Jakobek Lidija, Kenjerić Daniela, Šoher Lidija, Matić Petra
Faculty of Food Technology Osijek, Josip Juraj Strossmayer University of Osijek, Franje Kuhaca 18, 31000 Osijek, Croatia.
Molecules. 2025 Jan 14;30(2):301. doi: 10.3390/molecules30020301.
Beneficial activities of phenolic compounds in the gastrointestinal tract, such as antiradical activity, are affected by the food matrix. The aim of this study was to investigate the influence of one constituent of the food matrix (dietary fiber β-glucan) on the release and antiradical activity of phenolic compounds from apples in gastrointestinal digestion. Simulated digestion in vitro was conducted on whole apples without or with added β-glucan. Antiradical activity was determined with the DPPH method. The total amount of released phenolic compounds in the stomach (563 mg kg fresh weight (fw), 85%) decreased in the intestine (314 mg kg fw, 47%) ( < 0.05). The presence of β-glucan decreased the release of phenolic compounds to 80 and 74% in the stomach and to 44 and 40% in the small intestine when there were lower and higher β-glucan amounts, respectively. A statistical analysis showed differences between release in digestion without or with β-glucan. B-glucan adsorbed up to 24 (stomach) and 32 mg g (small intestine) of the phenolics. Phenolic compounds scavenged more free radicals in the small intestine than in the stomach, and β-glucan decreased this activity, but not significantly. The interaction between β-glucan and phenolic compounds should be considered when explaining the beneficial effects in the stomach and small intestine.
酚类化合物在胃肠道中的有益活性,如抗自由基活性,会受到食物基质的影响。本研究的目的是调查食物基质的一种成分(膳食纤维β-葡聚糖)对苹果中酚类化合物在胃肠道消化过程中的释放及抗自由基活性的影响。对添加或未添加β-葡聚糖的完整苹果进行体外模拟消化。采用DPPH法测定抗自由基活性。胃中释放的酚类化合物总量(563毫克/千克鲜重(fw),85%)在肠道中减少(314毫克/千克fw,47%)(P<0.05)。当β-葡聚糖含量较低和较高时,β-葡聚糖的存在分别使胃中酚类化合物的释放量降至80%和74%,小肠中降至44%和40%。统计分析表明,有无β-葡聚糖时消化过程中的释放量存在差异。β-葡聚糖吸附的酚类物质最多可达24毫克/克(胃)和32毫克/克(小肠)。酚类化合物在小肠中清除的自由基比在胃中更多,β-葡聚糖降低了这种活性,但不显著。在解释胃和小肠中的有益作用时,应考虑β-葡聚糖与酚类化合物之间的相互作用。