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Polyphenols are the secondary metabolic products of plants and are considered as active constituents to possess therapeutic effects. To date, a vast number of scientific literature addressed the potential of polyphenols as bio-efficient compounds owing to their structural diversity. Due to the presence of several hydroxyl groups, they are metabolized quickly due to conjugation reaction and thus, readily produce toxic metabolites as a defense material against many pathogens, reflecting their safety strategy. This review focuses on the anti-quorum sensing and biofilm inhibition activity of polyphenols, which display their potential to treat bacterial infections by combating the virulence caused by pathogenic agents. Thus, for mitigating quorum sensing-controlled pathogenesis, the use of polyphenol-based phytochemicals holds immense potential to cure infections. The application of polyphenol as sensitizing agent/ adjuvant therapeutics which act in synergism with antibiotics is highly remarkable.
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Genus Vitex is largely used throughout the world (Benin, Burkina Faso, Ethiopia, Ghana, India, Lesotho, Nigeria, Senegal, South Africa) for various care such as: anti-inflammatory, antibacterial, hepatocuractive, intestinal troubles. Among the plurality of known Vitex, the most exploited in Burkina Faso are Vitex diversifolia Bak and Vitex doniana Sweet. Then, the aim of this study is to summarize traditional uses, phytochemistry and pharmacological activities of 2 local species of Vitex. The results of this study show that the species of this genus are rich in polyphenolic compounds, minerals and vitamins. These founding can justify the many uses in traditional medicine.
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Objective: Both Lycium barbarum L. (LB) and Lycium ruthenicum Murr. (LR) belong to the Lycium genus of Solanaceae family but their fruits have significant phenotypic differences in terms of color and shapes. This study is aimed to investigate the inter-species difference of their fruit polyphenol composition. Methods: The polyphenol composition of fresh and dried fruits of two Lycium species were comprehensively analyzed using ultra-high performance liquid chromatography-electrospray ionization-quadrupole-time of flight mass spectrometry (UHPLC-ESIQ- TOF-MS). Results: 35 polyphenolic compounds were detected and quantified in the fresh and dried Lycium fruits including phenolic acids, anthocyanins and phenolamides (i.e., the amide-adducts of polyphenolic acids and polyamines). For both species, the dried fruits had more polyphenolic compounds than their fresh fruits with significant inter-species difference; for both fresh and dried fruits, LR had more polyphenolic compounds than LB. Conclusion: There are significant inter-species differences between these two Lycium in both fresh and dried fruits. These results offer essential information for further understanding of the biological functions of these two Lycium fruits as phytomedicines and functional food.
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<p><b>OBJECTIVE</b>Anabasis aretioides (Coss & Moq.), a Saharan plant belonging to Chenopodiaceae family, is widely distributed in semi-desert areas from the Tafilalet region of Morocco. This plant is extensively used by local population against diabetes and cardiovascular disorders. The purpose of the study was to investigate the effect of the aqueous A. aretioides extract on lipid metabolism in normal and streptozotocin (STZ)-induced diabetic rats and to identify the polyphenolic compounds present. In addition, the in vitro antioxidant activity of the aqueous A. aretioides extract was also evaluated.</p><p><b>METHODS</b>The effect of an aerial part aqueous extract (APAE) of A. aretioides (5 mg/kg of lyophilized A. aretioides APAE) on plasma lipid profile was investigated in normal and STZ-induced diabetic rats (n = 6) after once daily oral administration for 15 days. The aqueous extract was tested for its 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical-scavenging activity. Polyphenolic compounds in the extracts were definitively characterized by high-performance liquid chromatography-diode array detection-electrospray ionization-mass spectrometry.</p><p><b>RESULTS</b>In diabetic rats, oral administration of A. aretioides APAE provoked a significant decrease in both plasma cholesterol and triglyceride levels from the first to the second week (P < 0.01). A significant decrease on plasma triglyceride levels was also observed in normal rats (P < 0.01), where the reduction was 53%. In addition, the phytochemical analysis revealed the presence of 12 polyphenolic compounds. Moreover, according to the DPPH radical-scavenging activity, the aqueous extract showed an in vitro antioxidant activity.</p><p><b>CONCLUSION</b>Aqueous A. aretioides APAE exhibits lipid-lowering and in vitro antioxidant activities. Many polyphenols were present in this extract and these phytoconstituents may be involved in the pharmacological activity of this plant.</p>
