Franco L, Velo G P
Institute of Pharmacology, University of Verona, Policlinico di Borgo Roma, Italy.
Inflamm Res. 1995 Mar;44(3):139-42. doi: 10.1007/BF01782025.
We investigated the effect of oral administration of graded doses of: nordihydroguaiaretic acid (NDGA), CuNSN, a bis(2-benzimidazolyl)thioether and CuCl2 on ethanol-induced gastric damage in the rat and the role of leukotrienes and prostaglandins in attenuating this damage. In the experiments we determined ex-vivo eicosanoid release in the rat gastric mucosa pretreated with the above-mentioned compounds. The results indicate that the gastric lesion is accompanied by an increase in mucosa-synthesize LTC4, while PGE2 formation remains unchanged. Pretreatment with NDGA, CuNSN and CuCl2, protects the gastric mucosa from damages and reduces the increase in LTC4 mucosal formation. CuNSN and CuCl2 increase the PGE2 release, while NDGA has no effect on this pathway. These results suggest that one of the possible mechanisms of the NDGA protective effect is related to the inhibition of LTC4 formation, while the PGE2 increase in synthesis together with the leukotriene inhibition could contribute to the protective effect of CuNSN and CuCl2.
我们研究了口服不同剂量的去甲二氢愈创木酸(NDGA)、CuNSN(一种双(2-苯并咪唑基)硫醚)和氯化铜对大鼠乙醇诱导的胃损伤的影响,以及白三烯和前列腺素在减轻这种损伤中的作用。在实验中,我们测定了用上述化合物预处理的大鼠胃黏膜中类花生酸的体外释放。结果表明,胃损伤伴随着黏膜合成LTC4的增加,而PGE2的形成保持不变。用NDGA、CuNSN和氯化铜预处理可保护胃黏膜免受损伤,并减少LTC4黏膜形成的增加。CuNSN和氯化铜增加了PGE2的释放,而NDGA对该途径没有影响。这些结果表明,NDGA保护作用的一种可能机制与抑制LTC4的形成有关,而PGE2合成的增加以及对白三烯的抑制可能有助于CuNSN和氯化铜的保护作用。