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鉴定(L.)medik的主要黄酮类化合物及其在糖尿病肾病治疗中的代谢产物。

Identification of the main flavonoids of (L.) medik and their metabolites in the treatment of diabetic nephropathy.

作者信息

Diao Zhipeng, Yu Hongmei, Wu Yapeng, Sun Yuanbo, Tang Haitao, Wang Mei, Li Nan, Ge Haitao, Sun Jianguo, Gu Harvest F

机构信息

Jiangsu Provincial Key Laboratory of Drug Metabolism and Pharmacokinetics, Research Unit of PK-PD Based Bioactive Components and Pharmacodynamic Target Discovery of Natural Medicine of Chinese Academy of Medical Sciences, China Pharmaceutical University, Nanjing, China.

Laboratory of Molecular Medicine, School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, China.

出版信息

Front Pharmacol. 2024 Jan 8;14:1290868. doi: 10.3389/fphar.2023.1290868. eCollection 2023.

Abstract

Huangkui capsule (HKC) is made from the ethanol extract of (L.) Medik [Malvaceae; abelmoschi corolla] and received approval from the China Food and Drug Administration (Z19990040) in 1999. Currently, HKC is used for treatment of the patients with diabetic nephropathy (DN) in China. The bioactive chemical constituents in HKC are total flavonoids of (L.) Medik (TFA). The present study aims to identify the primary flavonoid metabolites in HKC and TFA and their metabolism fates in db/db mice, the animal model for the study of type 2 diabetes and DN. HKC (0.84 g/kg/d) and TFA (0.076 g/kg/d) or vehicle were respectively administered daily via oral gavage in db/db mice for 4 weeks. The metabolism fate of the main metabolites of HKC in serum, liver, kidney, heart, jejunum, colon, jejunal contents, colonic contents, and urine of db/db mice were analyzed with a comprehensive metabolite identification strategy. In db/db mice administered with HKC and TFA, 7 flavonoid prototypes and 38 metabolites were identified. The related metabolic pathways at Phases I and II reactions included dehydroxylation, deglycosylation, hydrogenation, methylation, glucuronidation, sulphation, and corresponding recombined reactions. Quercetin, isorhamnetin, quercetin sulphate, quercetin monoglucuronide, and isorhamnetin monoglucuronide presented a high exposure in the serum and kidney of db/db mice. Thereby, the present study provides a pharmacodynamic substance basis for better understanding the mechanism of (L.) Medik for medication of DN.

摘要

黄葵胶囊(HKC)由黄蜀葵(锦葵科;黄蜀葵的花冠)的乙醇提取物制成,并于1999年获得中国食品药品监督管理总局批准(国药准字Z19990040)。目前,在中国黄葵胶囊用于治疗糖尿病肾病(DN)患者。黄葵胶囊中的生物活性化学成分是黄蜀葵总黄酮(TFA)。本研究旨在鉴定黄葵胶囊和黄蜀葵总黄酮中的主要黄酮类代谢产物及其在db/db小鼠(一种用于研究2型糖尿病和糖尿病肾病的动物模型)中的代谢命运。将黄葵胶囊(0.84 g/kg/d)和黄蜀葵总黄酮(0.076 g/kg/d)或赋形剂分别每日经口灌胃给予db/db小鼠,持续4周。采用综合代谢产物鉴定策略分析db/db小鼠血清、肝脏、肾脏、心脏、空肠、结肠、空肠内容物、结肠内容物和尿液中黄葵胶囊主要代谢产物的代谢命运。在给予黄葵胶囊和黄蜀葵总黄酮的db/db小鼠中,鉴定出7种黄酮类原型和38种代谢产物。I相和II相反应的相关代谢途径包括脱羟基、去糖基化、氢化、甲基化、葡萄糖醛酸化、硫酸化以及相应的重组反应。槲皮素、异鼠李素、槲皮素硫酸盐、槲皮素单葡萄糖醛酸苷和异鼠李素单葡萄糖醛酸苷在db/db小鼠的血清和肾脏中呈现高暴露水平。因此,本研究为更好地理解黄蜀葵治疗糖尿病肾病的机制提供了药效学物质基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fab/10836608/f7c0f5618de0/fphar-14-1290868-g001.jpg

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