154 research outputs found

    Amino acid, Antioxidant and Ion Profiles of Carpolobia lutea Leaf (Polygalaceae)

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    Purpose: To evaluate the amino acid, antioxidant and ionic profiles of Carpolobia lutea leaf (Polygalaceae) extract (CLL).Methods: The powdered leaf was macerated and subjected to gradient solvent extraction with nhexane, chloroform, ethyl acetate and ethanol for 72 h to obtain their respective fractions. Amino acid analysis was by cation-exchange chromatography using automated amino acid analyser. Antioxidant potential was obtained by spectrophotometric assay using 2, 2-Diphenyl-1-picrylhydrazyl DPPH while elemental and ionic analyses were carried out by atomic absorption spectrophotometry and potentiometric titration, respectively.Results: Proline, alanine, serine, valine, glycine, glutamate and lysine were found in the ethanol fraction while lysine, phenyl alanine, glycine and serine were present in the ethyl acetate fraction but not in the non-polar fractions, n-hexane and chloroform. The ethyl acetate fraction contained more lysine, phenyl alanine, glycine and serine the other leaf fractions. Minimal radical scavenging activity of all the fractions was recorded. The most abundant cations in the extract were potassium and phosphorus (2.16 ± 0.05 and 1.90 ± 0.06 mg/g, respectively) while the most abundant anion was phosphate with a concentration of 23.23 ± 4.61 mg/g for the aqueous leaf fractionConclusion: The study shows that CLL fractions contain variety of amino acids which could promote wound healing, as well as major and minor elemental ions which, as essential body electrolytes, are required for various metabolic processes in the body.Keywords: Carpolobia leaf, Polygalaceae, Amino acid, Antioxidant, Ionic profile

    Antidiarrheal Mechanism And Ionic Profile Of Carpolobia Lutea Ethanolic Stem-Bark Extract In Rats.

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    Background: The stem-bark extract of Carpolobia lutea (Polygalaceae), used in ethno-medicine as anti-diarrhea was pharmacologically evaluated. This was the first report of assessment of the ethanolic stem extract (ESE), of C. lutea as anti-diarrhoeal agent in rats. The anti-diarrhoeal effects, acute toxicity and ionic profile are investigated and reported.Materials and Methods: The acute toxicity was established using Lock’s method. The anti-diarrhoeal effects were demonstrated using castor oilinduced diarrheal and fluid accumulation and its effect on normal intestinal transit. The mechanism elucidated using yohimbine, isosorbide dinitrate, and diphenoxylate. The elemental and ionic profile of ESE was established using inductively coupled argon-plasma emission spectrometer and potentiometric titration respectively. The finger print of ESE was revealed by Jasco (Tokyo, Japan), HPLC and active compounds by phytochemical screening using standard procedure.Results: The LD50 obtained is 866.025 mg/kg (i.p). The doses of 43.3, 86.6, and 173.2 mg/kg of ESE showed inhibition of castor oil–induced diarrheal (p<0.05 - 0.001). The most abundant cations in the extract are potassium and phosphorus (1.00 ±0.01 and 0.80 ± 0.030 mg/g respectively); while the most abundant anions are phosphate and sulphate (33.50±7.09 and 7.19±3.29 mg/g respectively). The HPLC fingerprint of ESE revealed UV spectra of biomolecules. Phytochemical screening revealed presence of saponins, polyphenols and glycosides.Conclusion: These investigations indicate presence of bioactive and elemental substances which could play major role in diarrheal management. This investigation justifies the use of stem-bark of C. lutea in illicit gin (akpatashi), among the Effiks in Nigeria as antidiarrheal.Key words: Carpolobia lutea, stem-bark extract, antidiarrheal, elemental and ionic profile

    Effects of tea from Turnera ulmifolia L. on mouse gastric mucosa support the Turneraceae as a new source of antiulcerogenic drugs

