
Afr J Med Med Sci ; 42(2): 131-42, 2013 Jun.
Article in English | MEDLINE | ID: mdl-24377198

ABSTRACT

BACKGROUND: Buchholzia coriacea, taken by elderly, has phytochemicals that have neuro-active metabolites, and the folklore documented its use in neuro-behavioural despairs. OBJECTIVE: This study was conducted to investigate the neuro-pharmacological potentials of Buchholzia coriacea (MEBC) seed extract in the laboratory rodents. METHODOLOGY: Methanol extract of the seeds on B. coriacea (MEBC) was evaluated for its antidepressant (Forced Swimming Test and Tail Suspension Test), anxiolytic (Light-Dark Test, Hole Board Test and Elevated Plus Maze), antinociceptive (Hot-Plate and Tail Flick test) and motor coordination (Rota Rod) functions in mice. RESULTS: Our findings showed antidepressant activity (P < 0.05) of MEBC that is dose-dependent. Secondly, MEBC showed significant anxiolytic property that is comparable with the standard drug (diazepam). Furthermore, MEBC significantly prolonged the latency on hot-plate and tail flick responses when compared with the control (P < 0.05). Finally, MEBC significantly prolonged mice endurance time (P < 0.05) on a revolving Rota rod. The results suggest antidepressant, anxiolytic and analgesic potentials of MEBC. CONCLUSION: Buchholzia coriacea may have a stabilizing effect on the motor activity and MEBC probably contains secondary metabolites with some therapeutic effects on neuro-physiological disorders like depression, anxiety and pain.


Subject(s)
Analgesics/pharmacology , Anti-Anxiety Agents/pharmacology , Antidepressive Agents/pharmacology , Behavior, Animal/drug effects , Capparaceae , Plant Extracts/pharmacology , Seeds , Animals , Anxiety , Depression , Disease Models, Animal , Male , Mice , Pain
4.
Niger J Physiol Sci ; 27(1): 65-71, 2012 Jun 07.
Article in English | MEDLINE | ID: mdl-23235310

ABSTRACT

Anacardium occidentalis (family: Anacardiaceae) is a plant of the tropical climate widely used by folklore to treat pain and inflammation. This study was conducted to evaluate the analgesic and anti-inflammatory effects of the leaf extracts in rat and mice using different models in other to confirm folkloric claims. The aqueous, hexane, dichloromethane and methanol extracts (AEAO, HEAO, DEAO and MEAO respectively) were investigated for analgesic effects in acetic acid induced pain in mice. They significantly reduced the number of writhing (p<0.001) and the highest analgesic effect was seen in DEAO extract. DEAO was further studied on various analgesic and anti-inflammatory models in graded doses. The extract significantly reduced writhing induced by acetic acid and the number and time of paw licking induced by formalin in a dose related manner. It inhibited the neurogenic and inflammatory phases of formalin. Analgesia was shown in the inhibition of nociception induced by tail immersion in 55oC hot water. The extract prolonged the latencies of tail withdrawal to a similar degree as pentazocine. The extract caused significant inhibition of carrageenan induced paw oedema in rats in a dose dependent manner. These findings suggest that the leaf extracts of Anacardium occidentalis are highly potent analgesic and anti-inflammatory agents. Phytochemical analysis showed that the leaf extracts contain alkaloids, tannins, saponins and cardenolides.


Subject(s)
Anacardium , Analgesics/therapeutic use , Plant Extracts/therapeutic use , Plant Leaves , Analgesics/isolation & purification , Analgesics/pharmacology , Animals , Anti-Inflammatory Agents, Non-Steroidal/isolation & purification , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Edema/drug therapy , Edema/pathology , Male , Mice , Pain/drug therapy , Pain/pathology , Pain Measurement/drug effects , Pain Measurement/methods , Plant Extracts/isolation & purification , Plant Extracts/pharmacology , Rats , Rats, Sprague-Dawley
5.
Niger J Physiol Sci ; 27(2): 165-9, 2012 Dec 18.
Article in English | MEDLINE | ID: mdl-23652231

ABSTRACT

The effects of methanol extract of Buchholzia coriacea seed was studied on male reproductive system of albino rats. Administration of 200mg/kg b.w.(p.o.) of the extract for 6 weeks resulted in significant reduction (P˂0.05) in the weight of the epididymis and seminal vesicle, but not the testes and prostate gland. Also the weight of the visceral organs- lungs, liver, heart and kidney were unaffected. A marked decrease (P<0.05) in sperm motility and volume was also observed in sperm collected from the caudal epididymis of the treated animals. Sperm count and morphology were not significantly affected (P<0.05). Total tissue protein of the epididymis and testes of the treated rats was significantly increased (P<0.05) and fertility was zero in the treated rats. Histological section showed that the epididymal ducts were mostly empty, though the epithelial lining appeared normal. There were fewer spermatozoa and late stage spermatids in the testes, with normal testicular epithelium. The results suggest that the extract of Buchholzia coriacea may have antifertility effects in male rats, the site of action most probably the epididymis.


