Evaluation of antidiarrhoeal activity of the stem bark of Cylicodiscus gabunensis (mimosaceae)

The ethyl acetate (EA) extract of the stem bark of Cylicodiscus gabunensis (CG) (Mimosaceae) was analysed for its anti-diarrhoeal activity. Like loperamide (3 mg/Kg body weight), a single oral dose of C.gabunensis ethyl acetate extract (CG-EA) (375, 750 mg/Kg body weight) produced a significant decrease in the severity of diarrhoea. To understand the mechanism of its anti-diarrhoeal activity, its effect was further evaluated on intestinal transit, castor oil induced intestinal fluid accumulation(enteropooling) and electrolyte concentration in the small intestinal fluid. CG-EA produced a decrease in intestinal transit (10.26-30.75%), and unlike atropine, it significantly inhibited castor oil induced enteropooling. However, it did not alter the electrolyte concentration in intestinal fluid as compared tocastor oil-treated rat

Piptaderol From Piptadenia africana

A new glyceryl derivative (Glyceryl-1-hexacosanoate) and a flavone derivative (methyletherapigenin) were isolated from the stem bark extract of Piptadenia africana, a western Cameroonian plant species. Common terpenes like sitosterol, β-amyrin and eicosane were also isolated. These compounds were identified using physical and spectroscopic methods including mp, IR, 1H and 13C-NMR, DEPT, COSY, HMQC, HMBC, EI MS, HREI MS as well as some chemical transformations. The antibacterial activity of the extract, the fractions and the pure compounds is also discussed. Keywords: Piptadenia africana, Leguminoseae, Glyceryl-1-hexacosanoate, Methyletherapigenin, Chemotaxonomy, Antibacterial activity.African Journal of Traditional and Complementary Medicine Vol. 4 (3) 2007: pp. 294-29

Evaluation of In Vitro Uterotonic Activities of Fruit Extracts of Ficus asperifolia in Rats

The aim of the present study was to determine the uterotonic activities of Ficus asperifolia and investigate its mechanism. The effects of aqueous and methanol extracts of the dried fruits of F. asperifolia (0.05–1.60 mg mL−1) were evaluated on estrogenized isolated rat uterus in the presence and absence of atropine (1.73–55.27 nM), pyrilamine maleate (1.25 × 10−3 to 40 × 10−3 M), indomethacin (0.06 × 10−5 to 2.00 × 10−5 M) or hexamethonium (0.66 × 10−4 to 21.43 × 10−4 M). Aqueous (EC50, 0.36 mg mL−1) and methanol (EC50, 0.22 mg mL−1) extracts as well as oxytocin (EC50, 0.02 nM), acetylcholine (EC50, 7.87 nM) and histamine (EC50, 0.76 nM) evoked concentration-dependent contractions of the uterus. Atropine, pyrilamine maleate and indomethacin concentration dependently blocked the response of the uterus to acetylcholine (IC50, 4.82 nM), histamine (IC50, 2.49 nM) and oxytocin (IC50, 0.07 nM), respectively, and to aqueous extract. Hexamethonium produced graded decreases in oxytocin-induced uterine contractions (IC50, 0.37 μM), but did not prevent the contractile effects of the aqueous extract (IC50, 9.88 μM). These results suggest that F. asperifolia-induced uterotonic effect is related to the release of prostaglandins and contraction of the myometrial cells through muscarinic, oxytocic and H1 histamine receptors. These data further give added value to the ethnic use of F. asperifolia for its abortificient and contraceptive properties

Hepato-protective, antioxidant activities and acute toxicity of a stem bark extract of Erythrina senegalensis DC.

This study aimed at evaluating the in vitro antioxidant and hepatoprotective activities of different stem bark extracts of Erythrina senegalensis prepared with ethanol, and the in vivo hepatoprotective activity and acute toxicity of the best extract. The 2, 4-diphenyl-1-picryl-hydrazil (DPPH) and microsomal lipid peroxidation (MLP) models, and the rat liver slices system were respectively used for the in vitro study. The Methylene chloride/methanol (1:1 v/v) (Emc) and 40% ethanolic (E40) extracts were more efficient in inhibiting MLP and in scavenging DPPH radical. However, E40 was most effective with regards to lactate dehydrogenase (LDH) leakage inhibition from rat liver slices intoxicated with carbon tetrachloride (CCl4). The in vivo hepatoprotective activity was evaluated against CCl4-induced hepatotoxicity in rats. The E40 extract (100 mg/Kg) significantly reduced the increase in ALT, AST and lipid peroxidation in liver homogenate, showing that the extract is as protective as silymarin at the same dose. Acute toxicity was evaluated in mice and E40 did not produce any behavioural changes or mortality even at an oral dose of 16 g/kg. The extract was found to contain antioxidant classes of compounds (flavonoids and polyphenols). In conclusion, the E40 extract of E. senegalensis could be an important source of hepatoprotective compounds.Key words: Erythrina senegalensis, stem bark extract, antioxidant, hepatoprotective, carbon tetrachloride