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    Turnera ulmifolia is a plant belonging to the family Turneraceae, popularly known in Brazil as chanana. This species is distributed from Guyana to southern Brazil where it is considered a weed. The plant occurs in tropical rain forest, fields, and gardens. Chanana tea is used in Brazilian folk medicine for the treatment of diseases related mainly to gastric dysfunction including gastric and duodenal ulcers. In this study, the ability of a lyophilized infusion, as an aqueous fraction (AqF) of the aerial parts of T. ulmifolia, was investigated for its ability to prevent ulceration of the gastric and duodenal mucosa was examined in mice and rats, respectively. The AqF significantly reduced the formation of lesions associated with HCl/ethanol administration by 39% and 46%, respectively, at doses of 500 mg/kg and 1000 mg/kg, p.o. The AqF also significantly reduced the incidence of gastric lesions induced by a combination of indomethacin and bethanechol by 58% and 72% at doses of 500 mg/kg and 1000 mg/kg, respectively. In stress-induced gastric ulcer, the inhibition by the AqF was 48%, 57%, and 58% at doses of 250 mg/kg, 500 mg/kg, and 1000 mg/kg, respectively (p<0.05). A pyloric ligature experiment showed that the highest dose of the AqF significantly affected the gastric juice parameters by increasing the pH from 2.5 (control) to 5.3 and decreasing the acid output from 11.3 (control) to 3.7 mEq/ml/4 h. The AqF had no significant effect on duodenal ulcers induced by cysteamine. Preliminary phytochemical screening confirmed that flavonoids were the major constituents of the AqF of T. ulmifolia. These results indicate that this extract has a significant antiulcerogenic effect, as popularly believed.25448749