Subject(s)
Animals , Humans , Male , Rats , Antioxidants , Chenopodiaceae , Chemistry , Cholesterol , Blood , Chromatography, High Pressure Liquid , Diabetes Mellitus, Experimental , Blood , Drug Therapy , Hypolipidemic Agents , Chemistry , Phytochemicals , Chemistry , Plant Extracts , Chemistry , Polyphenols , Chemistry , Rats, Wistar , Streptozocin , Tandem Mass Spectrometry , Triglycerides , BloodABSTRACT
Objective:To reach the recovery and identification of antioxidant polyphenolic compounds from Nephelium lappaceum L. (Mexican variety) husk using ultrasound-assisted extraction and liquid chromatography/mass spectrometry as well as the in vitro antioxidant activity.Methods:Rambutan husk extracts were obtained by ultrasound-assisted extraction, mass/ volume ratio, water/ethanol percentage and extraction time were evaluated. Once the best extraction condition of polyphenolic compounds was defined, a polyphenolic fraction was recovered using Ambetlite XAD-16. The total content of antioxidant polyphenolic compounds was determined by summation of the total hydrolysable polyphenol and total condensed polyphenol contents. Recovered compounds were identified by FTIR (ATR) spectroscopy and HPLC/ESI/MS. The antioxidant activity was carried out by ABTS, DPPH and lipid oxidation inhibition in vitro methods.Results:In Mexican variety rambutan husk, the total polyphenolic content was 487.67 mg/g, after ultrasound-assisted extraction. According to the HPLC/ESI/MS analysis 12 antioxidant polyphenolic compounds were identified, mostly ellagitannins such as geraniin, corilagin and ellagic acid. The antioxidant activity determined by ABTS, DPPH and lipid oxidation inhibition methods was demonstrated. The main functional groups of the identified compounds were determined by FTIR analysis.Conclusions:It was demonstrated that ultrasound-assisted extraction was effective and allowed the extraction and recovery of antioxidant polyphenolic compounds. Furthermore Mexican variety rambutan husk is an important source for recovering polyphenolic compounds with antioxidant activity, these compounds have potential application for the treatment/prevention of various diseases related to cancer and pathogenic microorganisms.
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Objective: To reach the recovery and identification of antioxidant polyphenolic compounds from Nephelium lappaceum L. (Mexican variety) husk using ultrasound-assisted extraction and liquid chromatography/mass spectrometry as well as the in vitro antioxidant activity. Methods: Rambutan husk extracts were obtained by ultrasound-assisted extraction, mass/volume ratio, water/ethanol percentage and extraction time were evaluated. Once the best extraction condition of polyphenolic compounds was defined, a polyphenolic fraction was recovered using Ambetlite XAD-16. The total content of antioxidant polyphenolic compounds was determined by summation of the total hydrolysable polyphenol and total condensed polyphenol contents. Recovered compounds were identified by FTIR (ATR) spectroscopy and HPLC/ESI/MS. The antioxidant activity was carried out by ABTS, DPPH and lipid oxidation inhibition in vitro methods. Results: In Mexican variety rambutan husk, the total polyphenolic content was 487.67 mg/g, after ultrasound-assisted extraction. According to the HPLC/ESI/MS analysis 12 antioxidant polyphenolic compounds were identified, mostly ellagitannins such as geraniin, corilagin and ellagic acid. The antioxidant activity determined by ABTS, DPPH and lipid oxidation inhibition methods was demonstrated. The main functional groups of the identified compounds were determined by FTIR analysis. Conclusions: It was demonstrated that ultrasound-assisted extraction was effective and allowed the extraction and recovery of antioxidant polyphenolic compounds. Furthermore Mexican variety rambutan husk is an important source for recovering polyphenolic compounds with antioxidant activity, these compounds have potential application for the treatment/prevention of various diseases related to cancer and pathogenic microorganisms.
