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The Polygonum hydropiper are dried whole grasses of Polygonum hydropiper L., which mainly contains the following chemical components, such asflavonoids, sesquiterpenoids, and volatile oils. The recent research of the pharmacological effects of Polygonum hydropiper showed that its effects include anti-oxidation, anti-inflammation, analgesic.
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Objective: To improve the survival status of wild Rheum tanguticum, which is threatened to meet the market demand, Illumina high-throughput sequencing technologies is used to bring new directions for relevant research. Methods The complete chloroplast genome of Rheum tanguticum was constructed with Illumina high-throughput sequencing technologies in this paper. Results: The genome was 161 054 bp in length, and exhibited a typical quadripartite structure of the large (LSC, 86 441 bp) and small (SSC, 12 745 bp) single-copy regions, separated by a pair of inverted repeats (IRs, 30 934 bp each). The chloroplast genome contained 132 genes, including 88 protein-coding genes, 36 transfer RNA genes, eight ribosomal RNA genes and two pseudogenes, 19 genes located in each IR area. Conclusion: The phylogenetic tree constructed with 11 sequences of seven Polygonaceae species and four other family species demonstrated a close relationship between R. tanguticum and R. palmatum in Polygonaceae, which was coincided with their morphological similarity, in addition, there were certain SNP sites in rpl32 and other genes, which provided a new basis for the effective identification of related species.
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Objective: To study the chemical constituents from Polygonum multiflorum. Methods: The constituents were isolated and purified by macroporous adsorbent resin (DM-8), gel chromatography, silica chromatography, and other modern separation methods, and the structures were identified by spectral analyses. Results: Ten compounds were isolated and identified as thunberginol C 6-O-β-D-glucopyranoside (1), p-hydroxybenzaldehyde (2), trans-N-caffeoyltyramine (3), (Z)-2,3,5,4'-tetrahydroxy-stilbene-2-O-β-D- glucoside (4), (E)-2,3,5,4'-tetrahydroxy-stilbene-2-O-β-D-glucoside (5), pieceid-2″-O-gallate (6), (E)-2,3,5,4'-tetrahydroxystilbene-2-O-β-D-(3″-galloyl)-glucoside (7), tricin-7-O-β-D-glucoside (8), torachrysone-8-O-β-D-glucoside (9), and emodin-8-O-β-D-glucoside (10). Conclusion: Compound 1 is a new compound named as polygonimitin D. Compounds 3 and 8 are isolated from this plant for the first time.
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A new napthalenone, rumexone A (1), was isolated from the roots of Rumex nepalensis. The structure of 1 was elucidated by extensive spectroscopic analyses, including 1D and 2D NMR spectra and MS data. Its cytotoxic effect was evaluated using four clinically relevant human cancer cell lines, gastric carcinoma SGC7901, breast carcinoma MDA-MB-231, lung carcinoma A549, and hepatocellular carcinoma HepG2.
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The aim of this current study was to evaluate phytochemistry along with pharmacological activities of the whole plant of Rumex maritimus L. (Family: Polygonaceae). Phytochemical analysis of the extract of R. maritimus indicates the presence of Reducing Sugar, Glycoside, Gum, Tannin and Alkaloid type compounds and the pharmacological attention of these compounds prompted us to check R. maritimus for possible anti-oxidant, antimicrobial and antidiarrheal activities in a dose dependent manner. The dried plants were subjected to successive extraction with methanol and the extract was used to investigate the activities. The extract of plants produced good diarrheal inhibition in castor oil induced diarrhea in mice (250mg/kg and 500mg/kg body weight) which was comparable to the standard drug Loperamide at the dose of 3 mg/kg of body weight. The alcoholic extract was showed anti-bacterial activity against the tested microorganisms (both gram positive as well as negative bacteria). This study reveals the potent anti-oxidant activity that is (IC50~80 μg/ml) to that of standard drug ascorbic acid (IC50 about ~7 μg/ml) in-vitro when tested in 1, 1-Diphenyl-2-picrylhydrazyl (DPPH) scavenging method. The obtained results provide a support for the use of this plant in traditional medicine and its further investigation.
