LDH and isoenzymes in platelets from man and from rats were studied during normal and abnormal thrombopoiesis. The LDH isoenzyme distribution (log H/M) was determined by disc polyacrylarnide electrophoresis, split‐gel technique, total LDH activity per platelet (LDH/platelet) by fluorometry.
In 15 normal subjects there was no correlation between log H/M and LDH/platelet or platelets/μl, whereas LDH/platelet was significant, negatively correlated to the platelet count.
Compared with 15 controls, 13 patients with metastasizing cancer showed a significantly lower log H/M, higher LDH/platelet, and higher platelet count. In platelets from 25 rats there was, during normal thrombopoiesis, no correlation between log H/M, LDH/platelet, and platelet count. M‐LDH activity constituted 97 % of the total LDH activity in rat platelets.
During bleeding‐induced thrombocytosis the LDH/platelet was significantly lower and the log H/M unchanged, i.e. the M‐LDH activity was lower compared with the prebleeding values. The change in LDH/platelet and M activity was significant, negatively correlated to the change in the platelet count. Platelet volume/platelet was unchanged. The normal and abnormal LDH and isoenzymes of the platelets are assumed to have originated in megakaryocyte cytoplasm.