Effect of thyrotoxicosis on liver blood flow and propranolol disposition after long-term dosing. 1983

P G Wells, and J Feely, and G R Wilkinson, and A J Wood

The effects of thyrotoxicosis on Liver blood flow and propranolol disposition were followed in five patients while thyrotoxic and when euthyroid. Propranolol was taken orally to achieve steady state and then radiolabeled drug was given simultaneously by intravenous injection. Thyrotoxicosis was associated with doubling of both oral and systemic clearances of unbound propranolol, which resulted in an approximately 50% reduction in blood concentrations after oral doses. These changes were attributable to increases in hepatic blood flow and drug-metabolizing activity of the liver. The propranolol elimination t 1/2 was not affected by thyrotoxicosis since the enhanced clearance was offset by a change in volume of distribution. These findings may explain the reduction of plasma propranolol concentration and many of the therapeutic failures reported in the treatment of thyrotoxicosis. The dose required to achieve therapeutic blood concentrations of propranolol in thyrotoxic patients is variable and will usually be substantially larger than that required for euthyroid patients.

UI MeSH Term Description Entries
D006980 Hyperthyroidism Hypersecretion of THYROID HORMONES from the THYROID GLAND. Elevated levels of thyroid hormones increase BASAL METABOLIC RATE. Hyperthyroid,Primary Hyperthyroidism,Hyperthyroidism, Primary,Hyperthyroids
D007275 Injections, Intravenous Injections made into a vein for therapeutic or experimental purposes. Intravenous Injections,Injection, Intravenous,Intravenous Injection
D008099 Liver A large lobed glandular organ in the abdomen of vertebrates that is responsible for detoxification, metabolism, synthesis and storage of various substances. Livers
D008102 Liver Circulation The circulation of BLOOD through the LIVER. Hepatic Circulation,Circulation, Liver,Circulation, Hepatic
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D011433 Propranolol A widely used non-cardioselective beta-adrenergic antagonist. Propranolol has been used for MYOCARDIAL INFARCTION; ARRHYTHMIA; ANGINA PECTORIS; HYPERTENSION; HYPERTHYROIDISM; MIGRAINE; PHEOCHROMOCYTOMA; and ANXIETY but adverse effects instigate replacement by newer drugs. Dexpropranolol,AY-20694,Anaprilin,Anapriline,Avlocardyl,Betadren,Dociton,Inderal,Obsidan,Obzidan,Propanolol,Propranolol Hydrochloride,Rexigen,AY 20694,AY20694,Hydrochloride, Propranolol
D005260 Female Females
D006207 Half-Life The time it takes for a substance (drug, radioactive nuclide, or other) to lose half of its pharmacologic, physiologic, or radiologic activity. Halflife,Half Life,Half-Lifes,Halflifes
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

P G Wells, and J Feely, and G R Wilkinson, and A J Wood
September 1982, The New England journal of medicine,
P G Wells, and J Feely, and G R Wilkinson, and A J Wood
January 1973, Drug metabolism and disposition: the biological fate of chemicals,
P G Wells, and J Feely, and G R Wilkinson, and A J Wood
May 2000, Journal of clinical pharmacology,
P G Wells, and J Feely, and G R Wilkinson, and A J Wood
June 1995, Circulation,
P G Wells, and J Feely, and G R Wilkinson, and A J Wood
January 1975, Comptes rendus des seances de la Societe de biologie et de ses filiales,
P G Wells, and J Feely, and G R Wilkinson, and A J Wood
January 2011, Journal of andrology,
P G Wells, and J Feely, and G R Wilkinson, and A J Wood
January 2018, Journal of the American Geriatrics Society,
P G Wells, and J Feely, and G R Wilkinson, and A J Wood
August 1976, The Journal of pharmacology and experimental therapeutics,
P G Wells, and J Feely, and G R Wilkinson, and A J Wood
January 1969, The Journal of clinical pharmacology and the journal of new drugs,
P G Wells, and J Feely, and G R Wilkinson, and A J Wood
March 1981, The New England journal of medicine,
Copied contents to your clipboard!