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1.
Braz. j. biol ; 80(2): 393-404, Apr.-June 2020. tab
Article in English | LILACS | ID: biblio-1132371

ABSTRACT

Abstract This paper reports the in vitro antiproliferative effects, antiprotozoal, anti-herpes and antimicrobial activities of 32 organic extracts of 14 marine sponges and 14 corals collected in northeast Brazilian coast. The ethanolic extracts of the sponges Amphimedon compressa and Tedania ignis, and the acetone extract of Dysidea sp. showed relevant results concerning the antiproliferative effects against A549, HCT-8, and PC-3 cell lines by sulforhodamine B assay, but also low specificity. Concerning the antiprotozoal screening, the ethanolic extract of Amphimedon compressa and the acetone and ethanolic extracts of Dysidea sp. were the most active against Leishmania amazonensis and Trypanosoma cruzi expressing β-galactosidase in THP-1 cells. In the preliminary anti-HSV-1 (KOS strain) screening, the ethanolic extracts of the sponges Amphimedon compressa, Haliclona sp. and Chondrosia collectrix inhibited viral replication by more than 50%. The most promising anti-herpes results were observed for the ethanolic extract of Haliclona sp. showing high selective indices against HSV-1, KOS and 29R strains (SI> 50 and >79, respectively), and HSV-2, 333 strain (IS>108). The results of the antibacterial screening indicated that only the ethanolic extract of Amphimedon compressa exhibited a weak activity against Enterococcus faecalis, Pseudomonas aeruginosa and Escherichia coli by the disk diffusion method. In view of these results, the extracts of Amphimedon compressa, Tedania ignis and Dysidea sp. were selected for further studies aiming the isolation and identification of the bioactive compounds with antiproliferative and/or antiprotozoal activities. The relevant anti-herpes activity of the ethanolic extract of Haliclona sp. also deserves special attention, and will be further investigated.


Resumo Este artigo reporta as atividades in vitro antiproliferativa, atiprotozoárica, anti-herpética e antimicrobiana de 32 extratos orgânicos provenientes de 14 esponjas marinhas e 14 corais coletados no litoral nordestino brasileiro. Os extratos etanólicos das esponjas Amphimedon compressa e Tedania ignis, e o extrato acetônico de Dysidea sp. demonstraram resultados promissores em relação aos efeitos antiproliferativos frente as linhagens celulares A549, HCT-8, PC-3 pelo método da sulforrodamina B, mas sem especificidade. Em relação à atividade antiprotozárica, os extratos etanólico de Amphimedon compressa e acetônico e etanólico de Dysidea sp. apresentaram atividade contra Leishmania amazonensis e Trypanosoma cruzi através do método de expressão de β-galactosidase em células THP-1. Na investigação preliminar de atividade antiviral frente ao vírus Herpes simplex tipo 1 (cepa KOS), os extratos etanólicos das esponjas Amphimedon compressa, Haliclona sp. e Chondrosia collectrix inibiram mais de 50% da replicação viral. O extrato etanólico da esponja Haliclona sp. demonstrou resultados promissores para atividade anti-herpética com altos índices de seletividade para as cepas KOS (IS >50) e 29R (IS>79) frente ao VHS-1 e cepa 333 (IS>108) frente ao VHS-2. O extrato etanólico da esponja Amphimedon compressa exibiu uma pequena atividade contra Enterococcus faecalis, Pseudomonas aeruginosa and Escherichia coli pelo método de difusão em disco. De acordo com os resultados apresentados, os extratos das esponjas Amphimedon compressa, Tedania ignis e Dysidea sp. serão selecionados para futuros estudos de isolamento e identificação dos compostos bioativos para as atividades antiproliferativa e antiprozoárica. O extrato etanólico de Haliclona sp. será investigado por possuir atividade relevante anti-herpética.


