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白皮杉醇,一种来自葡萄的天然多酚,通过靶向抑制其分泌的脲酶发挥抑制作用。

Piceatannol, a Natural Polyphenol From Grape, Inhibits Through Targeted Suppression of Its Secreted Urease.

作者信息

Lu Qiang, Xie Yuhong, Wang Xuefei, Chen Haohui, Xu Yifei, Li Cailan

机构信息

Department of Pharmaceutical Sciences Zunyi Medical University Zhuhai People's Republic of China.

Department of Pharmacology Zunyi Medical University Zhuhai People's Republic of China.

出版信息

Food Sci Nutr. 2025 Sep 8;13(9):e70932. doi: 10.1002/fsn3.70932. eCollection 2025 Sep.

Abstract

infection, mediated largely through its urease enzyme, causes chronic gastric inflammation that can progress to severe pathology. This study investigates the inhibitory effects of piceatannol (PIC), a polyphenol from grape peels, on growth and its urease activity. PIC remarkably inhibited the growth of three strains, with MIC values ranging from 100 to 150 μg/mL. Furthermore, PIC exerted a potent inhibitory effect on urease (HPU) and jack bean urease (JBU) with IC values of 0.67 ± 0.02 mM and 0.47 ± 0.01 mM, respectively. Kinetic studies revealed that PIC acts as a slow-binding, mixed inhibitor of HPU and a slow-binding, non-competitive inhibitor for JBU. The use of thiol-blocking substances observably delayed the deactivation of HPU and JBU, whereas the synergistic effect of PIC with competitive inhibitors of Ni further restrained urease activity. These results indicated that the sulfhydryl group in the active site may be the key binding site for PIC to inhibit HPU and JBU. Molecular docking simulations further support the inhibitory mechanism. Additionally, the inactivation of HPU and JBU caused by PIC was reversible. In conclusion, PIC significantly suppresses the growth of and the activity of its major virulence factor, urease. Further investigation into the kinetic properties and mechanisms revealed that the inhibition of urease by PIC may target the active site sulfhydryl group.

摘要

感染主要通过其尿素酶介导,可导致慢性胃炎症,进而发展为严重病变。本研究调查了葡萄皮中的多酚白藜芦醇(PIC)对幽门螺杆菌生长及其尿素酶活性的抑制作用。PIC显著抑制了三种菌株的生长,MIC值在100至150μg/mL之间。此外,PIC对幽门螺杆菌尿素酶(HPU)和刀豆尿素酶(JBU)具有强大的抑制作用,IC值分别为0.67±0.02 mM和0.47±0.01 mM。动力学研究表明,PIC作为HPU的慢结合型混合抑制剂和JBU的慢结合型非竞争性抑制剂。使用巯基阻断物质可显著延迟HPU和JBU的失活,而PIC与镍竞争性抑制剂的协同作用进一步抑制了尿素酶活性。这些结果表明,活性位点中的巯基可能是PIC抑制HPU和JBU的关键结合位点。分子对接模拟进一步支持了这种抑制机制。此外,PIC引起的HPU和JBU失活是可逆的。总之,PIC显著抑制幽门螺杆菌的生长及其主要毒力因子尿素酶的活性。对动力学性质和机制的进一步研究表明,PIC对尿素酶的抑制作用可能靶向活性位点的巯基。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b8f/12417329/a1ce1408c5dd/FSN3-13-e70932-g002.jpg

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