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单次静脉注射后大鼠体内NG-硝基-L-精氨酸药代动力学的剂量范围研究。

Dose-ranging study of NG-nitro-L-arginine pharmacokinetics in rats after bolus intravenous administration.

作者信息

Piotrovskij V, Kállay Z, Horecký J, Trnovec T, Krumpl G, Krejcy K

机构信息

Institute of Preventive and Clinical Medicine, Bratislava, Slovakia.

出版信息

Xenobiotica. 1994 Jul;24(7):663-9. doi: 10.3109/00498259409043268.

Abstract
  1. NG-nitro-L-arginine (10, 30 and 100 mg/kg) was administered intravenously to the male Wistar rat. Plasma was collected over 48, 72 and 120 h and was analysed for the drug by hplc. Pharmacokinetic parameters were calculated using a non-compartmental method. 2. Drug concentration-time profiles of individual rats after all doses studied exhibited secondary peaks, while geometric mean concentration-time curves showed plateaus. 3. NG-nitro-L-arginine plasma concentrations divided by dose almost coincided. Pharmacokinetic parameters were not dose-dependent in the range of 10-30 mg/kg, but changed after 100 mg/kg of NG-nitro-L-arginine indicating some decline from linearity. 4. NG-nitro-L-arginine is a low-extracted drug in rat as the total clearance was low (0.05-0.07 l/h/kg). Half-life and mean residence time were found to be long (17-30 and 23-40 h, respectively). Despite its low lipophilicity, NG-nitro-L-arginine exhibited large steady-state and terminal volumes of distribution (1.4-2.2 l/kg and 1.4-2.4 l/kg, respectively). Together with the double peak phenomenon, these results may be explained by assuming NG-nitro-L-arginine is involved in a recirculation process in the body.
摘要
  1. 将NG-硝基-L-精氨酸(10、30和100毫克/千克)静脉注射给雄性Wistar大鼠。在48、72和120小时内采集血浆,并用高效液相色谱法分析药物。使用非房室方法计算药代动力学参数。2. 在所研究的所有剂量下,各只大鼠的药物浓度-时间曲线均出现二次峰,而几何平均浓度-时间曲线显示为平台期。3. NG-硝基-L-精氨酸的血浆浓度除以剂量几乎一致。在10-30毫克/千克范围内,药代动力学参数与剂量无关,但在给予100毫克/千克的NG-硝基-L-精氨酸后发生变化,表明线性关系有所下降。4. NG-硝基-L-精氨酸在大鼠体内是一种低摄取药物,因为总清除率较低(0.05-0.07升/小时/千克)。发现半衰期和平均驻留时间较长(分别为17-30小时和23-40小时)。尽管其脂溶性较低,但NG-硝基-L-精氨酸表现出较大的稳态分布容积和终末分布容积(分别为1.4-2.2升/千克和1.4-2.4升/千克)。连同双峰现象,这些结果可以通过假设NG-硝基-L-精氨酸参与体内再循环过程来解释。

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