23 research outputs found

    Endothelium/Nitric Oxide Mediates the Vasorelaxant and Antihypertensive Effects of the Aqueous Extract from the Stem Bark of Mammea africana

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    This study evaluates the vasorelaxant and antihypertensive effects of the aqueous extract from the stem bark of M. africana (AEMA). AEMA was tested in vitro on intact or endothelium-denuded rats’ aorta rings precontracted with KCl or norepinephrine in absence or in presence of L-NAME or glibenclamide. The effect of a single concentration (300 μg/mL) of AEMA was also examined on the concentration-response curve of KCl. In vivo, the antihypertensive effects of AEMA (200 mg/kg/day) were evaluated in male Wistar rats treated with L-NAME (40 mg/kg/day) for 4 weeks. AEMA relaxed aorta rings precontracted with NE or KCl with respective EC50 values of 0.36 μg/mL and 197.60 μg/mL. The destruction of endothelium or pretreatment of aorta rings with L-NAME shifted the EC50 of AEMA from 0.36 μg/mL to 40.65 μg/mL and 20.20 μg/mL, respectively. The vasorelaxant activity of M. africana was significantly inhibited in presence of glibenclamide. AEMA also significantly inhibited the concentration-response curve of KCl. Administered orally, AEMA induced acute and chronic antihypertensive effects and normalized renal NO level. These results show that the vasorelaxant activity of AEMA might be mediated by the activation of the NO-cGMP-ATP-dependent potassium channels pathway and might predominantly account for its antihypertensive effect

    Prevalence of viral and non-viral hepatitis in Menoua Division, West Region, Cameroon: a retrospective hospital-based study

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    Introduction: the paucity of data on hepatitis' epidemiology in Menoua Division, west region, Cameroon, prompted us to assess the prevalence of viral and non-viral hepatitis in this area. Methods: a retrospective exhaustive study based on records of patients from January 2008 to June 2014 was conducted in 9 health centres in Menoua Division. Targeted subjects were patients who did not receive hepatitis vaccines for the past year and have been screened for hepatitis B virus (HBV), hepatitis C virus (HCV) and/or a blood transaminase. Associations between variables were quantified with odd ratios (OR) and 95% confidence interval (CI). Cochran-Armitage test of linear trend was used for testing proportions of ordinal variables. Fisher's exact test was used for testing the association between 2 qualitative variables when expected counts were less than 5. Results: the overall prevalence were 9.6% and 6.7% for HBV and HCV respectively. HBV mostly infected people aged 21-30 (12.4%) while the prevalence of HCV increased with age up to 35.4% (p=0.03). A 0.6% co-infection was observed. Thirty percent of positive HBV or HCV had high transaminase while 13% of patients with elevated transaminase showed negative viral serology. Conclusion: these results show that hospital-based prevalence of HCV and HBV in Menoua Division is under the Cameroon's national range but point out the fact that non-viral hepatitis might be a serious case of concern in this area. There is therefore, a need to identify the risk-factors of non-viral hepatitis

    Acute and sub-chronic oral toxicity assessment of the leaf aqueous extract of Kalanchoe crenata (Crassulaceae)

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    Previous studies demonstrated that the leaves of Kalanchoe crenata (Crassulaceae) possess analgesic, anti-inflammatory, anticonvulsant and cardiovascular activities but nothing is known about the toxicity of this plant material. The objective of the present study was to evaluate the acute and sub-chronic toxicities of the aqueous extract of the leaves of K. crenata (AEKC) prepared as a dry leaves decoction. Acute oral toxicity of the AEKC was evaluated in mice at doses 2, 4, 6, and 8 g/kg. Animals were observed for 3 hours post administration for signs and symptoms of intoxication. Survivors were followed up for 14 days after treatment. Wistar rats of both sexes were used for sub-chronic toxicity. They were orally treated with the AEKC at doses of 300, 600 and 1200 mg/kg/day for 4 consecutive weeks. They were further euthanized and blood was collected for biochemical and hematological analyses. A single acute administration of AEKC reduced the sensitivity to pain and the mobility of animals. These behavioral modifications disappeared 3 hours after administration. Only the dose of 8 g/kg caused the death of one female mouse out of 6, inferring a LD50 greater than 8 g/kg. The daily administration of AEKC did not induce mortality, behavioral modifications, significant variations of body weight, relative weights of the liver and kidney and plasma content of Alanine amino transferase (ALAT) and aspartate amino transferase (ASAT). Besides, no significant difference was observed on glomerular filtration rate and other parameters of renal excretion. Meanwhile, at the dose of 300 mg/kg/day, a significant increase in total bilirubin, free bilirubin and a significant decrease in conjugated bilirubin and plasma creatinine were registered. These results suggest that the aqueous extract of the leaves of K. crenata can be classified as a non-toxic substance. However, attention should be paid on the hepatic function.Keywords: Acute and sub-chronic toxicity, aqueous extract, Kalanchoe crenata, Crassulacea

    Hypoglycemic Properties of the Aqueous Extract from the Stem Bark of Ceiba pentandra in Dexamethasone-Induced Insulin Resistant Rats

