1. Investigación

A 24-h fast induced different patterns of change in the amino acid concentrations of liver, muscle, plasma and blood cells. Starvation produced generalized increases in blood amino acids despite decreases in plasma, thus increasing the blood cells amino acid pool. Muscle increased amino acid levels with fasting, while the changes were much more buffered in liver. The fraction of essential amino acids carried by the blood was considerably greater than that of muscle and liver. The size of muscle pool in the whole rat was much greater than that of liver and more than two orders of magnitude higher than that of the whole blood. Fasting-induced changes agree with the known transport of amino acids from muscle and other peripheral tissues towards the liver and other splanchnic organs.

Rats chronically treated with two daily doses of tolbutamide, glibenclamide or glipentide were compared with animals treated with placebo. Plasma individual amino acids were determined at 0, 3, 7, 10, 12, 14, 17, 24, 27 and 29 days of treatment 16 hours after the administration of the drug. Rats were fasted for 48 h periods at days 10 to 12 and 27 to 29 of the experiment. Sulfonylurea treated animals show minor changes in the plasma aminogram, although glipentide and glibenclamide produced greater effects than tolbutamide. At the 3rd day after the onset of the treatment, plasma levels of glutamate+ glutamine, arginine and histidine appeared significantly reduced in glipentide and glibenclamide treated animals. When plasma samples were collected 3 h after the drug administration at the 24th day of treatment, the only observed change was a decrease in the levels of arginine in the glipentide treated animals. Fasting produced decreases in plasma levels of alanine, pro line, cysteine, tyrosine, methionine +ornithine and tryptophan, there were no changes in serine, aspartate + asparagine, threonine citruline, arginine and lysine; and glycine, glutamate+ glutamine and leucine + isoleucine show increases. These changes were rapidly compensated with refeeding, appearing a "rebound effect" in certain amino acids. Both fasting and refeeding affect very little the effect of sultonylureas on plasma amino acid levels, although for some individual amino acid they reduce or enhance the effect of the fasting. These small effect of sulfonylureas on plasma amino acid levels could be the result of the juxtaposition of different factors, including the effects of these drugs on circulating insulin levels, on protein biosynthesis and amino acids transamination and hepatic gluconeogenesis.

Plasma amino acid concentrations, together with other metabolic parameters were determined in thyroidectomized rats treated with daily injections of sal ins (hypothyroid), and 250 ,ug/kg L-T4 {hypothyroid). Data were compared with sham-operated controls. TherP. is a genera! incre'!SE> in plasma amino acid concentrations in hyperthyroidism, a limited in· crease only in several amino acid r.oncentrations in hypothyroid rats as compared with controls, and a considerable difference between the plasma aminograms of both groups. Amino acid homeostasis seems to be subject to greater modification in hyperthyroidism than in hypothyroidism.

The effects of food deprivation for up to 24 hours on plasma metabolic parameters in the rat have been studied. Liver dry weight and glycogen content dropped significantly from a hours of food deprivation onwards. Total muscle glycogen supplied about as much glycosyl residues or precursors as did the liver. Plasma glucose, urea, lactate and total and essential amino acids decreased significantly from 3 hours of fasting onwards. Glycerol, free fatty acids, beta-hydroxybutyrate and acetoacetate showed significant increases with fasting. Alanine, serine, arginine, threonine, aspartate plus asparagine and proline showed significant decreases with fasting. Several other amino acids showed almost nc change with fasting. Lysine, leucine plus isoleucine and taurine showed biphasic changes in their concentrations with a minimum at 6 hours and a transient recovery at 12 hours of fasting. Essential amino acids decreased more than the non essential ones. With fasting there is a shift in ammonia disposal with lower urea concentrations as nitrogen is better conserved. The results seem to suggest that there i~ a constant release of substrates, through liver and peripheral tissue proteolysis, that is counteracted by differential utilization of amino acids during fasting.

Female rats were treated with two daily equihypoglycemic doses (as observed in acute treatment) of tolbutamide, glibenclamide or glipentide . by stomach tube, and were compared with control ammals treated with the suspending medium alone. On day 29 the rats were subjected to a 48 h fast and then were injected intraperitoneally with 100 .μMoles of C' -alanine. Blood samples were collected before and 5, 15 and 30 minutes after the alanine injection, at which time the animals were killed. Blood glucose levels increased after the injection of alanine in all groups, but at the different times stll:died, both the glibenclamide and glipentide treated_ anu_n~ls showed hypoglycemia versus controls. The rad10act1:"1ty found in blood glucose and liver glycogen and glycendeglycerol decreased in the glibenclamide treated anima~s compared with controls while in the other groups 1t was similar. The increase in liver glycogen after the injection of alanine was also diminished in the_ glibenclamide treated animals. Alanine produced an mcrease in the plasma levels of gluconeogenic, basic, aromatic and sulphur-containing amino acids in the controls, while in the animals treated with glipentide the alanine effect was less pronounced. The results show an impairment of gluconeogenic function in glibenclamide treated animals. The effects of both tolbutamide and glipentide were less dramatic. Nevertheless, the findings hinted at an effect of both drugs upon glycogen metabolism in liver.

In food-restricted normal rats plasma and brain amino acid concentrations also differed from values in normal controls but they were of different magnitude and/or direction than those of diabetics. In vitro 3 H-Leucine incorporation into proteins by brain postmitochondrial dialyzed supematants was unaffected in both diabetic and food-restricted rats, whereas in liver preparations the same parameter was significantly reduced in both groups and insulin treatment of the diabetics decreased this difference. Results indicate that brain amino acid concentrations in diabetic aminals are a secondary consequence of their circulating levels and of potential modifications of brain amino acid metabolism other than protein synthesis, which is unaffected.