Ent-kaurene and ent-beyerene diterpenoids and other constituents of Thecacoris batesii

Two novel diterpenoids, thecacorins A (1) and B (2), were isolated from Thecacoris batesii and their structures were established as ent-3b,20-epoxy-16-kaurene-3a,12b-diol and ent-15-beyerene-2b,3b-diol, respectively, on the basis of extensive spectroscopic analysis, especially, 1D NMR spectra, in conjunction with 2D experiments, COSY, NOESY, HMQC and HMBC. KEY WORDS: Diterpenoids, Thecacorin A, Thecacorin B, Ent-3b,20-epoxy-16-kaurene-3a,12b-diol, Ent-15-beyerene-2b,3b-diol, Thecacoris batesii  Bull. Chem. Soc. Ethiop. 2007, 21(1), 89-94

Anti-endometriotic Effects of the Mixture of Erigeron floribundus (Asteraceae) and Tragia benthamii (Euphorbiaceae) Extracts in Peritoneal Endometriosis in Wistar Rats

Endometriosis is a frequent pathology in gynecology. This study was aimed at investigating the curative effects of the mixture of Erigeron floribundus and Tragia benthamii aqueous extracts on experimental endometriosis in rat. Twenty endometriosic rats were randomly distributed into four groups of five animals each and orally treated during four weeks with either distilled water (10 ml/kg), raloxifene hydrochloride (10 mg/kg) or aqueous extract of plant mixture (130 or 260 mg/kg). Vaginal smear was daily checked throughout the experiments and, blood and sexual organs were collected after sacrifice. Body and sexual organ weights, sexual hormones, prostaglandin E2, oxidative stress markers and uterine histology were measured. Results showed a disrupted estrus cycle, an increase in MDA concentration, implant weight and implantation surface in the untreated endometriosic rats. On the contrary, in the plant extracts-treated endometriosic animals and raloxifene, the estrus stage frequency was increased while the endometriosis lesions were significantly (p<0.001) regressed. Plant extracts also decreased the level of estradiol, progesterone, MDA and catalase, and increased the activities of SOD and peroxidase compared to the untreated rats. Prostaglandin E2 concentration and the uterine architecture remained statistically unchanged after treatments. In conclusion, the aqueous extract of the mixture of E. floribundus and T. benthamii alleviates the endometriosic alterations in rats

Synthesis of novel stilbene–coumarin derivatives and antifungal screening of monotes kerstingii-specialized metabolites against fusarium oxysporum

Fusarium is one of the most toxigenic phytopathogens causing diseases and reduced agricultural productivity worldwide. Current chemical fungicides exhibit toxicity against non-target organisms, triggering negative environmental impact, and are a danger to consumers. In order to explore the chemical diversity of plants for potential antifungal applications, crude extract and fractions from Monotes kerstingii were screened for their activity against two multi-resistant Fusarium oxysporum strains: Fo32931 and Fo4287. Antifungal activity was evaluated by the determination of minimum inhibitory concentration (MIC) by broth dilution of fermentative yeasts using kinetic OD600 nm reading by a spectrophotometer. The n-butanol fraction showed the best activity against Fo4287. We screened eleven previously reported natural compounds isolated from different fractions, and a stilbene–coumarin 5-[(1E)-2-(4-hydroxyphenyl)ethenyl]-4,7-dimethoxy-3-methyl-2H-1-benzopyran-2-one (1) was the most active compound against both strains. Compound 1 was employed as a nucleophile with a selection of electrophilic derivatizing agents to synthesize five novel stilbene–coumarin analogues. These semisynthetic derivatives showed moderate activity against Fo32931 with only prenylated derivative exhibiting activity comparable to the natural stilbene–coumarin (1), demonstrating the key role of the phenolic group

Semen quality among men attending urology services in the Dschang Health District, west Cameroon: A retrospective study on 379 cases

