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首页> 外文期刊>Alcohol and alcoholism: international journal of the Medical Council on Alcoholism >Inhibitory mechanism of costunolide, a sesquiterpene lactone isolated from Laurus nobilis, on blood-ethanol elevation in rats: involvement of inhibition of gastric emptying and increase in gastric juice secretion.
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Inhibitory mechanism of costunolide, a sesquiterpene lactone isolated from Laurus nobilis, on blood-ethanol elevation in rats: involvement of inhibition of gastric emptying and increase in gastric juice secretion.

机译:从月桂属中分离出倍半萜内酯的木香内酯对大鼠血液中乙醇含量的抑制作用:抑制胃排空和增加胃液分泌。

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摘要

Basic inhibitory mechanisms of costunolide and its active component, alpha-methylene-gamma-butyrolactone (alpha-MGBL), on blood-ethanol elevation were investigated in rats. In normal rats, blood-ethanol elevation (30 min later) induced by 20% (v/v) ethanol [5 ml/kg, per os (p.o.)] was strongly inhibited by pretreatment (30 min earlier) with costunolide and alpha-MGBL (50 mg/kg, p.o.). In pylorus-ligated rats given ethanol, blood-ethanol level (30 min) was barely elevated compared with that of normal rats. Neither costunolide nor alpha-MGBL affected the blood-ethanol elevation in pylorus-ligated rats or that induced by intraperitoneal and intraduodenal ethanol administration. Moreover, these compounds given orally induced no irreversible changes in alcohol dehydrogenase activity in rat liver. We continuously investigated the rate of gastric emptying in rats given various test meals. Costunolide and alpha-MGBL suppressed gastric emptying in rats given 20% ethanol and 1% sodium carboxymethyl cellulose. alpha-MGBL (50 mg/kg), but not costunolide, suppressed gastric emptying in 20% glucose-loaded rats. In an in vitro experiment, alpha-MGBL contracted the pylorus strip at a high concentration (20 mM), which was the estimated concentration in the stomach when the substance was given orally in vivo. These findings suggested that alpha-MGBL constricted the pylorus and caused delay of gastric emptying. Moreover, both compounds increased gastric fluid secretion with pepsin and mucus. In conclusion, the inhibitory effects of costunolide and alpha-MGBL on blood-ethanol elevation were based on inhibition of gastric emptying and dilution of the ethanol concentration by the increased gastric fluid.
机译:在大鼠中研究了木香酚及其活性成分α-亚甲基-γ-丁内酯(α-MGBL)对血液中乙醇升高的基本抑制机制。在正常大鼠中,通过用木香酚内酯和α-苯甲酸酯预处理(30分钟之前)可强烈抑制20%(v / v)乙醇[5 ml / kg,每os(po)]引起的血液乙醇升高(30分钟后)。 MGBL(50 mg / kg,口服)。在幽门结扎的大鼠中加入乙醇,与正常大鼠相比,血液-乙醇水平(30分钟)几乎没有升高。 Costunolide或alpha-MGBL均不影响幽门结扎大鼠的血乙醇升高或腹膜内和十二指肠内乙醇诱导的升高。而且,口服给予的这些化合物在大鼠肝脏中没有引起乙醇脱氢酶活性的不可逆变化。我们不断研究给予各种试验餐的大鼠胃排空的速率。在使用20%乙醇和1%羧甲基纤维素钠的情况下,Costunolide和α-MGBL抑制了大鼠的胃排空。 α-MGBL(50 mg / kg)可抑制20%葡萄糖负荷大鼠的胃排空,但不能抑制木香酚。在体外实验中,alpha-MGBL以高浓度(20 mM)收缩了幽门条,这是在体内口服该物质时胃中的估计浓度。这些发现表明,α-MGBL收缩了幽门并导致胃排空延迟。此外,两种化合物均增加胃蛋白酶和胃蛋白酶和粘液的分泌。总之,木香酚内酯和α-MGBL对血中乙醇升高的抑制作用是基于抑制胃排空和增加胃液稀释乙醇浓度。

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