    Byrsonima Crassa Niedenzu (ik): Antimicrobial Activity And Chemical Study

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    The methanolic extract of leaves from Byrsonima crassa, a Brazilian medicinal plant, was analyzed by CC and HPLC. Four constituents were isolated and identified as quercetin, methyl gallate, (-)-epigallocatechin gallate and quercetin-3-O-(2″-galloyl)-α-L-arabinopyranoside. The methanolic and hydromethanolic extract, as well as fractions, were evaluated regarding their possible antimicrobial activity using in vitro methods. Results showed that both extracts and fractions exhibited significant antimicrobial activity against all tested strains.2617175Agrawal, P.K., (1989) Carbon 13NMR of Flavonoids, , Amsterdam:ElsevierAlzoreky, N.S., Nakahara, K., Antibacterial activity of extracts from some edible plants commonly consumed in Asia (2003) Int J Food Microbiol, 80, pp. 223-230Amarqiuise, A., Che, C.T., Bejar, E., Malone, M.H., Fong, H.H.S., A New Glycolipid from Byrsonima crassifolia (1994) Planta Med, 60, pp. 85-86Basile, A., Sorbo, S., Giordano, S., Ricciardi, L., Ferrara, S., Montesano, D., Cobianchi, R.C., Ferrara, L., Antibacterial and allelopathic activity of extract from Castanea sativa leaves (2000) Fitoterapia, 71, pp. S110-S116Bauer, A.W., Kirby, M.D.K., Sherries, J.C., Truck, M., Antibiotic susceptibilities testing by standard single disc diffusion method (1966) Am J Clin Pathol, 45, pp. 493-496Bejar, E., Amarquaye, A., Che, C.T., Malone, M.H., Fong, H.H.S., Constituents of Byrsonima crassifolia and their spasmogenic activity (1995) Int J Pharmacog, 33, pp. 25-32Binutu, O.A., Cordell, G.A., Gallic acid derivatives from Mezoneuron benthamianum leaves (2000) Pharm Biol, 38, pp. 284-286Djipa, C.D., Delmee, M., Quetin-Leclercq, J., Antimicrobial activity of bark extracts of Syzygium jambos (L.) Alston (Myrtaceae) (2000) J Ethnopharmacol, 71, pp. 307-313Geiss, F., Heinrich, M., Hunkler, D., Rimpler, H., Heinrich, M., Proanthocyanidins with (+)-epicatechin units from Byrsonima crassifolia bark (1995) Phytochemistry, 39, pp. 635-643Gottlieb, O.R., Henriques Mendes, P., Taveira Magalhães, M., Triterpenoids from Byrsonima verbascifolia (1975) Phytochemistry, 14, pp. 1456-1456Harborne, J.B., (1996) The Flavonoids: Advances in Research since 1986, , New York:Chapman & HallLopez, A., Hudson, J.B., Towers, G.H.N., Antiviral and antimicrobial activities of Colombian medicinal plants (2001) J Ethnopharmacol, 77, pp. 189-196Martínez-Vasquéz, M., González-Esquinca, A.R., Cazares Luna, L., Moreno Gutiérrez, M.N., García-Argáez, A.N., Antimicrobial activity of Byrsonima crassifolia (L.) H.B.K (1999) J Ethnopharmacol, 66, pp. 79-82Mendes, C.C., Cruz, F.G., David, J.M., Nascimento, I.P., David, J.P., Triterpenes esterified with fatty acid and triterpene acids isolated from Byrsonima microphylla (1999) Quím Nova, 22, pp. 185-188Nascimento, G.G.F., Locatelli, J., Freitas, P.C., Silva, G.L., Antibacterial activity of plants extracts and phytochemicals on antibiotic-resistant bacteria (2000) Braz J Microbiol, 31, pp. 247-256(2003) Performance Standards for Antimicrobial Disc Susceptibility Tests, , Approved Standard M2-A7, Pennsylvania:WaynePenna, C., Marino, S., Vivot, E., Cruanes, M.C., Munoz, J.D., Cruanes, J., Ferraro, G., Martino, V., Antimicrobial activity of Argentine plants used in the treatment of infectious diseases. Isolation of active compounds from Sebastiania brasiliensis (2001) J Ethnopharmacol, 77, pp. 37-40Pretorius, J.C., Magama, S., Zietsman, P.C., Purification and identification of antibacterial compounds from Euclea crispa subsp crispa (Ebenaceae) leaves (2003) S Afr J Bot, 69, pp. 579-586Rastrelli, L., De Tommasi, N., Berger, I., Caceres, A., Saravia, A., De Simone, F., Glycolipids from Byrsonima crassifolia (1997) Phytochemistry, 45, pp. 647-650Sannomiya, M., Rodrigues, C.M., Coelho, R.G., Santos, L.C., Hiruma-Lima, C.A., Souza Brito, A.R.M., Vilegas, W., Application of preparative high-speed counter-current chromatography for the separation of flavonoids from the leaves of Byrsonima crassa Niedenzu (IK) (2004) J Chromatogr A, 1035, pp. 47-51Sannomiya, M., Fonseca, V.B., Da Silva, M.A., Rocha, L.R.M., Dos Santos, L.C., Souza, H.C.A., Brito, A.R.M., Vilegas, W., Flavonoids and antiulcerogenic activity from Byrsonima crassa leaves extracts (2005) J Ethnopharmacol, 97, pp. 1-6Silva, S.R., Silva, A.P., Munhoz, C.B., Silva Jr., M.C., Medeiros, M.B., (2001) Guia de Plantas Do Cerrado Utilizadas Na Chapada Dos Veadeiros, , Brasília:WWF58pSrinivasan, D., Nathan, S., Suresh, T., Perumalsamy, P.L., Antimicrobial activity of certain Indian medicinal plants used in folkloric medicine (2001) J Ethnopharmacol, 74, pp. 217-220Wagner, H., Bladt, H., Zgainski, E.M., (1984) Plant Drug Analysis, , Berlin:Springer320

    Avaliação da atividade mutagênica do extrato etanólico bruto de Paepalanthus latipes (Eriocaulaceae) e dos compostos flavonoídicos 7-metoxilados relacionados

