High altitude hypoxia and blood pressure dysregulation in adult chickens

E. A. Herrera, Carlos E. Salinas Salmón, C. E. Blanco, M. Villena, D. A. Giussani

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Although it is accepted that impaired placental perfusion in complicated pregnancy can slow fetal growth and programme an increased risk of cardiovascular dysfunction at adulthood, the relative contribution of reductions in fetal nutrition and in fetal oxygenation as the triggering stimulus remains unclear. By combining high altitude (HA) with the chick embryo model, we have previously isolated the direct effects of HA hypoxia on embryonic growth and cardiovascular development before hatching. This study isolated the effects of developmental hypoxia on cardiovascular function measured in vivo in conscious adult male and female chickens. Chick embryos were incubated, hatched and raised at sea level (SL, nine males and nine females) or incubated, hatched and raised at HA (seven males and seven females). At 6 months of age, vascular catheters were inserted under general anaesthesia. Five days later, basal blood gas status, basal cardiovascular function and cardiac baroreflex responses were investigated. HA chickens had significantly lower basal arterial PO2 and haemoglobin saturation, and significantly higher haematocrit than SL chickens, independent of the sex of the animal. HA chickens had significantly lower arterial blood pressure than SL chickens, independent of the sex of the animal. Although the gain of the arterial baroreflex was decreased in HA relative to SL male chickens, it was increased in HA relative to SL female chickens. We show that development at HA lowers basal arterial blood pressure and alters baroreflex sensitivity in a sex-dependent manner at adulthood.

Original languageEnglish
Pages (from-to)69-76
Number of pages8
JournalJournal of Developmental Origins of Health and Disease
Volume4
Issue number1
DOIs
StatePublished - Feb 2013

Keywords

  • baroreflex
  • cardiovascular disease
  • chronic hypoxia
  • fetal programming

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