9 results match your criteria: "Research Centre of Animal Production[Affiliation]"

Monocytes and macrophages belong to the mononuclear phagocyte system and play important roles in both physiological and pathological processes. The cells belonging to the monocyte/macrophage system are structurally and functionally heterogeneous. Several subsets of monocytes have been previously identified in mammalian blood, generating different subpopulations of macrophages in tissues.

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Interrelationship between feeding level and the metabolic hormones leptin, ghrelin and obestatin in control of chicken egg laying and release of ovarian hormones.

Comp Biochem Physiol A Mol Integr Physiol

June 2015

Department of Functional Genomics and Bioregulation, Ïnstitute of Animal Genetics, Friedrich-Loeffler Institut (FLI), Mariensee, 31535 Neustadt, Germany. Electronic address:

The aim of the present experiment is to examine the role of nutritional status, metabolic hormones and their interrelationships in the control of chicken ovarian ovulatory and secretory activity. For this purpose, we identified the effect of food restriction, administration of leptin, ghrelin 1-18, obestatin and combinations of food restriction with these hormones for 3days on chicken ovulation (egg laying) rate and ovarian hormone release. The release of progesterone (P), testosterone (T), estradiol (E) and arginine-vasotocin (AVT) by isolated and cultured ovarian fragments was determined by EIA.

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The purpose of the present study was to identify the role of age, nutritional state and some metabolic hormones in control of avian hypothalamic and ovarian ghrelin/ghrelin receptor system. We examined the effect of food restriction, administration of ghrelin 1-18, ghrelin antagonistic analogue (D-Lys-3)-GHRP-6, obestatin and combinations of them on the expression of ghrelin and ghrelin receptor (GHS-R1a) in hypothalamus and ovary of old (23months of age) and young (7months of age) chickens. Expression of mRNAs for ghrelin and GHS-R1a in both hypothalamus and largest ovarian follicle was measured by RT-PCR.

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Comparison of effects of leptin and ghrelin on porcine ovarian granulosa cells.

Domest Anim Endocrinol

July 2010

Research Centre of Animal Production, Slovak Agricultural Research Centre, 949 92, Nitra, Slovakia.

The aim of our studies was to compare the roles of leptin and ghrelin in the direct control of proliferation, apoptosis, and secretory activity by porcine ovarian cells. In our in vitro experiments, we analyzed the effects of leptin and ghrelin treatments (at 0, 1, 10, or 100ng/mL medium) on the accumulation of proliferation-related peptides (PCNA, cyclin B1, MAP kinase [MAPK]) and apoptosis-associated peptides (Bax, caspase 3, p53), and on progesterone secretion by cultured porcine granulosa cells, using immunocytochemistry, SDS PAGE-Western immunoblotting, and radioimmunoassay (RIA). Leptin stimulated proliferation (PCNA, cyclin B1, MAPK), apoptosis (Bax, p53), and progesterone secretion.

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The duodenal passages of non-ammonia nitrogen (NAN), amino acid N (AA-N) and microbial N (MN) were measured in seven duodenal fistulated dairy cows (6130 kg FCM/305 d) during lactation receiving 30 different rations similar to those used in dairy practice. The rations consisted of roughage (protein-rich silages, hay) and concentrate mixture (corn, barley, oat) in a ratio of 60:40 on a DM basis or roughage/concentrate mixture/fodder beets in the proportions 60:20:20 or 60:0:40 respectively. N supplements consisted of soya bean meal and peas meal (untreated or treated with formaldehyde in each case), rapeseed meal, fish meal and urea.

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In an experiment with 3 pigs (initial live weight 30 kg, each fitted with 2 re-entrant fistulas in duodenum and ileum, one labelled with 15N), the duodenal and ileum digesta was exchanged. The N and 15N contents were estimated in faeces, urine, duodenal and ileum digesta of all experimental animals as well as in special organs and in the contents of different tract sections. The 15N excess (15N') of N compounds secreted into the gut lumen was determined using the 15N' in pancreas, gut mucosa and TCA-soluble blood serum.

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An experiment was carried out using pigs weighing approximately 30 kg. The animals were fitted with two re-entrant cannulas in duodenum and ileum. During a 5 day period the passage of digesta through duodenum and ileum as well as the excretion by urine and faeces was estimated, taking an aliquot of 5% for N analysis.

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Gene transfer experiments in cattle.

J Reprod Fertil Suppl

November 1989

Research Centre of Animal Production, Academy of Agricultural Sciences of GDR.

Various methods for gene transfer in cattle are described. Four vectors containing (1) the bovine papilloma virus DNA, (2) the alcohol dehydrogenase gene of Drosophila melanogaster, and the human (3) and the bovine (4) growth hormone gene were used for gene injection in bovine zygotes. The period between 78 and 82 h after prostaglandin treatment was determined as the optimum time for collection of bovine zygotes.

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