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Functionalization of C-aryl glycals and studies toward the total synthesis of 5-hydroxyaloin AProcko, Kristen Jean 16 February 2015 (has links)
In the context of ongoing efforts toward C-aryl glycoside synthesis, a recently developed approach to form C-aryl glycals from 2-deoxysugar lactones was expanded to form novel substrates. This approach has been applied to the synthesis of various furyl glycals, allowing access to C-aryl glycals via a benzyne furan (4+2) cycloaddition methodology. The hydroboration-oxidation of said C-aryl glycals has allowed access to C(2)-oxygenated C-aryl glycosides via the benzyne cycloaddition approach. An approach to the total synthesis of 5-hydoxyaloin A is detailed, in which regioselective benzyne furan (4+2) cycloadditions were achieved via the use of a silicon tether. Two approaches to the anthrone core have been applied; one in which an unsymmetrically-substituted aryl ring is first constructed by means of a silicon tether, and one in which the unsymmetrically-substituted ring is formed last, also utilizing a silicon tether. The latter approach has allowed access to the anthrone core of 5-hydroxyaloin A, and only a final desulfurization remains in order to access the natural product. / text
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The population status of the threatened endemic plant Aloe peglerae in the Magaliesberg mountain range.Phama, Justin Onkemetse. January 2013 (has links)
Thesis (MTech. Nature Conservaion) -- Tshwane University of Technology 2013. / The aim of this study was to determine the current population status of Aloe peglerae in the Magaliesberg Mountain Range.
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Regulation of hyperhydricity in Aloe polyphylla propagated in vitro.Ivanova, Mariyana Vasileva. January 2009 (has links)
Micropropagation of Aloe polyphylla, an endangered species with a high ornamental and medicinal value, is an important part of its conservation. However, the in vitro culture was hindered by the phenomenon of hyperhydricity. The research reported in this thesis was undertaken for two reasons. Firstly, to understand the role of various culture factors involved in the process of hyperhydricity in A. polyphylla and to identify the in vitro conditions, under which this disorder can be prevented. Secondly, we conducted an investigation into the underlying mechanisms of this phenomenon by probing if it was mediated through internal cytokinins. Ammonium (NH4 +) ions, applied cytokinins (CKs) and CK concentrations were tested in multifactorial combinations and significantly influenced the regeneration rate and occurrence of hyperhydricity. Shoots were grown on media with different NH4 + concentrations (10.3, 20.6 and 61.8 mM) and supplemented with BA, zeatin or TDZ at 0, 5 or 15 ìM. Elevating the levels of NH4 +, in the absence of CKs, could not induce hyperhydricity. Similarly, very low hyperhydricity was observed when CKs were added to media containing low NH4 + (10.3 mM). However, in the presence of higher NH4 + concentrations, CKs increased hyperhydricity in a concentrationdependant manner, suggesting that they were capable of inducing this syndrome only when other factors in the culture system were not optimised. High numbers of healthy looking shoots were produced on media with low NH4 + and low BA or zeatin (5 ìM). The use of TDZ resulted in the formation of buds, which did not develop into shoots. In view of the fact that NH4 + was supplied in the form of NH4NO3, it was difficult to determine if NH4 + or nitrate (NO3 -) ions were associated with the increase in hyperhydricity. We further examined the role of nitrogen (N) supplied as inorganic NH4 + or NO3 -, or organic glutamine. The omission of total N from the culture medium resulted in low multiplication and hindered shoot growth. Ammonium as the sole source of N depressed shoot regeneration and growth and escalated the frequency of hyperhydricity to ca. 50%. When NO3 - was used as the sole N source, shoots of fine quality were produced and hyperhydricity was completely eliminated. Overall, the MS N mix was superior to any single N source for multiplication and growth of shoots, suggesting a synergistic effect between NH4 + and NO3 - on shoot regeneration. Furthermore, not only the absolute amount of N, but also the relative amounts of NH4 + and NO3 - influenced the multiplication rate, frequency of hyperhydricity and shoot quality. The highest regeneration was obtained with NH4 + : NO3 - ratios (mM) of 20 : 40, 30 : 30 and 40 : 20. Decreasing the ratio of NH4 + : NO3 - lowered the occurrence of hyperhydricity. The potential of glutamine as the sole source of N was also demonstrated, since its application resulted in the production of good quality shoots and almost no hyperhydricity. Shoot explants