Summary
The total content of phenolic compounds in purple sweet potato (PSP) was determined and the release of such compounds from PSP in gastrointestinal digestion was studied in vitro. The extraction conditions for the maximum recovery of free phenol (FP) and bound phenol (BP) from PSP were determined by response surface methodology (RSM). The maximum recovery of FPPSP was 14.16 ± 0.87 mg GAE per g short for dry weight (DW), which was obtained using 60% (v/v) ethanol maceration with a liquid–solid ratio of 57.21:1 (mL g−1) at 51.93 °C for 2.12 h. The maximum recovery for BPPSP was 7.54 mg GAE per g DW, which was obtained upon hydrolysis with 1.87 mol L−1 NaOH at a liquid–solid ratio of 35.93:1 (mL g−1) for 4.74 h. The maximum phenolic content was released after 1 and 2 h for the in vitro gastric and intestinal digestion respectively. The release of the phenolics was promoted by pepsin and gastric acid during gastric digestion, while it was further promoted by trypsin during intestinal digestion.
A-type voltage-dependent K + currents IC 50 Half maximal inhibitory concentration IK Intermediate-conductance calcium-activated potassium (channel) iNOS Inducible nitric oxide synthase K 2 P Two-pore-domain potassium (channel) K ATP ATP-sensitive potassium (channel) K Ca Calcium-activated potassium (channel) Kir Inwardly rectifying potassium (channel) K V Voltage-gated potassium (channel) LTCC L-type voltage-gated calcium channel MgTx Margatoxin mito-K ATP Mitochondrial ATP-sensitive potassium (channel) mTOR Mammalian target of rapamycin Na V Voltage-gated sodium (channel) NMDAR N-methyl-D-aspartate receptor NO Nitric oxide PD Parkinson's disease PGC Peroxisome proliferator-activated receptor-gamma coactivator PIP 2 Phosphatidylinositol 4,5-bisphosphate PKA Protein kinase A PM Plasma membrane has not been copyedited and formatted. The final version may differ from this version.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.