Hiruma-Lima C A, Spadari-Bratfisch R C, Grassi-Kassisse D M, Brito A R
Departamento de Fisiologia e Biofísica, Universidade Estadual de Campinas, São Paulo, Brasil.
Planta Med. 1999 May;65(4):325-30. doi: 10.1055/s-1999-13995.
The bark of Croton cajucara Benth, is used in Brazilian folk medicine as an infusion to treat gastrointestinal disorders. The aim of the present study was to assess the mechanisms involved in the antiulcerogenic activity of dehydrocrotonin (DHC), a diterpene isolated from C. cajucara bark. We studied the effects of DHC on pylorus ligature (Shay) in mice treated with the drug (100 mg/kg) by the intraduodenal route. DHC did not induce any alteration in gastric volume in Shay mice but modified the pH and total acid concentration of gastric juice. Incubation of gastric juice with DHC did not reduce gastric acidity compared to control. We also investigated the effects of DHC on the response to histamine of right atria isolated from guinea pigs and on the response to carbachol of stomach fundus strips from rats. The concentration-response curves for the chronotropic effect of histamine in guinea pig right atria were shifted to the right, with a significant decrease in the maximum response, in the presence of DHC. Similar results were obtained with DHC (30 microM) for the concentration-response curves to carbachol in the isolated rat stomach. The ability of DHC to increase PGE2 release from rat stomach mucous cells was also studied. We observed that DHC induced a significant increase in PGE2 production (60% compared to control). In addition, the effects of DHC on the healing of acetic acid-induced gastric ulcer in rats were evaluated 14 days after acid injection. Oral administration of DHC (100 mg/kg per day) for 14 consecutive days had no effect on gastric ulcer healing in rats. Thus, the protective effect of DHC on induced gastric lesions could be due to synergistic effects, e.g., an increase in PGE2 release and non-competitive antagonism of H2-receptors and of muscarinic receptors. Whereas the former result represents an increase in the protective factors, the latter one shows a decrease in the aggressive factors against the gastric mucosa.
巴豆叶巴豆(Croton cajucara Benth)的树皮在巴西民间医学中被用作浸剂来治疗胃肠道疾病。本研究的目的是评估脱氢巴豆素(DHC)的抗溃疡活性机制,DHC是从巴豆叶巴豆树皮中分离出的一种二萜。我们通过十二指肠途径研究了DHC(100 mg/kg)对幽门结扎(Shay)小鼠的影响。DHC对Shay小鼠的胃容量没有引起任何改变,但改变了胃液的pH值和总酸浓度。与对照组相比,DHC与胃液孵育并没有降低胃酸度。我们还研究了DHC对豚鼠离体右心房组胺反应以及大鼠胃底条带对卡巴胆碱反应的影响。在存在DHC的情况下,豚鼠右心房组胺变时效应的浓度-反应曲线向右移动,最大反应显著降低。对于离体大鼠胃中卡巴胆碱的浓度-反应曲线,DHC(30 microM)也得到了类似的结果。我们还研究了DHC增加大鼠胃黏液细胞释放PGE2的能力。我们观察到DHC诱导PGE2产生显著增加(与对照组相比增加60%)。此外,在酸注射14天后评估了DHC对大鼠乙酸诱导的胃溃疡愈合的影响。连续14天口服DHC(每天100 mg/kg)对大鼠胃溃疡愈合没有影响。因此,DHC对诱导性胃损伤的保护作用可能是由于协同作用,例如PGE2释放增加以及对H2受体和毒蕈碱受体的非竞争性拮抗作用。前者结果代表保护因子增加,而后者显示针对胃黏膜的攻击因子减少。