» Articles » PMID: 41661

Role of the Lung in Total Body Clearance of Circulating Drugs

Overview
Specialty Pharmacology
Date 1979 Sep 1
PMID 41661
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

Attention in recent years has focused upon the ability of lung to accumulate and/or to metabolise circulating hormones, drugs and other xenobiotic agents. Although often studied in broken cell preparations, such functions must be examined in intact lung before extrapolation to the situation in vivo is possible. The role of lung in total body clearance of xenobiotic agents is often considered to be small, as compared with the liver it usually has much lower concentrations of degradative enzymes and a smaller mass. However, consideration of such factors as organ blood flow or stimulation of drug metabolising enzymes suggests that the contribution of the lung to total body clearance of some drugs is greater than previously recognised. This may explain some of the alterations in drug clearance seen clinically. For example, cigarette smoking may increase the clearance of certain xenobiotic compounds by stimulating pulmonary drug metabolising enzymes. Pulmonary drug disposition may also be altered by conditions affecting cardiac output, such as exercise, hypoxia, and circulatory shock, or those affecting acid-base balance, such as hyperventilation. In addition, pneumotoxicants may affect pulmonary clearance of circulating drugs and xenobiotics.

Citing Articles

Physical activity and cancer prevention : pathways and targets for intervention.

Rogers C, Colbert L, Greiner J, Perkins S, Hursting S Sports Med. 2008; 38(4):271-96.

PMID: 18348589 DOI: 10.2165/00007256-200838040-00002.


Effect of cardiopulmonary bypass on the pharmacokinetics of drugs.

Holley F, Ponganis K, Stanski D Clin Pharmacokinet. 1982; 7(3):234-51.

PMID: 7047043 DOI: 10.2165/00003088-198207030-00004.


Effect of halothane on metabolism of 5-hydroxytryptamine by rat lungs perfused in situ.

WATKINS C, Wartell S, Rannels D Biochem J. 1983; 210(1):157-66.

PMID: 6847641 PMC: 1154201. DOI: 10.1042/bj2100157.


Uptake, distribution, metabolism, and elimination of styrene in man. A comparison between single exposure and co-exposure with acetone.

Wigaeus E, Lof A, Nordqvist M Br J Ind Med. 1984; 41(4):539-46.

PMID: 6498116 PMC: 1009382. DOI: 10.1136/oem.41.4.539.


Inhalation pharmacokinetics of 1,2-dichloroethane after different dietary pretreatments of male Sprague-Dawley rats.

Igwe O, Hee S, Wagner W Arch Toxicol. 1986; 59(3):127-34.

PMID: 3813877 DOI: 10.1007/BF00316320.


References
1.
Zampaglione N, MANNERING G . Properties of benzpyrene hydroxylase in the liver, intestinal mucosa and adrenal of untreated and 3-methylcholanthrene-treated rats. J Pharmacol Exp Ther. 1973; 185(3):676-85. View

2.
Aberg G . Toxicological and local anaesthetic effects of optically active isomers of two local anaesthetic compounds. Acta Pharmacol Toxicol (Copenh). 1972; 31(4):273-86. View

3.
Gaddum J, HEBB C, Silver A, Swan A . 5-Hydroxytryptamine; pharmacological action and destruction in perfused lungs. Q J Exp Physiol Cogn Med Sci. 1953; 38(4):255-62. DOI: 10.1113/expphysiol.1953.sp001037. View

4.
Hayes A, Cooper R . Studies on the absorption, distribution and excretion of propranolol in rat, dog and monkey. J Pharmacol Exp Ther. 1971; 176(2):302-11. View

5.
Branch R, Nies A, SHAND D . The disposition of propranolol. 8. General implications of the effects of liver blood flow on elimination from the perfused rat liver. Drug Metab Dispos. 1973; 1(5):687-90. View