Tsurumi K, Fujimura H
Jpn J Pharmacol. 1983 Feb;33(1):165-73. doi: 10.1254/jjp.33.165.
Prostaglandins (PGs) increase the intestinal fluid to result in diarrhea. Some laxatives are known to exert their actions partially by stimulating the PGs biosynthesis. On the other hand, it is well documented that nonsteroidal anti-inflammatory drugs (NSAID) inhibit markedly the PGs biosynthesis. Since endotoxin (ETX) also produces diarrhea similarly in all species of experimental animals, we investigated the effect of various NSAID and steroidal anti-inflammatory drugs (SAID) on ETX-induced diarrhea in mice. ETX given p.o. did not produce diarrhea, but it could induce it after parenteral administration, especially intravenous injection. ALL NSAID and SAID tested inhibited ETX-induced diarrhea at dose levels similar to or lower than those commonly producing an acute anti-inflammatory effect. The anti-diarrheal effects were found in not only acidic NSAID, but also in basic NSAID and SAID which did not inhibited ultraviolet erythema, acute death induced by arachidonic acid injection and PGs biosynthesis. Therefore, this test using ETX-induced diarrhea in mice may be used as a new and desirable method for screening or evaluating anti-inflammatory drugs. The mechanism of diarrheogenic action of ETX is poorly understood, but may be attributed to inhibition of PGs biosynthesis besides other unknown actions.
前列腺素(PGs)可增加肠液分泌导致腹泻。已知一些泻药部分通过刺激PGs生物合成发挥作用。另一方面,有充分文献记载非甾体抗炎药(NSAID)可显著抑制PGs生物合成。由于内毒素(ETX)在所有实验动物物种中均能类似地引起腹泻,我们研究了各种NSAID和甾体抗炎药(SAID)对ETX诱导的小鼠腹泻的影响。口服ETX不会引起腹泻,但经胃肠外给药,尤其是静脉注射后可诱导腹泻。所有测试的NSAID和SAID在与通常产生急性抗炎作用相似或更低的剂量水平下均能抑制ETX诱导的腹泻。不仅在酸性NSAID中发现了止泻作用,在碱性NSAID和SAID中也发现了该作用,而这些药物并不抑制紫外线红斑、花生四烯酸注射诱导的急性死亡以及PGs生物合成。因此,这种利用ETX诱导小鼠腹泻的试验可作为筛选或评估抗炎药物的一种新的理想方法。ETX致泻作用的机制尚不清楚,但除其他未知作用外,可能归因于对PGs生物合成的抑制。