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Objective To determinate the recovery of total polyphenolic compounds content, in vitro antioxidant activity and HPLC/ESI/MS characterization of extract from Nephelium lappaceum L. (Mexican rambutan). Methods The rambutan husk extract was obtained by aqueous extraction and a polyphenolic fraction was recovered using Amberlite XAD-16. The total polyphenolic compounds content was determined by the Folin Ciocalteu and butanol-HCI methods. In vitro antioxidant activity was performed using ABTS and ferric reducing antioxidant power methods. Results Mexican rambutan husk showed a total polyphenolic content of 582 mg/g and an evident antioxidant activity by ABTS and ferric reducing antioxidant power analysis. The HPLC/ESI/MS assay allowed the identification of 13 compounds, most of which belong to ellagitannins. Geraniin, corilagin and ellagic acid were present in the sample; the mineral composition was also evaluated. Conclusions Rambutan husk cultivated in Mexico is a promising source for the recovery of added value bioactive compounds with antioxidant activity, which have potential applications as bioactive antioxidant agents for the treatment of diseases.
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OBJECTIVE@#To determinate the recovery of total polyphenolic compounds content, in vitro antioxidant activity and HPLC/ESI/MS characterization of extract from Nephelium lappaceum L. (Mexican rambutan).@*METHODS@#The rambutan husk extract was obtained by aqueous extraction and a polyphenolic fraction was recovered using Amberlite XAD-16. The total polyphenolic compounds content was determined by the Folin Ciocalteu and butanol-HCI methods. In vitro antioxidant activity was performed using ABTS and ferric reducing antioxidant power methods.@*RESULTS@#Mexican rambutan husk showed a total polyphenolic content of 582 mg/g and an evident antioxidant activity by ABTS and ferric reducing antioxidant power analysis. The HPLC/ESI/MS assay allowed the identification of 13 compounds, most of which belong to ellagitannins. Geraniin, corilagin and ellagic acid were present in the sample; the mineral composition was also evaluated.@*CONCLUSIONS@#Rambutan husk cultivated in Mexico is a promising source for the recovery of added value bioactive compounds with antioxidant activity, which have potential applications as bioactive antioxidant agents for the treatment of diseases.
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BACKGROUND/OBJECTIVES: Mulberry leaves contain quercetin derivatives, which have the effects of reducing obesity and improving lipid and glucose metabolism in mice with obesity. It is not clear whether or not mulberry leaves can directly affect metabolic disorders, in the presence of obesity, because of the interaction between obesity and metabolic disorders. The aim of the current study was to assess the direct action of quercetin derivatives on metabolic disorders in non-obese conditions in short-term high-fat diet fed mice. MATERIALS/METHODS: C57BL/6N mice were fed a high-fat diet, supplemented with either 0% (control), 1%, or 3% mulberry leaf powder (Mul) or 1% catechin powder for five days. Anthropometric parameters and blood biochemistry were determined, and hepatic gene expression associated with lipid and glucose metabolism was analyzed. RESULTS: Body and white fat weights did not differ among the four groups. Plasma triglycerides, total cholesterol, and free fatty acids in the 1%, 3% Mul and catechin groups did not differ significantly from those of the controls, however, plasma glucose and 8-isoprostane levels were significantly reduced. Liver gene expression of gp91phox, a main component of NADPH oxidase, was significantly down-regulated, and PPAR-alpha, related to beta-oxidation, was significantly up-regulated. FAS and GPAT, involved in lipid metabolism, were significantly down-regulated, and Ehhadh was significantly up-regulated. Glucose-metabolism related genes, L-PK and G6Pase, were significantly down-regulated, while GK was significantly up-regulated in the two Mul groups compared to the control group. CONCLUSIONS: Our results suggest that the Mul quercetin derivatives can directly improve lipid and glucose metabolism by reducing oxidative stress and enhancing beta-oxidation. The 1% Mul and 1% catechin groups had similar levels of polyphenol compound intake (0.4 x 10(-5) vs 0.4 x 10(-5) mole/5 days) and exhibited similar effects, but neither showed dose-dependent effects on lipid and glucose metabolism or oxidative stress.
