Why the study?
Do phenothiazines (promazine and thioridazine) reduce potassium loss and prevent ventricular fibrillation in isolated perfused rat hearts?
Do phenothiazines (promazine and thioridazine) reduce potassium loss and prevent ventricular fibrillation in isolated perfused rat hearts?
Phenothiazines such as promazine and thioridazine reduce potassium permeability and can prevent ouabain-induced ventricular fibrillation in isolated rat hearts.
Answers are grounded in this paper and cite their sources.
No clinical adoption warranted for arrhythmia prevention; leaves open mechanistic effects in isolated heart models.
Electrically stimulated isolated rat hearts were perfused with a Ringer solution containing a low concentration of K + . At the end of a control period of 20 min. the cumulative K + loss from the hearts was approximately 30 meq./kg dry weight. This value was used in each experiment as reference (100 per cent) for the total loss found after a subsequent additional test period of 30 min. The addition of promazine and thioridazine to the perfusate at the end of the control period reduced the further K + loss. The values found in the different groups at the end of the test period were: Control group (10 hearts): 154 ± 11.6 per cent; with promazine 10 ‐5 M added (8 hearts): 103 ± 5.6 per cent; with promazine 2.5 × 10 ‐5 M added (10 hearts): 74 ± 10.5 per cent and with thioridazine 10 ‐5 M added (8 hearts): 110 ± 5.8 per cent. In another type of experiments, ouabain 1.5 × 10 ‐6 M was added at the end of the control period. This drug caused an increased K + loss (181 ± 14.2 per cent) and ventricular fibrillation in 6 out of 8 hearts. Promazine 2.5 × 10 ‐5 M added before ouabain, prevented the development of fibrillation in another group of 7 hearts, and also markedly reduced the K + loss. It is concluded that phenothiazines reduce the K + permeability of the heart muscle membranes.
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Knud Landmark (1971) studied this question.
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