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    Paepalanthus latipes (Silveira) é uma das plantas brasileiras nativas da Serra do Cipó, Minas Gerais, conhecida como sempre-vivas e muito exportada para os Estados Unidos, Europa e Japão, por seu valor ornamental. Poucos resultados são relatados quanto à atividade biológica destas plantas. Este trabalho teve como objetivo avaliar a atividade mutagênica do extrato etanólico bruto de P. latipes e de dois flavonóides 7-metoxilados dele isolados (7-metilquercetagetina e 7-metilquercetagetina-4'-O-β-D-glicopiranosídeo), através do teste de Ames, utilizando linhagens mutantes de Salmonella typhimurium TA98 e TA100. A atividade mutagênica das amostras testadas, em concentrações variando de 62,5 a 375 μg/placa, foi determinada com ativação metabólica (utilizando-se a fração microssomal S9) e na ausência dessa. Os resultados demonstraram que, tanto o extrato etanólico bruto de P. latipes quanto os flavonóides 7-metoxilados testados, não induziram atividade mutagênica nas linhagens TA98 e TA100.Paepalanthus latipes (Silveira) is one of the native Brazilian plants from Serra do Cipó, Minas Gerais, known as sempre-vivas which is exported to the United States, Europe and Japan because of its ornamental value. Few results were reported in relation to the biological activity of these plants. In this work, the mutagenicity of the crude ethanolic extract of P. latipes and isolated 7-methoxyflavonoids (7-methylquercetagetin and 7-methylquercetagetin-4'-O-β-D-glucopyranoside) was evaluated by using the Ames test with Salmonella typhimurium TA98 and TA100 strains, at concentrations from 62.5 to 375 μg/plate, with and without metabolic activation (using microsomal S9 fraction). Results demonstrated that both the extract of P. latipes as well as the tested 7-methoxyflavonoids did not induce mutagenicity at the experimental tested conditions

    Antiulcerogenic activity of four extracts obtained from the bark wood of Quassia amara L. (Simaroubaceae)

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    Quassia amara L., a neotropical forest shrub of the Simaroubaceae family, is widely used in Caribbean folk medicine and in some northern states of Brazil for the treatment of gastric ulcers. This plant is a source of numerous compounds including both beta-carbonile and cantin-6 alkaloids as well as, primarily, the bitter compounds known as quassinoids. We analyzed the possible antiulcerogenic activities of four extracts of different polarities: 70% ethanol (70% EtOH), 100% EtOH, 100% dichloromethane (DCM), and 100% hexane (HEX) obtained from Quassia amara bark. All extracts, administered at doses of 5000 mg/kg orally and 1000 mg/kg intraperitoneally, caused neither toxicity or death. In the indomethacin[bethanechol-induced gastric ulcer, 70% EtOH, 100% EtOH, DCM and HEX extracts, 100 mg/kg, p.o., inhibited the gastric ulcer (22.5, 23.4, 50.5, 46.8%, respectively). 70% EtOH, 100% EtOH, DCM, and HEX extracts reduced the gastric injury induced by the hypothermic restraint-stress test in mice (70.7, 80, 60, 82.7%, respectively). In the pylorus ligature of the mouse stomach, following pre-treatment with a single intraduodenal administration of 100 mg/kg of each extract, only 70% EtOH did not change the biochemical parameters of gastric juice. 100% EtOH, DCM and HEX extracts presented decreased gastric juice content, increased pH values and decreased acid output. We also determined the antiulcerogenic activity on HCl-EtOH-induced gastric ulcers in mice at four doses (25, 50, 75, 100 mg/kg, p.o.), then evaluated the possible dose-dependent relation and calculated the ED50 values. Except for 70% EtOH at a dose of 25 mg/kg, the other extracts showed significantly activity (p<0.05). The free mucous amount in the gastric stomach content was also evaluated. All extracts showed significant increases (p<0.05) of free mucous. This effect was abolished when the animals were pre-treated with indomethacin. Prostaglandin synthesis was evaluated by the administration of HEX extracts by the oral route (100 mg/kg). Prostaglandin synthesis was significantly, increased by 52.3% (p<0.05), and this effect was abolished with prior administration of indomethacin. We concluded that Quassia amara is a probable source for a new drug to treat gastric ulcers, and the mechanism of its activity relates to cytoprotective factors, such as mucous and prostaglandins, but there is still the possibility that antisecretory activity is involved in its antiulcerogenic effect.2591151115

