Department of Pharmacology and Nutritional Sciences University of Kentucky Lexington KY USA.
Department of Biomedical Sciences Cedars-Sinai Medical Center Los Angeles CA USA.
J Am Heart Assoc. 2024 Jan 2;13(1):e029511. doi: 10.1161/JAHA.123.029511. Epub 2023 Dec 29.
We have previously reported that male mice exposed to maternal separation and early weaning (MSEW), a model of early life stress, show sympathetic activation and increased blood pressure in response to a chronic high-fat diet. The goal of this study was to investigate the contribution of the renin-angiotensin-aldosterone system to the mechanism by which MSEW increases blood pressure and vasomotor sympathetic tone in obese male mice.
Mice were exposed to MSEW during postnatal life. Undisturbed litters served as controls. At weaning, both control and MSEW offspring were placed on a low-fat diet or a high-fat diet for 20 weeks. Angiotensin peptides in serum were similar in control and MSEW mice regardless of the diet. However, a high-fat diet induced a similar increase in angiotensinogen levels in serum, renal cortex, liver, and fat in both control and MSEW mice. No evidence of renin-angiotensin system activation was found in adipose tissue and renal cortex. After chronic treatment with enalapril (2.5 mg/kg per day, drinking water, 7 days), an angiotensin-converting enzyme inhibitor that does not cross the blood-brain barrier, induced a similar reduction in blood pressure in both groups, while the vasomotor sympathetic tone remained increased in obese MSEW mice. In addition, acute boluses of angiotensin II (1, 10, 50 μg/kg s.c.) exerted a similar pressor response in MSEW and control mice before and after enalapril treatment.
Overall, elevated blood pressure and vasomotor sympathetic tone remained exacerbated in MSEW mice compared with controls after the peripheral inhibition of angiotensin-converting enzyme, suggesting a mechanism independent of angiotensin II.
我们之前报道过,雄性小鼠在经历母体分离和早期断奶(MSEW),即早期生活应激模型后,对慢性高脂肪饮食的反应会出现交感神经激活和血压升高。本研究的目的是探讨肾素-血管紧张素-醛固酮系统(RAAS)在 MSEW 增加肥胖雄性小鼠血压和血管运动性交感神经张力的机制中的作用。
在产后生活中,小鼠经历了 MSEW。未受干扰的同窝仔鼠作为对照。在断奶时,对照组和 MSEW 后代都被置于低脂饮食或高脂饮食中 20 周。无论饮食如何,对照组和 MSEW 小鼠的血清血管紧张素肽相似。然而,高脂饮食会导致对照组和 MSEW 小鼠的血清、肾皮质、肝脏和脂肪中的血管紧张素原水平相似增加。在脂肪组织和肾皮质中未发现肾素-血管紧张素系统的激活。在接受慢性依那普利(2.5mg/kg/天,饮用水,7 天)治疗后,一种不穿过血脑屏障的血管紧张素转换酶抑制剂,在两组中均能引起相似的血压降低,而肥胖的 MSEW 小鼠的血管运动性交感神经张力仍然升高。此外,在依那普利治疗前后,急性给予血管紧张素 II(1、10、50μg/kg 皮下注射)在 MSEW 和对照组小鼠中产生相似的升压反应。
总的来说,与对照组相比,外周抑制血管紧张素转换酶后,MSEW 小鼠的血压和血管运动性交感神经张力仍然升高,这表明存在独立于血管紧张素 II 的机制。