Background: Infertility is a common condition affecting at least 15% of couples worldwide, and male factors are involved in about half of this prevalence rate. In Cameroon, about 20%-40% of couples are the victims. However, the sperm characteristics of infertile men are yet to be described in the health districts in Cameroon for better management of male infertility. Objective: The present study was designed to assess the sperm profile and related sociodemographic factors of men attending the urology services at the Dschang Health District. Materials and Methods: It consisted of a 10 yr retrospective study carried out in the Dschang Health District. The results of patients’ semen analysis (SA) were computed using Epi Info software and expressed as qualitative and quantitative spermogram state as described by the clinician and sociodemographic features of those patients. Results: Out of the 379 patients studied, 83.91% had abnormal spermogram. Patients older than 50 yr were the most affected when grouped into age categories. With regard to patient’s profession, 52.51% had specified their profession and from that group, although farmers (9.31%) represented the lowest size category, they were the most affected with 94.74% having abnormal spermogram. Conclusion: This study indicates that the sperm damage is the major cause of male infertility in the Dschang Health District. It also shows that farmers are the most affected category and it could be linked to the long-term exposure to pesticides. These results call for the assessment of the reproductive toxicity of locally used pesticides. Key words: Sperm damage, Male infertility, Semen analysis, Dschang Health District

Aphrodisiac property of aqueous and methanolic extracts of Raphia vinifera (Arecaceae) in sexually experienced male rats

Background: Raphia vinifera (Arecaceae) is a medicinal plant commonly used as a sexual enhancer. Objective: To investigate the aphrodisiac potential of aqueous extract (AE) and methanolic extract (ME) of R. vinifera in sexually experienced male rats. Materials and Methods: Thirty male Wistar rats were randomly distributed into six groups (5 rats per group) and administered for 14 days with distilled water (10 ml/kg), sildenafil citrate (1.44 mg/kg), and AE or ME of R. vinifera (100 or 500 mg/kg). The copulatory activity was tested on days 0, 7, and 14 using receptive females. Further, on day 14, rats were sacrificed and biochemical analyses (testosterone, total protein, and acid phosphatase) were performed. Results: Sildenafil citrate significantly decreased the intromission latency (day 14, p = 0.04) and frequency (days 7 and 14, p = 0.03) but increased the mount frequency (day 14, p = 0.04), compared with control. Remarkably, R. vinifera enhanced the sexual activity by significantly decreasing the intromission latency (AE and ME, 500 mg/kg, day 14, p = 0.04) and increasing the mount frequency (AE and ME, 100 mg/kg, day 7, p = 0.02) compared with control. Moreover, R. vinifera improved plasmatic (AE, 100 mg/kg, p = 0.03; AE, 500 mg/kg, p = 0.001; ME, 100 mg/kg, p = 0.01) and testicular (AE, 100 mg/kg, p = 0.001; AE, 500 mg/kg, p = 0.01; ME, 100 mg/kg, p = 0.001; ME, 500 mg/kg, p = 0.01) testosterone levels as well as plasmatic total proteins concentration (ME, 500 mg/kg, p = 0.04). Conclusion: These findings showed that R. vinifera possesses an aphrodisiac property which could further justify its folkloric use in traditional medicine as a sexual enhancer

Amaranthus hybridus (Amaranthaceae) prevents the detrimental effects of cyclophosphamide on ovarian function in Wistar rats: An experimental study

Background: Cyclophosphamide (CP) is an anticancer agent, but its chronic administration induces ovarian toxicity Objective: We evaluated the effects of aqueous extract (AE) and methanol extract (ME) of Amaranthus hybridus (A. hybridus) on CP-induced ovarian toxicity in rats. Materials and Methods: 40 female Wistar rats (10 wk, 170-200 gr) were distributed into 8 groups (n = 5/each) as follows: 1) healthy control; 2) CP+distilled water (10 ml/kg/d); 3) CP+3%-tween 80 (10 mL/kg/d); 4) CP+clomiphene citrate (2 mg/kg/d); 5, 6) CP+AE of A. hybridus (55 and 110 mg/kg/d); and 7, 8) CP+ME of A. hybridus (55 and 110 mg/kg/d). After 28 days of treatment, estrus cyclicity, ovarian and uterine weights as well as estradiol levels and ovarian histology were determined. Results: CP induced ovarian toxicity after 28 days of exposure. More specifically, CP disturbed the estrus cycle, decreased ovary and uterus weights (p = 0.04), and the 17-β estradiol level (p = 0.04), and induced severe ovarian damages. Remarkably, A. hybridus significantly increased (p = 0.03) the ovarian weight (AE and ME at all doses) and uterus weight (ME at 110 mg/kg/d), compared with the CP-treated rats. Moreover, the 17-β estradiol level was significantly elevated (p = 0.02) in rats given clomiphene citrate and A. hybridus (AE 110 mg/kg/d; ME 55 mg/kg/d). Finally, the ovaries of rats given plant extracts had many corpus luteum and normal follicles, and no cystic follicles. Conclusion: A. hybridus prevented the detrimental effects of CP on ovarian function, which could support its traditional use as a fertility enhancer. Key words: Cyclophosphamide, Amaranthus hybridus, Toxicity, Estradiol, Rat