Subject(s)
Animals , Porifera , Brazil , Plant Extracts , Enterococcus faecalis , Anti-Bacterial Agents
2.
Braz J Biol ; 80(2): 393-404, 2020.
Article in English | MEDLINE | ID: mdl-31389485

ABSTRACT

This paper reports the in vitro antiproliferative effects, antiprotozoal, anti-herpes and antimicrobial activities of 32 organic extracts of 14 marine sponges and 14 corals collected in northeast Brazilian coast. The ethanolic extracts of the sponges Amphimedon compressa and Tedania ignis, and the acetone extract of Dysidea sp. showed relevant results concerning the antiproliferative effects against A549, HCT-8, and PC-3 cell lines by sulforhodamine B assay, but also low specificity. Concerning the antiprotozoal screening, the ethanolic extract of Amphimedon compressa and the acetone and ethanolic extracts of Dysidea sp. were the most active against Leishmania amazonensis and Trypanosoma cruzi expressing ß-galactosidase in THP-1 cells. In the preliminary anti-HSV-1 (KOS strain) screening, the ethanolic extracts of the sponges Amphimedon compressa, Haliclona sp. and Chondrosia collectrix inhibited viral replication by more than 50%. The most promising anti-herpes results were observed for the ethanolic extract of Haliclona sp. showing high selective indices against HSV-1, KOS and 29R strains (SI> 50 and >79, respectively), and HSV-2, 333 strain (IS>108). The results of the antibacterial screening indicated that only the ethanolic extract of Amphimedon compressa exhibited a weak activity against Enterococcus faecalis, Pseudomonas aeruginosa and Escherichia coli by the disk diffusion method. In view of these results, the extracts of Amphimedon compressa, Tedania ignis and Dysidea sp. were selected for further studies aiming the isolation and identification of the bioactive compounds with antiproliferative and/or antiprotozoal activities. The relevant anti-herpes activity of the ethanolic extract of Haliclona sp. also deserves special attention, and will be further investigated.


Subject(s)
Porifera , Animals , Anti-Bacterial Agents , Brazil , Enterococcus faecalis , Plant Extracts
3.
Article in English | LILACS-Express | LILACS, VETINDEX | ID: biblio-1467306

ABSTRACT

Abstract This paper reports the in vitro antiproliferative effects, antiprotozoal, anti-herpes and antimicrobial activities of 32 organic extracts of 14 marine sponges and 14 corals collected in northeast Brazilian coast. The ethanolic extracts of the sponges Amphimedon compressa and Tedania ignis, and the acetone extract of Dysidea sp. showed relevant results concerning the antiproliferative effects against A549, HCT-8, and PC-3 cell lines by sulforhodamine B assay, but also low specificity. Concerning the antiprotozoal screening, the ethanolic extract of Amphimedon compressa and the acetone and ethanolic extracts of Dysidea sp. were the most active against Leishmania amazonensis and Trypanosoma cruzi expressing -galactosidase in THP-1 cells. In the preliminary anti-HSV-1 (KOS strain) screening, the ethanolic extracts of the sponges Amphimedon compressa, Haliclona sp. and Chondrosia collectrix inhibited viral replication by more than 50%. The most promising anti-herpes results were observed for the ethanolic extract of Haliclona sp. showing high selective indices against HSV-1, KOS and 29R strains (SI> 50 and >79, respectively), and HSV-2, 333 strain (IS>108). The results of the antibacterial screening indicated that only the ethanolic extract of Amphimedon compressa exhibited a weak activity against Enterococcus faecalis, Pseudomonas aeruginosa and Escherichia coli by the disk diffusion method. In view of these results, the extracts of Amphimedon compressa, Tedania ignis and Dysidea sp. were selected for further studies aiming the isolation and identification of the bioactive compounds with antiproliferative and/or antiprotozoal activities. The relevant anti-herpes activity of the ethanolic extract of Haliclona sp. also deserves special attention, and will be further investigated.


