Key result
Phosphate depletion in rats impairs myocardial energy metabolism and mitochondrial respiration.
Why the study?
The effects of phosphate depletion on myocardial energy metabolism and its molecular basis for altered myocardial function were not fully understood.
Answers are grounded in this paper and cite their sources.
Phosphate depletion impairs rat myocardial energetics; leaves open relevance to human hypophosphatemia or heart failure.
The effects of phosphate depletion (PD) of 4, 8, and 12 wk duration on myocardial energy metabolism were studied in rats fed a phosphate-deficient diet and compared with rats pair-fed a normal phosphate diet. Myocardial biopsies were examined for high-energy phosphate bonds. The results show that PD causes a significant reduction in myocardial concentration of inorganic phosphorus at 4 wk of PD and creatine phosphate at 8 wk of PD, while adenine nucleotides were significantly reduced only after 12 wk of PD. The changes in cellular inorganic phosphorus and creatine phosphate displayed a significant correlation with serum phosphorus levels. Mitochondrial respiration was impaired early in PD. Total cellular, mitochondrial, and myofibrillar creatine kinase activities were significantly reduced at 4 wk of PD and fell further at 8 and 12 wk. These data show that chronic PD is associated with reduced mitochondrial capacity to produce ATP, impaired transport via the creatine phosphate shuttle, and reduced myofibrillar ability to utilize ATP. These abnormalities indicate that all steps of myocardial energetics are impaired in PD and provide the molecular basis for the altered myocardial function seen in PD.
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Brautbar et al. (1982) studied Phosphate depletion. Phosphate-deficient diet vs. Normal phosphate diet (pair-fed) was evaluated on Myocardial energy metabolism (inorganic phosphorus, creatine phosphate, adenine nucleotides, creatine kinase activities). Phosphate depletion in rats significantly reduced myocardial inorganic phosphorus, creatine phosphate, and adenine nucleotides, and impaired mitochondrial respiration and creatine kinase activities.
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