黄酮类化合物的提取[j];对弹性酶、胰蛋白酶和凝乳胰蛋白酶的体外抑制活性。2. 体内血管保护活性比较[j]。

Journal de pharmacologie Pub Date : 1986-01-01
M Jonadet, M T Meunier, F Villie, J P Bastide, J L Lamaison
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引用次数: 0

摘要

采用体外实验研究了黑荆和紫荆提取物(A1 + A2, A1, A2)对蛋白酶弹性酶、胰蛋白酶和α -凝乳胰蛋白酶活性的抑制作用。在合成底物浓度分别为0.56 mg/ml和0.16 mg/ml时,猪胰脏弹性酶活性降低50%。抑制胰蛋白酶和α -凝乳胰蛋白酶活性的效果较差。除炼金草A2部位无明显活性外,其余化合物均有明显的体内血管保护作用。结果表明,这些抑制剂可能在保护受蛋白水解酶不利影响的结缔组织和弹性组织方面发挥作用。另一个优点是它们没有毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Flavonoids extracted from Ribes nigrum L. and Alchemilla vulgaris L.: 1. In vitro inhibitory activities on elastase, trypsin and chymotrypsin. 2. Angioprotective activities compared in vivo].

In vitro experiments were conducted on the inhibitory properties of extracts from Ribes nigrum L. and Alchemilla vulgaris L. (fractions A1 + A2, A1, A2) on activity of the proteolytic enzymes elastase, trypsin and alpha-chymotrypsin. Extracts from Ribes Nigrum L. and Alchemilla Vulgaris L. (Fraction A1) inhibited 50% of the activity of porcine pancreas elastase at concentrations of 0.56 mg/ml and 0.16 mg/ml, respectively, against a synthetic substrate. Inhibition was less effective on activity of trypsin and alpha-chymotrypsin. Marked in vivo angioprotective properties were shown by the compounds studied, except Fraction A2 of Alchemilla vulgaris L. which had no significant activity. The results suggest a possible role by these inhibitors in the protection of conjunctive and elastic tissues adversely affected by proteolytic enzymes. An additional advantage is their lack of toxicity.

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