Adrenergic mediation of vasopressin secretion in newborn pigs.

Abstract

Effects of inhibition of alpha 1-(prazosin) and alpha 2-(yohimbine) adrenoreceptors on plasma lysine vasopressin concentration during normotension and hemorrhagic hypotension were studied in unanesthetized newborn pigs. During the normotensive period, treatment with prazosin and yohimbine both increased plasma lysine vasopressin concentration (vehicle = 3.4 +/- 1.21 microU/ml; prazosin = 35.8 +/- 10.8 microU/ml; and yohimbine = 20.1 +/- 9.5 microU/ml). Prazosin caused a decline in arterial pressure (vehicle = 60 +/- 6 mmHg; prazosin = 49 +/- 5 mmHg), which may account for the increase in plasma lysine vasopressin concentration, whereas yohimbine increased arterial pressure (73 +/- 3 mmHg). On hemorrhage to equivalent arterial pressure, plasma lysine vasopressin concentration increased to similar levels in vehicle- (110.3 +/- 28.7 microU/ml) and prazosin-treated (92.6 +/- 14.2 microU/ml) piglets. In contrast, on hemorrhage of yohimbine-treated piglets, the increase in plasma lysine vasopressin concentration was augmented remarkably (527.0 +/- 103.2 microU/ml) in comparison to the other groups. We conclude that, in unanesthetized newborn pigs, treatment with the alpha 2-adrenoreceptor antagonist yohimbine increased plasma lysine vasopressin concentration and markedly accentuated the vasopressin response to hemorrhage. An alpha 2-adrenergic receptor-mediated mechanism appears to be an important inhibitory component in the vasopressin secretory system of the newborn pig.

• Authors: C W Leffler, D W Busija, L Share, J T Crofton, D P Brooks, D G Beasley, R S Green, R Mirro
• Journal: The American journal of physiology (Am J Physiol) Vol. 253 Issue 3 Pt 2 Pg. R489-93 (Sep 1987) ISSN: 0002-9513 [Print] United States
• PMID: 2820251 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Receptors, Adrenergic, alpha
• Yohimbine
• Lypressin
• Prazosin

Topics

• Animals
• Animals, Newborn (physiology)
• Blood Pressure (drug effects)
• Hemorrhage (physiopathology)
• Hydrogen-Ion Concentration
• Lypressin (metabolism)
• Prazosin (pharmacology)
• Receptors, Adrenergic, alpha (physiology)
• Secretory Rate (drug effects)
• Yohimbine (pharmacology)