Literature DB >> 19632662

Effect of intrauterine fetal programming on response to postnatal shaker stress in endothelial nitric oxide knockout mouse model.

Maged M Costantine1, Francesca Ferrari, Giusseppe Chiossi, Esther Tamayo, Gary D V Hankins, George R Saade, Monica Longo.   

Abstract

OBJECTIVE: To determine whether the intrauterine environment affects the postnatal vascular response to stress in a model of fetal programming induced by endothelial nitric oxide synthase deficiency. STUDY
DESIGN: Homozygous nitric oxide synthase knockout and wild-type controls were crossbred to obtain maternally and paternally derived heterozygous offspring. At 14 weeks of age, in vivo blood pressure measurements by telemetry, and in vitro carotid arteries vascular reactivity studies were performed in male offspring after subjecting them to shaker stress.
RESULTS: Maternally derived heterozygous offspring, compared with paternally derived heterozygous offspring, had significantly higher systolic blood pressure, mean arterial blood pressure, and pulse pressure before, as well as after introduction of the shaker stress. The difference in the latter between maternally and paternally derived heterozygous offspring was accentuated after stress. Maternally derived heterozygous offspring also had significantly higher contractile responses to phenylephrine when compared with paternally derived heterozygous offspring, and this was abolished after incubation with L-NAME.
CONCLUSION: The adverse uterine environment affects the postnatal vascular response to stress.

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Year:  2009        PMID: 19632662      PMCID: PMC2748249          DOI: 10.1016/j.ajog.2009.05.040

Source DB:  PubMed          Journal:  Am J Obstet Gynecol        ISSN: 0002-9378            Impact factor:   8.661


  29 in total

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  3 in total

1.  Effect of age and gender on the progression of adult vascular dysfunction in a mouse model of fetal programming lacking endothelial nitric oxide synthase.

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2.  Fetal programming of blood pressure in a transgenic mouse model of altered intrauterine environment.

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