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Molecular Pharmacology, Vol 19, 520-524, Copyright © 1981 by the American Society for Pharmacology and Experimental Therapeutics
1 Departments of Physiology and Anesthesia, The Milton S. Hershey Medical Center, The Pennsylvania State University,
Hershey, Pennsylvania 17033
The effect of halothane exposure on synthesis of lung proteins was investigated. In rat lungs perfused in situ with Krebs-Henseleit bicarbonate buffer containing plasma levels of 19 amino acids, 690 µM [14C]phenylalanine, 5.6 mM glucose, and 4.5% bovine serum albumin, protein synthesis was linear for at least 4 hr. Halothane (1-4% equilibrated with O2/N2/CO2, 4:15:1) rapidly inhibited protein synthesis in a dose-dependent manner, with about a 10% depression of the rate for each 1% increment in halothane. The inhibition was rapidly and completely reversed when halothane delivery was stopped; it was not associated with depletion of tissue ATP or with nonspecific changes in cellular permeability. A similar reversible and dose-dependent inhibition of protein synthesis was observed in primary cultures of mixed lung cells incubated in Dulbeccos minimal essential medium containing 10% donor calf serum. These results suggested a significant but reversible inhibition of protein synthesis, exerted at the cellular level, in lungs exposed to halothane.
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ACKNOWLEDGMENT
The authors thank Ms. Patricia A. Gering for typing the manuscript.
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