Pinto Lorraine Aparecida, Cordeiro Kátia Wolff, Carrasco Viviane, Carollo Carlos Alexandre, Cardoso Cláudia Andréa Lima, Argadoña Eliana Janet Sanjinez, Freitas Karine de Cássia
School of Health Sciences, Federal University of Grande Dourados, Dourados, Mato Grosso do Sul, Brazil.
Naunyn Schmiedebergs Arch Pharmacol. 2015 Mar;388(3):305-17. doi: 10.1007/s00210-014-1069-y. Epub 2014 Nov 25.
The purpose of the present study was to evaluate the gastroprotective and healing effects of the methanolic extract of the seed of the papaya Carica papaya L. (MECP) in rats. Models of acute gastric ulcer induction by ethanol and indomethacin and of chronic ulcer by acetic acid were used. The gastric juice and mucus parameters were evaluated using the pylorus ligation model, and the involvement of sulfhydryl compounds (GSH) and nitric oxide in the gastroprotective effect was analyzed using the ethanol model. The toxicity was assessed through toxicity tests. No signs of toxicity were observed when the rats received a single dose of 2000 mg/kg of extract. The MECP in doses of 125, 250, and 500 mg/kg significantly reduced the gastric lesion with 56, 76, and 82 % inhibition, respectively, and a dose of 30 mg/kg lansoprazole showed 79 % inhibition in the ethanol model. MECP (125, 250, 500 mg/kg) and cimetidine (200 mg/kg) reduced the gastric lesion in the indomethacin model, with 62, 67, 81, and 85 % inhibition, respectively. The MECP (500 mg/kg) and cimetidine (200 mg/kg) treatments showed a reduction in ulcerative symptoms induced by acetic acid by 84 and 73 %, respectively. The antiulcerogenic activity seems to involve GSH because the inhibition dropped from 72 to 13 % in the presence of a GSH inhibitor. Moreover, the MECP showed systemic action, increasing the mucus production and decreasing gastric acidity. Treatments with MECP induce gastroprotection without signs of toxicity. This effect seems to involve sulfhydryl compounds, increased mucus, and reduced gastric acidity.
本研究的目的是评估番木瓜(Carica papaya L.)种子甲醇提取物(MECP)对大鼠的胃保护和愈合作用。采用乙醇和吲哚美辛诱导急性胃溃疡模型以及乙酸诱导慢性胃溃疡模型。使用幽门结扎模型评估胃液和黏液参数,并使用乙醇模型分析巯基化合物(GSH)和一氧化氮在胃保护作用中的参与情况。通过毒性试验评估毒性。当大鼠接受单剂量2000 mg/kg提取物时,未观察到毒性迹象。剂量为125、250和500 mg/kg的MECP分别显著降低胃损伤,抑制率为56%、76%和82%,在乙醇模型中,30 mg/kg兰索拉唑的抑制率为79%。MECP(125、250、500 mg/kg)和西咪替丁(200 mg/kg)在吲哚美辛模型中降低胃损伤,抑制率分别为62%、67%、81%和85%。MECP(500 mg/kg)和西咪替丁(200 mg/kg)处理分别使乙酸诱导的溃疡症状减少84%和73%。抗溃疡活性似乎涉及GSH,因为在存在GSH抑制剂的情况下,抑制率从72%降至13%。此外,MECP显示出全身作用,增加黏液分泌并降低胃酸度。用MECP治疗可诱导胃保护且无毒性迹象。这种作用似乎涉及巯基化合物、增加的黏液和降低的胃酸度。