Prolonged melatonin administration in 6-month-old Sprague-Dawley rats: metabolic alterations.

The aim of this work was to evaluate the effect of prolonged melatonin administration on chosen metabolic and hormonal variables in male and female Sprague-Dawley rats. Melatonin was administered in tap water (4 microg/ml) daily from the 6th month of age. Rats were fed a standard type of diet ad libitum and were kept in a light regimen L:D--12:12h. The experiment was terminated after 12 weeks of melatonin administration. Melatonin decreased body mass during the whole experiment in females and from the 42nd day of the experiment in males. Relative heart muscle weight in females and absolute/relative thymus weight in males were increased after melatonin administration. Melatonin decreased glycaemia, heart muscle glycogen concentration in females and liver glycogen concentration in both sexes. Serum insulin concentration in males was decreased; serum corticosterone concentration was increased in both males and females. Serum triacylglycerol and heart muscle cholesterol concentration in females were decreased, however in males serum and heart muscle cholesterol concentration was increased. Liver phospholipid concentration in females was decreased and heart muscle phospholipid concentration in males was increased. Melatonin increased malondialdehyde concentration in heart muscle in males and in liver in both sexes. Melatonin induced prominent sex-dependent changes in both carbohydrate and lipid metabolism.

Thymus lipids in continuously irradiated rats.

Male Wistar rats were irradiated continuously with a daily dose of 0.19 Gy (120 days), 0.57 Gy (90 days) and 0.96 Gy (35 days) of gamma rays. An other group of rats was irradiated continuously with graded doses of gamma rays, up to total exposures ranging from 3.83-19.15 Gy. Depending on both the daily dose and total exposure, there was a decrease in phospholipid content in the thymus which correlated well with thymus weight changes. The decrease in triacylglycerol content was a less reliable sign of radiation damage. The phospholipid content reflecting the patterns of organ cellularity is a valuable indicator of the extent as well as recovery from radiation-induced injury to the thymus.

Circaseptan rhythm of corticosterone and lipids in the serum of male rats.

After adaptation to standard conditions and to a 12:12 h light: dark regimen, groups of young SPF male Wistar rats were killed at 8 h on 17 consecutive days and their serum corticosterone and lipid concentrations were determined. Using a combination of a Fourier harmonic analysis and an analysis of variance, the circaseptan rhythm of corticosterone, total cholesterol and triacylglycerol oscillations was determined; it is unlikely that the nonesterified fatty acid concentration has a 7-day rhythm. The circaseptan variation of metabolic and hormonal indicators is evidently adaptive in character and its existence ought to be taken particularly into account in the evaluation of long-term experiments.

Correlation of circadian changes in tyrosine aminotransferase and tryptophan-2-3-dioxygenase in rat liver to irradiation at different times of the day.

Male SPF Wistar rats adapted to a 12:12 h light: dark regimen were irradiated at 3-hour intervals in the course of 24 h with a dose of 14.35 Gy X-rays; 24 h after irradiation or sham irradiation and starvation for the same length of time, and also in fed intact rats, tyrosine aminotransferase and tryptophan-2-3-dioxygenase activity in the liver and the serum corticosterone level were determined. Although lethal irradiation modified the given enzyme activities, it did not abolish their circadian rhythm, evidently in association with the low sensitivity in association with the low sensitivity of the liver to ionizing radiation. In irradiated animals (compared with sham-irradiated animals), the serum corticosterone concentration fell during the light part of the day and at the beginning of the dark part.

Circadian rhythm of ketone bodies in the blood of fasting rats.

SPF male Wistar rats were kept under standard conditions with a light: dark schedule of 12:12 h. The total ketone body concentration was determined in the blood, and the non-esterified fatty acid level in the serum, of fed rats and of animals which had fasted 24 and 48 h. The amount of ketone bodies in fed rats rose in the second half of the light period and fell with the onset of the dark period. After a 24 h fast, the amount of ketone bodies in the blood rose, but the basic characteristics of the curve and the rhythm remained the same as in fed animals. After a 48 h fast, the mean ketone body concentration was decoupled, a significant phase shift occurred and the rhythm was lost. No relationship between the oscillations of the total ketone body concentration in the blood and the oscillations of the serum non-esterified fatty acid level was found.

Circadian oscillations of thyroid hormones, insulin and glucagon in the blood of laboratory rats in the course of the year.

The concentration of thyroid hormones and insulin in the serum that of glucagon in the plasma and glucose in the blood was determined at 3-hour intervals, in the course of one day, at different times of the year, in adult male rats (Wistar strain) of a conventional breed kept under standard conditions with a 12:12 h light:dark regimen. The lowest thyroid hormone and glucagon concentrations and the highest insulin and blood glucose levels were found in the winter. In various seasons, circadian oscillations of the thyroid hormones culminated in the dark part of the day and that of glucagon in the light part, with the exception of the autumn. Circadian oscillation of insulin levels culminated at different times of day during the year. The pronounced changes found in the examined hormones in the laboratory rat at various times of the year are evidently the outcome of adaptation to changes in external environmental conditions during phylogenesis. In the polarity of changes in these indicators between the winter and the summer or the spring, the laboratory rat bears the closest resemblance to wild mammals.

Effect of food synchronization on the circadian rhythm of bone marrow and thymus lipids in rats.

Young male Wistar rats reared under standard laboratory conditions with a 12:12 h light:dark regimen were fed ad libitum or were allowed access to food for only 2 h in the first half of the light or the dark part of the day. In rats fed ad libitum, marked circadian oscillation of the bone marrow triacylglycerol and phospholipid concentration and oscillation of the same fractions in the thymus were found. The restricted feeding time raised the triacylglycerol concentration in the bone marrow, but did not noticeably affect the time course of the circadian curves. The mean lipid values in the thymus of animals with a shortened feeding time did not alter, but the acrophase of the two basic fractions shifted.

Circadian rhythm of the lactate and pyruvate concentration in rat liver and blood.

Diurnal changes in the blood and liver lactate and pyruvate concentration and in the blood glucose, serum insulin and liver glycogen level were studied in the spring, at 3-hour intervals, in adult ad libitum fed male Wistar rats adapted to standard laboratory conditions and a 12:12 h light and dark regimen (7-19 and 19-7 h). The marked liver and blood lactate oscillations attained maximum values during the dark period, together with the serum insulin oscillations. The pyruvate concentration oscillations culminated in the light part of the day in the liver and in the dark part in the blood; they were not very pronounced, probably owing to rapid metabolization. The curve for the liver lactate/pyruvate index resembled the lactate curve and attained the maximum in the dark period; the blood curve for this index was different, because of the different times at which the two substrates pass from the liver and other tissues into the blood stream. The blood glucose circadian oscillations culminated in the second half of the light period, parallel with the first serum insulin maximum. The oscillations of the liver glycogen values were typical, with the maximum at the end of the dark period and the beginning of the light period. The circadian oscillations of the given substances furnish information on the time sequence of period metabolic processes dependent on the illumination or alimentary regimen, on the waking and sleep cycle and on other synchronizers.