grown in static liquid media became hyperhydric and lost their ability to regenerate. The type of gelling agent used to solidify the medium affected greatly hyperhydricity and shoot multiplication. Gelrite resulted in a significantly lower multiplication rate and four times higher hyperhydricity (64.7%) compared to when agar was used. Gelrite was further selected to test the hypothesis if hyperhydricity can be overcome by decreasing the relative matric potential of the media, and respectively the availability of water, as represented by increasing gelrite concentrations. Satisfactory reduction in hyperhydricity was achieved only at 16 g l-1 gelrite, however the regeneration also decreased. The nature of the gelling agent is therefore essential for the successful control of this phenomenon. It appears that a crucial prerequisite for the reduction of hyperhydricity in tissue cultures of A. polyphylla is the gaseous exchange between the in vitro atmosphere and the outside environment. In ventilated cultures, achieved by using a modified lid with a hole (d = 7 mm) covered with polyester or cotton mesh, hyperhydricity was completely eliminated, irrespectively of the type of gelling agent. Ventilation was further advantageous for the in vitro regenerants by increasing their leaf chlorophyll content as well as epicuticular wax deposition, the last one being indicative of the development of the water loss regulation mechanisms of explants. The increased culture ventilation, however, was negatively correlated with the regeneration rate and shoot growth. Endogenous CKs were measured in in vitro regenerants after an eight-week cycle to examine whether the hyperhydricity-inducing effect of exogenous CKs and gelling agents is associated with changes in the endogenous CK content. The content of endogenous CKs, determined by HPLC-mass spectrometry, in the shoots grown on CK-free media comprised isopentenyladenine-, trans-zeatin- and cis-zeatin-type CKs. The application of exogenous CKs resulted in an increase in the CK content of the shoots. Following application of zeatin, dihydrozeatin-type CKs were also detected in the newly-formed shoots. Application of BA to the media led to a transition from isoprenoid CKs to aromatic CKs in the shoots. Shoots grown on gelrite media contained higher levels of endogenous CKs compared to those on agar media. Total CK content of hyperhydric shoots was higher than that of normal shoots grown on the same medium. We suggest that the ability of exogenous CKs and gelrite to induce hyperhydricity in shoots of Aloe polyphylla is at least partially due to up-regulation of endogenous CK levels. However, hyperhydricity is a multifactor process in which different factors intervene. / Thesis (Ph.D.)-University of KwaZulu-Natal, Pietermaritzburg, 2009.
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Extração e avaliação das propriedades físicas, quimicas e biológicas do gel de aloe vera para aplicação em ecografia.SILVA NETO, Oscar Gomes da. 21 June 2018 (has links)
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Previous issue date: 2018-06-21 / A ecografia é um dos métodos de diagnóstico por imagem mais versátil e difundido na
atualidade, de aplicação relativamente simples, basear-se no fenômeno de interação de
uma onda mecânica com os tecidos corporais, ou seja, observa as propriedades
mecânicas dos tecidos ao longo da propagação da onda pelos mesmos, necessitando de
um gel de acoplamento acústico para aumentar o contato entre a pele e o aparelho. A
Aloe vera (Aloe barbadensis Miller) é uma planta suculenta perene, que desenvolve um
tecido de armazenamento de água no interior das folhas, o gel, para sobreviver em zonas áridas de pluviosidade baixa ou irregular. Desta forma, este trabalho objetivou a extração do gel de Aloe vera, com subsequente análise de suas propriedades físicas, químicas e biológicas. Foram realizados testes de avaliação da sua funcionalidade para aquisição de imagens por ecografia e, por fim, realizado estudo comparativo com imagens ecográficas adquiridas com o gel de Aloe vera e com o gel comercial atualmente utilizado. O gel de Aloe Vera a 100% foi extraído da própria planta, processado e caracterizado por espectroscopia na Região do Infravermelho com Transformada de Fourier (FTIR), espectroscopia por Energia Dispersiva de raios X (EDS), Ensaio de Citotoxicidade e Ecografia. As análises foram realizadas no Laboratório de Desenvolvimento e Avaliação de Biomateriais (CERTBIO). O gel de Aloe vera quando utilizado para fins de obtenção de imagem, apresentou resultado igual ou superior às imagens obtidas com o gel comercial, podendo ter ocorrido devido a menor resistência oferecida pelo mesmo e consequentemente maior condutividade, provavelmente pela maior quantidade de íons livres, permitindo a diminuição da impedância do transdutor em relação à pele, promovendo a propagação do ultrassom desde o transdutor até os órgãos avaliados. Com base nos resultados obtidos nos ensaios de Espectroscopia na Região do Infravermelho com Transformada de Fourier, Espectroscopia por Energia Dispersiva de raios X, Citotoxicidade e Exames Ecográficos, pode-se concluir que os materiais
