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The distribution of ammonia between hepatocytes and extracellular fluid.

1. Some factors determining the distribution of ammonia between hepatocytes and the suspension medium and between mitochondria and cell cytosol were examined. 2. Intracellular [ammonia] of isolated hepatocytes was similar to that in freeze-clamped rat liver. The intra- to extracellular [ammonia] ratio ('ammonia ratio') of cells incubated without added substrates was as great as 70. 3. High ammonia ratios were found only within the physiological range of extracellular [ammonia] i.e. 0.03 mM. At higher external [NH4Cl] the ammonia ration decreased until at 20 mM it approached 1.0. 4. On addition of NH4Cl (10.0 mM) ammonia entered hepatocytes rapidly until at about 2.5 min internal and external ammonia concentration were similar. The final steady state distribution of ammonia was not reached until 60 min, when the internal concentration was slightly higher than that externally. 5. Intracellular [K+] decreased when intracellular [ammonia] increased. The sum of intracellular [K+] plus [NH4(+)] remained approximately constant. 6. In anaerobic cells the high endogenous ammonia ratio was not maintained. 7. The high physiological ammonia ratio was not abolished by ouabain. Thus the (Na+ + K+)-ATPase does nt appear to be responsible for the maintenance of the ammonia ratio. 8. A high ammonia ratio also existed between hepatocyte cytosol and mitochondria. 9. On addition of fructose, which depletes the cells of Pi and adenine nucleotides, the ammonia content of the cells decreased parallel with Pi and ATP. In the presence of fructose much ammonia was removed by the formation of alanine. However, when pyruvate was added to stimulate alanine formation there was no effect on the ammonia distribution. This showed that alanine formation alone was not responsible for decreased intracellular [ammonia] with fructose. 10. Incubation with adenosine led to a large increase in intracellular ATP and ammonia content as well as in the ammonia ratio. Incubation with alanine also led to increased intracellular ammonia production but in this case ammonia was released into the medium and high ammonia ratios did not occur. 11. Some mechanisms for maintenance of a high ammonia ratio between cells and medium are discussed.

Ammonia↗

Oxygen and extracellular fluid restriction in cultured heart cells: electron microscopy studies.

STUDY OBJECTIVE: To evaluate the effects of "simulated ischaemia" on the structure of cultured heart cells. DESIGN: Cultured heart cells were subjected for 2 h either to anoxia or to anoxia with simultaneous extracellular volume restriction ("simulated ischaemia"). Cells maintained under normoxic conditions served as controls. The cells were then fixed in situ in Petri dishes with formaldehyde-glutaraldehyde. EXPERIMENTAL MATERIALS: Heart cells from one day old rats on day 5 in culture were used. MEASUREMENTS AND RESULTS: Electron microscope studies were carried out on control and injured cells. "Mildly ischaemic" cells featured raffled and invaginated cell surfaces, reduced matrix density, disorientated mitochondrial cristae due to swelling, and giant mitochondria. Dilatation of rough endoplasmic reticulum and electron dense membrane bound vesicles were observed in the cytoplasm. CONCLUSIONS: The model of simulated ischaemia is in keeping with the classical picture of irreversible cell damage caused by ischaemic injury.

Animals↗

Studies on oxygen and extracellular fluid restrictions in cultured heart cells: high energy phosphate metabolism.

Although cultured heart cells are increasingly used for the study of cardiac metabolism, relatively little is known about their energy turnover. We studied the effects of anoxia with simultaneous restrictions of the volume of the extracellular medium ("ischaemia") on high energy phosphate catabolism in cells from neonatal rat ventricles, cultured for 5 days. The cells were incubated for up to 4 h in Ham-F10 medium either in the presence or in the absence of glucose. High energy phosphates in cell extracts and AMP catabolites in the incubation medium were measured by high pressure liquid chromatography. ATP and creatine phosphate content in normoxic cells did not change significantly, either in the presence or absence of glucose, and the values were similar to those found in the heart in vivo. Energy rich phosphates decreased during anoxia, and were more rapidly depleted during simultaneous oxygen deprivation and volume restriction. Glucose delayed the decline in high energy phosphates. In the presence of glucose, hypoxanthine uptake was higher during normoxia than in anoxia, whereas in "ischaemic" conditions some hypoxanthine was produced. In the absence of glucose, only minor changes were observed in hypoxanthine levels during anoxia, but hypoxanthine production was marked when anoxia was coupled with extracellular volume restriction. Adenosine levels were below the limit of detection. Inosine release was relatively low under all conditions, Xanthine release did not show variation, and anoxia suppressed urate production. Oxygen and glucose deprivation thus led to various degrees of ATP and creatine phosphate breakdown in cultured neonatal heart cells both during anoxia and in simulated "ischaemia".

Adenosine Monophosphate↗