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    Parts of Ceiba pentandra are wildly used in Africa to treat diabetes and previous works have demonstrated their in vivo antidiabetic effects on type 1 diabetes models. In addition, it has been recently shown that the decoction and the methanol extract from the stem bark of C. pentandra potentiate in vitro, the peripheral glucose consumption by the liver and skeletal muscle slices. But nothing is known about its effect on type II diabetes, especially on insulin resistance condition. We investigated herein the antihyperglycemic, insulin-sensitizing potential, and cardioprotective effects of the dried decoction from the stem bark of Ceiba pentandra (DCP) in dexamethasone-induced insulin resistant rats. DCP phytochemical analysis using LC-MS showed the presence of many compounds, including 8-formyl-7-hydroxy-5-isopropyl-2-methoxy-3-methyl-1,4-naphthaquinone, 2,4,6-trimethoxyphenol, and vavain. Wistar rats were given intramuscularly (i.m.) dexamethasone (1 mg/kg/day) alone or concomitantly with oral doses of DCP (75 or 150 mg/kg/day) or metformin (40 mg/kg/day) for 9 days. Parameters such as body weight, glycemia, oral glucose tolerance, plasma triglycerides and cholesterol, blood pressure, and heart rate were evaluated. Moreover, cardiac, hepatic and aortic antioxidants (reduced glutathione, catalase, and superoxide dismutase), malondialdehyde level, and nitric oxide content were determined. DCP decreased glycemia by up to 34% and corrected the impairment of glucose tolerance induced by dexamethasone but has no significant effect on blood pressure and heart rate. DCP reduced the total plasma cholesterol and triglycerides as compared to animals treated only with dexamethasone. DCP also increased catalase, glutathione, and NO levels impaired by dexamethasone, without any effect on SOD and malondialdehyde. In conclusion, the decoction of the stem bark of Ceiba pentandra has insulin sensitive effects as demonstrated by the improvement of glucose tolerance, oxidative status, and plasma lipid profile. This extract may therefore be a good candidate for the treatment of type II diabetes

    Hypoglycaemic activity of the leaves extracts of Bersama engleriana in rats

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    The hypoglycaemic properties of the aqueous and methanol extracts of the leaves of Bersama engleriana were evaluated in normoglycaemic rats in order to scientifically validate its traditional therapeutic use. With a dose of 300 mg/kg b.w. only the aqueous extract appeared to be significantly effective while at high dose, 600 mg/kg b.w., the aqueous and methanol extracts of Bersama engleriana reduced the blood glucose level by 37.7% and 49.11% after 8h of treatment of rats respectively. These results confirm the hypoglycaemic properties of some extracts of the leaves of Bersama engleriana with the aqueous extract appearing more active

    Endothelium/Nitric Oxide Mediates the Vasorelaxant and Antihypertensive Effects of the Aqueous Extract from the Stem Bark of Mammea africana Sabine (Guttiferae)

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    This study evaluates the vasorelaxant and antihypertensive effects of the aqueous extract from the stem bark of M. africana (AEMA). AEMA was tested in vitro on intact or endothelium-denuded rats' aorta rings precontracted with KCl or norepinephrine in absence or in presence of L-NAME or glibenclamide. The effect of a single concentration (300 μg/mL) of AEMA was also examined on the concentration-response curve of KCl. In vivo, the antihypertensive effects of AEMA (200 mg/kg/day) were evaluated in male Wistar rats treated with L-NAME (40 mg/kg/day) for 4 weeks. AEMA relaxed aorta rings precontracted with NE or KCl with respective EC50 values of 0.36 μg/mL and 197.60 μg/mL. The destruction of endothelium or pretreatment of aorta rings with L-NAME shifted the EC50 of AEMA from 0.36 μg/mL to 40.65 μg/mL and 20.20 μg/mL, respectively. The vasorelaxant activity of M. africana was significantly inhibited in presence of glibenclamide. AEMA also significantly inhibited the concentrationresponse curve of KCl. Administered orally, AEMA induced acute and chronic antihypertensive effects and normalized renal NO level. These results show that the vasorelaxant activity of AEMA might be mediated by the activation of the NO-cGMP-ATPdependent potassium channels pathway and might predominantly account for its antihypertensive effect

    Short Communication: The antiulcer effects of the methanol extract of the leaves of Aspilia africana (Asteraceae) in rats

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    Aspilia Africana (Asteraceae) is a plant currently used in Cameroon ethnomedicine for the treatment of stomach ailments. The methanol extract of the leaves of A. africana was investigated against gastric ulcerations induced by HCl/ethanol and pylorus-ligation. With both methods, the extract inhibited gastric ulcerations in a dose-related manner. Oral administration of the plant extract at the doses of 0.5 and 1 g/kg reduced gastric lesions induced by HCl/ethanol by 79% and 97% respectively. The extract at the dose of 1 g/kg reduced gastric lesion in the pylorus ligated rats by 52% although the gastric acidity remained higher as compared to the control. These findings show that methanol extract of the leaves of A. Africana possess potent antiulcer properties. Key words: Aspilia Africana, antiulcer, rat Afr. J. Trad. Comp. Alt. Med. Vol.2(3) 2005: 233 - 23
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