首页> 外文期刊>Naunyn-Schmiedeberg's Archives of Pharmacology >Antiulcerogenic activity of extract, fractions, and some compounds obtained from Polygala cyparissias St. Hillaire & Moquin (Polygalaceae).
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Antiulcerogenic activity of extract, fractions, and some compounds obtained from Polygala cyparissias St. Hillaire & Moquin (Polygalaceae).

机译:提取物,部分和一些化合物的抗溃疡活性,该化合物来自远志圣希勒尔和莫昆(远志科)。

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摘要

The present study evaluates the gastroprotective properties of acetone extract, chloroform, and methanol fractions, alpha-spinasterol (1); 1,3-dihydroxy-7-methoxyxanthone (2); and 1,7-dihydroxy-2,3-methylenedioxyxanthone (3) obtained from Polygala cyparissias (Polygalaceae). Gastroprotective assays were performed in mice using ethanol/HCl and nonsteroidal anti-inflammatory drug (NSAID)/bethanechol-induced ulcer models. Chloroformic fraction showed no interesting results. On the other hand, in the ethanol/HCl-induced ulcer model, the treatment using doses of 50, 125, and 250 mg/kg promoted ulcer inhibition of 45.19+/-12.93%, 62.99+/-3.49%, and 67.40+/-4.75% for acetone extract and 43.70+/-5.12%, 64.56+/-5.64%, and 74.49+/-6.13% for methanol fraction. In the model of NSAID/bethanechol-induced ulcer, the ulcer inhibitions in the same doses were 28.12+/-12.45%, 60.16+/-6.58%, and 77.86+/-7.18% for the acetone extract and 46.09+/-6.92%, 67.45+/-4.36%, and 75.00+/-2.92% for the methanol fraction. In view of the antiulcer potential of the acetone extract and its high yield and xanthone content, it was submitted to chromatographic procedures, giving compounds 1-3, which were also evaluated in the ethanol-induced ulcer model. The results showed that at a dose of 50 mg/kg, these compounds reduced the percentage of ulcer by around 71.26+/-9.40%, 81.10+/-5.75%, and 86.22+/-3.42%, for compounds 1, 2, and 3, respectively. The antiulcerogenic activity of P. cyparissias may be attributed, at least in part, to these compounds.
机译:本研究评估了丙酮提取物,氯仿和甲醇馏分α-spinasterol(1)的胃保护性能。 1,3-二羟基-7-甲氧基黄酮(2);购自圆柏(Polygala cyparissias)(Polygalaceae)的1,7-二羟基-2,3-亚甲基二氧基黄酮(3)。使用乙醇/ HCl和非甾体抗炎药(NSAID)/苯乙二酚诱导的溃疡模型在小鼠中进行了胃保护性测定。氯仿分数未显示有趣的结果。另一方面,在乙醇/ HCl诱发的溃疡模型中,以50、125和250 mg / kg的剂量进行治疗可促进溃疡抑制45.19 +/- 12.93%,62.99 +/- 3.49%和67.40+对于丙酮提取物,为--4.75%,对于甲醇馏分,为-43.70 +/- 5.12%,64.56 +/- 5.64%和74.49 +/- 6.13%。在非甾体抗炎药/安息香引起的溃疡模型中,相同剂量的溃疡提取物对丙酮提取物的抑制作用分别为28.12 +/- 12.45%,60.16 +/- 6.58%和77.86 +/- 7.18%,以及46.09 +/- 6.92对于甲醇馏分,分别为%,67.45 +/- 4.36%和75.00 +/- 2.92%。考虑到丙酮提取物的抗溃疡潜力及其高收率和x吨酮的含量,将其进行色谱分析,得到化合物1-3,其也在乙醇诱导的溃疡模型中进行了评估。结果表明,对于化合物1、2,这些化合物以50 mg / kg的剂量可使溃疡百分率降低约71.26 +/- 9.40%,81.10 +/- 5.75%和86.22 +/- 3.42%。和3。 cy。parparissias的抗溃疡活性可能至少部分归因于这些化合物。

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