Resumo Este artigo reporta as atividades in vitro antiproliferativa, atiprotozoárica, anti-herpética e antimicrobiana de 32 extratos orgânicos provenientes de 14 esponjas marinhas e 14 corais coletados no litoral nordestino brasileiro. Os extratos etanólicos das esponjas Amphimedon compressa e Tedania ignis, e o extrato acetônico de Dysidea sp. demonstraram resultados promissores em relação aos efeitos antiproliferativos frente as linhagens celulares A549, HCT-8, PC-3 pelo método da sulforrodamina B, mas sem especificidade. Em relação à atividade antiprotozárica, os extratos etanólico de Amphimedon compressa e acetônico e etanólico de Dysidea sp. apresentaram atividade contra Leishmania amazonensis e Trypanosoma cruzi através do método de expressão de -galactosidase em células THP-1. Na investigação preliminar de atividade antiviral frente ao vírus Herpes simplex tipo 1 (cepa KOS), os extratos etanólicos das esponjas Amphimedon compressa, Haliclona sp. e Chondrosia collectrix inibiram mais de 50% da replicação viral. O extrato etanólico da esponja Haliclona sp. demonstrou resultados promissores para atividade anti-herpética com altos índices de seletividade para as cepas KOS (IS >50) e 29R (IS>79) frente ao VHS-1 e cepa 333 (IS>108) frente ao VHS-2. O extrato etanólico da esponja Amphimedon compressa exibiu uma pequena atividade contra Enterococcus faecalis, Pseudomonas aeruginosa and Escherichia coli pelo método de difusão em disco. De acordo com os resultados apresentados, os extratos das esponjas Amphimedon compressa, Tedania ignis e Dysidea sp. serão selecionados para futuros estudos de isolamento e identificação dos compostos bioativos para as atividades antiproliferativa e antiprozoárica. O extrato etanólico de Haliclona sp. será investigado por possuir atividade relevante anti-herpética.

4.
Neuroscience ; 292: 13-21, 2015 Apr 30.
Article in English | MEDLINE | ID: mdl-25681522

ABSTRACT

Yerba-mate (Ilex paraguariensis St. Hil.) is the most used beverage in Latin America with approximately 426 thousand of tons consumed per year. Considering the broad use of this plant, we aimed to investigate the anxiety-like and stimulant activity of both the hydroethanolic (HE) and aqueous (AE) extracts from leaves of I. paraguariensis. Swiss mice were treated with I. paraguariensis HE or AE chronically or acutely, respectively, followed by evaluation in the elevated plus-maze (EPM; anxiety-like paradigm), open field (OF; locomotor activity) or the step-down avoidance task (memory assessment). Following behavioral protocols the brains were collected for evaluation of acetylcholinesterase (AChE) activity ex vivo. Chronic treatment with HE induced an anxiolytic-like effect and increased motor activity besides augmented AChE activity. Additionally, acute treatment with AE prevented the scopolamine-induced memory deficit in the step-down avoidance task. Overall, our results indicate the importance of the I. paraguariensis-induced CNS effects, since it is a widely used nutraceutical. We have reported anxiolytic, stimulant and neuroprotective effects for this plant species. These effects are potentially modulated by the cholinergic system as well as by caffeine.


Subject(s)
Anti-Anxiety Agents/pharmacology , Central Nervous System Stimulants/pharmacology , Ilex paraguariensis , Neuroprotective Agents/pharmacology , Plant Extracts/pharmacology , Plant Leaves , Acetylcholinesterase/metabolism , Animals , Anti-Anxiety Agents/chemistry , Anxiety/drug therapy , Avoidance Learning/drug effects , Brain/drug effects , Brain/enzymology , Caffeine/chemistry , Caffeine/pharmacology , Central Nervous System Stimulants/chemistry , Cholinergic Agents/chemistry , Cholinergic Agents/pharmacology , Exploratory Behavior/drug effects , Ilex paraguariensis/chemistry , Male , Memory Disorders/prevention & control , Mice , Motor Activity/drug effects , Neuroprotective Agents/chemistry , Phototherapy , Plant Extracts/chemistry , Plant Leaves/chemistry , Scopolamine
5.
Phytomedicine ; 21(5): 670-5, 2014 Apr 15.
Article in English | MEDLINE | ID: mdl-24548722

