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A pronounced and significant stimulatory effect on erythropoiesis was observed in anemic uremic rats receiving either T3 (50 micrograms/kg/day) or Ep (7.5 and 15 U[units]/day) for ten days. A lack of erythropoietic response was seen after the administration of testosterone (5 mg/kg/day) for the same period of time. Renal failure and anemia were studied in partially nephrectomized rats that had received nephrotoxic doses of kanamycin (500 mg/kg/day). The marked increase in red blood cell production produced by T3 and Ep in anemic uremic rats was evident, not only from increased hemoglobin and hematocrit values in peripheral blood, but also from an elevated number of circulating reticulocytes and generally increased absolute counts of nucleated erythroid cells per milligram of bone marrow. The effects of T3 on erythropoiesis in anemic rats with renal insufficiency are in accordance with our previous report demonstrating the direct effect of thyroid hormones on marrow erythroid precursors. This effect can occur only when high levels of the free active forms of T3 are present in plasma, as can happen in the uremic rats receiving daily doses of T3. Since the possibility of producing large amounts of Ep for the treatment of the anemia associated with chronic renal failure is unlikely in the near future, utilization of T3, mainly compounds without calorigenic effects, may be a potential therapeutic alternative.

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