Comparison of metabolic effect of ammonia and adrenaline infusions in sheep
- PMID: 256166
- DOI: 10.1113/expphysiol.1979.sp002455
Comparison of metabolic effect of ammonia and adrenaline infusions in sheep
Abstract
Intravenous infusions of ammonium chloride (62.3 mumol.kg-1.min-1) for 30 min caused a significant increase in blood glucose, lactate, pyruvate and free fatty acid (FFA) levels. A similar effect was also observed during infusion of adrenaline. Propanolol--a beta-receptor blocking agent--completely prevented the rise of blood pyruvate and lactate after adrenaline when 8.3 microgram.kg-1.min-1 of propranolol were infused, but not after NH4Cl administration. Lipolytic actions of adrenaline were completely prevented but that of NH4Cl was only significantly diminished by blockade of beta-receptors with propranolol. It was concluded that the influence of ammonium ions on blood lactate and pyruvate and FFA was not entirely mediated by adrenaline.
Similar articles
-
The effect of adrenal denervation on the metabolic effects of hyperammonemia in sheep.Can J Physiol Pharmacol. 1989 Sep;67(9):1062-6. doi: 10.1139/y89-168. Can J Physiol Pharmacol. 1989. PMID: 2598130
-
Effect of hyperammonaemia on blood glucose and plasma insulin levels in sheep.Q J Exp Physiol Cogn Med Sci. 1979 Jan;64(1):31-7. doi: 10.1113/expphysiol.1979.sp002456. Q J Exp Physiol Cogn Med Sci. 1979. PMID: 256167
-
The influence of phentolamine on the hyperglycaemic and lipolytic effects of ammonia in sheep.Q J Exp Physiol Cogn Med Sci. 1975 Apr;60(2):89-94. doi: 10.1113/expphysiol.1975.sp002306. Q J Exp Physiol Cogn Med Sci. 1975. PMID: 1040939
-
[Changes in the concentration of glucose, fructose, insulin and free fatty acids in the blood plasma as well as of lactate and pyruvate in the blood of cattle after i.v. adrenaline, insulin and noradrenaline infusion].Arch Exp Veterinarmed. 1980;34(2):247-57. Arch Exp Veterinarmed. 1980. PMID: 7006551 German.
-
Dissociation o epinephrine-induced free fatty acid and glycerol release by adrenergic blocking drugs.Biochem Pharmacol. 1968 Oct;17(10):2205-13. doi: 10.1016/0006-2952(68)90195-0. Biochem Pharmacol. 1968. PMID: 5696886 No abstract available.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous