ABSTRACT
Abstract This study aimed to evaluate the anthelmintic and ultrastructural effects of Calotropis procera latex on Haemonchus contortus. C. procera latex was twice centrifuged at 10,000×g and dialyzed to obtain a fraction rich in proteins, named LP (latex protein), and at 3,000 rpm to obtain a fraction rich in secondary metabolites, named LNP (latex non-protein). Specimens of H. contortus exposed to LNP, LP and PBS in the Adult Worm Motility Test (AWMT) were submitted to scanning (SEM) and transmission (TEM) electron microscopy to verify changes in their ultrastructure. Phytochemical tests in the LNP indicated the presence of phenols, steroids, alkaloids and cardenolides. High-Performance Liquid Chromatography (HPLC) characterized the presence of the compounds gallic acid and quercetin in the LNP. The protein content in the LP was 43.1 ± 1.1 mg/mL and 7.7 ± 0.3 mg/mL in LNP. In AWMT, LNP and LP inhibited the motility of 100% of the nematodes, with LNP being more effective than LP and ivermectin more effective than both (p <0.05). Cuticle changes were observed by SEM and TEM in nematodes treated with LP and LNP. Calotropis procera latex has anthelmintic effects against H. contortus, causing damage to its cuticle and other alterations in its ultrastructure.
Resumo Este estudo objetivou avaliar os efeitos anti-helmínticos e ultraestruturais do látex de Calotropis procera sobre Haemonchus contortus. Látex de C. procera foi centrifugado duas vezes à a 10.000xg e dialisado para obter uma fração rica em proteínas, denominada proteínas do látex (LP). E centrifugado e centrifugado a 3.000 rpm, para obter uma fração rica em metabólitos secundários, denominada LNP (látex não proteico). Espécimes de H. contortus expostos à LNP, LP e PBS no Teste de Motilidade dos Nematoides Adultos (TMNA) foram submetidos a microscopia eletrônica de varredura (MEV) e de transmissão (MET), para verificar alterações em sua ultraestrutura. Testes fitoquímicos em LNP indicaram a presença de fenóis, esteroides, alcaloides e cardenolídeos. A presença dos compostos ácido gálico e quercetina em LNP foi caracterizada por Cromatografia Líquida de Alta Eficiência (CLAE). O conteúdo de proteínas em LP foi de 43,1 ± 1,1 mg/mL e de 7,7 ± 0,3 mg/mL em LNP. No TMNA, LNP e LP inibiram a motilidade de 100% dos nematoides, sendo LNP mais eficaz que LP, e a ivermectina mais eficaz que ambos (p <0,05). Alterações na cutícula de nematoides tratados com LP e LNP foram observadas por MEV e MET. O látex de C. procera apresenta efeito anti-helmíntico sobre H. contortus, causando danos à sua cutícula e outras alterações em sua ultraestrutura.
Subject(s)
Animals , Calotropis/chemistry , Haemonchus/drug effects , Haemonchus/ultrastructure , Latex/chemistry , Anthelmintics/pharmacology , Phenols/chemistry , Phytosterols/chemistry , Saponins/chemistry , Sheep Diseases/parasitology , Tannins/chemistry , Triterpenes/chemistry , In Vitro Techniques , Brazil , Drug Resistance , Sheep/parasitology , Microscopy, Electron, Scanning , Cardenolides/chemistry , Chromatography, High Pressure Liquid , Alkaloids/chemistry , Haemonchiasis/veterinary , Haemonchus/isolation & purification , Haemonchus/physiology , Latex/isolation & purification , Anthocyanins/chemistryABSTRACT
Wild and tissue culture raised regenerants of Artemisia amygdalina, a critically endangered and endemic plant of Kashmir and North West Frontier Provinces of Pakistan were screened for the amount of bioactive principles and in particular antimalarial compound artemesinin. Phytochemical screening of extracts revealed the presence of terpenes, alkaloids, phenolics, tannins [polyphenolics], cardiac glycosides and steroids in wild [aerial, inflorescence] and tissue culture regenerants [in vitro grown plant, callus and green house acclimatized plants]. HPLC of Artemisia amygdalina revealed the presence of artemesinin in petroleum ether extracts of wild aerial part, tissue culture raised plant and green house acclimatized plants. Acetonitrile and water in 70:30 ratios at flow rate of 1ml/min was standardised as mobile phase. Retention time for standard chromatogram was 6.7. Wild inflorescences and callus does not produce artemesinin. This is the first report of phytochemical screening and artemesinin estimation of wild and tissue culture raised regenerants of Artemisia amygdalina
Subject(s)
Biological Factors/chemistry , Cardiac Glycosides/chemistry , Phenols/chemistry , Plant Extracts/chemistry , Steroids/chemistry , Tannins/chemistry , Terpenes/chemistry , Tissue Culture Techniques/methods , Alkaloids/chemistry , AntimalarialsABSTRACT
