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Introduction: For centuries, mosses have been used in traditional medicine due to their antibacterial, antifungal, and antiviral activities. Objective: The present study was designed to evaluate the antibacterial activity of ethanolic extracts obtained from 12 moss species: Brachythecium albicans, Bryum argenteum, Ceratodon purpureus, Dicranum scoparium, Dryptodon pulvinatus, Orthotrichum anomalum, Oxyrrhynchium hians, Plagiomnium undulatum, Polytrichum juniperinum, P. piliferum, Schistidium crassipilum, and Syntrichia ruralis. Methods: The antimicrobial activity of extracts was investigated against three Gram(+) bacteria (Enterococcus faecalis, Staphylococcus aureus, and Streptococcus pyogenes) and two Gram(-) bacteria (Escherichia coli and Klebsiella pneumoniae), using the agar disc-diffusion method. Results: The high activity against all investigated bacteria was determined for extracts of D. pulvinatus, P. undulatum, B. argenteum, S. crassipilum, O. anomalum (mean inhibition zone: 11.3–13.1 mm) and to a lesser extent in the case of D. scoparium (8.3 mm). Extracts from P. juniperinum and P. piliferum showed activity only against Gram-positive bacteria, with an inhibition zone from 7.3 to 9.7 mm. Four species: B. albicans, C. purpureus, O. hians, and S. ruralis had not antibacterial properties. Conclusions: The obtained results indicate that mosses could be a significant source of antibacterial agents. For the first time, we presented antibacterial activity of ethanolic extracts from S. crassipilum and O. anomalum.
The purpose of the present study is to investigate whether the alcoholic extract of Graptophyllum pictum (L.) Griff. could decrease the intensity of nephrotoxicity in albino rats. Cisplatin at a single dose of 12 mg/kg body weight was administered intraperitonially to albino male Wistar rats. Nephrotoxicity was assessed by determining the serum creatinine and urea levels as well as renal antioxidant status in rats after cisplatin administration. Ethanolic extract of G. pictum at 150 and 300 mg/kg body weight was administered orally after cisplatin injection for 15 days. The extracts could significantly reduce the elevated serum creatinine and urea levels. Renal antioxidant defence systems, such as superoxide dismutase, catalase, glutathione peroxidase activities and reduced glutathione level, depleted by cisplatin therapy were restored to normal by treatment with the extract. Cisplatin induced lipid peroxidation was also found markedly reduced by treatment with the extract. This result indicated that ethanolic extract of G. pictum rendered significant preventive effect against cisplatin induced nephrotoxicity.
β-sitosterol and two triterpenoids: ursolic acid acetate and platanic acid have been isolated from ethanolic extract of Vitex trifola leaves. β-sitosterol was previously isolated from the leaves, stem and seeds of Vitex trifolia. Ursolic acid acetate has been isolated for the first time in this plant species. Platanic acid has been reported for the first time in Vitex trifolia and even in the family of this plant: Verbenaceae. These compounds were characterized using spectroscopic methods including 1D-1HNMR, 13CNMR, ESIMS and 2D-NMR (HSQC, HMBC, COSY) experiments and confirmed by comparison of their NMR data with those from the literature. A preliminary molluscicidal test for ethanol, chloroform and n-hexane extracts of leaves of Vitex trifolia against Biomphalaria alexandrina adult snails showed that ethanol extract of leaves with LC50 value 26.42 mg/l (27.92 mg/l – 24.99 mg/l) was more effective than n-hexane extract with LC50 value 35.48 mg/l (43.81 mg/l – 28.72mg/l) and chloroform extract with LC50 value 46.77 mg/l (53.59 mg/l – 43.81 mg/l) after 24 h exposure.
Wound infection has become a major medical problem in recent years. This study was conducted to evaluate the healing activity of Capparis spinosa against surgical wounds infected by Escherichia coli. Twenty male rats were divided into two groups. Excisions were created surgically on the animals’ skin and then infected with E coli. Group 1 was treated with C spinosa while Group 2 was untreated. Wound biopsy specimens were collected on days 5, 10 and 16 and analyzed. Results showed that the hydroxyproline content in treatment group was significantly higher in various post wounding days. Protein content increased gradually in ten days. Results of histopathological studies showed moderate to intense granulation tissue formation in treated group on day 10. The histopathological studies showed, that the new epidermis in treated group was thicker than in control group on day 16 post wounding. The present study has demonstrated that ethanol extract of C spinosa includes properties that accelerate wound healing activities.
