Yan Jing-chao, Liu Zhao-ming, Wang Tian-ming, Shi Rong, Ma Yue-ming
Laboratory of Pharmacokinetics, Shankhai University of Traditional Chinese Medicine, Shanghai 201203, China.
Yao Xue Xue Bao. 2007 Jul;42(7):722-9.
To study the pharmacokinetics of flavonoids from Xiexin decoction in rats. SD rats were given a single ig dose of Xiexin decoction 12 g x kg(-1), plasma and urine were collected before and after dosing. Flavonoids components in plasma and urine were measured by HPLC. Pharmacokinetic parameters were determined from the plasma concentration-time data and urinary excretion-time data with the DAS software package. Baicalin was incubated with the rat renal homogenate to investigate its metabolism in vitro. After oral administration of Xiexin decoction baicalin and wogonoside were quickly absorbed and exhibited double peak phenomena in their plasma concentrations. The first peaks in plasma concentrations of baicalin and wogonoside reached Cmax1 of (10 +/- 8) and (1.5 +/- 0.5) mg x L(-1) at Tmax1 of (0.27 +/- 0.09) and (0.17 +/- 0.00) h, while the second peaks reached Cmax2 of (3. 9 0. 5) and (0. 74 +/- 0.11) mg x L(-1) at Tmax2 of (7.6 +/- 2.6) and (16.0 +/- 0.0) h, respectively. The T(1/2) of baicalin and wogonoside were (7 +/- 3) and (6.4 +/- 2.1) h, AUC(0-infinity) were (57 +/- 12) and (15 +/- 3) mg x h x L(-1), respectively. After oral administration of Xiexin decoction, not only baicalin and wogonoside but also baicalein and wogonin can be detected in the urine. The amounts of baicalin, wogonoside, baicalein and wogonin excreted from urine during 0-72 h were (1.4 +/- 0.3), (3.4 +/- 1.3), (2.2 +/- 0.97), (10 +/- 4)% of dose given in rats, respectively. The excretion T(1/2) of the four flavonoids were (6.9 +/- 2.1), (9 +/- 4) , (8.2 +/- 2.0) and (7.2 +/- 1.8) h, respectively. Baicalin was metabolized into baicalein in the rat renal homogenate in vitro, and the kinetic parameters were measured as Vmax = 702 nmol x min(-1) x g(-1) (protein) and Km=135 micromol x L(-1). After oral administration of Xiexin decoction, flavonoids can be absorbed quickly. Only a small quantity of baicalin, wogonoside, baicalein and wogonin were excreted from urine. Baicalin may be metabolized into baicalein in the rat kidney.
研究泻心汤中黄酮类成分在大鼠体内的药代动力学。将SD大鼠单次ig给予12 g·kg⁻¹泻心汤,给药前后采集血浆和尿液。采用高效液相色谱法测定血浆和尿液中的黄酮类成分。用DAS软件包根据血浆浓度 - 时间数据和尿排泄 - 时间数据确定药代动力学参数。将黄芩苷与大鼠肾匀浆孵育以研究其体外代谢。口服泻心汤后,黄芩苷和汉黄芩苷迅速吸收,血浆浓度出现双峰现象。黄芩苷和汉黄芩苷血浆浓度的第一个峰分别在(0.27±0.09)和(0.17±0.00) h达到Cmax1为(10±8)和(1.5±0.5) mg·L⁻¹,而第二个峰分别在(7.6±2.6)和(16.0±0.0) h达到Cmax2为(3.9±0.5)和(0.74±0.11) mg·L⁻¹。黄芩苷和汉黄芩苷的T(1/2)分别为(7±3)和(6.4±2.1) h,AUC(0 - ∞)分别为(57±12)和(15±3) mg·h·L⁻¹。口服泻心汤后,尿液中不仅可检测到黄芩苷和汉黄芩苷,还可检测到黄芩素和汉黄芩素。0 - 72 h内从尿液中排泄的黄芩苷、汉黄芩苷、黄芩素和汉黄芩素的量分别为大鼠给药剂量的(1.4±0.3)、(3.4±1.3)、(2.2±0.97)、(10±4)%。这四种黄酮类成分的排泄T(1/2)分别为(6.9±2.1)、(9±4)、(8.2±2.0)和(7.2±1.8) h。黄芩苷在大鼠肾匀浆中体外代谢为黄芩素,动力学参数测定为Vmax = 702 nmol·min⁻¹·g⁻¹(蛋白),Km = 135 μmol·L⁻¹。口服泻心汤后,黄酮类成分可迅速吸收。只有少量的黄芩苷、汉黄芩苷及黄芩素和汉黄芩素从尿液中排泄。黄芩苷可能在大鼠肾脏中代谢为黄芩素。