Unknown

Dataset Information

0

Inhibitory Effects of Siegesbeckia orientalis Extracts on Advanced Glycation End Product Formation and Key Enzymes Related to Metabolic Syndrome.


ABSTRACT: Metabolic syndrome typically includes Type 2 diabetes associated with hyperglycemia, central obesity, dyslipidemia and hypertension. It is highly related to oxidative stress, formation of advanced glycated end products (AGEs) and key enzymes, such as carbohydrate digesting enzymes like pancreatic ?-amylase and intestinal ?-glucosidase, pancreatic lipase and angiotensin I-converting enzyme (ACE). This study used an in vitro approach to assess the potential of four extracts of Siegesbeckia orientalis linne on key enzymes relevant to metabolic syndrome. In this research, S. orientailis was firstly extracted by ethanol. The ethanol extract (SE) was then partitioned sequentially with hexane, ethyl acetate and methanol, and these extracts were named SE-Hex, SE-EA and SE-MeOH, respectively. The experimental results showed that SE-EA had the highest total phenolic content (TPC, 76.9 ± 1.8 mg/g) and the total flavonoids content (TFC, 5.3 ± 0.3 mg/g). This extract exhibited the most significant antioxidant activities, including DPPH radical-scavenging capacity (IC50 = 161.8 ± 2.4 ?g/mL), ABTS radical-scavenging capacity (IC50 = 13.9 ± 1.5 ?g/mL) and reducing power. For anti-glycation activities, SE-EA showed the best results in the inhibition of AGEs, as well as inhibitory activities against ?-glucosidase (IC50 = 362.3 ± 9.2 ?g/mL) and ?-amylase (IC50 = 119.0 ± 17.7 ?g/mL). For anti-obesity activities, SE-EA indicated the highest suppression effect on pancreatic lipase (IC50 = 3.67 ± 0.52 mg/mL). Finally, for anti-hypertension activity, SE-EA also demonstrated the strongest inhibitory activity on ACE (IC50 = 626.6 ± 15.0 ?g/mL). Close relationships were observed among the parameters of TPC, antioxidant activities, inhibitory activities on ?-amylase, ?-glucosidase, lipase and ACE (R > 0.9). Moderate correlations were found among the parameters of TFC, antioxidant activities, and suppression of dicarbonyl compounds formation (R = 0.5-0.9). Taken together these in vitro studies reveal the therapeutic potential of SE-EA extract in the prevention and treatment of metabolic disorders.

SUBMITTER: Hung WC 

PROVIDER: S-EPMC6151556 | biostudies-literature | 2017 Oct

REPOSITORIES: biostudies-literature

altmetric image

Publications

Inhibitory Effects of Siegesbeckia orientalis Extracts on Advanced Glycation End Product Formation and Key Enzymes Related to Metabolic Syndrome.

Hung Wei-Chin WC   Ling Xue-Hua XH   Chang Chi-Chang CC   Hsu Hsia-Fen HF   Wang Shih-Wei SW   Lee Yi-Chen YC   Luo Ci C   Lee Yun-Tzu YT   Houng Jer-Yiing JY  

Molecules (Basel, Switzerland) 20171021 10


Metabolic syndrome typically includes Type 2 diabetes associated with hyperglycemia, central obesity, dyslipidemia and hypertension. It is highly related to oxidative stress, formation of advanced glycated end products (AGEs) and key enzymes, such as carbohydrate digesting enzymes like pancreatic α-amylase and intestinal α-glucosidase, pancreatic lipase and angiotensin I-converting enzyme (ACE). This study used an in vitro approach to assess the potential of four extracts of <i>Siegesbeckia orie  ...[more]

Similar Datasets

| S-EPMC6768434 | biostudies-literature
| S-EPMC3150472 | biostudies-literature
| S-EPMC4191044 | biostudies-literature
| S-EPMC4607637 | biostudies-literature
| S-EPMC6378764 | biostudies-literature
| S-EPMC7653286 | biostudies-literature
2010-11-22 | GSE24885 | GEO