AI Article Synopsis

  • - The study explored how early life stress from maternal separation and early weaning (MSEW) impacts blood pressure in obese male mice, focusing on the role of the renin-angiotensin-aldosterone system.
  • - Both control and MSEW mice on a high-fat diet showed similar increases in angiotensinogen levels, but there was no activation of the renin-angiotensin system in their fat or kidneys.
  • - Despite a reduction in blood pressure after treating with an angiotensin-converting enzyme inhibitor, MSEW mice still experienced heightened sympathetic tone, indicating that other mechanisms beyond angiotensin II contribute to their elevated blood pressure.

Article Abstract

Background: 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.

Methods And Results: 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.

Conclusions: 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10863837PMC
http://dx.doi.org/10.1161/JAHA.123.029511DOI Listing

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