Storage of retinoids and beta-carotene in the genital organs of Japanese quail

The present study was designed to investigate the effect of a one-month feeding of retinyl acetate (RA) on the retinol (ROL), retinyl palmitate (RP) and (-carotene (BC) levels in the blood, testicles and ovarian follicles of adult Japanese quails. The basal diet (containing vitamin A at 10 × 103IU/kg) was supplemented with 100 ×, 500 × and 1000 × 103IU/kg RA in Groups I, II and III in both sexes. Plasma vitamin A levels rose in all groups. The elevations were caused basically by the RP fraction. The ROL concentration increased only slightly, indicating saturation of the blood binding/transport system. Plasma BC was depressed in both sexes. RA feeding resulted in high RP concentration in the genital organs (testicles and ovarian follicles), indicating subclinical hypervitaminosis, while the BC content of genital organs decreased considerably. The retinoid and BC concentration of ovarian follicles (F1-F5) was in the same range, indicating continuous retinoid and carotene transport during the fast maturation period. Retinoid content of the genital organs was higher in layers than in roosters. BC deposition was decreased both in the testicles and in the follicles, indicating a competition between RP and BC for the storage capacity of organs

Effect of large dietary doses of ß-carotene on plasma retinoid and ß-carotene levels and ON progesterone production in the granulosa cells of Japanese quail

An experiment was conducted to study the effect of large-dose (-carotene supplementation on blood retinoid and (-carotene levels as well as on the progesterone secretion of the granulosa cells in Japanese quail. Laying quails were assigned to three dietary groups. The control group (Group C) received the basal diet (laying feed containing 9000 IU vitamin A/kg). In the treated groups (Groups BC1 and BC2) the basal diet was supplemented with 102and 103mg/kg (-carotene (BC), respectively. At the end of the two-week feeding period, 10 birds from each group were euthanised. Blood samples were analysed for retinol, retinyl palmitate and (-carotene concentrations. Granulosa cells were isolated from ovarian follicles (F1and F2), and PMSG-inducedin vitroprogesterone (P4) secretion was measured. Similar retinol concentrations were found in both (-carotene supplemented groups, indicating saturation of the retinol-transporting system. (-carotene supplementation was accompanied by hypercarotenaemia, but did not increase the retinyl palmitate levels in the blood. PMSG-induced P4production of the granulosa cells decreased significantly in Groups BC1 and BC2 in a dose-dependent manner

Relationships between force-feeding and some physiological parameters in geese bred for fatty liver

The susceptibility of geese of different genotypes and sexes to force-feeding, some plasma biochemical parameters (thyroid hormones, cholesterol, retinoids, total protein and albumin) of force-fed geese, and the relationship between force-feeding, fat storage and the above-mentioned parameters were studied. Sixty (30 male and 30 female) geese of three genotypes (Hungarian, Landes and their crossbred called Babat Hybrid) were divided in two groups at 12 weeks of age. Geese in one group (5 males and 5 females from each genotype) received mixed feedingad libitum. Birds in the other group were force-fed with maize. After 3 weeks all birds were bled, blood samples were taken, and the above-mentioned plasma parameters were determined. Thyroxine (T4) levels were significantly lower in force-fed (11.6 ± 3.5 ng/ml) than in control geese (22.7 ± 4.09 ng/ml). Plasma triiodothyronine (T3) level was also lower in the force-fed than in the control group, but the difference was not significant (1.87 ± 0.23 ng/ml and 2.11 ± 0.28 ng/ml, respectively). Plasma total protein (TP, 45.2 ± 4.5 g/l), albumin (ALB, 16.51 ± 2.8 g/l), (-carotene (BC, 3504 ± 3107 µg/l), retinol (ROL, 1160 ± 505 µg/l), retinyl palmitate (RP, 1745 ± 405 µg/l) and total cholesterol (TCh, 4.32 ± 0.55 mmol/l) levels were elevated in the force-fed group as compared to the control (TP = 36.4 ± 5.1 g/l, ALB = 15.6 ± 0.9 g/l, BC = 1657 ± 1681 µg/l, ROL = 687 ± 375 µg/l, RP = 1398 ± 607 µg/l, and TCh = 2.83 ± 1.98 mmol/l). All differences were significant except those found for albumin and (-carotene. No significant sex- or genotype-related effects were observed for these parameters

A new, modern, cost-saving micro/macro method for the determination of serum fructosamine

