Abstract
In reviewing the literature1, 2 on the pharmacodynamic activity and importance of ergot, it was found that its constituents, so far as the activity is concerned, may be divided into 2 groups: (1) specific alkaloids: ergotamine and ergotoxine, and (2) nonspecific amines: histamine and possibly tryramine. The specific alkaloids, to which I shall limit attention, are reported to produce a slow but persistent rise in blood pressure, diminishing with repeated dosage due to vasomotor paralysis until a condition is reached in which there is no rise, or else there is a fall which cannot be raised by epinephrine. Ergotoxine and ergotamine are pharmacodynamically identical. The researches of Brown, 3 and Barker 4 and their colleagues suggested the possibility that quantitative data on the actual changes in blood flow to the periphery brought about by this drug might be of some general interest. So far as I know, no such data are available.
The blood flow was measured by the thermo-stromuhr method developed by Rein. 5 The method permits quantitative observations under normal physiologic conditions in the intact animal. The femoral blood pressure was measured and recorded in the usual manner. All operative procedures were carried out under local anesthesia. The blood flow was measured in one femoral artery, and the blood pressure in the other femoral artery.
The dogs had been trained to lie quietly throughout all observations. After the normal blood flow and blood pressure were established, either 1.0 or 0.5 mg. of ergotamine tartrate (gynergen) was injected intravenously. The results of several experiments are given in the table. In 4 of the 6 experiments the blood flow was reduced to 25.5% of its normal value, on the average. The remaining 2 reductions were only 57 and 35%.
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