BackgroundType 2 diabetes is a serious problem for developed and developing countries. Prevention of prediabetes progression to type 2 diabetes with the use of natural products appears to be a cost-effective solution. Zingiber mioga has been used as a traditional food in Asia. Recent research has reported the potential health benefits of Zingiber mioga, but the blood glucose reducing effect has not been yet evaluated.MethodsIn this study Zingiber mioga extracts (water and ethanol) were investigated for their anti-hyperglycemic and antioxidant potential using both in vitro and animal models. The in vitro study evaluated the total phenolic content, the oxygen radical absorbance capacity (ORAC) and the inhibitory effect against carbohydrate hydrolyzing enzymes (porcine pancreatic α-amylase and rat intestinal sucrase and maltase) of both Zingiber mioga extracts. Also, the extracts were evaluated for their in vivo post-prandial blood glucose reducing effect using SD rat and db/db mice models.ResultsOur findings suggest that the ethanol extract of Zingiber mioga (ZME) exhibited the higher sucrase and maltase inhibitory activity (IC50, 3.50 and 3.13 mg/mL) and moderate α-amylase inhibitory activity (IC50, >10 mg/mL). Additionally, ZME exhibited potent peroxyl radical scavenging linked antioxidant activity (0.53/TE 1 μM). The in vivo study using SD rat and db/db mice models also showed that ZME reduces postprandial increases of blood glucose level after an oral administration of sucrose by possibly acting as an intestinal α-glucosidase inhibitor (ZME 0.1 g/kg 55.61 ± 13.24 mg/dL)ConclusionThe results indicate that Zingiber mioga extracts exhibited significant in vitro α-glucosidase inhibition and antioxidant activity. Additionally, the tested extracts demonstrated in vivo anti-hyperglycemic effects using SD rat and db/db mice models. Our findings provide a strong rationale for the further evaluation of Zingiber mioga for the potential to contribute as a useful dietary strategy to manage postprandial hyperglycemia.
Brassica juncea var. integrifolia, known as mustard leaf, is used as a medicinal plant in Asia, however, knowledge for their health benefits is limited. Here, we evaluate the total phenolic contents, phenolic profile, and antioxidant activity of green and red mustard leaves (EG and ER, respectively). Additionally, the inhibitory activity of EG and ER against rat intestinal α‐glucosidase and porcine‐pancreatic α‐amylase were investigated. The total phenolic contents of EG and ER were 1,228.48 ± 36.81 and 850.75 ± 28.88mg/100 g, respectively. The total phenolic contents correlated to the observed antioxidant activities. ER had significant α‐glucosidase but low α‐amylase inhibitory activity. Using an Sprague‐Dawley‐Rat model, ER appeared to have better glucose‐lowering effect when compared to EG, after a sucrose‐loading test. This is the first report evaluating mustard leaves for potential glucose‐lowering effects. Our observations suggest that ER has better potential for this bioactivity and this observation possibly correlates with the sinigrin contents observed in both extracts. Practical applications Mustard seeds are widely used for the production of food products and have been evaluated for their health benefits. Currently, mustard leaves are considered a low‐value by‐product of the mustard plant and are significantly underutilized. To support the sustainable utilization of mustard plant, it is important to initiate the utilization of mustard leaves. Value addition in mustard leaves through research efforts that define possible health benefits of this resource will significantly assist toward the possible utilization of this low‐value, underutilized raw material to produce high‐value, health beneficial, food ingredients.
We selected 3 kinds of water soluble vitamins such as vitamin B₄, vitamin B₆, and vitamin C using Sprague Dawley(SD) rat model. The concentration of vitamin B₄and vitamin B₆ for sucrose loading test was 50 mg/kg, vitamin C was 0.1 and 0.5 g/kg. The effect of as vitamin B₄, vitamin B₆, and vitamin C on the postprandial blood glucose increase after meal was investigated in SD rats fed on sucrose. Three vitamin samples significantly reduced the postprandial blood glucose levels after sucrose loading. These results indicate that vitamin B₄, vitamin B₆, and vitamin C may have anti‐hyperglycemic effect by suppressing carbohydrate absorption in the gastrointestinal level, and thereby reducing the postprandial increase of blood glucose. These results indicate that vitamin B₄, vitamin B₆, and vitamin C may improve postprandial in blood glucose and glucose homeostasis since it inhibits intestinal sucrase and thus delays carbohydrate absorption, although clinical trials are needed.
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