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1.
J Appl Microbiol ; 129(4): 906-915, 2020 Oct.
Article in English | MEDLINE | ID: mdl-32350955

ABSTRACT

AIMS: The objective of the study was to evaluate the antimicrobial interactions between two volatile agents, Cinnamomum cassia essential oil (CCEO) and 8-hydroxyquinoline (8-HQ) against Staphylococcus aureus strains in liquid and vapour phases. METHODS AND RESULTS: In vitro antimicrobial effect of CCEO in combination with 8-HQ was evaluated against 12 strains of S. aureus by broth volatilization chequerboard method. Results show additive effects against all S. aureus strains for both phases. In several cases, sums of fractional inhibitory concentration values of our test combinations were lower than 0·6, which can be considered as a strong additive interaction. Moreover, composition of CCEO was analysed by gas chromatography-mass spectrometry analysis. In the CCEO, 26 compounds in total were identified, where (E)-cinnamaldehyde was the predominant compound, followed by cinnamyl acetate, α-copaene, bornyl acetate and caryophyllene. CONCLUSIONS: Results showed additive in vitro growth-inhibitory effect of CCEO and 8-HQ combination against various standard strains and clinical isolates of S. aureus. SIGNIFICANCE AND IMPACT OF THE STUDY: This is the first report on antibacterial effect of 8-HQ and CCEO combination in liquid and vapour phases. Results of the study suggest these agents as potential candidates for development of new anti-staphylococcal applications that can be used in the inhalation therapy against respiratory infections.


Subject(s)
Cinnamomum aromaticum/chemistry , Oils, Volatile/pharmacology , Oxyquinoline/pharmacology , Staphylococcus aureus/drug effects , Acrolein/analogs & derivatives , Acrolein/chemistry , Anti-Bacterial Agents/pharmacology , Gas Chromatography-Mass Spectrometry , Microbial Sensitivity Tests
2.
Eur J Med Chem ; 89: 683-90, 2015 Jan 07.
Article in English | MEDLINE | ID: mdl-25462275

ABSTRACT

Chagas disease, caused by the protozoa parasite Trypanosoma cruzi, is an example of extended parasitaemia with unmet medical needs. Current treatments based on old-featured benznidazole (Bz) and nifurtimox are expensive and do not fulfil the criteria of effectiveness, and a lack of toxicity devoid to modern drugs. In this work, a group of abietic acid derivatives that are chemically stable and well characterised were introduced as candidates for the treatment of Chagas disease. In vitro and in vivo assays were performed in order to test the effectiveness of these compounds. Finally, those which showed the best activity underwent additional studies in order to elucidate the possible mechanism of action. In vitro results indicated that some compounds have low toxicity (i.e. >150 µM, against Vero cell) combined with high efficacy (i.e. <20 µM) against some forms of T. cruzi. Further in vivo studies on mice models confirmed the expectations of improvements in infected mice. In vivo tests on the acute phase gave parasitaemia inhibition values higher those of Bz, and a remarkable decrease in the reactivation of parasitaemia was found in the chronic phase after immunosuppression of the mice treated with one of the compounds. The morphological alterations found in treated parasites with our derivatives confirmed extensive damage; energetic metabolism disturbances were also registered by (1)H NMR. The demonstrated in vivo activity and low toxicity, together with the use of affordable starting products and the lack of synthetic complexity, put these abietic acid derivatives in a remarkable position toward the development of an anti-Chagasic agent.


Subject(s)
Abietanes/chemistry , Abietanes/pharmacology , Antiprotozoal Agents/pharmacology , Chagas Disease/drug therapy , Disease Models, Animal , Trypanosoma cruzi/drug effects , Abietanes/chemical synthesis , Animals , Antiprotozoal Agents/chemical synthesis , Antiprotozoal Agents/chemistry , Chagas Disease/parasitology , Chlorocebus aethiops , Dose-Response Relationship, Drug , Female , Mice , Mice, Inbred BALB C , Molecular Conformation , Parasitic Sensitivity Tests , Structure-Activity Relationship , Vero Cells
3.
Z Naturforsch C J Biosci ; 56(5-6): 430-6, 2001.
Article in English | MEDLINE | ID: mdl-11421461

ABSTRACT

Labial gland secretions of 22 males of the bumblebee Bombus pomorum, collected in the Czech Republic, were analysed separately for each individual. The secretions contained 70 compounds among which saturated and unsaturated hydrocarbons strongly dominated. The proportion of hydrocarbons in the secretion was unusually high (85-100%) compared to other bumblebee species studied so far (3-15%). Methyl and ethyl esters of fatty acids, known from many other bumblebee species, formed only minor components (less than 1% in sum) of the secretions of several B. pomorum individuals. No terpenic compounds, typical for males' marking secretion of many bumblebee species, were detected in B. pomorum. The absolute quantities of hydrocarbons present in the labial gland extracts were comparable with those usually present in other species. The composition of hydrocarbons found in the labial glands was different from the profile of the cuticular hydrocarbons. Despite our expectations in species exhibiting a regular patrolling and scent-marking behaviour, the labial gland extracts obtained from B. pomorum males were unusually low concentrated and their chemical composition was atypical with respect of the proportions of hydrocarbons when compared with other patrolling species. This is the first report on the analysis of the labial gland secretion of the B. pomorum males.


Subject(s)
Bees/physiology , Exocrine Glands/metabolism , Hydrocarbons/chemistry , Animals , Carboxylic Acids/analysis , Carboxylic Acids/chemistry , Czech Republic , Esters/analysis , Esters/chemistry , Hydrocarbons/analysis , Male
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