Subject(s)
Animals , Mice , Adipose Tissue, White , Biochemistry , Blood Glucose , Catechin , Cholesterol , Diet, High-Fat , Fatty Acids, Nonesterified , Gene Expression , Glucose , Lipid Metabolism , Liver , Metabolism , Morus , NADPH Oxidases , Obesity , Oxidative Stress , Plasma , Quercetin , Triglycerides , Weights and MeasuresABSTRACT
BACKGROUND/OBJECTIVES: Mulberry leaves contain quercetin derivatives, which have the effects of reducing obesity and improving lipid and glucose metabolism in mice with obesity. It is not clear whether or not mulberry leaves can directly affect metabolic disorders, in the presence of obesity, because of the interaction between obesity and metabolic disorders. The aim of the current study was to assess the direct action of quercetin derivatives on metabolic disorders in non-obese conditions in short-term high-fat diet fed mice. MATERIALS/METHODS: C57BL/6N mice were fed a high-fat diet, supplemented with either 0% (control), 1%, or 3% mulberry leaf powder (Mul) or 1% catechin powder for five days. Anthropometric parameters and blood biochemistry were determined, and hepatic gene expression associated with lipid and glucose metabolism was analyzed. RESULTS: Body and white fat weights did not differ among the four groups. Plasma triglycerides, total cholesterol, and free fatty acids in the 1%, 3% Mul and catechin groups did not differ significantly from those of the controls, however, plasma glucose and 8-isoprostane levels were significantly reduced. Liver gene expression of gp91phox, a main component of NADPH oxidase, was significantly down-regulated, and PPAR-alpha, related to beta-oxidation, was significantly up-regulated. FAS and GPAT, involved in lipid metabolism, were significantly down-regulated, and Ehhadh was significantly up-regulated. Glucose-metabolism related genes, L-PK and G6Pase, were significantly down-regulated, while GK was significantly up-regulated in the two Mul groups compared to the control group. CONCLUSIONS: Our results suggest that the Mul quercetin derivatives can directly improve lipid and glucose metabolism by reducing oxidative stress and enhancing beta-oxidation. The 1% Mul and 1% catechin groups had similar levels of polyphenol compound intake (0.4 x 10(-5) vs 0.4 x 10(-5) mole/5 days) and exhibited similar effects, but neither showed dose-dependent effects on lipid and glucose metabolism or oxidative stress.
