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本文引用的文献

1
Increased intestinal absorption of foreign organic compounds in the presence of ethylenediaminetetraacetic acid (EDTA).在乙二胺四乙酸(EDTA)存在的情况下,外来有机化合物的肠道吸收增加。
Biochem Pharmacol. 1961 Dec;8:421-2. doi: 10.1016/0006-2952(61)90061-2.
2
ALTERATIONS IN THE ABSORPTION OF SULFISOXAZOLE FROM GUINEA PIG INTESTINE.豚鼠肠道中磺胺异恶唑吸收的变化
J Pharm Sci. 1965 Feb;54:314. doi: 10.1002/jps.2600540235.
3
OXIMES ANTAGONISTIC TO INHIBITORS OF CHOLINESTERASE. I.对胆碱酯酶抑制剂有拮抗作用的肟类化合物。I.
J Pharm Sci. 1964 Sep;53:995-1007. doi: 10.1002/jps.2600530902.
4
ELECTRICAL POTENTIALS ASSOCIATED WITH INTESTINAL SUGAR TRANSFER.与肠道糖分转运相关的电势
J Physiol. 1964 Jun;171(2):316-38. doi: 10.1113/jphysiol.1964.sp007379.
5
2-Hydroxyiminomethyl-N-methylpyridinium methanesulphonate (P2S), an antidote to organophosphorus poisoning. Its preparation, estimation and stability.2-羟基亚胺甲基-N-甲基吡啶甲磺酸盐(P2S),一种有机磷中毒的解毒剂。其制备、测定及稳定性。
J Pharm Pharmacol. 1959 Aug;11:485-90. doi: 10.1111/j.2042-7158.1959.tb12586.x.
6
The influence of experimental procedures and dose on the intestinal absorption of an onium compound, benzomethamine.实验程序和剂量对一种鎓化合物苯甲胺肠道吸收的影响。
J Pharmacol Exp Ther. 1961 Mar;131:319-27.
7
In vitro method for the study of the rate of intestinal absorption of sugars.研究糖类肠道吸收速率的体外方法。
J Appl Physiol. 1958 Jan;12(1):145-6. doi: 10.1152/jappl.1958.12.1.145.
8
The absorption of water and of some small solute molecules from the isolated small intestine of the rat.大鼠离体小肠对水和一些小分子溶质的吸收。
J Physiol. 1955 Dec 29;130(3):655-64. doi: 10.1113/jphysiol.1955.sp005433.
9
Diffusion potentials across the small intestine.小肠上的扩散电位。
Nature. 1966 Oct 8;212(5058):189-90. doi: 10.1038/212189a0.
10
Intestinal absorption of pralidoxime and other aldoximes.解磷定及其他醛肟类药物的肠道吸收
Nature. 1966 Jan 15;209(5020):269-71. doi: 10.1038/209269a0.

吡啶醛肟肠道吸收的体外研究。

An in vitro study of the intestinal absorption of pyridinium aldoximes.

作者信息

Crone H D, Keen T E

出版信息

Br J Pharmacol. 1969 Feb;35(2):304-12. doi: 10.1111/j.1476-5381.1969.tb07989.x.

DOI:10.1111/j.1476-5381.1969.tb07989.x
PMID:4975356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1703236/
Abstract
  1. The transfer rates of three pyridinium aldoximes, a non-quaternary pyridine aldoxime and choline across the wall of sacs from the jejunum of rats were measured in vitro.2. The transfer rates observed for any one of the quaternary compounds could be inversely correlated with the transmural potential of the particular sac studied, but there was no correlation with the rates of water or glucose transfer.3. 2-hydroxyiminomethyl-N-methylpyridinium iodide (PAM) had a transfer rate seven times less than that of its non-quaternary analogue, 2-hydroxyiminomethyl pyridine.4. Neither neostigmine nor EDTA affected the transfer rate of PAM in the conditions used.5. It was concluded that the transfer of the quaternary compounds could be explained by diffusion through aqueous pores.
摘要
  1. 在体外测量了三种吡啶醛肟、一种非季铵化吡啶醛肟和胆碱通过大鼠空肠囊壁的转运速率。

  2. 观察到的任何一种季铵化合物的转运速率都可能与所研究的特定囊的跨膜电位呈负相关,但与水或葡萄糖的转运速率无关。

  3. 2-羟基亚胺甲基-N-甲基碘化吡啶(PAM)的转运速率比其非季铵类似物2-羟基亚胺甲基吡啶低七倍。

  4. 在所用条件下,新斯的明和乙二胺四乙酸(EDTA)均未影响PAM的转运速率。

  5. 得出的结论是,季铵化合物的转运可以通过通过水孔的扩散来解释。