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5,7-二羟基黄酮作用于内皮型一氧化氮合酶,从而在自发性高血压大鼠中实现降压效果。

5,7-Dihydroxyflavone acts on eNOS to achieve hypotensive effects in spontaneously hypertensive rats.

作者信息

Shen Zi-Han, Ye Tongjie, Chen Baozhen, Wan Congchao, Lu Xiaolin, Chen Ting-Hsu, Lin Shuang, Ye Jia-Xin, Xie Liping, Fu Yaw-Syan

机构信息

College of Clinical Medicine, Xiamen Medical College, Xiamen, Fujian, China.

College of Pharmacy, Xiamen Medical College, Xiamen, Fujian, China.

出版信息

Sci Rep. 2025 Jan 2;15(1):594. doi: 10.1038/s41598-024-84259-6.

Abstract

Hypertension is one of the most serious chronic diseases. This study will focus on the systemic antihypertensive mechanisms of 5,7-dihydroxyflavone from in silico simulations to in vivo validations. In-silico studies were applied by network pharmacology, molecular docking, and molecular dynamic simulation. Based on the information of network pharmacology, 5,7-dihydroxyflavone could act on several different blood pressure regulating pathways, molecular docking results confirmed it might direct binding on the active pocket of eNOS, and the average molecular distance between 5,7-dihydroxyflavone -eNOS is less than 0.4 Å by molecular dynamic simulation. The in vivo studies were carried by SHRs oral administrated with 10 mg/kg 5,7-dihydroxyflavone that could alleviate hypertensive symptoms within 30 min, but if SHRs pretreated with L-NAME (10 mg/kg, an eNOS inhibitor) can erase the anti-hypertensive effects of 5,7-dihydroxyflavone, but no affected by aminoguanidine pretreatment (100 mg/kg, the selective antagonist of iNOS). Furthermore, oral administration of 5,7-dihydroxyflavone does not affect the heart rate and pulse pressure difference in SHR rats. In conclusion, the effects of 5,7-dihydroxyflavone on blood pressure regulation may act on eNOS as an agonist to achieve its acute antihypertensive effects. These acute antihypertensive effects suggest that 5,7-dihydroxyflavone has the potential to be a candidate medication for urgently lowering blood pressure requirements without posing hypertensive risks.

摘要

高血压是最严重的慢性疾病之一。本研究将聚焦于5,7 - 二羟基黄酮从计算机模拟到体内验证的全身降压机制。通过网络药理学、分子对接和分子动力学模拟进行计算机研究。基于网络药理学信息,5,7 - 二羟基黄酮可作用于多种不同的血压调节途径,分子对接结果证实其可能直接结合于内皮型一氧化氮合酶(eNOS)的活性口袋,且通过分子动力学模拟5,7 - 二羟基黄酮与eNOS之间的平均分子距离小于0.4埃。体内研究采用自发性高血压大鼠(SHRs)口服10 mg/kg的5,7 - 二羟基黄酮进行,其可在30分钟内缓解高血压症状,但如果用L - 精氨酸甲酯(L - NAME,10 mg/kg,一种eNOS抑制剂)预处理SHRs,则可消除5,7 - 二羟基黄酮的降压作用,而氨基胍预处理(100 mg/kg,诱导型一氧化氮合酶(iNOS)的选择性拮抗剂)则无此影响。此外,口服5,7 - 二羟基黄酮对SHR大鼠的心率和脉压差无影响。总之,5,7 - 二羟基黄酮对血压调节的作用可能是作为激动剂作用于eNOS以实现其急性降压效果。这些急性降压作用表明,5,7 - 二羟基黄酮有潜力成为一种在不带来高血压风险的情况下满足紧急降低血压需求的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94cd/11695686/d5669d734e5b/41598_2024_84259_Fig1_HTML.jpg

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