apresentam características semelhantes, indicando que o gel de Aloe vera possa ser utilizado em exames de ultrassonografia. / Ultrasound is a diagnostic methods for more versatile and widespread image today,
relatively simple application, be based on the interaction phenomenon of a mechanical wave with body tissues, ie observe the mechanical properties of tissues along the Wave propagation through the same, necessitating an acoustic coupling gel to increase the contact between the skin and the device. Aloe vera (Aloe barbadensis Miller) is a succulent perennial plant which develops a water storage tissue sheets within the gel, to survive in arid zones of low rainfall or irregular. Thus, this study aimed to extract the gel of Aloe vera, with subsequent analysis of their physical, chemical and biological properties, as well as evaluation tests were carried out of its functionality for image acquisition by ultrasound and finally performed study comparison with ultrasound images acquired with the gel of Aloe vera and commercial gel currently used. The gel of Aloe Vera 100% was extracted from the plant itself, processed and characterized by Spectroscopy in Infrared Region Fourier Transform (FTIR) Spectroscopy Energy Dispersive X-ray (EDS), Cytotoxicity and ultrasound test. The analyzes were performed at the Development Laboratory and Biomaterials Assessment (CERTBIO). The Aloe vera gel when used for the purpose of obtaining image presented results equal to or better than the images obtained with the commercial gel and this may be due to lower resistance of the same and therefore higher conductivity and this can probably allow the reduction of the impedance of the transducer relative to the skin, promoting the propagation of ultrasound from the transducer to the evaluated organs. Since based on the results obtained in tests spectroscopy in the infrared Fourier transform spectroscopy, by Energy Dispersive X-ray, ultrasound examinations and cytotoxicity, it can be concluded that the materials have similar characteristics indicative that the aloe vera gel may be used on ultrasound examination.
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Análise da citotoxicidade e genocitoxicidade da Aloe vera associada a medicamento endodôntico e fotobiomodulação a laserCarvalho, Nayane Chagas 02 December 2016 (has links)
This study aims to evaluate the effect of a drug in order to avoid the appearance of side effects of human pulp fibroblasts. The groups were divided into: CTR with culture medium with fibroblasts; CL, FTL only; AA, Aloe vera with distilled water; AL, Aloe vera with distilled water and FTL; HA, calcium hydroxide P.A. With distilled water; HL, calcium hydroxide P.A. With distilled water and FTL; HAA, calcium hydroxide P.A. With Aloe vera and distilled water; HAL, calcium hydroxide P.A. With Aloe vera, distilled water and FTL. Cytotoxicity evaluation was performed with the MTT reagent at 24, 48 and 72 h, for the evaluation of genotoxicity the micronucleus test was used in 24 h. At 24 h, the CL group presented a greater media of cellular viability, and the HA showed lower mean but stimulated greater number of cell division. At 48 h, the CL group presented a higher medium of cellular viability of high genotoxicity, and the HAL showed lower mean. The AL group showed a higher percentage of surviving cells in 72 h with statistic different from the HA and HL groups (p <0.05). (P <0.001) and to the AA group (p <0.01). The AL group exhibited high genotoxicity with significant results when the CTR group (p <0.001) and the AA group (p <0.01). It is concluded that Aloe vera allowed a greater cell viability in human pulp fibroblasts in the presence of calcium hydroxide, with the increase of the genotoxicity increase in this association. Calcium hydroxide and an FTL showed higher cytotoxicity. / Este estudo objetiva avaliar in vitro o efeito da Aloe vera associada a medicamento de uso endodôntico combinados ou não a FTL em fibroblastos pulpares humanos FP6. Os grupos foram divididos em: CTR com meio de cultura com fibroblastos; CL, apenas FTL; AA, Aloe vera com água destilada; AL, Aloe vera com água destilada e FTL; HA, hidróxido de cálcio P.A. com água destilada; HL, hidróxido de cálcio P.A. com água destilada e FTL; HAA, hidróxido de cálcio P.A. com Aloe vera e água destilada; HAL, hidróxido de cálcio P.A. com Aloe vera, água destilada e FTL. A avaliação da citotoxicidade sucedeu-se com o reagente MTT em 24, 48 e 72 h e, para avaliação da genotoxicidade utilizou-se o teste de micronúcleo em 24 