ABSTRACT

The Cecropia genus is widely distributed in Latin America including at least 60 species, and some of them are commonly used in traditional medicine for the treatment of several diseases. We used Cecropia pachystachya Trécul to search for quorum sensing (QS) inhibitors compounds and found that the aqueous extract of C. pachystachya leaves is a promising source of substances with this activity. Using as biosensor Chromobacterium violaceum ATCC 31532 and Escherichia coli pSB403, the compounds chlorogenic acid (2), isoorientin (3), orientin (4), isovitexin (6), vitexin (7), and rutin (9) were identified as QS inhibitors. None of these compounds inhibited the growth of neither the used biosensors nor the microorganisms Staphylococcus aureus ATCC 23591, Escherichia coli ATCC 25922 and Saccharomyces cerevisiae, used here as growth inhibition controls. Along with the rutin, here we presented for the first time the QS-inhibition potential of the C-glycosyl flavonoids. The prospective of this evidence lead to the use of these compounds as antipathogenic drugs or antifoulants.


Subject(s)
Anti-Bacterial Agents/isolation & purification , Cecropia Plant/chemistry , Flavonoids/pharmacology , Glucosides/pharmacology , Quorum Sensing/drug effects , Biosensing Techniques , Flavonoids/isolation & purification , Glucosides/isolation & purification , Microbial Sensitivity Tests
6.
Phytother Res ; 25(12): 1783-8, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21480409

ABSTRACT

Five saponins purified from the leaves of three Ilex species (saponins 1 and 2 from I. dumosa; saponin 3 from I. argentina; saponin 4 from I. paraguariensis) and from Passiflora alata (saponin 5) were evaluated for their in vitro haemolytic activity and in vivo immunostimulatory ability in a mouse model using tetanus toxoid (TT) as a model antigen. The assayed saponins showed very weak or no haemolytic activity over the tested concentration range. Mice were immunized twice with TT formulated with pure saponins 1-5, or with a mixture of saponins from Quillaja saponaria, aluminum hydroxide gel or saline, which were used as controls. The elicited humoral response was evaluated by means of the time course of specific serum antibody levels up to day 131 post-priming (total IgG and isotypes); the cellular response was tested through a delayed-type hypersensitivity (DTH) assay. The assayed saponins, in particular saponins 3 and 5, showed an adjuvant effect similar to that of alum for all tested parameters. The immunostimulating potential of these compounds deserves further investigation, especially taking into account that some Ilex spp. and Passiflora alata are native crops of widespread use and economical importance in Latin America.


Subject(s)
Adjuvants, Immunologic/pharmacology , Ilex/chemistry , Passiflora/chemistry , Saponins/immunology , Alum Compounds/pharmacology , Animals , Hemolysis , Hypersensitivity, Delayed/immunology , Immunity, Cellular , Immunity, Humoral , Male , Mice , Mice, Inbred BALB C , Quillaja/chemistry , Saponins/pharmacology , Tetanus Toxoid
7.
Lett Appl Microbiol ; 51(2): 143-8, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20572924

ABSTRACT

AIMS: To investigate the in vitro antiherpes effects of the crude aqueous extract obtained from Cecropia glaziovii leaves and their related fractions, the n-butanol fraction (n-BuOH) and the C-glycosylflavonoid-enriched fraction (MeOH(AMB)), and to determine the viral multiplication step(s) upon which this C-glycosylflavonoid-enriched fraction acts. METHODS AND RESULTS: The antiviral activity was evaluated against human herpes virus types 1 and 2 (HHV-1, HHV-2) by plaque reduction assay. The mode of action of the most active fraction was investigated by a set of assays, and the results demonstrated that MeOH(AMB) fraction exerts anti-herpes action by the reduction of viral infectivity (only against HHV-2); by the inhibition of virus entry into cells; by the inhibition of cell-to-cell virus spread as well as by the impaired levels of envelope proteins of HHV-1. The high-performance liquid chromatography (HPLC)-photo-diode array (PDA) analysis showed that the C-glycosylflavonoids are the major constituents of this fraction. CONCLUSIONS: These data showed that the MeOH(AMB) fraction has an antiviral activity against HHV types 1 and 2. The C-glycosylflavonoids are the major constituents of this fraction, which suggests that they could be one of the compounds responsible for the detected anti-herpes activity. SIGNIFICANCE AND IMPACT OF THE STUDY: The MeOH(AMB) fraction can be regarded as a phytopharmaceutical candidate for the treatment of herpetic infections.