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Medicinal plants and herbal preparations are gaining renowned interest in scientific communities nowadays due to their reliable pharmacological actions and affordability to common people which makes them effective in control of various diseases. Polygonum minus (Polygonaceae) locally known as kesum is an aromatic plant commonly used in Malay delicacies. The plant is having potential applications due to its high volatile oil constituents in perfumes and powerful antioxidant activity. It has been used traditionally to treat various ailments including dandruff. The research has been carried out by various researchers using different in vitro and in vivo models for biological evaluations to support these claims. This review paper may help upcoming research activities on Polygonum minus by giving up to date information on the phytochemical constituents and medicinal properties of kesum to a possible extent with relevant data.
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Medicinal plants and herbal preparations are gaining renowned interest in scientific communities nowadays due to their reliable pharmacological actions and affordability to common people which makes them effective in control of various diseases. Polygonum minus (Polygonaceae) locally known as kesum is an aromatic plant commonly used in Malay delicacies. The plant is having potential applications due to its high volatile oil constituents in perfumes and powerful antioxidant activity. It has been used traditionally to treat various ailments including dandruff. The research has been carried out by various researchers using different in vitro and in vivo models for biological evaluations to support these claims. This review paper may help upcoming research activities on Polygonum minus by giving up to date information on the phytochemical constituents and medicinal properties of kesum to a possible extent with relevant data.
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Medicinal plants and herbal preparations are gaining renowned interest in scientific communities nowadays due to their reliable pharmacological actions and affordability to common people which makes them effective in control of various diseases. Polygonum minus (Polygonaceae) locally known as kesum is an aromatic plant commonly used in Malay delicacies. The plant is having potential applications due to its high volatile oil constituents in perfumes and powerful antioxidant activity. It has been used traditionally to treat various ailments including dandruff. The research has been carried out by various researchers using different in vitro and in vivo models for biological evaluations to support these claims. This review paper may help upcoming research activities on Polygonum minus by giving up to date information on the phytochemical constituents and medicinal properties of kesum to a possible extent with relevant data.
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Rumex hastatus is fairly common small shrub, growing on dry slopes, rocks and walls between 700-2500 m, typically in North Indian hill station. Roots of Rumex hastatus have been used in Ayurveda and other folk medicines for the treatment of diarrhoea. To justify its folklore, present study was undertaken to investigate the antidiarrhoeal activity of the ethanolic extract from the roots of Rumex hastatus (EERH). Preliminary phytochemical screening, acute toxicity study and antidiarrhoeal activity of were studied on castor oil induced diarrhoea and normal gastrointestinal models of rats at 100, 150 and 200mg/kg body weight. The preliminary phytochemical screening of the ethanolic extract from the roots of Rumex hastatus (EERH) results with the presence of anthraquinone glycoside, tannins, flavonoids etc., LD50> 2000mg/kg. The doses of EERH significantly decreased (P<0.001) the total number of diarrhoeal faeces. PI decreases doses dependentally (100, 150 and 200mg/kg orally) of EERH and was comparable with standard drug atropine sulphate. Conclusively, EERH has the antidiarrhoeal activity in experimental rats.
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The common everyday use of medicinal plants is an ancient, and still very widespread practice, whereby the need for studies on their possible toxicity and mutagenic properties. The species Coccoloba mollis has been much used in phytotherapy, mainly in cases involving loss of memory and stress. In order to investigate its genotoxic and mutagenic potential, ethanolic extracts from the leaves and roots underwent Salmonella/microsome assaying (TA98 and TA100 strains, with and without exogenous metabolism - S9), besides comet and micronucleus tests in vivo.There was no significant increase in the number of revertants/plate of Salmonella strains in any of the analyzed root-extract concentrations, although the extract itself was extremely toxic to the Salmonella TA98 strain in the tests carried out with S9 (doses varying from 0.005 to 0.5 µg/plate). On the other hand, the leaf-extract induced mutations in the TA98 strain in the absence of S9 in the highest concentration evaluated, although at very low mutagenic potency (0.004 rev/µg). Furthermore, there was no statistically significant increase in the number of comets and micronuclei, in treatments involving Swiss mice. It was obvious that extracts of Coccoloba mollis, under the described experimental conditions, are not mutagenic.
