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本文引用的文献

1
Endothelium-dependent impairments to cerebral vascular reactivity with type 2 diabetes mellitus in the Goto-Kakizaki rat.2 型糖尿病 Goto-Kakizaki 大鼠脑血管反应性的内皮依赖性损伤。
Am J Physiol Regul Integr Comp Physiol. 2019 Jul 1;317(1):R149-R159. doi: 10.1152/ajpregu.00088.2019. Epub 2019 May 15.
2
Middle cerebral artery geometric features are associated with plaque distribution and stroke.大脑中动脉的几何特征与斑块分布和中风有关。
Neurology. 2018 Nov 6;91(19):e1760-e1769. doi: 10.1212/WNL.0000000000006468. Epub 2018 Oct 5.
3
Mind the gap: mechanisms regulating the endothelial barrier.留意间隙:调节内皮屏障的机制。
Acta Physiol (Oxf). 2018 Jan;222(1). doi: 10.1111/apha.12860. Epub 2017 Mar 22.
4
The Endothelium Solves Problems That Endothelial Cells Do Not Know Exist.内皮解决了内皮细胞未知其存在的问题。
Trends Pharmacol Sci. 2017 Apr;38(4):322-338. doi: 10.1016/j.tips.2017.01.008. Epub 2017 Feb 16.
5
Cardiovascular consequences of metabolic syndrome.代谢综合征的心血管后果。
Transl Res. 2017 May;183:57-70. doi: 10.1016/j.trsl.2017.01.001. Epub 2017 Jan 9.
6
The Link Between Angiogenesis and Endothelial Metabolism.血管生成与内皮代谢之间的联系。
Annu Rev Physiol. 2017 Feb 10;79:43-66. doi: 10.1146/annurev-physiol-021115-105134. Epub 2016 Dec 15.
7
Metabolic syndrome impairs reactivity and wall mechanics of cerebral resistance arteries in obese Zucker rats.代谢综合征损害肥胖Zucker大鼠脑阻力动脉的反应性和血管壁力学。
Am J Physiol Heart Circ Physiol. 2015 Dec 1;309(11):H1846-59. doi: 10.1152/ajpheart.00691.2015. Epub 2015 Oct 16.
8
Cerebral Cortical Microvascular Rarefaction in Metabolic Syndrome is Dependent on Insulin Resistance and Loss of Nitric Oxide Bioavailability.代谢综合征中大脑皮质微血管稀疏依赖于胰岛素抵抗和一氧化氮生物利用度的丧失。
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9
Effects of gadolinium chloride on basal flow and compression-induced rapid hyperemia in the rabbit masseter muscle.氯化钆对兔咬肌基础血流及压迫诱导的快速充血的影响。
J Physiol Pharmacol. 2014 Jun;65(3):409-15.
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Prevalence of metabolic syndrome in Brazilian adults: a systematic review.代谢综合征在巴西成年人中的流行情况:一项系统综述。
BMC Public Health. 2013 Dec 18;13:1198. doi: 10.1186/1471-2458-13-1198.

肌源性张力能否保护血管内皮功能?代谢性疾病时整合肌源性激活与扩血管反应性以评估脑阻力血管。

Can Myogenic Tone Protect Endothelial Function? Integrating Myogenic Activation and Dilator Reactivity for Cerebral Resistance Arteries in Metabolic Disease.

机构信息

Departments of Medical Biophysics, Schulich School of Medicine and Dentistry, University of Western Ontario, London, Ontario, Canada.

Department of Physiological Sciences, Oklahoma State University, Stillwater, Oklahoma, USA.

出版信息

J Vasc Res. 2021;58(5):286-300. doi: 10.1159/000516088. Epub 2021 May 10.

DOI:10.1159/000516088
PMID:33971663
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8478702/
Abstract

The obese Zucker rat (OZR) manifests multiple risk factors for impaired cerebrovascular function, including hypertension and insulin resistance although how they combine to produce integrated vascular function is unclear. As studies have suggested that myogenic activation (MA) severity for middle cerebral arteries (MCAs) may be proportional to hypertension severity, we hypothesized that MA will negatively correlate with dilator reactivity in OZR. MA of MCA from OZR was divided into low, medium, and high based on the slope of MA, while MCA reactivity and vascular metabolite bioavailability were assessed in all groups. Endothelium-dependent dilation of MCA in OZR was attenuated and correlated with the MA slope. Treatment of OZR MCA with TEMPOL (antioxidant) improved dilation in low or medium MA groups, but had less impact on high MA. Alternatively, treatment with gadolinium to normalize MA in OZR had reduced impact on dilator reactivity in MCA from low and medium MA groups, but improved responses in the high group. Treatment with both agents resulted in dilator responses that were comparable across all groups. These results suggest that, under conditions with stronger MA, endothelial function may receive some protection despite the environment, potentially from the ability of MCA to reduce wall tension despite increased pressure.

摘要

肥胖型 Zucker 大鼠(OZR)表现出多种脑血管功能受损的风险因素,包括高血压和胰岛素抵抗,尽管它们如何共同导致血管功能的综合变化尚不清楚。由于研究表明,大脑中动脉(MCA)的肌源性激活(MA)严重程度可能与高血压严重程度成正比,我们假设 MA 将与 OZR 中的舒张反应呈负相关。根据 MA 的斜率,将 OZR 的 MCA 的 MA 分为低、中、高,同时评估所有组的 MCA 反应性和血管代谢物生物利用度。OZR 的 MCA 的内皮依赖性舒张功能减弱,并与 MA 斜率相关。在低或中 MA 组中用 TEMPOL(抗氧化剂)处理 OZR 的 MCA 可改善舒张功能,但对高 MA 影响较小。或者,用钆处理以使 OZR 的 MA 正常化,对低和中 MA 组的 MCA 舒张反应的影响较小,但对高 MA 组的反应有所改善。用两种药物联合治疗可使所有组的舒张反应相当。这些结果表明,在 MA 较强的情况下,尽管存在这种环境,内皮功能仍可能受到一定程度的保护,这可能是由于 MCA 有能力降低壁张力,尽管压力增加。