Subject(s)
Antiviral Agents/isolation & purification , Antiviral Agents/pharmacology , Herpesvirus 1, Human/drug effects , Herpesvirus 2, Human/drug effects , Plant Extracts/isolation & purification , Plant Extracts/pharmacology , Urticaceae/chemistry , Antiviral Agents/chemistry , Chromatography, High Pressure Liquid , Flavonoids/analysis , Herpesvirus 1, Human/growth & development , Herpesvirus 1, Human/pathogenicity , Herpesvirus 2, Human/growth & development , Herpesvirus 2, Human/pathogenicity , Humans , Photometry , Plant Extracts/chemistry , Plant Leaves/chemistry , Viral Plaque Assay , Virus Attachment/drug effects , Virus Internalization/drug effects , Virus Release/drug effects
8.
Fitoterapia ; 78(2): 112-9, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17215089

ABSTRACT

The aqueous leaves extracts of Passiflora alata (100-300 mg/kg, i.p.) and Passiflora edulis (100-1000 mg/kg, i.p.) possess a significant antiinflammatory activity on carrageenan-induced pleurisy in mice. Treatment with the extracts inhibited leukocyte migration and reduced the formation of exudate. Moreover, a significant inhibition of myeloperoxidase and adenosine-deaminase activities was observed at the doses tested (100 or 250 mg/kg, i.p.). At the same doses, a significant decrease of serum C-reactive protein was observed.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Passiflora , Phytotherapy , Plant Extracts/pharmacology , Pleurisy/drug therapy , Animals , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , C-Reactive Protein/drug effects , Carrageenan , Disease Models, Animal , Dose-Response Relationship, Drug , Female , Male , Mice , Plant Extracts/administration & dosage , Plant Extracts/therapeutic use , Plant Leaves , Pleurisy/blood , Pleurisy/chemically induced
9.
Rev. bras. farmacogn ; 15(3): 229-236, jul.-set. 2005. tab
Article in Portuguese | LILACS | ID: lil-570923

ABSTRACT

No presente trabalho foi descrita a comparação da aplicabilidade das metodologias preconizadas na Farmacopéia Brasileira (1988) para a determinação de água em drogas vegetais. Foi realizada, ainda, a validação da determinação de água em analisador de umidade. As matérias-primas vegetais analisadas foram Calendula officinalis L. (calêndula), Foeniculum vulgare Miller (funcho), Maytenus ilicifolia Mart. ex. Reissek (espinheira-santa) e Passiflora alata Curtis (maracujá). A análise dos resultados obtidos mostrou que há diferenças estatisticamente significativas (p < 0,05) entre as metodologias "Determinação de água por destilação azeotrópica" e "Determinação de água em drogas vegetais" em estufa, assim como, entre a "Determinação da perda por dessecação" para as drogas vegetais calêndula e funcho. No entanto, não foram observadas diferenças estatisticamente significativas (p < 0,05) entre as duas metodologias de secagem em estufa. Quanto à validação da determinação de água em analisador de umidade, não foram observadas diferenças estatisticamente significativas (p<0,05) entre os resultados das análises em analisador de umidade e os obtidos através da "Determinação da perda por dessecação". Além disso, não foram verificadas diferenças estatisticamente significativas (p < 0,05) para as análises referentes à repetibilidade, precisão intermediária e reprodutibilidade da técnica, o que comprova a exatidão e a precisão da metodologia proposta.


