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Biomedical subjects

G Lac

Publications and source records attributed to G Lac.

40 records · Page 3Linked to original sources

[Spermatogenesis in the prepuberty Wistar rat during protein-energy malnutrition followed by balanced refeeding].

Protein-calorie malnutrition was induced by giving a 2% casein diet to a strain of post-weaning male Wistar rats from 26 to 56 days of age. They were then rehabilitated by a 15% casein diet till 86 days of age. Body and testis weights, diameter of seminiferous tubules and spermatogenetic score were compared to those of controls fed with the 15% casein diet. The unbalanced diet retarded growth by 30 days. Although rehabilitation of body and testis weights was incomplete, the spermatogenetic function equalled that of the controls at the end of the experiment. This aspect has been discussed.

Animals↗

[Course of the levels of myofibrillar proteins in the cardiac ventricles of adult rats in protein malnutrition followed by a balanced diet].

Adult male Wistar rats weighing 320 +/- 20 g at the beginning of the experiment were divided into two equal lots. A reference lot (T) was fed on a balanced diet containing 23,5 p. 100 mixed protein, for 60 days. A deficient lot (E) was fed on a low protein diet (3 p. 100 cereal protein) for 30 days (malnutrition), then on a balanced diet for 30 days (refeeding). When the food intake was expressed in 100 g of body weight/day, both lots ate about the same amount throughout the experiment. On the contrary, the amount of N ingested/100 mg of body weight/day by the E rats was only 11 p. 100 of that of the T lot. After 30 days of refeeding, the mean weight of the E rats equalled 90 p. 100 of that of the T rats. In the E lot, during malnutrition, the nitrogen balances were always positive and their nitrogen CDU were ranged between 73-83 p. 100 in comparison with 86-88 p. 100 in the T lot. The protein concentration of cardiac ventricles was the similar in both lots of rats, during malnutrition and refeeding periods. On the contrary, the myofibrillar protein concentration was increased in the E rats during these two phases. After separation of subunits sizes of muscle proteins by sodium dodecyl sulphate gel electrophoresis, we observed that the concentrations of myosin, actin, troponin-tropomyosin complex, myosin light chains, evolved in the same way that the total myofibrillar proteins. A relative degree of cardiac myocontractile protein sparing is suggested in our chronic protein malnutrition of adult rats.

Animals↗

[Course of minimal oxygen consumption in the young rat during protein energy malnutrition followed by return to a balanced diet].

Growth and resting oxygen consumption (VO2 minimal) were studied on two strains of six post-weaning male rats during 60 days. The first strain was fed with a balanced diet (15% casein) for 60 days, the second received a 2% casein diet for 30 days, and then the balanced diet for the remaining 30 days. The 2% casein diet completely stopped the body weight and VO2 minimal increases. When return to a balanced diet, these parameters show an evolution similar to that of controls of the same body weight. The VO2 minimal had the same kind of evolution as body weight and was well correlated with growth speed. The protein restriction involves a strong and temporary reduction of the VO2 minimal, which will correspond to a nutritional stress.

Animals↗

Steroid assays in saliva: a method to detect plasmatic contaminations.

Plasmatic and salivary levels of six steroid hormones in adult males and females are given and compared to the data of the literature. These steroids are: cortisol (F), dehydroepiandrosterone (DHA) and its sulphate (DHAS), androstenedione (A), testosterone (T) and 11 beta OH androstenedione (OHA). The salivary assay of the last compound is an original. The correlations between salivary and plasmatic values are presented and confirm that this method is a reliable alternative for hormonal investigations. From these data and from those of the literature, the salivary versus plasmatic ratio are calculated. From the fact that high concentrations of DHAS in saliva generally stem from blood contamination, we derive a method to estimate the amount of this contamination and its impact on other steroids measured on the same saliva sample.

Adult↗