Subject(s)
Anti-Infective Agents/toxicity , Capparaceae/toxicity , Genitalia, Male/drug effects , Plant Extracts/toxicity , Reproduction/drug effects , Animals , Female , Male , Rats , Rats, Wistar
6.
Afr J Med Med Sci ; 41 Suppl: 35-8, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23678634

ABSTRACT

In this study, the effects of ethanol extract of Ocimum gratissimum (EEOG) on both basal and stimulated gastric acid secretion and gastric mucus secretion were investigated in Albino rats treated with the extract. Four groups of animals were used. Sub-group 1A serves as control. Animals in Group 2A, 3B and 4B were pretreated with 200 mg/kg of (E3EOG) for 1, 7 and 14 days respectively. Basal gastric effluents were collected from all the groups of animals at intervals of 10 mins for 60 mins. Thereafter, Subgroups 1A, 2A, 3A and 4A were administered with 50 micro/kg b.w. of carbachol (i.p.) intraperitonialy and effluents collected. Animals in Sub-group B were used for gastric mucus study. Carbachol stimulates gastric acid secretion in animals pretreated with the extract for 1, 7 and 14 days. 50-400 mg/kg b.w. doses of the extract significantly increase gastric mucus secretion. These results indicate the mechanism of anti-ulcer activity of the extract may be due to stimulation of gastric mucus secretion amongst pathways.


Subject(s)
Gastric Acid/metabolism , Gastric Mucosa , Ocimum , Phytotherapy/methods , Plant Extracts , Animals , Anti-Ulcer Agents/administration & dosage , Anti-Ulcer Agents/pharmacokinetics , Biological Availability , Carbachol/pharmacology , Cholinergic Agonists/pharmacology , Dose-Response Relationship, Drug , Gastric Acidity Determination , Gastric Mucosa/drug effects , Gastric Mucosa/metabolism , Male , Plant Extracts/administration & dosage , Plant Extracts/pharmacokinetics , Rats , Rats, Wistar , Time Factors , Treatment Outcome
7.
Pharmacognosy Res ; 3(1): 2-8, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21731388

ABSTRACT

BACKGROUND: The present study was undertaken to evaluate the anti-ulcer and antioxidant activities of the ethanol extract of Lagenaria breviflora (EELB) whole fruit in laboratory rats. METHODS: The anti-ulcer property of the ethanolic extract of the whole fruit of Lagenaria breviflora (LB) was assessed using the cold-restraint stress-induced (CRU) gastric ulcer, pyloric ligation-induced (PL) gastric ulcer, aspirin-induced (ASP) gastric ulcer and alcohol-induced (AL) gastric ulcer models. The scavenging activity of the LB extract was examined with 1, 1-diphenyl-2-picryl-hydrazyl (DPPH), Nitric oxide, Hydroxyl radical and Superoxide anion scavenging models. RESULTS: EELB (50, 100, 150 and 200 mg/kg, b.w.) protected against the CRU gastric ulcer dose dependently. Similarly, 150 mg/kg b.w. of the LB extract protected against the PL gastric ulcer, ASP gastric ulcer and AL gastric ulcer and was comparable to omeprazole (10 mg/kg b.w.) or Suscralfate (500 mg/kg b.w.), respectively. The in vitro antioxidant activity of LB was demonstrated by its ability to quench free radicals generated by nitric oxide and superoxide anion with a concomitant scavenging potential against DPPH-induced radical formation. CONCLUSION: Taken together, the study showed that the whole fruit extract possess potent anti-ulcer and antioxidant activities.