h. Em 24 h, o grupo CL apresentou a maior média de viabilidade celular, e o HA mostrou menor média mas estimulou maior número de divisão celular. Em 48 h, o grupo CL apresentou a maior média de viabilidade celular apesar da elevada genotoxicidade, e o HAL mostrou menor média. O grupo AL demonstrou maior percentual de células sobreviventes em 72 h com diferença estatística dos grupos HA e HL (p<0,05). O grupo AL exibiu alta genotoxicidade tendo resultados significantes quando em comparação com o grupo CTR (p<0,001) e ao grupo AA (p<0,01). Conclui-se que a Aloe vera permitiu uma maior viabilidade celular em fibroblastos pulpares humanos na presença do hidróxido de cálcio, contudo houve aumento da genotoxicidade nessa associação. Já o hidróxido de cálcio e a FTL apresentaram maior citotoxicidade.
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Contributions to the systematics and biocultural value of Aloe L. (Asphodelaceae)Grace, Olwen Megan 13 July 2009 (has links)
Aloe L. (Asphodelaceae) is a monocotyledonous group of considerable popularity among succulent plant collectors and with a long history of medicinal use. It comprises ca. 500 species occurring throughout Africa, the Arabian Peninsula and western Indian Ocean islands. The first comprehensive ethnobotanical study of Aloe (excluding the cultivated A. vera) was undertaken using the literature as a surrogate for data gathered by interview methods. Over 1400 use records representing 173 species were collated, the majority (74%) of which described medicinal uses, including species used for natural products. In southern Africa, 53% of approximately 120 Aloe species in the region are used for health and wellbeing. Consensus ratios indicated that the uses of Aloe spp. for medicine and pest control are of the greatest biocultural importance. Utility has contributed to the recognition of diversity, taxonomic complexity, and conservation concerns, in Aloe. A systematic evaluation of the problematic maculate (spotted) species complex, section Pictae, was undertaken. New sequences were acquired of the nuclear ribosomal internal transcribed spacer (ITS), chloroplast trnL intron, trnL–F spacer and matK gene in 29 maculate species of Aloe. A well supported monophyletic (holophyletic) maculate group was recovered in phylogenetic trees of comparable topology generated by parsimony analysis and Bayesian inference. A representative of the related section Paniculatae, A. striata, was recovered in the maculate group, whereas doubtful maculate species with unusual floral morphology (A. leptosiphon and A. suffulta) comprised a sister group. Analogous patterns were identified in chemosystematic and comparative morphological studies of 34 and 36 maculate species, respectively, and insights were gained into interspecific relationships. The flavonoids isoorientin and isovitexin, and a new C-glycosylanthrone, 6′-malonylnataloin, were characterised using hyphenated chromatographic techniques and nuclear magnetic resonance (NMR) spectroscopy. Leaf surface sculpturing, stomata and lobes surrounding the epistomatal pore observed under a scanning electron microscope (SEM) are of potential taxonomic significance. Available evidence indicates that floral characters, namely a basally swollen perianth with constriction above the ovary, are of greater significance than maculate leaves as synapomorphies for section Pictae. An evolutionary hypothesis for section Pictae excludes marginal maculate species with unusual flowers. / Thesis (PhD)--University of Pretoria, 2009. / Plant Science / unrestricted
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Micropropagação e acompanhamento bioquímico, fisiológico e nutricional da babosa (Aloe vera (L.) Burm. f.) cultivada ex vitro em doses de nitrogênio / Micropropagation and biochemical, physiological and nutritional aspects of Aloe vera (L.) burm.f cultivated ex vitro under nitrogen ratesOliveira, Enio Tiago de 14 December 2007 (has links)
A babosa (Aloe vera (L.) Burm. f.), família Asphodelaceae, reconhecida e explorada mundialmente pela indústria farmacêutica e cosmética devido aos princípios medicinais de seus compostos fenólicos e principalmente ao gel de polissacarídeos específicos, foi submetida a dois experimentos interligados. O primeiro, refere-se a micropropagação no qual foram avaliados tratamentos de desinfestação de ápices caulinares, multiplicação in vitro e condições de aclimatação ex vitro. O segundo experimento refere-se ao cultivo das plantas em areia lavada e irrigada com solução nutritiva, em condições controladas de casa de vegetação, onde foram testados os efeitos de doses (105; 210 e 315 ppm) de nitrogênio avaliados aos 90; 180 e 270 dias de cultivo. Os efeitos foram avaliados em função dos teores foliares dos macronutrientes e dos micronutrientes boro, cobre, ferro manganês e zinco, de proteínas totais