Maria A O, Wendel G H, Guzman J A, Giordano O S, Guerreiro E
Departamento de Química Orgánica, Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis.
Pharmacol Res. 1998 Apr;37(4):281-4. doi: 10.1006/phrs.1998.0291.
Previously we reported that dehydroleucodine (DhL), a sesquiterpene lactone, shows gastric and duodenal cytoprotective activity. The mechanism is not mediated by antiacid secretory action; DhL stimulated mucus production and indomethacin pretreatment reduced cytoprotective action. In the present study we demonstrated that the gastric cytoprotective effect is antagonized by the nitric oxide (NO) synthase inhibitor, NG-nitro-L-arginine. The inhibitory action of NG-nitro-L-arginine is reversed by L-arginine, but not D-arginine. The findings suggest that NO is involved in the gastroprotection induced by DhL.
此前我们报道过,倍半萜内酯脱氢白苞蒿素(DhL)具有胃和十二指肠细胞保护活性。其作用机制并非通过抗酸分泌作用介导;DhL刺激黏液分泌,吲哚美辛预处理可降低细胞保护作用。在本研究中,我们证明一氧化氮(NO)合酶抑制剂NG-硝基-L-精氨酸可拮抗胃细胞保护作用。L-精氨酸可逆转NG-硝基-L-精氨酸的抑制作用,而D-精氨酸则不能。这些发现表明,NO参与了DhL诱导的胃保护作用。