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1.
J Agric Food Chem ; 65(33): 7192-7199, 2017 Aug 23.
Artículo en Inglés | MEDLINE | ID: mdl-28753316

RESUMEN

Assays of the inhibitory potential against enzymes involved in carbohydrate and lipid digestion (α-amylase, α-glucosidase, and lipase) as well as the total contents of phenolics and anthocyanins, anthocyanin profile, and antioxidant capacity revealed significant differences (p < 0.05) between five varieties of red cabbage. Among the varieties, the highest inhibitory activity against α-glucosidase (IC50 = 3.87 ± 0.12 mg dry weight (DW) of cabbage/mL) and lipase (IC50 = 1.57 ± 0.06 mg DW/mL) was exhibited by the Koda variety, which showed the highest antioxidant capacity in ABTS (Trolox equivalent antioxidant capacity (TEAC) = 141 ± 4.71 µmol/g DW) and ferric-reducing antioxidant power (TEAC = 125 ± 1.94 µmol/g DW) assays and had the highest total phenolics level (19.6 ± 0.48 mg/g DW). The highest total anthocyanin content (12.0 ± 0.16 mg/g DW) and inhibitory activity against α-amylase (IC50 = 69.0 ± 3.65 mg DW of cabbage/mL) was shown by the Kissendrup variety. The anthocyanin profiles of these two varieties were characterized by the highest percentages of diacylated cyanidin derivatives. There was no correlation between the contents of phenolic compounds and lipase inhibitory activity, but inhibition of α-amylase was correlated with concentrations of monoacylated and diacylated anthocyanins, while inhibition of α-glucosidase increased with total phenolics and diacylated anthocyanins levels.


Asunto(s)
Brassica/química , Diabetes Mellitus Tipo 2/enzimología , Inhibidores Enzimáticos/química , Obesidad/enzimología , Extractos Vegetales/química , alfa-Glucosidasas/química , Diabetes Mellitus Tipo 2/tratamiento farmacológico , Inhibidores de Glicósido Hidrolasas/química , Humanos , Lipasa/antagonistas & inhibidores , Lipasa/química , Lipasa/metabolismo , Obesidad/tratamiento farmacológico , alfa-Amilasas/antagonistas & inhibidores , alfa-Amilasas/química , alfa-Amilasas/metabolismo , alfa-Glucosidasas/metabolismo
2.
Curr Top Med Chem ; 15(23): 2431-44, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26088348

RESUMEN

Type 2 diabetes mellitus, which is usually a result of wrong dietary habits and reduced physical activity, represents 85-95% of all diabetes cases and among other diet related diseases is the major cause of deaths. The disease is characterized mainly by hyperglycemia, which is associated with attenuated insulin sensitivity or beta cells dysfunction caused by multiple stimuli, including oxidative stress and loss of insulin secretion. Since polyphenols possess multiple biological activities and constitute an important part of the human diet, they have recently emerged as critical phytochemicals in type 2 diabetes prevention and treatment. Their hypoglycemic action results from their antioxidative effect involved in recovering of altered antioxidant defenses and restoring insulin secreting machinery in pancreatic cells, or abilities to inhibit the activity of carbohydrates hydrolyzing enzymes (α-amylase and α-glucosidase) or protein tyrosine phosphatase 1B (PTP1B), which is known as the major negative regulator in insulin signaling. This study investigates the total phenolic content (Folin-Ciocalteu and HPLC methods) and antioxidant capacity (ABTS) of 20 polyphenolic extracts obtained from selected edible plants, which were screened in terms of α -amylase, α - glucosidase and protein tyrosine phosphatase 1B inhibitors or protective agents against oxidative stress induced by tertbutylhydroperoxide (t-BOOH) in ßTC3 pancreatic beta cells used as a model target for antidiabetes drugs. The study concludes that Chaenomeles japonica, Oenothera paradoxa and Viburnum opulus may be promising natural sources for active compounds with antidiabetic properties.


