We tested the hypothesis that exposure of high-altitude (HA) rats to a period of postnatal normoxia has long-term consequences on the ventilatory and hematological acclimatization in adults. Male and female HA rats (3,600 m, Po(2) ≃ 100 Torr; La Paz, Bolivia) were exposed to normal room air [HA control (HACont)] or enriched oxygen (32% O(2); Po(2) ≃ 160 Torr) from 1 day before to 15 days after birth [HA postnatal normoxia (HApNorm)]. Hematocrit and hemoglobin values were assessed at 2, 12, and 32 wk of age. Cardiac and lung morphology were assessed at 12 wk by measuring right ventricular hypertrophy (pulmonary hypertension index) and lung air space-to-tissue ratio (indicative of alveolarization). Respiratory parameters under baseline conditions and in response to 32% O(2) for 10 min (relieving the ambient hypoxic stimulus) were measured by whole body plethysmography at 12 wk. Finally, we performed a survival analysis up to 600 days of age. Compared with HACont, HApNorm rats had reduced hematocrit and hemoglobin levels at all ages (both sexes); reduced right ventricular hypertrophy (both sexes); lower air space-to-tissue ratio in the lungs (males only); reduced CO(2) production rate, but higher oxygen uptake (males only); and similar respiratory frequency, tidal volume, and minute ventilation. When breathing 32% O(2), HApNorm male rats had a stronger decrease of minute ventilation than HACont. HApNorm rats had a marked tendency toward longer survival throughout the study. We conclude that exposure to ambient hypoxia during postnatal development in HA rats has deleterious consequences on acclimatization to hypoxia as adults.

Download full-text PDF

Source
http://dx.doi.org/10.1152/japplphysiol.01043.2011DOI Listing

Publication Analysis

Top Keywords

postnatal normoxia
12
po2 ≃
8
hematocrit hemoglobin
8
ventricular hypertrophy
8
air space-to-tissue
8
space-to-tissue ratio
8
hacont hapnorm
8
hapnorm rats
8
minute ventilation
8
rats
7

Similar Publications

Pulmonary hypertension (PH) increases the mortality of preterm infants with bronchopulmonary dysplasia (BPD). There are no curative therapies for this disease. Lung endothelial carnitine palmitoyltransferase 1a (Cpt1a), the rate-limiting enzyme of the carnitine shuttle system, is reduced in a rodent model of BPD.

View Article and Find Full Text PDF

A rat model establishment of bronchopulmonary dysplasia-related lung & brain injury within 28 days after birth.

BMC Neurosci

November 2024

Department of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu, China.

Purpose: Lung injury associated with bronchopulmonary dysplasia (BPD) and its related neurodevelopmental disorders have garnered increasing attention in the context of premature infants. Establishing a reliable animal model is essential for delving into the underlying mechanisms of these conditions.

Methods: Newborn rats were randomly assigned to two groups: the hyperoxia-induced BPD group and the normoxia (NO) group.

View Article and Find Full Text PDF
Article Synopsis
  • * In experiments using Wistar rats, antibiotics led to increased miscarriages and reduced weight gain, while offspring exhibited impaired neurodevelopment and increased neuroinflammation.
  • * The study suggests that caution is needed when using antibiotics during pregnancy due to potential long-term effects on the brain development of children, highlighting the need for future research on preventive measures like probiotics.
View Article and Find Full Text PDF
Article Synopsis
  • Preterm infants often need oxygen right after birth, but too much oxygen can harm their developing lungs due to harmful free radicals.
  • Research using a mouse model tested how different oxygen levels during pregnancy affect lung health after exposure to high levels of oxygen at birth.
  • The study found that exposing mice to low oxygen before birth protected their lungs from damage during high oxygen exposure after birth, indicating hypoxic preconditioning could improve postnatal lung development.
View Article and Find Full Text PDF

Gut microbiome and inflammation in response to increasing intermittent hypoxia in the neonatal rat.

Pediatr Res

September 2024

Department of Pediatrics, Division of Neonatal-Perinatal Medicine, State University of New York, Downstate Health Sciences University, Brooklyn, NY, USA.

Background: Intermittent hypoxia (IH) and oxidative stress play key roles in gut dysbiosis and inflammation. We tested the hypothesis that increasing numbers of daily IH episodes cause microbiome dysbiosis and severe gut injury.

Methods: Neonatal rats were exposed to hyperoxia (Hx), growth restriction, and IH.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!