A comparison of the Brazilian pharmacopeial methodologies for water determination in plant raw materials is presented for the following species: Calendula officinalis, Foeniculum vulgare, Maytenus ilicifolia e Passiflora alata. In addition, the validation of water determination by infrared drying was carried out for these species. The results obtained using the azeotropic distillation method (Brazilian Pharmacopoeia - "Determination of Water by Azeotropic Distillation") were significantly different (p<0.05) than those obtained using two different gravimetric methods (Brazilian Pharmacopoeia - "Determination of Water in Vegetable Drugs" and "Determination of loss on Drying"). However, no significant statistical difference was observed between the two gravimetric methodologies. After optimization of operating conditions, the results of water determination by infrared drying were not significantly different than those obtained using the loss on drying pharmaceutical method. Also, no statistically significant differences were observed for repeatability, intermediate precision and reproducibility of the method, demonstrating the accuracy and precision of the proposed methodology.

10.
Nat Prod Res ; 18(2): 153-7, 2004 Apr.
Article in English | MEDLINE | ID: mdl-14984089

ABSTRACT

A new abietane diterpene, the 19-O-beta-D-glucopyranoside of 16-hydroxylambertic acid was isolated from the leaves of Quillaja brasiliensis together with a known prosapogenin (3-O-beta-D-glucuronopyranosyl-quillaic acid), quercetin, and rutin. The new compound was identified by chemical and spectroscopic methods.


Subject(s)
Glucosides/isolation & purification , Phenanthrenes/isolation & purification , Quillaja/chemistry , Saponins/isolation & purification , Glucosides/chemistry , Phenanthrenes/chemistry , Plant Leaves/chemistry , Quercetin/isolation & purification , Rutin/isolation & purification , Saponins/chemistry , Spectrum Analysis
11.
Nat Prod Lett ; 16(6): 401-6, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12462345

ABSTRACT

Two new saponins were isolated from the leaves of Ilex psammophila. Their structure was established by chemical and spectroscopic methods as 28-O-beta-D-glucopyranosylester of 20(S)-ilexgenin A ([structure: see text]) and 28-O-beta-D-glucopyranosylester of 20(S)-3beta,19alpha,24-trihydroxyurs-12-ene-23, 28-dioic acid ([structure: see text]).


Subject(s)
Ilex/chemistry , Saponins/isolation & purification , Triterpenes/isolation & purification , Brazil , Chromatography, Thin Layer , Hydrolysis , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Plant Leaves/chemistry , Saponins/chemistry , Stereoisomerism , Triterpenes/chemistry , Ursolic Acid
12.
Rev. bras. farmacogn ; 12(2): 75-83, jul.-dez. 2002. tab
Article in Portuguese | LILACS | ID: lil-526497

ABSTRACT

Com o objetivo de avaliar a qualidade das bulas de medicamentos fitoterápicos em relação à presença das frases obrigatórias por lei, bem como de informações específicas exigidas pela legislação de medicamentos fitoterápicos, foram selecionados 65 produtos em farmácias de Porto Alegre contendo pelo menos uma das seguintes plantas medicinais: maracujá, boldo, alcachofra, guaraná e sene. Através de um formulário, analisou-se a presença das frases exigidas pela Portaria 110/97 da ANVS, que regulamenta as bulas de medicamentos, e das informações exigidas pela Resolução RDC 17/00 da ANVS, sobre registro de medicamentos fitoterápicos. A maioria dos produtos analisados não possui bula, e em nenhum deles verificou-se a presença de todas a frases e demais informações exigidas pela legislação vigente. Especialmente significante foi a inexistência de dados sobre reações adversas, contra-indicações e advertências. Foi possível concluir que as bulas de medicamentos fitoterápicos analisados não seguem as normas legais, são incompletas e deficientes de informações, podendo induzir a sérios problemas de saúde.


Sixty-five products with one of the following medicinal plants: passion flower, boldus, artichoke, guarana and senne were acquired in drugstores of Porto Alegre, RS, Brazil. These products were analyzed in order to evaluate the quality of phytomedicines package inserts in relation to the obligatory informations required by the Brazilian drug legislation. Most of the products did not have package inserts, and none of them presented all informations required by the legislation. Furthermore, most of them omitted the potential occurrence of adverse effects, contra-indications and precautions. In conclusion, the analyzed package inserts did not followed the Brazilian drug regulation, were incomplete and showed deficiencies which can induce health consumer problems.