solúveis (PTS), de açúcares redutores (AR) e açúcares totais solúveis (ATS) e sobre o crescimento por meio do índice de área foliar (IAF), da taxa de assimilação líquida (TAL), taxa de crescimento relativo (TCR), taxa de crescimento absoluto (TCA) e incrementos de massas de matérias fresca (IMMF) e seca (IMMS). Todos os dados foram analisados estatisticamente. Em relação a micropropagação, a eficiência de desinfestação foi aumentada em torno de 40% na obtenção de ápices caulinares verdes em início de brotação quando as plantas colhidas a campo foram previamente desinfestadas por lavagem com solução de hipoclorito de sódio com 0,5% de cloro ativo ou com solução de dicloroisocianurato de sódio (Sumaveg®) 0,66%. p.v-1 e os ápices caulinares submetidos a imersões alternadas nas soluções dos dois produtos utilizados. A fase multiplicativa da microproagação em meio MS apresentou um rendimento de 1:5,3 a cada intervalo de 30 dias de multiplicação. A partir de 136 ápices caulinares desinfestados, verdes, em início de brotação, foram obtidas 40.495 microplantas. Classificadas em pequenas, médias e grandes, foram submetidas a condições de aclimatação observando-se que bandejas de 64 células com 40 cm3 de substrato apresentaram economia em torno de 50% de substrato e em espaço físico na casa-de-vegetação com micro-aspersão e exaustão de ar em sistema \"pad-house\", e durante o processo de aclimatação e transporte das microplantas aclimatadas. Em relação ao cultivo das plantas em doses de nitrogênio, apesar de algumas variáveis responderem melhor à dose de 105 ppm e outras à dose de 315 ppm, a dose de 210 ppm de nitrogênio favoreceu as melhores respostas para os teores de açúcares totais solúveis (504,21 mgATS.g-1 de MMS), que são diretamente relacionados ao conteúdo de polissacarídeos específicos, de interesse comercial da cultura de Aloe vera. Esses teores, por sua vez, foram propiciados pelos melhores valores de IAF, TCA, IMMF e IMMS, todos observados aos 270 dias de cultivo, ratificando a significância do fator tempo e da dose de 210 ppm de nitrogênio no cultivo dessa espécie vegetal. / Aloe vera (L.) Burm. f., family Asphodelaceae, worldwide renowned and explored by pharmaceutics and cosmetics industries due to its phenolics bearing medicinal principles and mainly to the specific polysaccharides present in the gel, was submitted to two interlinked experiments. The first one refers to apical shoot micropropagation evaluating different disinfection treatments of the explants, the in vitro bud multiplication and ex vitro acclimatization of the microplants. The second one refers to cultivation in greenhouse of the micropropagated plants in washed sand and irrigated with nutritive solution, in the presence of three nitrogen rates (105, 210 and 315 ppm); the plant material was harvested at 90-, 180- and 270-day. All data were statistically analyzed. The effects of nitrogen were evaluated on the content of the macronutrients, the following micronutrients: B, Cu, Fe, Mn and Zn and total soluble proteins, reducing sugars, total soluble sugars; the growth of the Aloe vera plants was measured through the foliar area index, the rate of liquid assimilation, rates of relative and absolute growth and increases in the fresh and dry weights. In regards to micropropagtion, the efficiency of the disinfection process was increased by 40% when the plants harvested in the field were previously washed either with sodium hypochloride (0.5% active chlorine) solution or sodium dichloroisocyanurate (Sumaveg®) 0.66% w.v-1 solution and the apical shoots explants were afterwards alternatively treated with the two disinfectants. The multiplication phase in MS medium showed a rate of 1:5.3 of microplant production at each 30-day interval with a production of 40.495 microplants out of the 136 initial disinfected apical shoots. The microplants were classified as small, medium and large plants and acclimatized in polyethylene trays bearing 64 cells with 40 cm3 of substrate each cell, a 50% saving in terms of substrate amount and free space in the greenhouse equipped with micro-aspersion irrigation, pad-house and air exhaustion systems and also in the transport of the acclimatized microplants. In regards to the effect of nitrogen rates on the development of Aloe vera plants, besides the fact that the best responses were observed either to 105 ppm or 315 ppm nitrogen by some variables, at 210 ppm nitrogen rates the best result was obtained for total soluble sugars (504.21 mg.g-1DW); the sugars are directly related to specific polysaccharides of Aloe vera and are of great importance for the industries. On the other hand, these values were favored by the best values reached by the physiological variables studied in this work at 270-day validate the significance of the time factor and the 210 ppm N rates in the Aloe vera production system.
