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1.
Chem Biodivers ; 12(7): 1105-14, 2015 Jul.
Article in English | MEDLINE | ID: mdl-26172330

ABSTRACT

Foeniculum vulgare Mill. (Apiaceae), known as fennel, is a widespread aromatic herbaceous plant, and its essential oil is used as additive in the food, pharmaceutical, cosmetic, and perfume industries. The in vitro antischistosomal activity and cytotoxic effects against V79 cells of the essential oil of F. vulgare cultivated in southeastern Brazil (FV-EO) was investigated. The FV-EO was obtained by hydrodistillation and characterized by GC-FID and GC/MS analyses. (E)-Anethole (69.8%) and limonene (22.5%) were identified as the major constituents. Its anthelmintic activity against Schistosoma mansoni was evaluated at concentrations of 10, 50, and 100 µg/ml, and it was found to be active against adult S. mansoni worms, although it was less effective than the positive control praziquantel (PZQ) in terms of separation of the coupled pairs, mortality, and decreased motor activity. However, FV-EO elicited an interesting dose-dependent reduction in the number of S. mansoni eggs. On their own, (E)-anethole and the limonene enantiomers were much less effective than FV-EO and PZQ. An XTT-cytotoxicity-based assay evidenced no FV-EO cytotoxicity against V79 cells. In summary, FV-EO displayed moderate in vitro schistosomicidal activity against adult S. mansoni worms, exerted remarkable inhibitory effects on the egg development, and was of low toxicity.


Subject(s)
Anthelmintics/pharmacology , Foeniculum/chemistry , Oils, Volatile/pharmacology , Plant Extracts/pharmacology , Schistosoma mansoni/drug effects , Animals , Anthelmintics/chemistry , Anthelmintics/isolation & purification , Brazil , Cell Line , Cricetinae , Dose-Response Relationship, Drug , Molecular Structure , Oils, Volatile/chemistry , Oils, Volatile/isolation & purification , Plant Extracts/chemistry , Plant Extracts/isolation & purification
2.
Rev. bras. farmacogn ; 22(1): 88-93, Jan.-Feb. 2012. graf, tab
Article in English | LILACS | ID: lil-607609

ABSTRACT

The in vitro schistosomicidal effects of the essential oil obtained from Tagetes erecta L. Asteraceae, leaves (TE-EO) collected in Brazil against Schistosoma mansoni worms are reported in this paper. The oil caused a significant decrease in the motor activity at 50 µg/mL as minimal concentration after 24 h. This oil also caused death of all the parasites and the separation of coupled pairs into individual male and female at 100 µg/mL after 24 h. The viability of adult worm groups treated with the TE-EO at 100 µg/mL was similar to that of groups treated with praziquantel (positive control). In addition, the oil promoted the inhibition of eggs development at all the tested concentrations. These data indicate that the TE-EO could be considered as a promising source for the development of new schistosomicidal agents.

3.
Parasitol Res ; 110(5): 1747-54, 2012 May.
Article in English | MEDLINE | ID: mdl-22006194

ABSTRACT

In this paper, cercariae, schistosomula, and adult Schistosoma mansoni worms were incubated in vitro with the essential oil of Piper cubeba (PC-EO) at concentrations from 12.5 to 200 µg/mL, and the viability was evaluated using an inverted microscopy. The effects of PC-EO at 100 and 200 µg/mL on the stages of S. mansoni were similar to those of the positive control (PZQ at 12.5 µg/mL), with total absence of mobility after 120 h. However, at concentrations from 12.5 to 50 µg/mL, PC-EO caused a reduction in the viability of cercariae and schistosomula when compared with the negative control groups (RPMI 1640 or dechlorinated water) or (RPMI 1640 + 0.1% DMSO or dechlorinated water + 0.1% DMSO). On the other hand, adult S. mansoni worms remained normally active when incubated with PC-EO at concentrations of 12.5 and 25 µg/mL, and their viabilities were similar to those of the negative control groups. In addition, at concentrations ranging from 50 to 200 µg/mL, separation of all the coupled adult worms was observed after 24 h of incubation, which is related to the fact of the reduction in egg production at this concentration. The main chemical constituents of PC-EO were identified by gas chromatography-mass spectrometry as being sabinene (19.99%), eucalyptol (11.87%), 4-terpineol (6.36%), ß-pinene (5.81%), camphor (5.61%), and δ-3-carene (5.34%). The cytotoxicity of the PC-EO was determined, and a significant cytotoxicity was only obtained in the concentration of 200 µg/mL after 24 h treatment. The results suggest that PC-EO possesses an effect against cercariae, schistosomula, and adult worms of the S. mansoni.