13.
Rev. bras. farmacogn ; 12(2): 51-62, jul.-dez. 2002. tab
Article in Portuguese | LILACS | ID: lil-526499

ABSTRACT

Foi realizado um levantamento das plantas medicinais utilizadas pela população do município de Ipê, RS, Brasil, visando uma investigação da medicina tradicional, melhoramento e racionalização das práticas medicinais populares, em um projeto envolvendo voluntários da comunidade. Foram entrevistadas 114 pessoas, que mencionaram 252 plantas, das quais foram identificadas 105 espécies, agrupadas em 48 famílias. As plantas coletadas e identificadas foram analisadas, de acordo com dados químicos, farmacológicos e/ou toxicológicos encontrados na literatura científica. Os resultados obtidos mostram que a população deste município faz uso de plantas que, ainda, não foram alvo de pesquisa química, farmacológica e/ou toxicológica e, também, que a mesma faz uso de onze espécies, que são reconhecidamente, responsáveis por efeitos colaterais indesejados, ou ainda, que são tóxicas.


Medicinal plants used by Brazilian people from Ipê city, in Rio Grande do Sul State, were the subject of a survey realized in order to investigate the traditional medicine in this comunity. The project involved 114 individuals who cited 252 medicinal plants. From these plants, 105 species were identified and classified into 48 botanical families. Assessments of all known plants were based on chemical, pharmacological and toxicological data searched in scientific literature. The results show that many of these plants were not yet chemically and/or pharmacologically and/or toxicologically studied, and eleven of them were related to be responsible for side effects or even toxicity in the consulted scientific literature.

15.
Allergy ; 56(11): 1077-80, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11703222

ABSTRACT

Nasal congestion is among the most bothersome of the symptoms of intermittent allergic rhinitis (IAR). Decongestants such as pseudoephedrine are often accompanied by adverse effects and should be avoided by patients with hypertension, arrhythmia, and other medical conditions. Most of the currently available antihistamines are ineffective for nasal congestion. Oral desloratadine, a new, potent H1-receptor antagonist, was examined for its ability to relieve nasal congestion/stuffiness in 346 patients (172 in the desloratadine group and 174 in the placebo group) with IAR. Desloratadine, administered once daily at a dose of 5 mg, demonstrated significant improvement in nasal congestion/stuffiness at all time points assessed in the study. This benefit was observed as early as the first patient evaluation on day 2 and continued throughout the 2 weeks of the study. Desloratadine is a new treatment option for patients with IAR and nasal congestion.


Subject(s)
Histamine H1 Antagonists/therapeutic use , Loratadine/analogs & derivatives , Loratadine/therapeutic use , Nasal Decongestants/therapeutic use , Nasal Mucosa/drug effects , Nasal Obstruction/drug therapy , Rhinitis, Allergic, Seasonal/drug therapy , Adolescent , Adult , Aged , Child , Circadian Rhythm/drug effects , Dose-Response Relationship, Drug , Double-Blind Method , Female , Histamine H1 Antagonists/administration & dosage , Humans , Loratadine/administration & dosage , Male , Middle Aged , Treatment Outcome , United States/epidemiology
16.
Rev Saude Publica ; 35(5): 415-20, 2001 Oct.
Article in Portuguese | MEDLINE | ID: mdl-11723511