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Micropropagação e acompanhamento bioquímico, fisiológico e nutricional da babosa (Aloe vera (L.) Burm. f.) cultivada ex vitro em doses de nitrogênio / Micropropagation and biochemical, physiological and nutritional aspects of Aloe vera (L.) burm.f cultivated ex vitro under nitrogen ratesEnio Tiago de Oliveira 14 December 2007 (has links)
A babosa (Aloe vera (L.) Burm. f.), família Asphodelaceae, reconhecida e explorada mundialmente pela indústria farmacêutica e cosmética devido aos princípios medicinais de seus compostos fenólicos e principalmente ao gel de polissacarídeos específicos, foi submetida a dois experimentos interligados. O primeiro, refere-se a micropropagação no qual foram avaliados tratamentos de desinfestação de ápices caulinares, multiplicação in vitro e condições de aclimatação ex vitro. O segundo experimento refere-se ao cultivo das plantas em areia lavada e irrigada com solução nutritiva, em condições controladas de casa de vegetação, onde foram testados os efeitos de doses (105; 210 e 315 ppm) de nitrogênio avaliados aos 90; 180 e 270 dias de cultivo. Os efeitos foram avaliados em função dos teores foliares dos macronutrientes e dos micronutrientes boro, cobre, ferro manganês e zinco, de proteínas totais solúveis (PTS), de açúcares redutores (AR) e açúcares totais solúveis (ATS) e sobre o crescimento por meio do índice de área foliar (IAF), da taxa de assimilação líquida (TAL), taxa de crescimento relativo (TCR), taxa de crescimento absoluto (TCA) e incrementos de massas de matérias fresca (IMMF) e seca (IMMS). Todos os dados foram analisados estatisticamente. Em relação a micropropagação, a eficiência de desinfestação foi aumentada em torno de 40% na obtenção de ápices caulinares verdes em início de brotação quando as plantas colhidas a campo foram previamente desinfestadas por lavagem com solução de hipoclorito de sódio com 0,5% de cloro ativo ou com solução de dicloroisocianurato de sódio (Sumaveg®) 0,66%. p.v-1 e os ápices caulinares submetidos a imersões alternadas nas soluções dos dois produtos utilizados. A fase multiplicativa da microproagação em meio MS apresentou um rendimento de 1:5,3 a cada intervalo de 30 dias de multiplicação. A partir de 136 ápices caulinares desinfestados, verdes, em início de brotação, foram obtidas 40.495 microplantas. Classificadas em pequenas, médias e grandes, foram submetidas a condições de aclimatação observando-se que bandejas de 64 células com 40 cm3 de substrato apresentaram economia em torno de 50% de substrato e em espaço físico na casa-de-vegetação com micro-aspersão e exaustão de ar em sistema \"pad-house\", e durante o processo de aclimatação e transporte das microplantas aclimatadas. Em relação ao cultivo das plantas em doses de nitrogênio, apesar de algumas variáveis responderem melhor à dose de 105 ppm e outras à dose de 315 ppm, a dose de 210 ppm de nitrogênio favoreceu as melhores respostas para os teores de açúcares totais solúveis (504,21 mgATS.g-1 de MMS), que são diretamente relacionados ao conteúdo de polissacarídeos específicos, de interesse comercial da cultura de Aloe vera. Esses teores, por sua vez, foram propiciados pelos melhores valores de IAF, TCA, IMMF e IMMS, todos observados aos 270 dias de cultivo, ratificando a significância do fator tempo e da dose de 210 ppm de nitrogênio no cultivo dessa espécie vegetal. / Aloe vera (L.) Burm. f., family Asphodelaceae, worldwide renowned and explored by pharmaceutics and cosmetics industries due to its phenolics bearing medicinal principles and mainly to the specific polysaccharides present in the gel, was submitted to two interlinked experiments. The first one refers to apical shoot micropropagation evaluating different disinfection treatments of the explants, the in vitro bud multiplication and ex vitro acclimatization of the microplants. The second one refers to cultivation in greenhouse of the micropropagated plants in washed sand and irrigated with nutritive solution, in the presence of three nitrogen rates (105, 210 and 315 ppm); the plant material was harvested at 90-, 180- and 270-day. All data were statistically analyzed. The effects of nitrogen were evaluated on the content of the macronutrients, the following micronutrients: B, Cu, Fe, Mn and Zn and total soluble proteins, reducing