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丙磺舒增加大鼠体内氯苯氧基乙酸的急性毒性及脑内浓度。

Increase in the acute toxicity and brain concentrations of chlorophenoxyacetic acids by probenecid in rats.

作者信息

Ylitalo P, Närhi U, Elo H A

机构信息

Department of Pharmacology and Toxicology, University of Kuopio, Finland.

出版信息

Gen Pharmacol. 1990;21(5):811-4. doi: 10.1016/0306-3623(90)91038-s.

Abstract
  1. Probenecid increased the acute toxicity of chlorophenoxyacetic acids (2,4-D, 2,4,5-T and MCPA) in rats. 2. Probenecid increased the brain to plasma ratios of all the three 14C-labelled chlorophenoxyacetic acids. The increase was due only partly to the displacement of chlorophenoxyacids from their binding sites in rat plasma proteins by probenecid. 3. Probenecid did not change significantly the intracerebral distribution pattern of 14C-labelled chlorophenoxyacetic acids.
摘要
  1. 丙磺舒增加了氯苯氧基乙酸(2,4-滴、2,4,5-涕和灭草灵)对大鼠的急性毒性。2. 丙磺舒增加了所有三种14C标记的氯苯氧基乙酸的脑血浆比。这种增加仅部分归因于丙磺舒将氯苯氧基酸从大鼠血浆蛋白中的结合位点置换出来。3. 丙磺舒未显著改变14C标记的氯苯氧基乙酸在脑内的分布模式。

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