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1.
Lett Appl Microbiol ; 74(3): 419-428, 2022 Mar.
Article in English | MEDLINE | ID: mdl-34860440

ABSTRACT

Microbial resistance to antibiotics affects the control of clinical infections and is a growing concern in global public health. One important mechanism whereby micro-organisms acquire resistance is biofilm formation. This context has led to the investigation of new antimicrobial substances from plants popularly used in folk medicine. In this work, we studied the antimicrobial and antibiofilm activity of Zinnia peruviana roots, ziniolide (major root metabolite) and aerial parts against Staphylococcus aureus, Staphylococcus epidermidis, Listeria monocytogenes, Escherichia coli, Pseudomonas aeruginosa and Candida albicans. The minimum inhibitory and minimum microbicidal concentration and inhibition of biofilm production was determined. All Z. peruviana extracts showed antimicrobial activity, but that corresponding to the roots was the most active one. The best inhibitory and microbicidal activity was detected against Gram-positive bacteria (0·039-0·078 mg ml-1 ). The acetonic extract from Z. peruviana leaves showed moderate activity against Gram-positive bacteria (0·625 mg ml-1 ). Acetonic extract of Z. peruviana flowers showed weak activity (1·25-5 mg ml-1 ). All the extracts tested showed inhibition of biofilm formation, as well as the ziniolide, however, roots and flowers extracts showed higher antibiofilm activity particularly against Staphylococcus, Listeria and Candida. The extracts tested may be a promising natural alternative for the control of microbial infections.


Subject(s)
Plankton , Plant Extracts , Anti-Bacterial Agents/pharmacology , Biofilms , Microbial Sensitivity Tests , Plant Extracts/pharmacology , Plant Leaves
2.
Bioorg Med Chem Lett ; 25(23): 5481-4, 2015 Dec 01.
Article in English | MEDLINE | ID: mdl-26525862

ABSTRACT

The Plant Kingdom is an excellent source for obtaining natural compounds with antiprotozoal activity. In the present work, we studied the effect of the diterpene 12-hydroxy-11,14-diketo-6,8,12-abietatrien-19,20-olide (HABTO) obtained from the aerial parts of Salvia cuspidata on Trypanosoma cruzi epimastigotes. This compound was found to inhibit parasite growth even at low concentrations (IC50 5 µg/mL) and with low toxicity on mammalian cells. In addition, this diterpene induced an intense vacuolization within the parasites. In order to obtain analogs with greater lipophilicity, chemical modifications on the enol moiety were carried out to obtain the acetyl (AABTO), the sylil (SABTO) and the allyl (ALLABTO) derivatives. We observed that the SABTO was the most effective one on the parasites, and the effect could be attributed to a greater lipophilicity of this compound. Taking into account these data we conclude that the increase of lipophilicity by chemical modifications is an adequate strategy for improving the trypanocidal activity of this kind abietane diterpenes.


Subject(s)
Abietanes/chemistry , Abietanes/pharmacology , Plant Extracts/chemistry , Plant Extracts/pharmacology , Salvia/chemistry , Trypanosoma cruzi/drug effects , Abietanes/isolation & purification , Animals , Cell Survival/drug effects , Chlorocebus aethiops , Molecular Structure , Trypanocidal Agents/chemistry , Trypanocidal Agents/isolation & purification , Trypanocidal Agents/pharmacology , Vero Cells
4.
Nat Prod Res ; 19(6): 625-31, 2005 Sep.
Article in English | MEDLINE | ID: mdl-16010831

ABSTRACT

Stereo- and regioselective hydroxylation of grindelane derivatives on position 3beta was catalyzed by cultures of Aspergillus niger. Grindelic acid (1), methyl grindelate (2), 15-hydroxy-7(8)-en-9alpha,13(S)-oxide-ent-labdane (3) and 7alpha,8alpha-epoxymethylgrindelate (4) were bioconverted into the corresponding 3beta-hydroxy derivatives as the only biotransformation products. 13(S),15-dihydroxy-8(9)-en-ent-labdane (5) remained unreacted under the same conditions. The conformational and electronic studies of the substrates are discussed.


Subject(s)
Aspergillus niger/chemistry , Diterpenes/chemistry , Biotransformation , Diterpenes/isolation & purification , Diterpenes/metabolism , Hydroxylation , Stereoisomerism
5.
Phytother Res ; 15(6): 529-31, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11536384

ABSTRACT

The antiinflammatory activities of ten organic extracts from the aerial parts of Baccharis medullosa DC., Baccharis rufescens S. and Laennecia sophiifolia (Kunth) G. L. Nesom were investigated in mice subjected to carrageenan induced paw oedema. Intraperitoneally administered organic extracts given at doses equivalent to 80 mg/kg of material inhibited the acute phases of inflammation in this model. Our results indicate that the most effective extracts were: n-hexane (I) from B. medullosa, acetone (V) and chloroform (VII) from L. sophiifolia, and acetone (VIII) and chloroform (X) from B. rufescens. All exerted the strongest effect at 5 h after injection of the phlogistic agent.


Subject(s)
Anti-Inflammatory Agents/pharmacology , Asteraceae/chemistry , Edema/drug therapy , Plant Extracts/pharmacology , Animals , Anti-Inflammatory Agents/isolation & purification , Anti-Inflammatory Agents/therapeutic use , Carrageenan/pharmacology , Edema/chemically induced , Herbal Medicine , Male , Mice , Phytotherapy , Plant Extracts/therapeutic use , Plant Structures
6.
Nat Prod Lett ; 15(6): 425-31, 2001.
Article in English | MEDLINE | ID: mdl-11838981

ABSTRACT

From the flowers of Baccharis medullosa DC (Asteraceae) two new ent-labdane-type diterpene glycosides were isolated. Structures were established by application of various spectroscopic techniques. The sugar residues were identified after acid hydrolysis of the isolated products.


Subject(s)
Asteraceae/chemistry , Diterpenes/isolation & purification , Glycosides/isolation & purification , Plants, Medicinal/chemistry , Argentina , Chromatography, Liquid , Diterpenes/chemistry , Gas Chromatography-Mass Spectrometry , Glycosides/chemistry , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Stereoisomerism
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