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Animals , Microsomes , Plants, Medicinal , Salmonella , Comet Assay , Micronucleus Tests , Mutagenicity Tests , PolygonaceaeABSTRACT
Polygonum hydropiperoides Michaux é uma espécie conhecida popularmente como "erva-de-bicho", amplamente utilizada na medicina tradicional como anti-hemorroidal, antiinflamatória e antidiarréica. O presente trabalho tem como objetivo a caracterização anatômica e histoquímica da folha, caule e raiz, que constituem a droga vegetal, visando estabelecer parâmetros para o controle de qualidade. O material vegetal foi fixado e submetido às técnicas usuais de microscopia de luz e aos testes histoquímicos. A folha é anfiestomática, dorsiventral e com estômatos paracíticos e anisocíticos. É comum a presença de estruturas secretoras como: tricomas glandulares capitados e glândulas epidérmicas e subepidérmicas em ambas as faces da lâmina foliar e também no caule. O material secretado pelas glândulas apresenta composição heterogênea de lipídios e flavonóides, segundo análises histoquímicas. Cristais de oxalato de cálcio e grãos de amido são freqüentes em células parenquimáticas da folha e do caule. Compostos fenólicos estão presentes na folha (parênquima paliçádico), no caule (parênquima cortical e floema) e na raiz (parênquima cortical).
P. hydropiperoides is popularly known as "erva-de-bicho", and it is used in traditional medicine as anti-hemorroidal, anti-inflammatory and antidiarrhoeic. The present work has as objective the anatomical and histochemical characterization of leaf, stem and root that are used as drug in order to offer elements for quality control. The botanical material was prepared for the usual optical and histochemical microtechniques. The leaf is amphistomatic, dorsiventral and paracytic and anisocytic stomata. It is common to find the presence of secretory structures as: capitate glandular trichomes and secretory glands on both epidermis, that are also present in stem. The secretion material is heterogeneous composition of lipids and flavonoids. Druses of calcium oxalate and starch are common in parenchyma cells of leaf and stem. Phenolic compounds are present in leaf (palisade parenchyma), in stem (cortical parenchyma and phloem) and root (cortical parenchyma).
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The antinociceptive, anti-inflammatory and diuretic properties of the extracts of P. barbatum (L.) Hara var. barbata, Polygonaceae, at the doses of 200 and 400 mg/kg body weight, were evaluated in mice/rat models using, respectively, the acetic-acid-induced writhing method, the carrageenan-induced edema test and the Lipschitz method. In the acetic-acid-induced writhing test in mice, all extracts displayed a dose dependent analgesic effect. The most potent analgesic activity was observed with the petroleum ether extract at the dose of 400 mg/kg body weight with an inhibition of writhing response 46.8 percent compared to 62.2 percent for the positive control aminopyrine. Petroleum ether extract at the dose of 400 mg/kg body weight also displayed the highest levels of anti-inflammatory activity after 2 h with the 39.3 percent inhibition of paw edema, and this effect was better than the effect observed by the conventional anti-inflammatory agent phenylbutazone (maximum inhibition of 38.3 percent after 4 h). All extracts increased urine volume in a dose-dependent manner, and the ethyl acetate extract showed a significant level of diuresis comparable to that of the standard diuretic agent furosemide.
As propriedades antinociceptiva, antiinflamatória e diurética dos extratos de P. barbatum (L.) Hara var. barbata, Polygonaceae, nas doses de 200 e 400 mg/kg de peso corpóreo foram avaliadas em modelos utilizando camundongos/ratos, respectivamente, o método de contorções induzidas por ácido acético, o teste de edema induzido por carragenina e o método de Lipschitz. No método de contorções induzidas por ácido acetic, todos os extratos apresentaram efeito nociceptivo dose dependente. O efeito nociceptivo mais potente foi observado com o extrato de éter de petróleo na dose de 400 mg/kg com uma inibição das contorções de 46,8 por cento comparado com o controle positivo de aminopirina de 62,2 por cento. O extrato de éter de petróleo na dose de 400 mg/kg também mostrou maior atividade antiinflammatoria após 2 h com 39,3 por cento de inibição do edema de pata, e este efeito foi maior que o observado para o agente antiinflamatório convencional fenilbutazona (inibição máxima de 38,4 por cento após 4 h). Todos os extratos aumentaram o volume de urina de maneira dose dependente e o extrato acetato de etila mostrou um nível de significância de diurese comparável ao agente diurético padrão, furosemida.
