Abstract
Widely conflicting opinion exists with regard to the effect of anesthetics on the resistance of red blood cells to hypotonic saline solutions. Since little of this is based on quantitative data, it was thought worth while to restudy the problem, using the quantitative method introduced by Simmel, 1 in which actual count is made of the number of cells remaining after uniform periods of contact with different grades of hypotonic solutions. The results are conveniently expressed as percentages of the total number of erythrocytes per cubic millimeter, where Hayem's solution has been used as the diluent. The normal variations likely to be encountered by this method have been studied by Leake and Pratt. 2
Dogs were used in all experiments. Blood was drawn by syringe from the femoral artery, through the intact skin. Ether or chloroform was administered by the drop method, and further samples of blood were drawn at various intervals up to one hour after the induction of the surgical stage of anesthesia. These were prepared for determination as soon as drawn.
After about 10 minutes of ether anesthesia, an apparent increased resistance was noted on the part of the erythrocytes to the hemolysing action of the different strengths of hypotonic Simmel's fluid. This may have been due either (a) to destruction of weaker cells, leaving only the more resistant ones in the circulation, or (b) to an influx of cells, from such reservoirs as the spleen, resulting from struggling or partial asphyxiation during induction. Studies are in progress to determine which is the more likely. After 30 minutes of ether anesthesia, the osmotic resistance of the red cells was much below the normal level, indicating injury to the stroma of all cells following prolonged contact with the ether.
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