Asunto(s)
Citoprotección/efectos de los fármacos , Hipoglucemiantes/farmacología , Células Secretoras de Insulina/efectos de los fármacos , Extractos Vegetales/farmacología , Plantas Comestibles/química , Proteína Tirosina Fosfatasa no Receptora Tipo 1/antagonistas & inhibidores , alfa-Amilasas/antagonistas & inhibidores , alfa-Glucosidasas/metabolismo , Animales , Técnicas de Cultivo de Célula , Línea Celular Tumoral , Proliferación Celular/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Diabetes Mellitus/tratamiento farmacológico , Diabetes Mellitus/enzimología , Diabetes Mellitus/patología , Hipoglucemiantes/aislamiento & purificación , Hipoglucemiantes/uso terapéutico , Ratones , Oenothera/química , Estrés Oxidativo/efectos de los fármacos , Extractos Vegetales/aislamiento & purificación , Extractos Vegetales/uso terapéutico , Polifenoles/química , Rosaceae/química , Viburnum/química
3.
J Agric Food Chem ; 62(20): 4610-7, 2014 May 21.
Artículo en Inglés | MEDLINE | ID: mdl-24785184

RESUMEN

Dietary inhibitors of fats and carbohydrates degrading enzymes can reduce obesity and type 2 diabetes. In this study, we screened crude extracts from 30 commonly consumed fruits to test their in vitro inhibitory effect against key enzymes relevant for obesity (pancreatic lipase) and type 2 diabetes (α-glucosidase and α-amylase), total phenolic content (Folin-Ciocalteu method), and antioxidant capacity (ABTS and FRAP). The IC50 values of the fruits tested varied from 39.91 to >400 mg/mL, from 1.04 to >80 mg/mL, and from 0.72 to 135.07 mg/mL against α-glucosidase, α-amylase, and pancreatic lipase, respectively. Antioxidant capacity ranged from 0.66 to 124.66 µmol of TE/g of fruit and strongly correlated with phenolic content, while the enzyme inhibition was poorly correlated with total phenolic and antioxidant capacity. Among fruits tested, blue honeysuckle and red gooseberry exhibited the highest inhibitory activity with respect to the carbohydrate degrading enzymes, while lingonberry had the strongest anti-lipase activity.


Asunto(s)
Antioxidantes/química , Inhibidores Enzimáticos/química , Frutas/química , Inhibidores de Glicósido Hidrolasas , Lipasa/antagonistas & inhibidores , Extractos Vegetales/química , alfa-Amilasas/antagonistas & inhibidores , Digestión , Humanos , Cinética , Lipasa/química , alfa-Amilasas/química , alfa-Glucosidasas/química
4.
Acta Biochim Pol ; 58(4): 449-60, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-22030557

RESUMEN

Angiogenesis, the formation of new capillaries from pre-existing vascular network, plays an important role in physiological and pathological processes such as embryonic development, wound healing, and development of atherosclerosis. Extension of the circulatory network is also considered to be one the most important factors during cancerogenesis. Inhibition of angiogenesis may lead to inhibition of tumor growth whereas stimulation may improve wound healing. Research achievements suggest the use of plants and their extracts as potential therapeutic agents with pro- or antiangiogenic activity. Since the anticancer and antiangiogenic properties of many phytomedicines have been amply reviewed elsewhere this paper will focus on the treatment of vascular insufficiency in wound healing. Globally accepted herbal drugs are thought to be safe and effective, however, there is a need for more evidence-based confirmation in controlled and validated trials. Among the most frequently studied proangiogenic phytochemicals are ginsenosides from Panax ginseng, beta-sitosterol from Aloe vera, calycosin from Radix Astragali, and extracts from Hippophae rhamnoides L. and Angelica sinensis.


Asunto(s)
Inductores de la Angiogénesis/uso terapéutico , Fitoterapia , Extractos Vegetales/uso terapéutico , Cicatrización de Heridas , Aloe/química , Inductores de la Angiogénesis/aislamiento & purificación , Ginsenósidos/uso terapéutico , Hippophae/química , Humanos , Sistema de Señalización de MAP Quinasas , Neovascularización Patológica/tratamiento farmacológico , Neovascularización Patológica/patología , Panax/química , Receptores de Factores de Crecimiento Endotelial Vascular/química , Factor A de Crecimiento Endotelial Vascular/química
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