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In vivo metabolism of Talosin A, new isoflavonol glycoside from Kitasatospora kifunensis, in rats

机译:大戟新奇异黄酮糖苷Talosin A在大鼠体内的体内代谢

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摘要

The isoflavonol glycoside Talosin A, genistein (GT)-7-α-L-6-deoxy talopyranose (GT-Tal), was first isolated from the culture broth of Kitasatospora kifunensis MJM341. The aim of the present study was to evaluate the oral absorption and metabolism of the newly isolated isoflavonol glycoside, GT-Tal compared to genistin (GT-7-O-β-D-glucopyranoside; GT-Glu). Free GT-Glu and GT-Tal could not be detected prior to enzymatic hydrolysis of the corresponding conjugates in rat plasma. Following oral administration of GT-Tal (15 min), GT-Tal was rapidly absorbed through the gastrointestinal tract and metabolized into GT-Tal conjugates with a mean Cmax of 2.74 µg/mL. GT-Tal was further metabolized to its aglycone, free GT and conjugated GT. After oral administration, GT-Glu was absorbed after being convereted to its aglycone and then further metabolized into its conjugate metabolites (free GT with a mean Cmax of 0.24 mg/mL at 1.25 h; conjugated GT with a mean Cmax of 1.31 mg/mL at 2.00 h). Significant differences in absorption and metabolism of GT-Tal and GT-Glu were observed. GT-Tal was metabolized into its corresponding conjugates or underwent deglycosylation to form GT, whereas GT-Glu was metabolized into its aglycone, GT.
机译:异黄酮醇苷Talosin A,染料木黄酮(GT)-7-α-L-6-脱氧塔洛吡喃糖(GT-Tal),首先从Kitasatospora kifunensis MJM341的培养液中分离得到。本研究的目的是评估与genistin(GT-7-O-β-D-吡喃葡萄糖苷; GT-Glu)相比,新分离的异黄酮糖苷GT-Tal的口服吸收和代谢。在大鼠血浆中相应的结合物进行酶水解之前,无法检测到游离的GT-Glu和GT-Tal。口服GT-Tal后(15分钟),GT-Tal迅速通过胃肠道吸收并代谢为GT-Tal偶联物,平均Cmax为2.74 µg / mL。 GT-Tal进一步代谢为其糖苷配基,游离GT和结合的GT。口服给药后,GT-Glu与其糖苷配基融合后被吸收,然后进一步代谢成其结合物代谢物(游离GT在1.25 h时的Cmax平均值为0.24 mg / mL;结合物GT的Cmax平均值为1.31 mg / mL在2.00 h)。观察到GT-Tal和GT-Glu的吸收和代谢存在显着差异。 GT-Tal被代谢成其相应的结合物或经过去糖基化反应形成GT,而GT-Glu被代谢成其糖苷配基GT。

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