8.
Niger J Physiol Sci ; 26(1): 71-6, 2011 Nov 28.
Article in English | MEDLINE | ID: mdl-22314991

ABSTRACT

The present study was conducted to evaluate the anti-nociceptive and anti-inflammatory properties of an ethanol extract of whole fruit of Lagenaria breviflora (LB) in rat and mice. Analgesic activity was measured by hot plate, formalin-induced paw licking, and acetic acid-induced abdominal writhing tests, while anti-inflammatory activity was determined by inhibition of carrageenan-induced paw oedema. Extract-treated animals exhibited significantly (P<0.05) higher pain threshold, lower number of licking of paws in response to formalin-induced irritation and writhing movements in response to acetic acid-induced writhing movement. There was significant (P<0.05) inhibition of carrageenan-induced paw oedema in rats pre-treated with the extract (50, 100, 200mg/kg) by 6.4%, 27.5%, 55.9% respectively. Analgesic effect of the extract (50, 100, 200mg/kg) in hot plate test was observable within 30 minutes of administration with maximum effect obtainable 90 minutes post-administration. Also, the effect of the extract (50, 100 and 200mg/kg) was dose dependent in both the early (88.17±6.21, 80.33±3.49 and 72.33±5.16) and late (72.50±3.95, 53.83±3.96 and 35.83±3.78) phases of formalin-induced paw licking, and in acetic acid-induced writhing with inhibition of 26.8%, 48.1% and 58.1% respectively. Its effect was comparable especially at 200mg/kg body weight to those of diclofenac, indomethacin and ibuprofen. It could be suggested from the findings of this experiment that the extract may be mediating its action as a central analgesic agent but the peripheral analgesic effect was preponderant based on its outcome from the pain models.


Subject(s)
Analgesics/pharmacology , Anti-Inflammatory Agents/pharmacology , Cucurbitaceae/chemistry , Ethanol/chemistry , Inflammation/prevention & control , Pain/prevention & control , Plant Extracts/pharmacology , Solvents/chemistry , Acetic Acid , Analgesics/isolation & purification , Animals , Anti-Inflammatory Agents/isolation & purification , Carrageenan , Disease Models, Animal , Dose-Response Relationship, Drug , Formaldehyde , Fruit , Hot Temperature , Inflammation/chemically induced , Inflammation/physiopathology , Male , Mice , Pain/etiology , Pain/physiopathology , Pain Measurement , Pain Threshold/drug effects , Plant Extracts/isolation & purification , Plants, Medicinal , Rats , Rats, Sprague-Dawley , Time Factors
9.
Niger J Physiol Sci ; 25(1): 37-46, 2010 Nov 25.
Article in English | MEDLINE | ID: mdl-22314901

ABSTRACT

Hedranthera barteri, anti-inflammatory activity, anti-nociceptive activity, anti-histaminic activityL. (HB) is used in the treatment of painful conditions and oedema amongst its folkloric use. The hexane and ethyl acetate fractions of the root of H. barteri were investigated for anti-nociceptive and antiinflammatory properties and probable mechanism of action. Hot plate, tail flick, formalin-induced oedema and acetic acidinduced writhing tests were employed to investigate the anti-nociceptive activity while the anti-inflammatory activity was investigated using carrageenan-induced paw oedema. Anti-histaminic potential of HB root extracts on the rat peritoneal mast cells (RPMCs) was explored through pectrofluorometric method. The root was screened for its phytochemical components. The HB root contains alkaloids,cardenolides and saponins. HXHBR exhibited higher anti-inflammatory potentials (P <0.001). HXHBR dose-dependently (P <0.01) reduced the histamine release from the rat peritoneal mast cells which is comparable with a standard anti-histaminic drug, ketotifen. These results showed that EAHBR and HXHBR possess anti-nociceptive and anti-inflammatory activities, and suggested its mechanism of action through the inhibition of histamine, an inflammatory mediator, usually released during the early phase of allergic responses and chronic phase of inflammatory pain. Flavonoids, alkaloids and/or saponins present in HB root may be responsible for its anti-nociceptive and anti-inflammatory properties.


