Yim H K, Kang H M, Lee M G, Kim Y C
College of Pharmacy, Seoul National University, South Korea.
Res Commun Mol Pathol Pharmacol. 1998 Sep;101(3):269-74.
Blood sampling site-dependent (the dorsal aorta, the jugular vein, and the retro-orbital sinus) plasma concentrations of acetaminophen and its glucuronide and sulfate conjugates, and acetaminophen-induced hepatotoxic parameters (such as ALT and SDH activity) in serum were evaluated after intraperitoneal administration of acetaminophen, 500 mg/kg body weight, to rats. The plasma concentrations and the resultant AUC0-12 h of acetaminophen, acetaminophen-glucuronide, and acetaminophen-sulfate were significantly higher when blood samples were collected from the retro-orbital sinus than those from the jugular vein. The serum ALT activity at 3 and 24 h after administration of acetaminophen were significantly higher when the blood samples were collected from the retro-orbital sinus than those from the dorsal aorta.
给大鼠腹腔注射500mg/kg体重的对乙酰氨基酚后,评估了采血部位(腹主动脉、颈静脉和眶后窦)对乙酰氨基酚及其葡萄糖醛酸和硫酸酯共轭物的血浆浓度,以及血清中对乙酰氨基酚诱导的肝毒性参数(如ALT和SDH活性)。从眶后窦采集血样时,对乙酰氨基酚、对乙酰氨基酚 - 葡萄糖醛酸和对乙酰氨基酚 - 硫酸酯的血浆浓度及由此得到的AUC0 - 12 h显著高于从颈静脉采集血样时。从眶后窦采集血样时,对乙酰氨基酚给药后3小时和24小时的血清ALT活性显著高于从腹主动脉采集血样时。