Introdução - Extrato bruto da casca de banana nanica (Musa acuminata); melhor fonte de enzima Polifenol oxidase (PFO) [EC.1.14.18.1] foi estudado como material biocatalítico para a oxidação aeróbica de substratos fenólicos. Materiais e Métodos - O extrato bruto de PFO foi obtido como em Perone et al.14 (2000). A atividade da enzima PFO e proteína total foram determinadas nesse extrato. Foi construído um biossensor desse extrato bruto da casca de banana nanica com 75 unidades de PFO, imobilizada com reagente glutaraldeído. Resultados - Esse biossensor, sensível a polifenóis, foi caracterizado e apresentou pH ótimo de imobilização da enzima igual a 6,5 e sensibilidade acentuada para o substrato catecol. Também foi utilizado no estudo da determinação da concentração de taninos em amostras de diversos tipos de chás. Conclusões - Foi verificado que a porcentagem de erro comparando com o método espectrofotométrico apresentou valores menores que 1,0% estando, portanto, de acordo com o procedimento padrão oficial. Comparando os resultados obtidos com esse biossensor e o de extrato bruto da polpa de banana nanica observamos, melhor tempo de armazenamento das membranas com a casca do que com a polpa, e uma diminuição significativa na quantidade de extrato imobilizado. Assim, conclui-se que o extrato de PFO da casca é melhor fonte de enzima do que a polpa e, portanto, será usado na construção dobiossensor. A vantagem do método amperométrico apresentado é possuir baixo custo, rapidez nas determinações e boa sensibilidade comparado com métodos cromatográficos.
Introduction - Crude extract of banana nanica (Musa acuminata); the best source of enzyme Poliphenol oxidase (PPO) [EC.1.14.18.1] was studied as biocatalytic material to the aerobic oxidation of phenolics substrates. Materials and Methods - The crude extract of I was done the same as at Perone et al.14 (2000). The activity from the enzyme PPO and total protein were determined in this extract. It has been built a biosensor of this crude extract from the peel of stunded banana with 75unities of PPO immobilized with glutaraldeyde reagent. Results - This biosensor, sensitive to poliphenol, was characterized and presented immobilizing optimium pH of the enzyme equal to 6.5and acute sensibility to its catechol substrate. It was also used at the study of the determination of tanines concentration in samples of many kinds of tea. Conclusions - It was verified that percentage of error comparing with the spectrophotometric method, has presented lower than 1,0% values according to the standard methods. Comparing the results obtained with this biosensor and the crude extract of the pulp of banana nanica, it was observed the better stock time of the membranes with the peel than with the pulp, and significative diminishing of the amount of immobilized extract. So, we conclude that the extract of PPO from the peel is better source of enzyme than the pulp and it will be used at the construction of the biosensor. The advantage of the amperometrics methods presented is to obtain low cost, fast determination and good sensibility compared to cromatographics methods.
Subject(s)
Phenolic Compounds/analysis , Plant Extracts/analysis , Tannins/analysis , Tannins/chemistry , Plants/enzymologyABSTRACT
The interactions between plant secondary metabolites (tannic acid, rutin, cinnamic acid and catechin) and glutathione transferase (GST) were investigated by fluorescence and UV-Vis absorption spectroscopy. Intrinsic fluorescence of GST was measured by selectively exciting their tryptophan (Trp) residues and quenching constants were determined using the Stern-Volmer equation. The binding affinity was found to be strongest for tannic acid and ranked in the order tannic acid>rutin>cinnamic acid>catechin. The pH values in the range of 6.7-7.9, except for tannic acid, did not affect significantly the affinity of rutin, cinnamic acid and catechin with GST. Results showed that the fluorescence quenching of GST was a static_quenching. Fluorescence quenching and UV-Vis absorption spectroscopy suggested that only the tannic acid changed the microenvironment of the Trp residues. Furthermore, the number of binding sites and binding constants at different pH values showed that tannic acid had strongest affinity towards GST and hydrogen bonding played an important role in the affinity between GST and the metabolites.