Subject(s)
Apocynaceae , Histamine Antagonists/therapeutic use , Pain/drug therapy , Plant Extracts/therapeutic use , Plant Roots , Animals , Histamine Antagonists/isolation & purification , Inflammation Mediators/isolation & purification , Inflammation Mediators/therapeutic use , Male , Mice , Mice, Inbred BALB C , Pain/metabolism , Pain Measurement/drug effects , Pain Measurement/methods , Plant Extracts/isolation & purification , Plant Extracts/pharmacology , Plants, Medicinal , Rats , Rats, Sprague-Dawley , Rodentia
10.
Afr J Med Med Sci ; 39 Suppl: 41-6, 2010 Dec.
Article in English | MEDLINE | ID: mdl-22416643

ABSTRACT

Kolaviron (KV), a biflavonoid fraction from the seeds of Garcinia kola has been shown to posess antiinflammatory properties in animal models of inflammation. In this study, the effect of KV on carrageenan-induced paw edema was investigated in mice. Furthermore, the effects of KV on the production of the pro-inflammatory mediators- nitric oxide (NO) and tumor necrosis factor alpha (TNF-alpha) were examined in an activated macrophage-like cell lines, RAW 264.7 cells. Administration of KV prior to injection of carrageenan significantly reduced the paw inflammation in a dose-dependent manner. KV consistently inhibited in-vitro production of NO and secretion of TNF-alpha in a dose-dependent manner. In addition, KV reduced the production of PGE2 in LPS-stimulated macrophages. Viability of cells at all concentrations studied was unaffected as determined MTT [3-(4,5- dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide] cytotoxicity assay. These results suggest that KV has inhibitory effects on LPS-induced TNF-alpha, NO and PGE2 production.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Dinoprostone/antagonists & inhibitors , Edema/drug therapy , Flavonoids/pharmacology , Nitric Oxide/antagonists & inhibitors , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Animals , Anti-Inflammatory Agents/isolation & purification , Carrageenan/administration & dosage , Carrageenan/pharmacology , Cell Line , Dinoprostone/biosynthesis , Dinoprostone/metabolism , Dose-Response Relationship, Drug , Edema/etiology , Enzyme-Linked Immunosorbent Assay , Garcinia kola/chemistry , Macrophages/drug effects , Macrophages/metabolism , Mice , Nitric Oxide/biosynthesis , Nitric Oxide/metabolism , Phytotherapy , Plant Extracts/isolation & purification , Plant Extracts/pharmacology , Seeds/chemistry , Treatment Outcome , Tumor Necrosis Factor-alpha/biosynthesis , Tumor Necrosis Factor-alpha/metabolism
11.
Afr J Med Med Sci ; 39 Suppl: 95-102, 2010 Dec.
Article in English | MEDLINE | ID: mdl-22416650

ABSTRACT

The protective effect of Garcinia kola (GK) crude extract on acetic acid induced colitis in rats was investigated. Colitis, a form of inflammatory bowel disease (IBD) is characterized by inflammation of colon. The pathology in colitis includes disruption of crypt architecture, inflammation of crypts, frank crypt abscesses, and hemorrhage or inflammatory cells in the lamina propria. Since oxidative stress plays an important role in the etiology of Inflammatory Bowel diseases,and Garcinia kola (GK), have been shown to reduce oxidative stress in the rat stomach.The present study was designed to investigate the effects of Garcinia kola on ulcerative colitis (UC) induced by acetic acid. Albino rats were divided into five groups; Group one served as control, group two received Normal saline, group three received 2.5% ethanol while groups four and five were given 20mg/kg and 100mg/kg of crude extract of Garcinia kolarespectively. In another experiment, rats were fed for 2 weeks on normal rat diets but specially composed to contain 12.5%, 25% and 50% by weight of G kola. Colitis was induced by intra-rectal administration of 6% acetic acid. The colonic damage was elucidated by macroscopic damage scores; colon wet weight, stool consistency and colonic edema (thickness of the colon). Intra-luminal administration of 6% acetic acid resulted in observable clinical and macroscopic signs of colitis.Pre-orally administered of crude extract of GK significantly reduced the colonic damage score (p<0.001), colon weight (p<0.001), thickness of the colon (p<0.001) and diarrhea (p<0.001).Histological examinations also indicated a marked reduction in tissue injury and inhibition in neutrophil infiltration in rats pretreated with crude extract of Garcinia kola. Results of this investigation provide experimental evidence of Garcinia kola as an anti-colitis agent.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Colitis, Ulcerative/drug therapy , Garcinia kola/chemistry , Plant Extracts/pharmacology , Acetic Acid/adverse effects , Administration, Oral , Animals , Colitis, Ulcerative/chemically induced , Colitis, Ulcerative/pathology , Colon/metabolism , Colon/pathology , Diet , Disease Models, Animal , Male , Oxidative Stress , Random Allocation , Rats , Rats, Wistar , Seeds
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