2017
DOI: 10.1016/j.fct.2017.03.015
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Pouteria torta epicarp as a useful source of α-amylase inhibitor in the control of type 2 diabetes

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Cited by 26 publications
(12 citation statements)
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“…Sebuah penelitian melaporkan bahwa proses fraksinasi memberikan nilai bioaktivitas yang bagus dimana Pouteria torta yang awalnya dimaserasi dengan etanol memberikan nilai IC 50 sebesar 73,6 µg/mL, tetapi saat ekstrak etanol difraksi sehingga menghasilkan 8 fraksi, setiap fraksi memberikan kemampuan inhibisi αamilase yang berbeda. Fraksi 2 dan fraksi 8 tidak menghasilkan aktivitas inhibisi, fraksi 6 memberikan aktivitas inhibisi tertinggi yaitu 77% dengan nilan IC 50 9 µg/mL (Sales et al, 2017). Aktivitas enzim diukur berdasarkan hasil absorbansi p-nitrofenol.…”
Section: Kemampuan Antihiperglikemikunclassified
“…Sebuah penelitian melaporkan bahwa proses fraksinasi memberikan nilai bioaktivitas yang bagus dimana Pouteria torta yang awalnya dimaserasi dengan etanol memberikan nilai IC 50 sebesar 73,6 µg/mL, tetapi saat ekstrak etanol difraksi sehingga menghasilkan 8 fraksi, setiap fraksi memberikan kemampuan inhibisi αamilase yang berbeda. Fraksi 2 dan fraksi 8 tidak menghasilkan aktivitas inhibisi, fraksi 6 memberikan aktivitas inhibisi tertinggi yaitu 77% dengan nilan IC 50 9 µg/mL (Sales et al, 2017). Aktivitas enzim diukur berdasarkan hasil absorbansi p-nitrofenol.…”
Section: Kemampuan Antihiperglikemikunclassified
“…In addition to their commercial importance, several species have been used in folk medicine to treat fevers, inflammations, ulcers, diabetes and nausea, among other applications [4] [5]. In addition, the extracts, semipurified fractions and isolated substances from the Pouteria species show anti-inflammatory activity [6], inhibition of the α-amylase and β-glucosidase enzymes [7] and antidiabetic activity [8]. Despite the occurrence of bioactive substances of pharmacological interest, such as carotenoids, flavonoids, triterpenes and cyanogenic glycosides, only about 15 Pouteria species have been investigated from a chemical point of view [5] [9] [10].…”
Section: Journal Of Biosciences and Medicinesmentioning
confidence: 99%
“…Inhibition of α‐amylase would slow the degradation of starch, thus reducing glucose release and controlling postprandial hyperglycemia (Ozer et al., 2018; Tan & Chang, 2017). One approach for treating type 2 diabetes is to inhibit the activities of carbohydrate‐hydrolyzing enzymes (de Sales et al., 2017; Johnson et al., 2011). Some commercial drugs characterized as carbohydrate‐hydrolyzing enzyme inhibitors (e.g., acarbose, voglibose, and miglitol) have been developed for diabetic patients; however, these drugs usually have side effects such as abdominal discomfort and diarrhea (de Sales et al., 2017; He et al., 2017; Lordan et al., 2013).…”
Section: Introductionmentioning
confidence: 99%
“…One approach for treating type 2 diabetes is to inhibit the activities of carbohydrate‐hydrolyzing enzymes (de Sales et al., 2017; Johnson et al., 2011). Some commercial drugs characterized as carbohydrate‐hydrolyzing enzyme inhibitors (e.g., acarbose, voglibose, and miglitol) have been developed for diabetic patients; however, these drugs usually have side effects such as abdominal discomfort and diarrhea (de Sales et al., 2017; He et al., 2017; Lordan et al., 2013). Therefore, it is important to find α‐amylase inhibitors from natural plants.…”
Section: Introductionmentioning
confidence: 99%