Ivorra M D, D'Ocon M P, Paya M, Villar A
Departamento de Farmacologia y Farmacotecnia, Facultad de Farmacia, Universitat de Valencia, Spain.
Arch Int Pharmacodyn Ther. 1988 Nov-Dec;296:224-31.
The effect of beta-sitosterol 3-beta-glucoside (antihyperglycemic principle isolated from the aerial part of Centaurea seridis L. var. maritima Lge.) and its aglycone on plasma insulin and glucose levels in normo- and hyperglycemic rats was investigated. The results indicate that oral treatment with the glycoside or with the beta-sitosterol increased the fasting plasma insulin levels. There was a corresponding decrease in fasting glycemia when beta-sitosterol was administered orally. In addition, these compounds improved the oral glucose tolerance test with an increase in glucose-induced insulin secretion. But when these products were administered orally, the effect of glycoside, either on fasting insulinemia or on glucose-induced insulin secretion, lasted longer than that of aglycone. The present study compared these effects with those of glibenclamide. It can be assumed that beta-sitosterol 3-beta-D-glucoside acts by increasing circulating insulin levels, and that this effect is due to their aglycone: beta-sitosterol.
研究了β-谷甾醇3-β-葡萄糖苷(从滨海矢车菊地上部分分离出的降血糖成分)及其苷元对正常血糖和高血糖大鼠血浆胰岛素和葡萄糖水平的影响。结果表明,口服该糖苷或β-谷甾醇可提高空腹血浆胰岛素水平。口服β-谷甾醇时,空腹血糖相应降低。此外,这些化合物改善了口服葡萄糖耐量试验,葡萄糖诱导的胰岛素分泌增加。但口服这些产品时,糖苷对空腹胰岛素血症或葡萄糖诱导的胰岛素分泌的作用持续时间比苷元更长。本研究将这些作用与格列本脲的作用进行了比较。可以推测,β-谷甾醇3-β-D-葡萄糖苷通过增加循环胰岛素水平起作用,且这种作用归因于其苷元:β-谷甾醇。