Literature DB >> 22902513

Acute regulation of hematocrit and blood acid-base balance during severe hypoxic challenges in late chicken embryos (Gallus gallus).

Hiroshi Tazawa1, Sarah J Andrewartha, Warren W Burggren.   

Abstract

Acid-base and hematocrit (Hct) responses of vertebrate embryos to severe hypoxia are as yet unknown, but may reveal the maturation process of physiological regulatory mechanisms. The present study elucidated how acute, severe hypoxia (10% O2, with and without 5% CO2) affects Hct and blood acid-base balance in late prenatal (days 11-19) chicken embryos. The time-course of the resulting Hct changes and blood acid-base disturbances was examined in detail in day 15 (d15) embryos to further understand the magnitude and time-components of these physiological changes. We hypothesized that Hct of developing embryos increases during severe hypoxia (10% O2) and hypercapnic hypoxia (5% CO2, 10% O2), due to increased mean corpuscular volume (MCV) and red blood cell concentration ([RBC]). We additionally hypothesized that 10% O2 would induce anaerobic glycolysis and the attendant increase in lactate concentration ([La-]) would create a severe metabolic acidosis. Hct increased in all embryos (d11-d19) during severe hypoxia (2h) but, with the exception of d19 embryos, the increase was due to increased MCV and was therefore unlikely related to O2 transport. The time-course of the d15 embryonic Hct response to hypoxic or hypercapnic hypoxic exposure was very rapid with MCV increasing within 30min. Severe metabolic acidosis occurred in all developing embryos (d11-d19) during 2h hypoxic exposure. Additionally, respiratory acidosis was induced in d15 embryos during hypercapnic hypoxia, with acid-base status recovering within 120 min in air. Throughout hypoxic exposure and recovery, changes in [HCO3-] were matched by those in [La-], indicating that anaerobic glycolysis is a key factor determining the metabolic alterations and overall acid-base status. Further, the blood gas and Hct values recovered in air and unchanged embryo mass suggest that the hypoxia-induced disturbances were only transient and may not affect long-term survival.
Copyright © 2012 Elsevier B.V. All rights reserved.

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Year:  2012        PMID: 22902513     DOI: 10.1016/j.resp.2012.08.002

Source DB:  PubMed          Journal:  Respir Physiol Neurobiol        ISSN: 1569-9048            Impact factor:   1.931


  6 in total

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Authors:  Travis Alvine; Warren W Burggren
Journal:  J Comp Physiol B       Date:  2013-09-05       Impact factor: 2.200

2.  Physiological Regulation of Growth, Hematology and Blood Gases in Chicken Embryos in Response to Low and High Incubation Humidity.

Authors:  Sylvia Branum; Hiroshi Tazawa; Warren Burggren
Journal:  Front Physiol       Date:  2022-05-24       Impact factor: 4.755

3.  Dynamics of acid-base metabolic compensation and hematological regulation interactions in response to CO2 challenges in embryos of the chicken (Gallus gallus).

Authors:  Casey Mueller; Hiroshi Tazawa; Warren Burggren
Journal:  J Comp Physiol B       Date:  2014-03-19       Impact factor: 2.200

4.  Phenotypic developmental plasticity induced by preincubation egg storage in chicken embryos (Gallus gallus domesticus).

Authors:  Sylvia R Branum; Hiroshi Tazawa; Warren W Burggren
Journal:  Physiol Rep       Date:  2016-02

5.  Critical developmental windows for morphology and hematology revealed by intermittent and continuous hypoxic incubation in embryos of quail (Coturnix coturnix).

Authors:  Warren W Burggren; Nourhan A Elmonoufy
Journal:  PLoS One       Date:  2017-09-19       Impact factor: 3.240

6.  Identifying Candidate Genes for Hypoxia Adaptation of Tibet Chicken Embryos by Selection Signature Analyses and RNA Sequencing.

Authors:  Xiayi Liu; Xiaochen Wang; Jing Liu; Xiangyu Wang; Haigang Bao
Journal:  Genes (Basel)       Date:  2020-07-20       Impact factor: 4.096

  6 in total

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