Subject(s)
Animals , Mice , Adipose Tissue, White , Biochemistry , Blood Glucose , Catechin , Cholesterol , Diet, High-Fat , Fatty Acids, Nonesterified , Gene Expression , Glucose , Lipid Metabolism , Liver , Metabolism , Morus , NADPH Oxidases , Obesity , Oxidative Stress , Plasma , Quercetin , Triglycerides , Weights and MeasuresABSTRACT
Aim: This study focused on finding molecules with inhibitory effects on Advanced Glycation End-products (AGEs) formation from Tanzanian some Clusiaceae plant species Study Design: Field study and Laboratory experimental tests. Place and Duration of Study: Institute of Traditional Medicine, Muhimbili University of Health and Allied Sciences, P.O. Box 65001, Dar es Salaam, Tanzania and PRES LUNAM, Université d’Angers, EA 921 SONAS, 16 Bd Daviers, 49045 Angers, France, between June 2011 and July 2013. Methodology: Three Clusiaceae plant species (Garcinia semseii, G. volkensii and Allanblackia ulugurensis) were collected and dried in the field with the assistance of a botanist. Extraction and concentration of plant samples to obtain crude extracts were done in the laboratory following standard procedures. The isolation of the phenolic compounds was carried out by using normal phase column chromatography as well as High performance liquid chromatography (HPLC). The isolated compounds were tested for anti- AGE activity using the in vitro automated assay. Results: Two polyphenolic compounds exhibiting phloroglucinol moieties [e.g. polyprenylated benzophenones, such as guttiferone F, 2 (18 mg)] or biflavonoids [such as morelloflavone, 1 (22mg)] were isolated and identified from A. ulugurensis and G. volkensis respectively. The results further indicated that compound 1 is an excellent inhibitor of AGE formation exhibiting an IC50 values of 78 and 64 μM at wavelength of 370/440 (vesperlysines-like AGEs) and 335/385 (pentosidine-like AGEs) respectively. Conclusion: Plants belonging to the Clusiaceae family commonly used in Tanzanian traditional medicine need to be considered as a potential source of molecules exhibiting pharmacological activities such as anti-AGE activity. Morelloflavone (1) and other biflavonoids prove to be very good anti-AGE compounds using our automated screening assay. Hence, our automated in vitro assay allows a fast, effective and quite inexpensive screening of natural compounds and can therefore be applied to high throughput screening projects.
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Objective: To evaluate the antioxidant and radical scavenging activities of Solanum anguivi fruit (SAG) and its possible effect on mitochondrial permeability transition pore as well as mitochondrial membrane potential (ΔΨm) isolated from rat liver. Methods: Antioxidant activity of SAG was assayed by using 2,2-diphenyl-1-picrylhydrazyl (DPPH), reducing power, iron chelation and ability to inhibit lipid peroxidation in both liver and brain homogenate of rats. Also, the effect of SAG on mitochondrial membrane potential and mitochondrial swelling were determined. Identification and quantification of bioactive polyphenolics was done by HPLC-DAD. Results: SAG exhibited potent and concentration dependent free radical-scavenging activity (IC50/DPPH=275.03±7.8 μg/mL). Reductive and iron chelation abilities also increase with increase in SAG concentration. SAG also inhibited peroxidation of cerebral and hepatic lipids subjected to iron oxidative assault. SAG protected against Ca2+ (110 μmol/L)-induced mitochondrial swelling and maintained theΔΨm. HPLC analysis revealed the presence of gallic acid [(17.54±0.04) mg/g], chlorogenic acid (21.90±0.02 mg/g), caffeic acid (16.64±0.01 mg/g), rutin [(14.71±0.03) mg/g] and quercetin [(7.39±0.05) mg/g]. Conclusions:These effects could be attributed to the bioactive polyphenolic compounds present in the extract. Our results suggest that SAG extract is a potential source of natural antioxidants that may be used not only in pharmaceutical and food industry but also in the treatment of diseases associated with oxidative stress.
