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Nitric oxide (NO) was analysed in expired air from 27 healthy human subjects. At rest the NO concentration was 10.5 +/- 0.9 ng 1-1 (mean +/- SEM) corresponding to 8.6 +/- 0.7 parts per billion (ppb). The expired NO concentration did not change when the subjects were switched from breathing NO-free tank gas to room air which contained 7.7 ng l-1 NO. Repeated measurements of expired NO with an interval of 1 day showed a mean variation of 2.2 +/- 0.7 ng l-1 NO. The NO concentration in the first portion in the expired tidal volume (44%) was insignificantly higher than in the latter expired portion, 6.9 +/- 1.9 vs. 5.1 +/- 1.0 ng l-1 (n = 5). During moderately heavy exercise on an ergometer bicycle (90 W for women, n = 4, 150 W for men, n = 4) the expired concentration of NO decreased, however because of increased minute ventilation, the expired amount of NO almost doubled (from 111 +/- 12 to 209 +/- 30 ng min-1). The source of the expired NO is not clear and both the airways and the pulmonary circulation may contribute.

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12hsiraci: Some pharmacological-toxicological effects of canatoxin, a toxic protein purified from the seeds of Canavalia ensiforrnis have been studied in mice and rats. The most obvious effect, a lethal tonic convulsion, was generally produced 10-15 rnin. after intravenous injection of 2-3 mg/kg of the highly purified protein (mol. wt. 88,000). After intraperitoneal, intramuscular or subcutaneous administration the convulsion produced by the same toxin dosis occurred within 24 hours. A spinal transection at the midthoracic level did not abolish the convulsions of the hindlimbs while destruction of the medulla below this level completely blocked the convulsions of the hindlimbs. The convulsions of the head and forelimbs were unaffected by these surgical pretreatments. The toxic protein did neither affect the isolated skeletal muscle nor did it potentiate nerve impulse induced contractions. The convulsive effect of canatoxin was potentiated by reserpine and attenuated by phenobarbital, diazepam, methenesine and also by haloperidol and spiroperidol. The total concentration of brain and spinal cord neurotransmitters seemed to remain unchanged after subconvulsive and convulsive doses of canatoxin. In the conscious rat the toxic protein did not change the blood pressure except for a shortlasting hypertensive response observed immediately before the onset of the convulsions. The heart frequency was lowered at subconvulsive and convulsive dosis but no effect was seen on the frequency of the rat isolated right atria exposed to high doses of canatoxin. The body temperature was lowered by a convulsive dosis of the toxic protein. The purified toxin did not show any haemagglutinating property or haemolytic phospholipase A2-like activity. The results strongly suggest a central nervous site for the action ofcanatoxin. However, if the effects are produced by the intact protein or not as well as its exact mode of action, remain unexplained.