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O estudo químico das frações neutra em hexano das folhas e em diclorometano do caule de Coccoloba mollis resultou no isolamento de um triterpeno pentacíclico (simiarenol), que pela primeira vez ocorre em Polygonaceae, dois fitoesteróides (sitostenona e sitosterol), um diterpeno (trans-fitol) e de um benzenóide (ácido vanílico) que está sendo descrito pela vez neste gênero. A identificação estrutural destes compostos foi feita com base na análise dos dados espectrais (IV, EM e RMN, incluindo DEPT e HMQC), bem como pela comparação com dados descritos na literatura.
This work describes the isolation of a pentacyclic triterpene (simiarenol), described for the first time in this family, two phytosteroids (sitostenone and sitosterol), a diterpene (trans-phytol) and a benzenoid (vanillic acid), described for the first time in this genus, from leaves and stem of Coccoloba mollis. These compounds were identified on basis of their spectral data (IR, MS and NMR, including DEPT and HMQC), as well as by comparison with literature data.
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The genus Coccoloba is represented in Brazilian Amazonia by twenty three species: Coccoloba acuminata Kunth, C. arborescens (Vell.) R. A. Howard, C. ascendens Duss ex Lindau, C. brasiliensis Nees & Mart., C. charitostachya Standl., C. conduplicata Maguire, C. coronata Jacq., C. declinata (Vell.) Mart., C. densifrons Mart. ex Meisn., C. excelsa Benth., C. gentryi R. A. Howard, C. latifolia Lam., C. lehmannii Lindau, C. lucidula Benth., C. marginata Benth., C. mollis Casar., C. ovata Benth., C. paraensis Meisn., C. parimensis Benth., C. ramosissima Wedd., C. savannarum Standl., C. striata Benth., and C. tenuiflora Lindau. Among that only C. paraensis occurs exclusively in Brazilian Amazonia. C. charitostachya, C. conduplicata, C. coronata, C. gentryi, C. lehmanni and C. savannarum are cited for the first time in Brazil. The major characters of taxonomic relevance are the petiole position in relation to ochrea, the inflorescence ramification, the relative dimensions of bracts and ochreolae, the fruiting perianth and pericarp characters. An identification key, descriptions, and illustrations are given for all taxa, as well as comments about geographic distribution, habitats and phenological dates.
O gênero Coccoloba está representado na Amazônia brasileira por 23 espécies: Coccoloba acuminata Kunth, C. arborescens (Vell.) R. A. Howard, C. ascendens Duss ex Lindau, C. brasiliensis Nees & Mart., C. charitostachya Standl., C. conduplicata Maguire, C. coronata Jacq., C. declinata (Vell.) Mart., C. densifrons Mart. ex Meisn., C. excelsa Benth., C. gentryi R. A. Howard, C. latifolia Lam., C. lehmannii Lindau, C. lucidula Benth., C. marginata Benth., C. mollis Casar., C. ovata Benth., C. paraensis Meisn., C. parimensis Benth., C. ramosissima Wedd., C. savannarum Standl., C. striata Benth. e C. tenuiflora Lindau, dentre as quais apenas C. paraensis ocorre exclusivamente na Amazônia brasileira, C. charitostachya, C. conduplicata, C. coronata, C. gentryi, C. lehmanni e C. savannarum, são citadas pela primeira vez para o Brasil. As características de maior relevância taxonômica são a posição do pecíolo em relação à ócrea, ramificação da inflorescência, tamanhos relativos das brácteas e ocréolas, perianto frutífero e pericarpo. São apresentadas chaves de identificação, descrições e ilustrações, bem como comentários sobre a distribuição geográfica, hábitats e dados fenológicos para todas as espécies estudadas.