In the present study Limonia acidissima Groff. ethanolic leaves extract was used for the detection of its antidermatophytic assay. It results broad spectrum of antifungals and antibacterial. Where the antimycotic activity against Trichophyton rubrum, Trichophyton tonsurans, Trichophyton mentagrophytes, Microsporium gypseum, Candida albicans and four Bacillus subtilis, Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa were more pronounced. The effective antidermatophytic activity observed against M. gypseum, T. tonsurans, E. coli and B. subtilis. Minimum Inhibitory Concentration of all the test microbes was determined using broth dilution technique. MFC, MBC also standardized. Preliminary Phytochemical tests were carried for the revealing basics antimicrobial responsible molecules of secondary metabolites.
Terminalia chebula, a plant rich with phytochemicals, was selected in the present investigation for evaluating its immunomodulatory activities. Extract of the leaves were prepared in various solvents. Ethanolic extract was found to contain significant amount of phytochemicals. Hence, it was selected to study immunomodualtory activity. Silica gel column chromatography of ethanolic extract was performed. The fractions were further subjected to TLC and most active fractions were administrated to balb/C mice for evaluating immunomodulatory studies. Out of the five fraction (S1 – S5), S3 was found to possess immunostimulant activity. Provision of Ethanol Extracts of Terminalia chebula on balb/C mice can increase the antibody titers IgM and IgG.
The antifungal activity of the ethanolic and aqueous fruit extracts of Zingiber officinale, Tetrapleura tetraptera, Garcinia kola and Cola nitida on the green rot fungus (Penicillium sp.) isolated from infected groundnut (Arachis hypogaea) seeds in storage were investigated in vitro. Various concentrations of the aqueous and ethanolic fruit extract ranging from 5g/100ml, 10g/100ml, and 15g/100ml were separately added to Potato Dextrose Agar (PDA) media. The fungus was inoculated into the media and incubated for seven days. Results of the in vitro studies showed that the ethanolic extracts had a significant inhibitory effect (p<0.05) on the radial growth of Penicillium sp. at all levels of concentration tested. Complete inhibition of the fungus was at 15g/100ml of ethanolic extracts of Garcinia kola and Tetrapleura tetraptera. The aqueous extracts showed less inhibitory effect as compared to the ethanolic extracts. The effective inhibition of ethanolic extracts as compared to the aqueous extracts may be attributed to the efficiency of the extraction solvent on the phytochemical content of the plant extracts. The application of botanical extracts for disease management could be less expensive, easily available, non-polluting and ecofriendly. The ethanolic fruit extracts of Garcinia kola and Tetrapleura tetraptera at the higher concentrations can be produced in large quantities and used as spray in controlling the green rot fungus of Arachis hypogaea in storage.
The research examined green tea ethanol extract, subjected to different purification processes with use of active carbon, bleaching earth, and mixture of acetone, acetic acid, water, with or without earlier hexane treatment. Purified extracts were examined according to total polyphenols content, antioxidant activity in linoleic acid emulsion and antiradical activity in DPPH• radical scavenging method. Highest polyphenol content was evaluated in the extract purified with bleaching earth, lowest however in purified with solvents mixture. Antioxidant activity of green tea extracts in linoleic acid emulsion indicated that highest antioxidative effectivity coefficient (Aec) values represented sample purified with active carbon and solvents mixture. Highest DPPH• radical scavenging activity was found in sample purified with solvents mixture, other samples however represented close activity. The present research indicated that plant extracts purification processes resulted in decrease of total polyphenols content, however without its antioxidant activity decrease
The purpose of the present study is to investigate whether the alcoholic extract of Sphaeranthus indicus could decrease the intensity of toxicity in albino rats. Gentamicin at a dose of 80mg/kg body weight was administered intraperitonially to albino male Wistar rats for 8 days. Then another set of animals were given the alcoholic extracts of S. indicus along with gentamicin treatment. The antioxidant levels, serum creatinine, serum urea etc were analyzed. The extracts could significantly decrease the gentamicin induced nephrotoxicity as inferred from the tissue antioxidant status in the drug administered animals. Remarkable change was observed in serum creatinine and urea levels. Lipid peroxidation in the kidney and liver tissues was also considerably reduced in S. indicus extract treated animals. The nephrotoxic rats showed lower activities of superoxide dismutase, catalase, glutathione transferase and reduced glutathione content in the liver and kidney which were restored to normal levels by treatment with S. indicus extract. The increased levels of lipid peroxidation in nephrotoxic rats were reverted back to normal levels after the treatment with S. indicus ethanol extract. These results suggest that it has protective effect against gentamicin induced nephrotoxicity which may be attributed to its antioxidant potential.
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