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黄芩素可预防糖尿病相关高血压:对血管反应性和僵硬度的影响。

Baicalein protects against hypertension associated with diabetes: effect on vascular reactivity and stiffness.

作者信息

El-Bassossy Hany M, Hassan Noura Ahmed, Mahmoud Mona Fouad, Fahmy Ahmed

机构信息

Department of Pharmacology and Toxicology, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia; Department of Pharmacology and Toxicology, Faculty of Pharmacy, Zagazig University, Zagazig, Egypt.

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Zagazig University, Zagazig, Egypt.

出版信息

Phytomedicine. 2014 Oct 15;21(12):1742-5. doi: 10.1016/j.phymed.2014.08.012. Epub 2014 Sep 19.

Abstract

The present work investigated the possible protective effect of baicalein, a natural lipoxygenase enzyme inhibitor, on both insulin deficiency (ID) and insulin resistance (IR)-induced macro-vascular impairment. ID and IR were induced by STZ or fructose for 8 or 12 weeks respectively while baicalein was administered in the last six weeks. Blood pressure (BP) was recorded and isolated aorta reactivity to phenylephrine (PE) and acetylcholine (ACh) were studied. Blood levels of glucose, insulin, advanced glycation end products (AGEs) and tumour necrosis factor-α (TNF-α) were determined. Aortic nuclear transcription factor-κB (NF-κB) activation was assessed. Both models resulted in elevated BP, increased vasoconstriction and impaired relaxation KCl, elevated TNF-α and AGEs, NF-κB activation, marked infiltration of leukocytes in the adventitia, pyknosis of endothelial cells and marked collagen deposition. Baicalein ameliorated elevations in BP in models, prevented exaggerated vasoconstriction IR model and improved relaxation in ID model. Baicalein reduced AGEs and TNF-α level, decreased NF-κB activation and inhibited histopathological changes in both models. Baicalein offsets the hypertensive and the vascular impairment associated with both diabetic models via ameliorating functional and structural derangements of blood vessels.

摘要

本研究探讨了天然脂氧合酶抑制剂黄芩苷对胰岛素缺乏(ID)和胰岛素抵抗(IR)诱导的大血管损伤的潜在保护作用。分别用链脲佐菌素(STZ)或果糖诱导ID和IR,持续8周或12周,而黄芩苷在最后六周给药。记录血压(BP),并研究离体主动脉对去氧肾上腺素(PE)和乙酰胆碱(ACh)的反应性。测定血糖、胰岛素、晚期糖基化终产物(AGEs)和肿瘤坏死因子-α(TNF-α)的血药浓度。评估主动脉核转录因子-κB(NF-κB)的激活情况。两种模型均导致血压升高、血管收缩增强、氯化钾舒张功能受损、TNF-α和AGEs升高、NF-κB激活、外膜白细胞明显浸润、内皮细胞固缩和胶原沉积明显。黄芩苷改善了模型中的血压升高,预防了IR模型中过度的血管收缩,并改善了ID模型中的舒张功能。黄芩苷降低了AGEs和TNF-α水平,降低了NF-κB激活,并抑制了两种模型中的组织病理学变化。黄芩苷通过改善血管的功能和结构紊乱,抵消了与两种糖尿病模型相关的高血压和血管损伤。

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