    Cissus Sicyoides: Pharmacological Mechanisms Involved In The Anti-inflammatory And Antidiarrheal Activities

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    The objective of this study was to evaluate the pharmacological mechanisms involved in anti-inflammatory and antidiarrheal actions of hydroalcoholic extract obtained from the leaves of Cissus sicyoides (HECS). The anti-inflammatory effect was evaluated by oral administration of HECS against acute model of edema induced by xylene, and the mechanisms of action were analysed by involvement of arachidonic acid (AA) and prostaglandin E2 (PGE2). The antidiarrheal effect of HECS was observed and we analyzed the motility and accumulation of intestinal fluid. We also analyzed the antidiarrheal mechanisms of action of HECS by evaluating the role of the opioid receptor, α2 adrenergic receptor, muscarinic receptor, nitric oxide (NO) and PGE2. The oral administration of HECS inhibited the edema induced by xylene and AA and was also able to significantly decrease the levels of PGE2. The extract also exhibited significant anti-diarrheal activity by reducing motility and intestinal fluid accumulation. This extract significantly reduced intestinal transit stimulated by muscarinic agonist and intestinal secretion induced by PGE2. Our data demonstrate that the mechanism of action involved in the anti-inflammatory effect of HECS is related to PGE2. The antidiarrheal effect of this extract may be mediated by inhibition of contraction by acting on the intestinal smoothmuscle and/or intestinal transit. © 2016 by the authors; licensee MDPI, Basel, Switzerland.17

    Antimicrobial activity of Byrsonima species (Malpighiaceae)

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    Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Byrsonima species, family Malpighiaceae, is popularly known as 'murici'. There are several properties attributed to the leaves of Byrsonima species including febrifuge, to treat gastrointestinal dysfunctions and skin diseases. In this work, the antimicrobial activity of Byrsonima fagifolia, B. basiloba and B. intermedia extracts obtained from the leaves were evaluated by using the disc-diffusion method. The results obtained showed that the methanol extracts of leaves had presented antimicrobial activity against all the microorganisms tested.18690695Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq

    Chronic administration of Abarema cochliacarpos attenuates colonic inflammation in rats

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    Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Inflammatory bowel diseases are characterized by a chronic clinical course of relapse and remission associated with self-destructive inflammation of the gastrointestinal tract. Active extracts from plants have emerged as natural potential candidates for its treatment. Abarema cochliacarpos (Gomes) Barneby & Grimes, Fabaceae (Barbatimao), is a native medicinal plant in to Brazil. Previously we have demonstrated in an acute colitis model a marked protective effect of a butanolic extract, so we decided to assess its anti-inflammatory effect in a chronic ulcerative colitis model induced by trinitrobenzensulfonic acid (TNBS). Abarema cochliacarpos (150 mg/day, v.o.) was administered for fourteen consecutive days. This treatment decreased significantly macroscopic damage as compared with TNBS. Histological analysis showed that the extract improved the microscopic structure. Myeloperoxidase activity (MPO) was significantly decreased. Study of cytokines showed that TNF-alpha was diminished and IL-10 level was increased after Abarema cochliacarpos treatment. In order to elucidate inflammatory mechanisms, expression of cyclooxygenase (COX)-2 and nitric oxide synthase (iNOS) were studied showing a significant downregulation. In addition, there was reduction in the JNK and p-38 activation. Finally, I kappa B degradation was blocked by Abarema cochliacarpos treatment being consistent with an up-regulation of the NF-kappaB-binding activity. These results reinforce the anti-inflammatory effects described previously suggesting that Abarema cochliacarpos could provide a source for the search for new anti-inflammatory compounds useful in ulcerative colitis treatment.214680690Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Universidade Estadual de Alagoas, BrazilInstituto Federal de Educacao Ciencia e Tecnologia-Sergipe, BrazilCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES
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