» Articles » PMID: 894534

Adrenal and Pancreatic Endocrine Responses to Hypoxia and Hypercapnia in the Calf

Overview
Journal J Physiol
Specialty Physiology
Date 1977 Jul 1
PMID 894534
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

1. Adrenal and pancreatic endocrine responses to hypoxia and hypercapnia, of differing degrees of intensity, have been examined in conscious, unrestrained calves 3-5 weeks after birth. 2. The outputs of cortisol and corticosterone from the right adrenal gland were found to vary inversely with arterial Po2 between 17 and 55 mmHg. Significant increase in mean adrenal blood flow was not observed at arterial oxygen tensions above about 30 mmHg. 3. Release of physiologically effective amounts of catecholamines from the adrenal medulla occurred only in response to intense hypoxia (arterial Po2 17-1 +/- 2-8 mmHg) and was effectively abolished by section of both splanchnic nerves. Release of pancreatic glucagon in response to such intense hypoxia was unaffected by section of both splanchnic nerves and administration of atropine. In contrast, the rise in plasma pancreatic glucagon concentration during less intense hypoxia was abolished by autonomic blockade. 4. Hypercapnia produced by inhalation of either 5% or 10% CO2 for 30 min stimulated maximal release of adrenal glucocorticoids and caused a substantial rise in plasma glucagon concentration. In contrast, the adrenal medulla was found to be extremely resistant to hypercapnia. Significant release of catecholamines was only observed during intense hypercapnia (inhalation of 10% CO2) and noradrenaline was invariably found to be the predominant amine. 5. The results of these experiments show how endocrine responses to hypoxia and hypercapnia are graded in the conscious calf. Of the mechanisms we have examined the pituitary-adrenal cortical axis is the most sensitive and the adrenal medulla the most resistant, while the pancreatic alpha cell occupies an intermediate position.

Citing Articles

Profiling endogenous adrenal function during veno-venous ECMO support in COVID-19 ARDS: a descriptive analysis.

Baumgartner C, Wolf P, Hermann A, Konig S, Maleczek M, Laxar D Front Endocrinol (Lausanne). 2024; 14:1321511.

PMID: 38333725 PMC: 10852060. DOI: 10.3389/fendo.2023.1321511.


Partial pressure of oxygen in the human body: a general review.

Ortiz-Prado E, Dunn J, Vasconez J, Castillo D, Viscor G Am J Blood Res. 2019; 9(1):1-14.

PMID: 30899601 PMC: 6420699.


Influence of Inhaled Amiloride on Lung Fluid Clearance in Response to Normobaric Hypoxia in Healthy Individuals.

Wheatley C, Baker S, Taylor B, Keller-Ross M, Chase S, Carlson A High Alt Med Biol. 2017; 18(4):343-354.

PMID: 28876128 PMC: 5743027. DOI: 10.1089/ham.2017.0032.


Ruminal, cardiorespiratory and adrenocortical sequelae of Na2EDTA-induced hypocalcaemia in calves.

Desmecht D, Linden A, Lekeux P Vet Res Commun. 1996; 20(1):47-60.

PMID: 8693701 DOI: 10.1007/BF00346577.


Autonomic control of adrenal function.

Edwards A, Jones C J Anat. 1993; 183 ( Pt 2):291-307.

PMID: 8300417 PMC: 1259909.


References
1.
MARKS B, BHATTACHARYA A, VERNIKOS-DANELLIS J . EFFECT OF HYPOXIA ON SECRETION OF ACTH IN THE RAT. Am J Physiol. 1965; 208:1021-5. DOI: 10.1152/ajplegacy.1965.208.5.1021. View

2.
Hirai K, Atkins G, MAROTTA S . 17-HYDROXYCORTICOSTEROID SECRETION DURING HYPOXIA IN ANESTHETIZED DOGS. Aerosp Med. 1963; 34:814-6. View

3.
Sarcione E, Back N, Sokal J, MEHLMAN B, KNOBLOCK E . Elevation of plasma epinephrine levels produced by glucagon in vivo. Endocrinology. 1963; 72:523-6. DOI: 10.1210/endo-72-4-523. View

4.
MILLAR R . Plasma adrenaline and noradrenaline during diffusion respiration. J Physiol. 1960; 150:79-90. PMC: 1363148. DOI: 10.1113/jphysiol.1960.sp006374. View

5.
Scian L, WESTERMANN C, VERDESCA A, HILTON J . Adrenocortical and medullary effects of glucagon. Am J Physiol. 1960; 199:867-70. DOI: 10.1152/ajplegacy.1960.199.5.867. View