sugars, total soluble sugars; the growth of the Aloe vera plants was measured through the foliar area index, the rate of liquid assimilation, rates of relative and absolute growth and increases in the fresh and dry weights. In regards to micropropagtion, the efficiency of the disinfection process was increased by 40% when the plants harvested in the field were previously washed either with sodium hypochloride (0.5% active chlorine) solution or sodium dichloroisocyanurate (Sumaveg®) 0.66% w.v-1 solution and the apical shoots explants were afterwards alternatively treated with the two disinfectants. The multiplication phase in MS medium showed a rate of 1:5.3 of microplant production at each 30-day interval with a production of 40.495 microplants out of the 136 initial disinfected apical shoots. The microplants were classified as small, medium and large plants and acclimatized in polyethylene trays bearing 64 cells with 40 cm3 of substrate each cell, a 50% saving in terms of substrate amount and free space in the greenhouse equipped with micro-aspersion irrigation, pad-house and air exhaustion systems and also in the transport of the acclimatized microplants. In regards to the effect of nitrogen rates on the development of Aloe vera plants, besides the fact that the best responses were observed either to 105 ppm or 315 ppm nitrogen by some variables, at 210 ppm nitrogen rates the best result was obtained for total soluble sugars (504.21 mg.g-1DW); the sugars are directly related to specific polysaccharides of Aloe vera and are of great importance for the industries. On the other hand, these values were favored by the best values reached by the physiological variables studied in this work at 270-day validate the significance of the time factor and the 210 ppm N rates in the Aloe vera production system.
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The efficacy and toxicological effects of aloe ferox mill. used in the management of constipation in Nkonkobe municipality of the Eastern Cape province, South AfricaWintola, Olubunmi Abosede A January 2011 (has links)
Herbal remedies are commonly used in developing countries for the treatment of various diseases, including constipation. The rationale for utilizing medicinal plants for the treatment of diseases rested largely on the belief that they are safe and free of side effects. However, there is limited scientific evidence on the safety and efficacy of these herbal medicines to back up their continued therapeutic application. Aloe ferox Mill. (Aspodelaceae), known as Cape aloe, locally called ikhala is a medicinal plant used by the people of the Eastern Cape Province for the treatment of gastrointestinal problems and constipation. The plant is a perennial shrub with thick succulent leaves bearing brown thorns on the margin and bright orange flowers arranged in oval lanceolate. It occurs in all weather in bush veld, road side, gardens and undisturbed places. According to the ethnomedicinal information, A. ferox is used as purgative. This research project was therefore designed to evaluate its ability in the treatment of constipation and to investigate its possible toxicological property. At the beginning of this programme, a survey of plants used for the treatment of constipation in Nkonkobe Municipality of the Eastern Cape Province was carried out using a questionnaire, which was administered to herbalists, traditional healers and rural dwellers. The study revealed 10 plant species from 8 families that are used for the treatment of constipation in the province. Four plants, Aloe ferox Mill, Boophone distischa L.f Herb, Alepidea amatybica Eckl and Artemisia afra Jacq, were repeatedly mentioned. Based on the frequency of usage, perceived efficacy and availability to the rural dwellers and the traditional healers, Aloe ferox was the most commonly used of the plants for the treatment of constipation. The plant was thus, chosen for the study. The invivo laxative effect of the aqueous extract of Aloe ferox in the treatment of loperamide-induced constipation in Wistar rats was investigated at varying concentrations. The leaf extract at all the dosages investigated (50, 100 and 200 mg/kg body weight) improved intestinal motility, increased fecal volume and normalized body weight in the constipated rats. This was an indication of its