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Obese Male Mice Exposed to Early Life Stress Display Sympathetic Activation and Hypertension Independent of Circulating Angiotensin II.
Dalmasso, Carolina; Ahmed, Nermin S; Ghuneim, Sundus; Cincinelli, Cole; Leachman, Jaqueline R; Giani, Jorge F; Cassis, Lisa; Loria, Analia S.
Affiliation
  • Dalmasso C; Department of Pharmacology and Nutritional Sciences University of Kentucky Lexington KY USA.
  • Ahmed NS; Department of Pharmacology and Nutritional Sciences University of Kentucky Lexington KY USA.
  • Ghuneim S; Department of Pharmacology and Nutritional Sciences University of Kentucky Lexington KY USA.
  • Cincinelli C; Department of Pharmacology and Nutritional Sciences University of Kentucky Lexington KY USA.
  • Leachman JR; Department of Pharmacology and Nutritional Sciences University of Kentucky Lexington KY USA.
  • Giani JF; Department of Biomedical Sciences Cedars-Sinai Medical Center Los Angeles CA USA.
  • Cassis L; Department of Pharmacology and Nutritional Sciences University of Kentucky Lexington KY USA.
  • Loria AS; Department of Pharmacology and Nutritional Sciences University of Kentucky Lexington KY USA.
J Am Heart Assoc ; 13(1): e029511, 2024 Jan 02.
Article in En | MEDLINE | ID: mdl-38156515
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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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Adverse Childhood Experiences / Hypertension Limits: Animals Language: En Journal: J Am Heart Assoc Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Adverse Childhood Experiences / Hypertension Limits: Animals Language: En Journal: J Am Heart Assoc Year: 2024 Document type: Article
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