Department of Histology and Cytophysiology, Medical University of Bialystok, 15-222 Bialystok, Poland.
Department of Experimental Physiology and Pathophysiology, Medical University of Bialystok, 15-222 Białystok, Poland.
Int J Mol Sci. 2023 Dec 20;25(1):84. doi: 10.3390/ijms25010084.
Hypertension is a global civilization disease and one of the most common causes of death in the world. Organ dysfunction is a serious health consequence of hypertension, which involves damage to the heart, kidneys and adrenals. The interaction of recently discovered multifunctional protein-CacyBP/SIP with ERK1/2 and p38 kinases by regulating the activity and intracellular localization of these kinases may play an important role in the signaling pathways involved in the pathogenesis of hypertension. Due to the lack of data on this subject, we decided to investigate the localization, expression and possible relationship between the studied parameters in the adrenals under arterial hypertension. The study was conducted on the adrenals of rats with spontaneous and DOCA-salt hypertension. The expression of CacyBP/SIP, p-ERK1/2 and p-p38 was detected by immunohistochemistry and qRT-PCR. The results show a statistically significant decrease in CacyBP/SIP expression in the adrenal glands of hypertensive rats. With ERK1/2, there was a decrease in cortical immunoreactivity and an increase in the adrenal medulla of primary hypertensive rats. In contrast, in the adrenals of DOCA-salt rats, ERK1/2 immunoreactivity increased in the cortex and decreased in the medulla. In turn, p38 expression was higher in the adrenal glands of rats with primary and secondary hypertension. The obtained results may suggest the involvement of CacyBP/SIP in the regulation of signaling pathways in which MAP kinases play an important role and provide new insight into molecular events in hypertension. Moreover, they show the participation of CacyBP/SIP in response to oxidative stress.
高血压是一种全球性文明病,也是世界上最常见的死亡原因之一。器官功能障碍是高血压的严重健康后果,涉及心脏、肾脏和肾上腺的损伤。最近发现的多功能蛋白-CacyBP/SIP 通过调节这些激酶的活性和细胞内定位与 ERK1/2 和 p38 激酶相互作用,可能在高血压发病机制涉及的信号通路中发挥重要作用。由于该主题缺乏数据,我们决定研究动脉高血压下肾上腺中研究参数的定位、表达和可能的关系。该研究在自发性和 DOCA-盐高血压大鼠的肾上腺上进行。通过免疫组织化学和 qRT-PCR 检测 CacyBP/SIP、p-ERK1/2 和 p-p38 的表达。结果表明,高血压大鼠肾上腺中 CacyBP/SIP 的表达明显降低。与 ERK1/2 相比,原发性高血压大鼠的皮质免疫反应性降低,肾上腺髓质增加。相反,在 DOCA-盐大鼠的肾上腺中,ERK1/2 免疫反应性在皮质中增加,在髓质中减少。反过来,原发性和继发性高血压大鼠的肾上腺中 p38 表达更高。所得结果可能表明 CacyBP/SIP 参与调节 MAP 激酶起重要作用的信号通路,并为高血压中的分子事件提供新的见解。此外,它们表明 CacyBP/SIP 参与了对氧化应激的反应。