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壳聚糖抑制脂肪消化的机制及抗坏血酸盐的协同作用。

Mechanism for the inhibition of fat digestion by chitosan and for the synergistic effect of ascorbate.

作者信息

Kanauchi O, Deuchi K, Imasato Y, Shizukuishi M, Kobayashi E

机构信息

Applied Bioresearch Center, Kirin Brewery Co. Ltd., Gunma, Japan.

出版信息

Biosci Biotechnol Biochem. 1995 May;59(5):786-90. doi: 10.1271/bbb.59.786.

Abstract

We investigated the mechanism for the inhibition of fat digestion by chitosan, and the synergistic effect of ascorbate. The important inhibition characteristics of fat digestion by chitosan from observations of the ileal contents were that it dissolved in the stomach and then changed to a gelled form, entrapping fat in the intestine. The synergistic effect of ascorbate (AsA) on the inhibition of fat digestion by chitosan is thought not to be acid-dependent but due to the specificity of AsA itself, according to the data resulting from using preparations supplemented with sodium ascorbate (AsN). The mechanism for the synergistic effect is considered to be 1) viscosity reduction in the stomach, which implies that chitosan mixed with a lipid is better than chitosan alone, 2) an increase in the oil-holding capacity of the chitosan gel, and 3) the chitosan-fat gel being more flexible and less likely to leak entrapped fat in the intestinal tract.

摘要

我们研究了壳聚糖抑制脂肪消化的机制以及抗坏血酸盐的协同作用。通过观察回肠内容物发现,壳聚糖抑制脂肪消化的重要特征是它在胃中溶解,然后转变为凝胶形式,在肠道中捕获脂肪。根据使用添加抗坏血酸钠(AsN)制剂所得到的数据,抗坏血酸盐(AsA)对壳聚糖抑制脂肪消化的协同作用被认为并非依赖于酸性,而是由于AsA自身的特性。协同作用的机制被认为是:1)胃中粘度降低,这意味着与脂质混合的壳聚糖比单独的壳聚糖更好;2)壳聚糖凝胶的持油能力增加;3)壳聚糖 - 脂肪凝胶更具柔韧性,在肠道中不太可能泄漏所捕获的脂肪。

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