Hubei Key Laboratory of Industrial Microbiology, Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Key Laboratory of Fermentation Engineering (Ministry of Education), National "111" Center for Cellular Regulation and Molecular Pharmaceutics, Hubei University of Technology, Wuhan 430068, Hubei, P. R. China.
State Key Laboratory of Tea Plant Biology and Utilization, Anhui Agricultural University, 130 Changjiang West Road, Hefei 230036, Anhui, P. R. China.
J Agric Food Chem. 2023 Aug 16;71(32):12311-12324. doi: 10.1021/acs.jafc.3c04265. Epub 2023 Aug 2.
Research on advanced glycation end product (AGEs) inhibition has generally focused on food processing, but many protein-AGEs will still be taken. Oligopeptide (OLP)-AGEs, as the main form after digestion, will damage human health once absorbed. Here, we investigated the ability of lotus seedpod oligomeric procyanidins (LSOPC) to inhibit the absorption of the OLP-AGEs and elucidated the underlying mechanism. Our results showed that the inhibition rate of LSOPC on the absorption of OLP-AGEs was about 50 ± 5.38%. 0.1, 0.2, and 0.3 mg/mL could upregulate the expression of ZO-1 and downregulate the expression of PepT1 and clathrin. Molecular docking showed that LSOPC could compete with the binding of OLP-AGEs to PepT1 and AP-2, thus inhibiting the absorption of OLP-AGEs. Furthermore, the interaction of LSOPC with the OLP-AGEs reduced the surface hydrophobicity of OLP-AGEs. It altered the secondary structure of the OLP-AGEs, thus weakening the affinity of the OLP-AGEs to the transporter protein to inhibit the absorption of OLP-AGEs. Together, our data revealed potential mechanisms by which LSOPC inhibit the absorption of OLP-AGEs and opened up new perspectives on the application of LSOPC in reducing the increasing health risks posed by OLP-AGEs.
对糖基化终产物(AGEs)抑制的研究通常集中在食品加工上,但仍会摄入许多蛋白质-AGEs。寡肽(OLP)-AGEs 作为消化后的主要形式,一旦被吸收,将损害人体健康。在这里,我们研究了莲子寡聚原花青素(LSOPC)抑制 OLP-AGEs 吸收的能力,并阐明了其潜在机制。结果表明,LSOPC 对 OLP-AGEs 吸收的抑制率约为 50±5.38%。0.1、0.2 和 0.3 mg/mL 可上调 ZO-1 的表达,下调 PepT1 和网格蛋白的表达。分子对接表明,LSOPC 可以与 OLP-AGEs 竞争与 PepT1 和 AP-2 的结合,从而抑制 OLP-AGEs 的吸收。此外,LSOPC 与 OLP-AGEs 的相互作用降低了 OLP-AGEs 的表面疏水性。它改变了 OLP-AGEs 的二级结构,从而削弱了 OLP-AGEs 与转运蛋白的亲和力,抑制了 OLP-AGEs 的吸收。总之,我们的数据揭示了 LSOPC 抑制 OLP-AGEs 吸收的潜在机制,为 LSOPC 应用于降低 OLP-AGEs 日益增加的健康风险开辟了新的视角。