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Canadian Journal of Anesthesia, Vol 9, 497-503, Copyright © 1962 by Canadian Anesthesiologists' Society

Changes in Histamine Blood Levels Following d-Tubocurarine Administration

H. D. WESTGATE M.D., M.S.1 and F. H. VAN BERGEN M.D., M.S.1

1 University of Minnesota Medical Center, Minneapolis, Minn., U.S.A.

The blood level of histamine was measured in six control patients scheduled for elective surgery. In eleven patients the histamine blood level was measured before and five minutes after the rapid intravenous injection of 0.44 mg. per kg.body weight of d-tubocurarine. There was no change in the histamine blood level of four patients, a rise in the histamine blood level of four patients, and a decrease in the histamine blood levels of three patients. The last group of patients all showed evidence of systolic hypotension, increased airway resistance, and skin erythema.

Histamine may be released from endogenous sources by d-tubocurarine. The significance of this release is determined by the sensitivity of the histamine effector cells and by the state of the histamine binding sites. When these are abnormal, such as in asthmatic or "ectopic" individuals, it is wise to use relaxants other than d-tubocurarine.

Note:

The work was supported by Research Grant No. H-1983 (C7) from the National Heart Institute, U.S. Public Health Service.







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Copyright © 1962 by the Canadian Anesthesiologists' Society.