Serum/plasma fructosamine (SeFa) concentration is a reliable indicator used in human diabetic control. Tests for monitoring the carbohydrate/energy metabolism of (farm) animals are less commonly performed in veterinary laboratories, since most of the reliable determinations, both automated and manual, are relatively expensive. The aim of this study was to develop a precise, money- (and time-) saving automated micro method for measuring SeFa. ELISA microplates (20 µL samples and 200 µL reagents) and an automatic microplate autoreader were used. The classical nitroblue tetrazolium (NBT) stain reagent solution of Johnson et al. (1982) was modified using a SIGMA reagent to render it stable for up to one year. SeFa concentrations measured by the new method in 30 human blood plasma samples were compared with values obtained by the standard (generally used) LaRoche kit procedure. Fifteen cow, 13 dog and 18 chicken plasma samples were assayed by the new automated ‘micro’ method as well as by the manual test tube ‘macro’ method commonly used earlier. The modified reagent was applied for both methods. The coefficient of correlation (r) between the results obtained by the two methods was consistently between 0.94 and 0.98 (p < 0.001)

Effect of beta-carotene and nucleotide base supplementation on blood composition and immune response in weaned pigs

The effect of synthetic beta-carotene and synthetic nucleotide base on daily weight gain, feed consumption and certain haematological, biochemical and immunological parameters of piglets were studied in a 3-week experiment. Beginning one week prior to weaning, the diet fed to one experimental group of piglets was supplemented with 10% Rovimix Beta-carotene at 875 mg/kg of diet. Synthetic uracil and adenine (98%, Sigma-Aldrich) were mixed into the diet of the other experimental group at doses of 500 mg/kg of diet for each substance. The control group received the basic diet without any supplementation. The changes observed over time in the haematological parameters and in certain biochemical variables could be regarded as physiological. By day 21 of the experiment, beta-carotene supplementation had significantly lowered the neutrophilic granulocyte percentage and elevated the lymphocyte percentage, while in the other two groups a change of opposite tendency occurred. At the end of the experimental period there was a decrease in plasma vitamin E concentration due to carotene supplementation (control: 6.1 ± 1.5, nucleotide: 6.3 ± 2.5, carotene: 2.3 ± 1.5 mg/L). Lymphocyte blastogenesis induced by phytohaemagglutinin and concanavalin A increased by 50 and 130%, respectively, in the nucleotide group and by 60 and 30%, respectively, in the carotene group, while it did not change in the control group. The supplements exerted no positive effect on the in vivo cellular immune response

A novel actin binding site of myosin required for effective muscle contraction

nature structural &amp; molecular biology advance online publication a r t i c l e s Several cellular motor functions, including cell proliferation and differentiation, muscle contraction and intracellular transport, are powered by different types of myosins, which act in complex with actin 1,2 . Myosins The pivotal question is, what is the molecular mechanism behind actin activation of myosin that determines the force and velocity of muscle contraction? The importance of understanding the actin activation of myosin extends beyond muscle function. This process probably resembles the activation of a wide array of NTPases by their own track system or activator. In support of this notion is the fact that allosteric activation is an evolutionarily conserved universal mechanism among motor proteins and signaling enzyme complexes, including kinesin-tubulin, G protein-guanine nucleotide exchange factor 7 and kinase-scaffold systems 8 . Although the phenomenon of actin activation has long been acknowledged, its mechanism and structural background are unknown. We believe that this process is related to a specific actin-myosin interaction. The atomic structure of actomyosin has not been determined, however, high resolution electron micrography 9,10 and in silico docking simulation

Tetrakis(trimethylsilyloxy)silane for nanostructured SiO2-like films deposited by PECVD at atmospheric pressure

We performed the thin films deposition using atmospheric pressure plasma enhanced chemical vapour deposition (AP-PECVD) by means of a radiofrequency and a microwave plasma jets operating with mixtures of argon and tetrakis(trimethylsilyloxy)silane (TTMS)

mTOR signalling, embryogenesis and the control of lung development

The existence of a nutrient sensitive “autocatakinetic” regulator of embryonic tissue growth has been hypothesised since the early 20th century, beginning with pioneering work on the determinants of foetal size by the Australian physiologist, Thorburn Brailsford-Robertson. We now know that the mammalian target of rapamycin complexes (mTORC1 and 2) perform this essential function in all eukaryotic tissues by balancing nutrient and energy supply during the first stages of embryonic cleavage, the formation of embryonic stem cell layers and niches, the highly specified programmes of tissue growth during organogenesis and, at birth, paving the way for the first few breaths of life. This review provides a synopsis of the role of the mTOR complexes in each of these events, culminating in an analysis of lung branching morphogenesis as a way of demonstrating the central role mTOR in defining organ structural complexity. We conclude that the mTOR complexes satisfy the key requirements of a nutrient sensitive growth controller and can therefore be considered as Brailsford-Robertson's autocatakinetic centre that drives tissue growth programmes during foetal development