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脂多糖诱导的炎症挑战对脉络丛β-葡萄糖醛酸酶活性以及其代谢产物槲皮素在脉络丛、血浆和脑脊液中浓度的影响。

Effect of Lipopolysaccharide-Induced Inflammatory Challenge on β-Glucuronidase Activity and the Concentration of Quercetin and Its Metabolites in the Choroid Plexus, Blood Plasma and Cerebrospinal Fluid.

机构信息

Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, 10-748 Olsztyn, Poland.

Faculty of Health Sciences, Lomza State University of Applied Sciences, 18-400 Lomza, Poland.

出版信息

Int J Mol Sci. 2021 Jul 1;22(13):7122. doi: 10.3390/ijms22137122.

Abstract

Quercetin-3-glucuronide (Q3GA), the main phase II metabolite of quercetin (Q) in human plasma, is considered to be a more stable form of Q for transport with the bloodstream to tissues, where it can be potentially deconjugated by β-glucuronidase (β-Gluc) to Q aglycone, which easily enters the brain. This study evaluates the effect of lipopolysaccharide (LPS)-induced acute inflammation on β-Gluc gene expression in the choroid plexus (ChP) and its activity in blood plasma, ChP and cerebrospinal fluid (CSF), and the concentration of Q and its phase II metabolites in blood plasma and CSF. Studies were performed on saline- and LPS-treated adult ewes ( = 40) receiving Q3GA intravenously ( = 16) and on primary rat ChP epithelial cells and human ChP epithelial papilloma cells. We observed that acute inflammation stimulated β-Gluc activity in the ChP and blood plasma, but not in ChP epithelial cells and CSF, and did not affect Q and its phase II metabolite concentrations in plasma and CSF, except Q3GA, for which the plasma concentration was higher 30 min after administration ( < 0.05) in LPS- compared to saline-treated ewes. The lack of Q3GA deconjugation in the ChP observed under physiological and acute inflammatory conditions, however, does not exclude its possible role in the course of neurodegenerative diseases.

摘要

槲皮素-3-葡萄糖醛酸苷 (Q3GA),是人体血浆中槲皮素 (Q) 的主要 II 期代谢物,被认为是一种更稳定的形式,可以与血液一起运输到组织中,在那里它可以被β-葡萄糖醛酸酶 (β-Gluc) 潜在地去共轭化为 Q 苷元,后者很容易进入大脑。本研究评估了脂多糖 (LPS) 诱导的急性炎症对脉络丛 (ChP) 中 β-Gluc 基因表达及其在血浆、ChP 和脑脊液 (CSF) 中的活性的影响,以及 Q 和其在血浆和 CSF 中的 II 期代谢物的浓度。对静脉注射 Q3GA 的生理盐水和 LPS 处理的成年母羊 ( = 40) 进行了研究 ( = 16),并对原代大鼠 ChP 上皮细胞和人 ChP 上皮乳头瘤细胞进行了研究。我们观察到,急性炎症刺激了 ChP 和血浆中的β-Gluc 活性,但不刺激 ChP 上皮细胞和 CSF 中的β-Gluc 活性,并且不影响血浆和 CSF 中的 Q 和其 II 期代谢物浓度,除了 Q3GA,其在 LPS 处理的母羊中的血浆浓度在给药后 30 分钟更高 ( < 0.05)。然而,在生理和急性炎症条件下观察到 ChP 中缺乏 Q3GA 的去共轭,并不排除其在神经退行性疾病过程中的可能作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9441/8268849/afbf38c4f295/ijms-22-07122-g001.jpg

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