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Introducción: el extracto acuoso de la corteza de Rhizophora mangle L. (mangle rojo) posee varias propiedades farmacológicas: en el tratamiento de la mastitis bovina, la curación de heridas,las infecciones uterinas y las úlceras gastroduodenales; debido a sus propiedades antiséptica, cicatrizante, antiinflamatoria y antioxidante. Sin embargo, no se han completado los estudios de la actividad antioxidante a todos los niveles de complejidad para dilucidar los mecanismos de acción involucrados en este efecto farmacológico. Objetivo: determinar el efecto del extracto acuoso de Rhizophora mangle y su fracción polifenólica sobre la producción de anión superóxido en una línea celular de macrófagos murinos RAW 264,7, estimulados con forbol 12-myristato 13-acetato o lipopolisacárido. Métodos: la evaluación de la actividad antioxidante del extracto de Rhizophora mangle y su fracción polifenólica sobre la producción de anión superóxido en macrófagos RAW 264.7, activados con lipopolisacárido o forbol 12-myristato 13-acetato, se determinó mediante el método de reducción del ferricitocromo c. Resultados: el extracto de Rhizophora mangle y su fracción polifenólica, inhibieron la producción de anión superóxido en macrófagos RAW 264,7, activados con ambos tipos de agentes de forma dependiente de la concentración de taninos. La comparación de las líneas de regresión reveló diferencias significativas (p< 0,05), resultando este efecto superior en la fracción para ambos tipos de agentes, y en presencia de lipopolisacárido para ambas muestras. Conclusiones: el extracto acuoso de Rhizophora mangle mostró actividad antioxidante a nivel celular, evidenciada por la reducción del estrés oxidativo en macrófagos mediante la inhibición de la producción de anión superóxido. A su vez se demostró que los compuestos polifenólicos presentes en el extracto fueron los principales responsables de los efectos antioxidantes observados en este estudio
Introduction: the aqueous extract of Rhizophora mangle L (red mangrove) bark has some pharmacological properties, that is, the treatment of bovine mastitis, wound healing, uterine infections and stomach ulcers, due to its antiseptic, healing, antiinflammatory and antioxidant properties. However, the studies of antioxidant activity at all complexity levels have not been completed in order to elucidate the mechanisms of action involved in this pharmacological effect. Objective: to determine the effect of Rhizophora mangle aqueous extract and its polyphenolic fraction on superoxide anion production in a cellular line of RAW 264,7 murine macrophages, stimulated with phorbol 12-myristate 13-acetate or lipopolysaccharide. Methods: the evaluation of the antioxidant activity of Rhizophora mangle extract and its polyphenolic fraction on superoxide anion production in RAW 264.7 macrophages activated with lipopolysaccharide or phorbol 12-myristate 13-acetate was made using the C ferricytochrome reduction method. Results: Rhizophora mangle extract and its polyphenolic fraction inhibit the superoxide anion production in RAW 264.7 macrophages activated with both types of agents depending on tannin concentration. The comparison of the regression lines showed significant differences (p< 0.05), resulting this effect higher in the fraction for both types of agents, and the presence of lipopolysaccharide for both samples. Conclusions: Rhizophora mangle aqueous extract showed antioxidant activity at cellular level, evidenced by reduction of oxidative stress in macrophages, through the inhibition of superoxide anion production. At the same time, it was shown that polyphenolic compounds, present in the extract, were the main responsible for the antioxidant effects observed in this study
Subject(s)
Antioxidants , Macrophages , Rhizophoraceae/chemistry , SuperoxidesABSTRACT
Al extracto acuoso de la corteza de Rhizophora mangle L se le ha demostrado un amplio espectro de usos medicinales: en el tratamiento de la mastitis bovina, la curación de heridas,las infecciones uterinas y las úlceras gastroduodenales; debido a sus propiedades antiséptica, cicatrizante, antiinflamatoria y antioxidante. Sin embargo, no se han completado los estudios de la actividad antioxidante a todos los niveles de complejidad para dilucidar los mecanismos de acción involucrados en este efecto farmacológico. Objetivo: determinar si el extracto acuoso de R. mangle y su fracción polifenólica protegen a las principales biomoléculas del daño oxidativo. La evaluación de la actividad antioxidante del extracto de R mangle y su fracción polifenólica sobre las principales biomoléculas se determinó mediante ensayo de daño oxidativo a la albúmina de suero bovino expuesta a los radicales hidroxilo generados en el sistema Fenton y ensayo de degradación oxidativa del ADN inducido por el sistema bleomicina-Fe3+.El extracto de R. mangle y su fracción polifenólica, a la máxima concentración ensayada, disminuyeron la oxidación de los grupos sulfidrilos en 87,3 y 89,1 por ciento; e inhibieron la degradación del ADN en 98,4 y 91,9 por ciento, respectivamente. El análisis de regresión mostró que ambos efectos fueron dependientes de la concentración de taninos en el extracto y su fracción. La comparación de las líneas de regresión reveló que el extracto y su fracción resultaron igualmente eficaces en proteger a la albúmina de suero bovino de la oxidación por los radicales hidroxilos, sin embargo, el extracto fue más eficaz en proteger al ADN de la degradación oxidativa que su fracción. El extracto acuoso de R. mangle mostró un efecto protector a las principales biomoléculas del daño oxidativo, evidenciado por la inhibición de la pérdida de grupos sulfidrilos en la albúmina de suero bovino y la disminución de la degradación del ADN...
