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影响高血压小鼠血压昼夜差异的基因。

Genes influencing circadian differences in blood pressure in hypertensive mice.

机构信息

Basic and Clinical Genomics Laboratory, School of Medical Sciences and Bosch Institute, The University of Sydney, Sydney, Australia.

出版信息

PLoS One. 2011 Apr 26;6(4):e19203. doi: 10.1371/journal.pone.0019203.

Abstract

Essential hypertension is a common multifactorial heritable condition in which increased sympathetic outflow from the central nervous system is involved in the elevation in blood pressure (BP), as well as the exaggerated morning surge in BP that is a risk factor for myocardial infarction and stroke in hypertensive patients. The Schlager BPH/2J mouse is a genetic model of hypertension in which increased sympathetic outflow from the hypothalamus has an important etiological role in the elevation of BP. Schlager hypertensive mice exhibit a large variation in BP between the active and inactive periods of the day, and also show a morning surge in BP. To investigate the genes responsible for the circadian variation in BP in hypertension, hypothalamic tissue was collected from BPH/2J and normotensive BPN/3J mice at the 'peak' (n = 12) and 'trough' (n = 6) of diurnal BP. Using Affymetrix GeneChip® Mouse Gene 1.0 ST Arrays, validation by quantitative real-time PCR and a statistical method that adjusted for clock genes, we identified 212 hypothalamic genes whose expression differed between 'peak' and 'trough' BP in the hypertensive strain. These included genes with known roles in BP regulation, such as vasopressin, oxytocin and thyrotropin releasing hormone, as well as genes not recognized previously as regulators of BP, including chemokine (C-C motif) ligand 19, hypocretin and zinc finger and BTB domain containing 16. Gene ontology analysis showed an enrichment of terms for inflammatory response, mitochondrial proton-transporting ATP synthase complex, structural constituent of ribosome, amongst others. In conclusion, we have identified genes whose expression differs between the peak and trough of 24-hour circadian BP in BPH/2J mice, pointing to mechanisms responsible for diurnal variation in BP. The findings may assist in the elucidation of the mechanism for the morning surge in BP in essential hypertension.

摘要

原发性高血压是一种常见的多因素遗传性疾病,其中中枢神经系统的交感神经输出增加与血压升高有关,以及高血压患者中与心肌梗死和中风风险相关的血压晨峰升高。Schlager BPH/2J 小鼠是一种高血压的遗传模型,其中下丘脑的交感神经输出增加在血压升高中起着重要的病因作用。Schlager 高血压小鼠在白天的活动期和不活动期之间血压变化很大,并且也表现出血压晨峰升高。为了研究导致高血压中血压昼夜变化的基因,从 BPH/2J 和正常血压的 BPN/3J 小鼠的下丘脑组织中采集了在昼夜血压的“高峰”(n = 12)和“低谷”(n = 6)时的组织。使用 Affymetrix GeneChip® Mouse Gene 1.0 ST Arrays,通过定量实时 PCR 进行验证,并使用一种调整时钟基因的统计方法,我们鉴定出 212 个在下丘脑组织中在高血压株中在“高峰”和“低谷”血压之间表达不同的基因。这些基因包括已知在血压调节中起作用的基因,如加压素、催产素和促甲状腺素释放激素,以及以前未被认为是血压调节剂的基因,包括趋化因子(C-C 基序)配体 19、食欲素和锌指和 BTB 结构域包含 16。基因本体论分析显示,炎症反应、线粒体质子转运 ATP 合酶复合物、核糖体结构成分等术语富集。总之,我们已经鉴定出在 BPH/2J 小鼠 24 小时昼夜血压的高峰和低谷之间表达不同的基因,这些基因可能是导致血压昼夜变化的机制。这些发现可能有助于阐明原发性高血压中血压晨峰升高的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0fd/3082552/2ec3a358c6aa/pone.0019203.g001.jpg

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