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O gênero Coccoloba está representado na Amazônia brasileira por 23 espécies: Coccoloba acuminata Kunth, C. arborescens (Vell.) R. A. Howard, C. ascendens Duss ex Lindau, C. brasiliensis Nees & Mart., C. charitostachya Standl., C. conduplicata Maguire, C. coronata Jacq., C. declinata (Vell.) Mart., C. densifrons Mart. ex Meisn., C. excelsa Benth., C. gentryi R. A. Howard, C. latifolia Lam., C. lehmannii Lindau, C. lucidula Benth., C. marginata Benth., C. mollis Casar., C. ovata Benth., C. paraensis Meisn., C. parimensis Benth., C. ramosissima Wedd., C. savannarum Standl., C. striata Benth. e C. tenuiflora Lindau, dentre as quais apenas C. paraensis ocorre exclusivamente na Amazônia brasileira, C. charitostachya, C. conduplicata, C. coronata, C. gentryi, C. lehmanni e C. savannarum, são citadas pela primeira vez para o Brasil. As características de maior relevância taxonômica são a posição do pecíolo em relação à ócrea, ramificação da inflorescência, tamanhos relativos das brácteas e ocréolas, perianto frutífero e pericarpo. São apresentadas chaves de identificação, descrições e ilustrações, bem como comentários sobre a distribuição geográfica, hábitats e dados fenológicos para todas as espécies estudadas.
The genus Coccoloba is represented in Brazilian Amazonia by twenty three species: Coccoloba acuminata Kunth, C. arborescens (Vell.) R. A. Howard, C. ascendens Duss ex Lindau, C. brasiliensis Nees & Mart., C. charitostachya Standl., C. conduplicata Maguire, C. coronata Jacq., C. declinata (Vell.) Mart., C. densifrons Mart. ex Meisn., C. excelsa Benth., C. gentryi R. A. Howard, C. latifolia Lam., C. lehmannii Lindau, C. lucidula Benth., C. marginata Benth., C. mollis Casar., C. ovata Benth., C. paraensis Meisn., C. parimensis Benth., C. ramosissima Wedd., C. savannarum Standl., C. striata Benth., and C. tenuiflora Lindau. Among that only C. paraensis occurs exclusively in Brazilian Amazonia. C. charitostachya, C. conduplicata, C. coronata, C. gentryi, C. lehmanni and C. savannarum are cited for the first time in Brazil. The major characters of taxonomic relevance are the petiole position in relation to ochrea, the inflorescence ramification, the relative dimensions of bracts and ochreolae, the fruiting perianth and pericarp characters. An identification key, descriptions, and illustrations are given for all taxa, as well as comments about geographic distribution, habitats and phenological dates.
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Classification , Amazonian Ecosystem , PolygonaceaeABSTRACT
Object To study the anthraquinone constituents in rhizoma and radix of Rheum sublanceolatum C Y Cheng et T C Kao Methods The constituents were isolated through column chromatography, and their structures elucidated through physicochemical and spectral analysis Results 6 anthraquinones were isolated and identified as chrysophanol (Ⅰ); physcion (Ⅱ); emodin (Ⅲ); emodin 8 O ? D glucopyranoside (Ⅳ); aloe emodin 8 O ? D glucopyranoside (Ⅴ) and citreorosein (Ⅵ) Conclusion All these compounds were isolated from R sublanceolatum for the first time
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Objective To isolate and determine the structures of chemical constituents from the roots and rootstalks of Rheum emodi.Methods The chemical constituents were isolated and purified by silica gel and polyamide column chromatography.Chemical methods and spectroscopic methods,such as 1H-NMR,13C-NMR,and MS spectra were used for the structure identification.Results Eighteen compounds were obtained.Sixteen of them were identified as:chrysophanol(1),physcion(2),?-sitosterol(3),emodin(4),aloe-emodin(5),rheumin(6),daucosterol(7),d-catechin(8),piceatannol(9),piceatannol-4'-O-?-D-glucopyranoside(10),piceatannol-4'-O-?-D-(6″-O-p-coumaroyl)-glucopyranoside(11),chrysophanol-8-O-?-D-glucopyranoside(12),physcion-1 and 8-O-?-D-glucopyranoside(13a and 13b),emodin-8-O-?-D-glucopyranoside(14),and sucrose(15).Meanwhile,one compound structure simi-lar to rhein was detected.Conclusion Compound 11 is a new compound named rheoside,compounds 13a and 13b are obtained from R.emodi for the first time.