The aqueous extract from Rhizophora mangle (L) bark has demonstrated a broad spectrum of medicinal uses; for example, in treating bovine mastitis, wound healing, uterine infections and gastroduodenal ulcers, due to its antiseptic, healing, anti-inflammatory and antioxidant properties. However, the antioxidant activity in its whole complexity has not been fully studied in order to elucidate the mechanisms of action involved in this pharmacological effect. Objective: to determine if R. mangle bark aqueous extract and its polyphenolic fraction protect the main biomolecules from oxidative damage. The antioxidant activity of R. mangle extract and its polyphenolic fraction on the main biomolecules was determined by the following methods: oxidative damage trial on bovine serum albumin exposed to hydroxyl radicals generated in the Fenton system and the bleomycin-Fe3+ system-induced DNA oxidative degradation trial. Results: the R. mangle bark extract and its polyphenolic fraction, at the highest tested concentration, reduced the sulfhydryl group oxidation by 87,3 percent and 89,1 percent and they also inhibited the DNA degradation by 98.4 percent and 91.9 percent respectively. The regression analysis demonstrated that both effects depended on tannin concentration in the extract and its fraction. The comparison of regression lines revealed that the extract and its fraction were equally effective in protecting bovine serum albumin from oxidation by hydroxyl radicals; however, the extract was more effective when protecting DNA from oxidative degradation than its fraction. The R mangle aqueous extract showed a protective effect on the main biomolecules from the oxidative damage, evidenced by inhibiting loss of sulfhydryl group in bovine serum albumin and decreasing the DNA degradation. At the same time, it was shown that polyphenolic compounds present in the extract were the main responsible for the antioxidant effects observed in this study
Subject(s)
Antioxidants/analysis , Rhizophoraceae/chemistryABSTRACT
Diabetes mellitus is a metabolic disorder characterized by chronic hyperglycaemia. There are many and diverse therapeutic strategies in the management of Type 2 diabetes. The inhibition of alpha-amylase activity is only one possibility to lower postprandial blood glucose levels. In our in-vitro studies we could demonstrate that different plants, mostly traditionally used in common diabetic therapy in Africa or Europe, are able to inhibit alpha-amylase, which is responsible for the breakdown of oligosaccharides into monosaccharides which are absorbed. An inhibition of alpha-amylase activity of 90 percent was seen with the extract of the leaves of Tamarindus indica. To quantify inhibtion rates, acarbose was used (IC50: 23.2 µM). Highest inhibition level of acarbose in our testmodel was about 85 percent. Additionally tests with pure polyphenolic compounds might explain the biological activity of the selected plants.
Diabetes mellitus é uma desordem metabólica caracterizada pela hiperglicemia crônica. Existem diversas estratégias terapêuticas no tratamento da diabetes Tipo 2. A inibição da atividade da a-amilase é apenas uma possibilidade de reduzir os níveis de glicose posprandiais. Nos nossos estudos in vitro pudemos demonstrar que diferentes plantas, especialmente as tradicionalmente usadas em terapia comum de diabetes na África ou Europa, são capazes de inibir a a-amilase, a qual é responsável pela quebra dos oligossacarídeos em monossacarídeos, os quais são absorvidos. Uma inibição da atividade da a-amilase da ordem de 90 por cento foi observada com o extrato das folhas de Tamarindus indica. Para quantificar os graus de inibição, acarbose foi usada (IC50: 23,2 mM). O maior grau de inibição de acarbose no nosso modelo de teste foi de cerca de 85 por cento. Adicionalmente testes com compostos polifenólicos puros poderão explicar a atividade biológica das plantas selecionadas.