laxative properties. However, the laxative property of the herb at 200 mg/kg body weight of the extract showed best efficacy and compares favourably well with senokot, a standard laxative drug. These findings have therefore, lent scientific credence to the folkloric use of the herb by the people of the Eastern Cape of South Africa as a laxative agent. Toxicological evaluation of aqueous leaf extract of Aloe ferox in loperamide-induced constipation was studied at 50, 100, and 200 mg/kg body weight. The oral administration of the extracts did not show any significant effect on the liver and kidney body weight ratios as well as the kidney and liver function indices. The extracts, at all the dosages investigated, did not alter the levels of creatinine, uric acid, urea, calcium and potassium ions. Similarly, the levels of total protein, albumin, bilirubin and gamma glutamyl transferase (GGT) were not significantly different from the control. The plant extract appreciably normalized the elevated activities of alkaline phosphatase (ALP), alanine transaminase (ALT) and aspartate transaminase (AST) in the untreated constipated rats following treatment with the extract. The extract did not show a significant effect on the hematological parameters except for the increase in the lymphocyte count in the untreated constipated rats, which was attenuated after administering the herb. ThThe available evidence in this study suggests that A. ferox may be safe as an oral remedy for constipation. Generally, the effect of the extract compared favourably well with senokot, a recommended drug for the treatment of constipation. The antioxidant activities against 1, 1 diphenyl- 2 picrylhydrazl (DPPH), 2,2’ – azinobis [3- ethylbenzothiazoline -6- sulfonic acid] diammonium salt (ABTS), hydrogen peroxide (H2O2), Nitric oxide (NO), lipid peroxidation and the ferric reducing agents were investigated spectrophotometrically. Alkaloids, saponins, tannins, total phenols, flavonoids, flavonols and proanthocyanidin were also determined to assess their effects on the antioxidants activity of this plant. The phytochemical content of the ethanol and acetone extracts were consistently high compared to other solvents extracts. The level of tannins was not significant (P > 0.05) as compared with other solvent extracts. The free radical scavenging activity of the extracts was high even at lower concentrations (0.025 mg/ml) except in DPPH and lipid peroxidation. The ferric reducing potential of the extracts was concentration dependent and significantly different from Vitamin C and butylated hydroxytoluene (BHT) that were used as standard drugs. The present study showed a high level of scavenging activity of the leaf extracts of Aloe ferox in all the solvent extracts. Both ethanol and methanolic extract showed potent antioxidant activities than acetone and aqueous extracts. The study indicated that the leaf extracts of Aloe ferox might be a valuable source of natural antioxidant for both medicine and food industries. A. ferox leaf consists of the gel, latex and mesophyll layer; however, the main active constituents of the latex and the leaf exudate of Aloe ferox are anthraquinones which are believed to be responsible for the laxative property. The laxative compound in Aloe ferox leaf extract was isolated and characterized by extracting the plant material in methanol and extract suspended in distilled water. Partitioning was done with n-hexane, ethyl acetate and butanol respectively and was co-spotted with the over-the-counter (OTC) laxative drugs. This led to the successive column chromatography and thin layer chromatography (TLC) of the most active ethyl acetate fraction on silica gel with benzene/ethanol/ammonia hydroxide (BEA: 90:10:1), ethyl acetate/methanol/water (EMW: 40:5.4:5) and chloroform/ethyl acetate/formic acid (CEF: 50:40:10) as the mobile phase. The successive chromatograph and TLC afforded two compounds of Rf 0.420 (blue) and 0.831 (yellow) with the over-the-counter (OTC) drugs. These compounds were not totally elucidated due to their small quantity and instability. However, hydroxyl (OH) and carboxyl groups (COOH) was established as common to the extracted compounds, which might be responsible for the biological activity recorded for the plant extract.
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