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采用大鼠和 Caco2 细胞比较氯化甲基汞和甲基汞半胱氨酸的体内与体外药代动力学的差异。

Comparison of in vivo with in vitro pharmacokinetics of mercury between methylmercury chloride and methylmercury cysteine using rats and Caco2 cells.

机构信息

Laboratory of Biopharmaceutics and Pharmacokinetics, Faculty of Pharmaceutical Sciences, Hiroshima International University, Hiro-koshingai, Kure, Hiroshima, Japan.

出版信息

Arch Environ Contam Toxicol. 2012 Nov;63(4):628-36. doi: 10.1007/s00244-012-9800-5. Epub 2012 Aug 30.

Abstract

The in vivo and in vitro pharmacokinetics of mercury (Hg) were compared between methylmercury chloride (MeHg·Cl) and methylmercury cysteine (MeHg-Cys) using rats and Caco2 cells because humans can be exposed to MeHg compounds through dietary fish. The in vivo pharmacokinetics of Hg immediately after the digestion of MeHg compounds are still obscure. In Caco2 cells, membrane uptake and subcellular distribution of MeHg compounds were examined. When rats received it intravenously, MeHg·Cl showed 20-fold greater plasma and 2-fold greater blood concentrations of Hg than MeHg-Cys, indicating that their pharmacokinetic properties are different. One hour later, however, Hg concentrations in plasma and blood became virtually identical between MeHg·Cl and MeHg-Cys, although blood Hg concentrations were >100-fold greater than those in plasma. When administered into the closed rat's jejunum loop, MeHg·Cl and MeHg-Cys were rapidly and efficiently taken up by intestinal membranes, and Hg was retained in intestinal membranes for a relatively long time. When administered orally, no difference was observed in plasma and blood Hg concentrations between MeHg·Cl and MeHg-Cys: plasma and blood Hg concentrations increased gradually and reached steady levels at 8 h after administration. In Caco2 cells, uptake of MeHg-Cys was significantly suppressed by L-leucine, although this was not seen with MeHg·Cl. In Caco2 cells, 81 % of Hg was recovered from cytosol fractions and 13 % of Hg from nuclear fractions (including debris) after a 2-h incubation with MeHg-Cys. In conclusion, the mechanism of membrane uptake and volume of distribution in the initial distribution phase were clearly different between MeHg·Cl and MeHg-Cys. However, such pharmacokinetic differences between them disappeared 1 h after intravenous and after oral routes of administration, possibly due to the metabolism in the body.

摘要

采用大鼠和 Caco2 细胞比较了氯化甲基汞(MeHg·Cl)和甲基汞半胱氨酸(MeHg-Cys)的体内和体外药代动力学,因为人类可能通过食用鱼类而接触到 MeHg 化合物。MeHg 化合物消化后立即进行的体内 Hg 药代动力学仍然不清楚。在 Caco2 细胞中,检查了 MeHg 化合物的膜摄取和细胞内分布。当大鼠静脉内给予时,MeHg·Cl 的血浆和血液中 Hg 浓度分别比 MeHg-Cys 高 20 倍和 2 倍,表明它们的药代动力学性质不同。然而,1 小时后,MeHg·Cl 和 MeHg-Cys 的血浆和血液中 Hg 浓度实际上变得相同,尽管血液中的 Hg 浓度是血浆中的 100 多倍。当将 MeHg·Cl 和 MeHg-Cys 给予到封闭的大鼠空肠袢中时,它们被肠膜迅速而有效地摄取,并且 Hg 在肠膜中保留了相对较长的时间。口服给予时,MeHg·Cl 和 MeHg-Cys 在血浆和血液中的 Hg 浓度没有差异:血浆和血液中的 Hg 浓度逐渐增加,在给药后 8 小时达到稳定水平。在 Caco2 细胞中,L-亮氨酸可显著抑制 MeHg-Cys 的摄取,而 MeHg·Cl 则未见这种情况。在 Caco2 细胞中,在用 MeHg-Cys 孵育 2 小时后,81%的 Hg 从胞质部分回收,13%的 Hg 从核部分(包括碎片)回收。总之,MeHg·Cl 和 MeHg-Cys 的膜摄取和初始分布阶段的分布体积的机制明显不同。然而,静脉内和口服途径给药后 1 小时,它们之间的这种药代动力学差异消失了,可能是由于体内的代谢。

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