Larger NMR magnets with relatively high field strengths have become available recently, allowing the application of magnetic resonance spectroscopy (MRS) in larger mammalian organs. The aim of this study was to develop and test a new and simple kidney perfusion model from slaughterhouse swine using a new 4.7-tesla/40-cm diameter system, with the intention behind to provide a human-like mammalian experimental kidney perfusion model, and to avoid sensitive in vivo animal experiments on higher-developed mammalians, 35 pig kidneys obtained 10-15 min post mortem were studied to evaluate and define conditions for optimum metabolic preservation with the following perfusion protocols: (1) immediate
plegia with cold
Collins solution, 1-3 h cold storage, P-31 MRS; (2) immediate
plegia, 1-3 h cold storage, blood reperfusion, P-31 MRS; (3) immediate blood reperfusion,
plegia, 1-3 h cold storage, blood reperfusion, P-31 MRS; (4) immediate blood reperfusion,
plegia, 24 h cold storage, blood reperfusion, P-31 MRS, P-31 MRS at 81 MHz with a double-tuned surface coil yielded the following results: [table: see text] Blood flow showed a weak correlation with beta-
ATP/
inorganic phosphate in protocols 3 and 4 of r = 0.64. Repeated reperfusion and
ischemia experiments of this model allowed the on-line observation of the metabolic response of the energy
phosphate pattern for several hours. In conclusion, slaughterhouse-harvested swine kidneys lend themselves to a simple, low-cost in vitro perfusion model, provided they are reperfused with arterial blood immediately after harvesting.(ABSTRACT TRUNCATED AT 250 WORDS)