ABSTRACT

OBJECTIVE: To describe drugs used during pregnancy by women attending prenatal clinics of the national public health system (SUS) in Brazilian cities. METHODS: Using a structured questionnaire, 5,564 pregnant women between the week 21 to 28 who attended prenatal visits of the SUS in six Brazilian cities were interviewed. The interview questions were grouped in "guided use" to cover pain, cramps, nausea, cough, and others, and "guided medicine" to cover vitamins, iron, and fluoride. The Food and Drug Administration gestational risk classification (1991-1995) was applied. RESULTS: Of a total of 5,564 women, 4,614 (83.8%) used at least one drug during pregnancy, with a total of 9,556 drugs used. The drugs most frequently used were vitamins associated with anti-anemics (33.5%), gastrointestinal drugs (31.3%), analgesics and anti-inflammatory drugs (22.2%), anti-anemics (19.8%), and antibiotics (11.1%). Regarding gestational risk, 3,243 drugs used (34%) belonged to category A risk, 1,923 (22.6%) to category B, 3,798 (39.7%) to category C, 289 (3.0%) to category D, and 55 (0.6%) to category X. CONCLUSIONS: A large variation in drug use across the cities was observed, especially for anti-anemics and vitamins associated with anti-anemics, revealing the lack of a national consensus regarding the use of these drugs during pregnancy. There was no literature data about safety during pregnancy for 12.9% of the drugs used. This percentage, plus the 26.9% of category C drugs, shows that 40% of the drugs used during pregnancy do not belong to the approved safety categories. However, only 3% of the 9,956 drugs used were clearly contraindicated during pregnancy.


Subject(s)
Drug Therapy/statistics & numerical data , Pregnancy , Adult , Brazil , Contraindications , Female , Humans , Pharmaceutical Preparations , Pregnancy Complications/drug therapy , Pregnancy Trimesters , Risk
17.
J Vet Diagn Invest ; 13(2): 170-2, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11289217

ABSTRACT

Cholangiohepatopathy was induced in 5 lambs by oral administration of extracts from signal grass (Brachiaria decumbens) in Brazil. Grossly there were pale foci multifocally distributed throughout the hepatic parenchyma in 4 lambs. The microscopic changes, which were similar to those produced by other steroidal sapogenins-containing plants such as Tribulus terrestris and Panicum spp., included multifocal cholangitis, bile duct proliferation, and the presence of crystals in the biliary system.


Subject(s)
Liver Diseases/veterinary , Panicum , Photosensitivity Disorders/veterinary , Poaceae , Sheep Diseases/pathology , Administration, Oral , Animals , Animals, Newborn , Chemical and Drug Induced Liver Injury , Liver Diseases/pathology , Photosensitivity Disorders/chemically induced , Plant Extracts/administration & dosage , Plant Extracts/pharmacology , Sheep
18.
Phytother Res ; 15(2): 162-4, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11268119

ABSTRACT

Several species of the genus Passiflora, known in Brazil as "maracujá", have widespread use in folk medicine as sedatives and tranquillizers. The anxiolytic activity of hydroethanol extracts of P. alata and P. edulis leaves was evaluated using the elevated plus-maze test. The extracts presented anxiolytic activity in dosages around 50, 100 and 150 mg/kg.


Subject(s)
Anti-Anxiety Agents/pharmacology , Maze Learning/drug effects , Plants, Medicinal , Rosales , Animals , Dose-Response Relationship, Drug , Male , Plant Extracts/pharmacology , Plant Leaves , Rats , Rats, Wistar
19.
Rev. bras. farmacogn ; 11(1): 21-35, 2001. tab
Article in Portuguese | LILACS | ID: lil-528789
20.
Rev. bras. farmacogn ; 11(2): 89-93, 2001. tab, ilus
Article in Portuguese | LILACS | ID: lil-528795

ABSTRACT

O gênero Croton possui seiscentas espécies e é originário de regiões tropicais. Croton gnaphelil é conhecida no sul do Brasil como infalivina, sendo utilizada popularmente nos distúrbios hepáticos. A substância majoritária presente nas partes aéreas desta planta foi isolada e identificada através de métodos espectroscópicos, sendo identificada como um glicosídeo acilado, o canferol‑3‑O‑(6"‑O‑p‑cumaroil)‑β‑D‑glicopyranose, também chamado de tilirosídeo.


Croton genus comprises six hundred species being native in tropical forests. Croton gnaphalliis popularly known as "infalivina" in South of Brazil and it is traditionally used for hepatic disorders. The major compound from aerial parts of this plant was isolated and its structure elucidated through spectroscopic analysis. It was identified as an acylglycoside, kaempferol‑3‑O‑(6"‑O‑p‑coumaroyl)‑ β ‑D‑glucopyranoside, known as tiliroside.

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