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二氢槲皮素和岩藻依聚糖抑制大鼠主动脉照射后血管紧张素转换酶活性的升高。

Dihydroquercetin and Fucoidin Inhibit the Increase of Angiotensin-Converting Enzyme Activity in the Rat Aorta after Irradiation.

作者信息

Korystova A F, Kublik L N, Kim Yu A, Levitman M Kh, Shaposhnikova V V, Korystov Yu N

机构信息

Institute of Theoretical and Experimental Biophysics, Russian Academy of Sciences, Pushchino, Moscow Region, Russia.

Institute of Cell Biophysics, Russian Academy of Sciences, Pushchino, Moscow Region, Russia.

出版信息

Bull Exp Biol Med. 2018 Jul;165(3):360-363. doi: 10.1007/s10517-018-4170-2. Epub 2018 Jul 12.

Abstract

The time course of angiotensin-converting enzyme activity in the rat aorta after fractionated exposure to ionizing radiation and the effects of dihydroquercetin and fucoidin on this parameter were studied. Male Wistar rats were exposed to single or repeated (fractionated) X-ray radiation in a dose of 2.5 Gy at 200 kV. Activity of angiotensin-converting enzyme in aorta segments was evaluated 2 h after the last exposure by hydrolysis of hippuryl-histidineleucin substrate. Enzyme activity in the rat aorta was higher than normally after all the studied doses of fractionated exposure (2.5 Gy per fraction) with the maximum effect after the total dose of 7.5 Gy (3 fractions). Fucoidin, a blocker of endothelium receptors realizing the leukocyte adhesion to the endothelium, and flavonoid dihydroquercetin inhibiting expression of adhesion molecules in the endothelium abolished the increase in activity of angiotensinconverting enzyme in the rat aorta after single exposure; moreover, dihydroquercetin reduced significantly the effect of fractionated exposure. These data indicate that leukocyte adhesion to the endothelium is an important factor contributing to the increase of angiotensin-converting enzyme activity in the aorta.

摘要

研究了分次暴露于电离辐射后大鼠主动脉中血管紧张素转换酶活性的时间进程,以及二氢槲皮素和岩藻依聚糖对该参数的影响。雄性Wistar大鼠接受200 kV、剂量为2.5 Gy的单次或重复(分次)X射线辐射。在最后一次暴露后2小时,通过水解马尿酰 - 组氨酸 - 亮氨酸底物评估主动脉段中血管紧张素转换酶的活性。在所有研究的分次暴露剂量(每次2.5 Gy)后,大鼠主动脉中的酶活性均高于正常水平,在总剂量为7.5 Gy(3次分次)后效果最为明显。岩藻依聚糖是一种内皮细胞受体阻滞剂,可实现白细胞与内皮细胞的黏附,而黄酮类化合物二氢槲皮素可抑制内皮细胞中黏附分子的表达,二者均可消除单次暴露后大鼠主动脉中血管紧张素转换酶活性的增加;此外,二氢槲皮素可显著降低分次暴露的影响。这些数据表明,白细胞与内皮细胞的黏附是导致主动脉中血管紧张素转换酶活性增加的一个重要因素。

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