Antonov Yegor V, Alexandrovich Yuriy V, Redina Olga E, Gilinsky Michael A, Markel Arcady L
a Laboratory of Genetics of Arterial Hypertension , Institute of Cytology and Genetics , Novosibirsk , Russia.
b Laboratory of Regulation of Adaptation Processes , Institute of Physiology and Fundamental Medicine , Novosibirsk , Russia.
Clin Exp Hypertens. 2016;38(5):415-23. doi: 10.3109/10641963.2015.1116546. Epub 2016 Jun 30.
Association between stress and hypertensive disease is still a matter of debate. Can stress be the cause of hypertensive disease and, if so, what mechanisms are involved? To clarify this question, the Inherited stress-induced arterial hypertensive rat strain (ISIAH rat strain) with a stress related arterial hypertension was developed by selection for the enhanced blood pressure response to 0.5 h restraint stress. The main intention of this work is to confirm that the adrenals are a main link between stress and hypertensive disease.
Hypertensive ISIAH and normotensive WAG rats have been studied. The in vivo secretion rate of corticosterone, aldosterone, 11-Deoxycorticosterone (DOC), and 11-dehydrocorticosterone was measured in anesthetized rats by adrenal vein cannulation. The Dexamethasone/Adrenocorticotropic hormone (DEX/ACTH) test was performed and mRNA expression of Cyp11b1 and Cyp11b2 genes in adrenals was evaluated by real-time PCR.
An increased secretion rate of corticosterone and DOC and higher peripheral plasma aldosterone concentration in ISIAH rats were revealed. Response of plasma aldosterone to the surgical stress (adrenal vein cannulation) in the ISIAH rats was significantly higher. The increase of corticosterone and aldosterone in response to ACTH was also higher in hypertensive rats. The basal mRNA expression of both Cyp11b1 and Cyp11b2 genes was increased in the ISIAH rats. The ratio 11-dehydrocorticosterone/corticosterone in ISIAH rats was low which indicates the weakening of 11-beta-Hydroxysteroid dehydrogenase (11-beta-HSD) type 2 converting corticosterone to cortisone.
ISIAH rats may serve as a living proof that stress may produce sustained hypertension, and genetically determined enhanced stress responsiveness of corticosterone and, especially, aldosterone may play a crucial role in the mechanism of hypertension development.
压力与高血压疾病之间的关联仍是一个有争议的问题。压力能否成为高血压疾病的病因?如果是,涉及哪些机制?为阐明这个问题,通过选择对0.5小时束缚应激的血压反应增强,培育出了具有与压力相关的动脉高血压的遗传性应激诱导性动脉高血压大鼠品系(ISIAH大鼠品系)。这项工作的主要目的是证实肾上腺是压力与高血压疾病之间的主要联系。
对高血压ISIAH大鼠和血压正常的WAG大鼠进行了研究。通过肾上腺静脉插管,在麻醉的大鼠中测量了皮质酮、醛固酮、11-脱氧皮质酮(DOC)和11-脱氢皮质酮的体内分泌率。进行了地塞米松/促肾上腺皮质激素(DEX/ACTH)试验,并通过实时PCR评估了肾上腺中Cyp11b1和Cyp11b2基因的mRNA表达。
发现ISIAH大鼠的皮质酮和DOC分泌率增加,外周血浆醛固酮浓度更高。ISIAH大鼠血浆醛固酮对手术应激(肾上腺静脉插管)的反应明显更高。高血压大鼠对ACTH反应时皮质酮和醛固酮的增加也更高。ISIAH大鼠中Cyp11b1和Cyp11b2基因的基础mRNA表达均增加。ISIAH大鼠中11-脱氢皮质酮/皮质酮的比值较低,这表明2型11-β-羟基类固醇脱氢酶(11-β-HSD)将皮质酮转化为可的松的能力减弱。
ISIAH大鼠可作为压力可能产生持续性高血压的有力证据,并且基因决定的皮质酮尤其是醛固酮应激反应性增强可能在高血压发展机制中起关键作用。