Subject(s)
Anthelmintics/pharmacology , Oils, Volatile/pharmacology , Piper/chemistry , Schistosoma mansoni/drug effects , Animals , Anthelmintics/chemistry , Anthelmintics/isolation & purification , Dose-Response Relationship, Drug , Gas Chromatography-Mass Spectrometry , Locomotion/drug effects , Mice , Mice, Inbred BALB C , Oils, Volatile/chemistry , Oils, Volatile/isolation & purification , Survival Analysis
4.
Chem Biodivers ; 8(11): 2149-57, 2011 Nov.
Article in English | MEDLINE | ID: mdl-22083928

ABSTRACT

The chemical composition and the in vitro schistosomicidal effects of the essential oil of Plectranthus neochilus (PN-EO) grown in Southeast Brazil was studied. ß-Caryophyllene (1; 28.23%), α-thujene (2; 12.22%), α-pinene (3; 12.63%), ß-pinene (4; 6.19%), germacrene D (5; 5.36%), and caryophyllene oxide (6; 5.37%) were the major essential oil constituents. This chemical composition differed from that previously reported for specimens harvested in Africa. Concerning the in vitro schistosomicidal activity against adult Schistosoma mansoni worms, PN-EO was considered to be active, but less effective than the positive control praziquantel (PZQ) in terms of separation of coupled pairs, mortality, decrease in the motor activity, and tegumental alterations. However, PN-EO caused an interesting dose-dependent reduction in the number and the percentage of developed S. mansoni eggs. These results suggest that PN-EO might be very promising for the development of new schistosomicidal agents.


Subject(s)
Oils, Volatile/isolation & purification , Plant Oils/isolation & purification , Plectranthus/chemistry , Schistosomicides/isolation & purification , Animals , Brazil , Dose-Response Relationship, Drug , Drug Design , Female , Gas Chromatography-Mass Spectrometry , Male , Molecular Structure , Oils, Volatile/chemistry , Oils, Volatile/pharmacology , Plant Leaves/chemistry , Plant Leaves/growth & development , Plant Oils/chemistry , Plant Oils/pharmacology , Plectranthus/growth & development , Schistosoma mansoni/drug effects , Schistosoma mansoni/growth & development , Schistosomicides/chemistry , Schistosomicides/pharmacology
5.
Molecules ; 16(1): 762-73, 2011 Jan 18.
Article in English | MEDLINE | ID: mdl-21245809

ABSTRACT

The in vitro schistosomicidal effects of the essential oil of Ageratum conyzoides L. (Ac-EO) against adult worms of Schistosoma mansoni is reported in this paper. Concerning this activity, Ac-EO was considered to be active, but less effective than the positive control (praziquantel, PZQ) in terms of separation of coupled pairs, mortality, decrease in motor activity, and tegumental alterations. However, Ac-EO caused an interesting dose-dependent reduction in the number of eggs of S. mansoni. Precocene I (74.30%) and (E)-caryophyllene (14.23%) were identified as the two major constituents of Ac-EO. These compounds were tested individually and were found to be much less effective than Ac-EO and PZQ. A mixture of the two major compounds in a ratio similar to that found in the Ac-EO was also less effective than Ac-EO, thus revealing that there are no synergistic effects between these components. These results suggest that the essential oil of A. conyzoides is very promising for the development of new schistosomicidal agents.


Subject(s)
Ageratum/chemistry , Oils, Volatile/pharmacology , Schistosoma mansoni/drug effects , Animals , Oils, Volatile/isolation & purification
6.
Rapid Commun Mass Spectrom ; 24(3): 295-308, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20049889

ABSTRACT

The fragmentation of six plumeran indole alkaloids (PIAs) previously isolated from Aspidosperma spruceanum has been investigated by electrospray ionization tandem mass spectrometry (ESI-MS/MS) in the positive ion mode. The fragmentation pathways have been established on the basis of MS/MS experiments using fragment ions generated in-source and deuterium-labeled alkaloids as precursor ions and on the basis of accurate mass measurements. Our results demonstrated that the fragmentation routes observed for the protonated PIAs are essentially derived from a pericyclic reaction and from the opening of rings D and E, followed by 1,4-hydrogen rearrangements. Product ions resulting from radical eliminations were also observed, contrary to the 'even-electron rule'. Our data reveals that some product ions from protonated PIAs provide crucial information for the characterization of the acyl substituent at N-1, the methoxyl and hydroxyl groups at the aromatic moiety, and give evidence of an ether bridge between C-18 and C-21. The data reported here were used for the dereplication of these compounds in a stem bark methanolic extract of Aspidosperma spruceanum.


Subject(s)
Aspidosperma/chemistry , Indole Alkaloids/analysis , Spectrometry, Mass, Electrospray Ionization , Indole Alkaloids/chemistry , Indole Alkaloids/isolation & purification , Molecular Structure , Plant Bark/chemistry , Protons
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