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The aim of our study was to investigate the effect of body condition on the number of ovarian follicles, the number and quality of COC-complexes and/or concentration of leptin (LEP), total and active ghrelin (TGHR and AGHR) in blood plasma and follicular fluids. Before slaughter all cows were divided into five classes according to their body condition scores (BCS). Body condition had no significant influence on the number of follicles and aspirated oocytes. The mean number of oocytes of a very good quality (Grade 1 and Grade 2) was 0.79 and 1.14 in cows with BCS 2.50 and 2.51-3.0, and was lower than 2.69, 2.66 and 2.0, respectively, aspirated from follicles in cows from group 3.01-3.5, 3.51-4.0 and > 4.0. Body condition influenced the number of COCs of a very good quality (Grade 1, P < 0.05). There was no relation between body condition and the number of oocytes grades 2 and 4. We found an interrelation between blood leptin concentration and its concentration in the follicular fluid (P < 0.01). No significant relationship exists between the BCS of cows and concentrations of leptin and active ghrelin in blood plasma and the follicular fluid.
The aim of the present study was to investigate the effect of exogenous leptin on somatotrophic axis regulation in prepubertal female lambs under conditions of acute undernutrition (72 h fasting). The analyses in fasted sheep revealed enhancement of immunoreactive (ir) somatostatin stores in perikarya of the periventricular (PEV) nucleus and in terminals of the median eminence (ME) (P<0.001), enhancement of growth hormone (GH) mRNA expression in the adenohypophysis, diminishing of ir GH stores in somatotrophs in the adenohypophysis (P<0.001), and a rise in GH pulsatility (P<0.05) in the blood in comparison with standard-fed sheep. In fasted sheep infused with leptin, additional enhancement of ir somatostatin stores in the PEV nucleus and in the ME (P<0.001), an increase in GH mRNA expression in the adenohypophysis (P<0.001), and augmentation of GH pulsatility (P<0.05) in the blood plasma were noted. In conclusion, acute undernutrition affects somatotrophic axis by enhancement of GH secretion via restraining of somatostatin output. Exogenous leptin additionally amplifies this effect by suppressing somatostatin release and increasing of GH secretion. The results provide evidence that leptin can regulate somatotrophic axis activity in prepubertal female lambs under conditions of acute fasting.
The aim of the study was to investigate the effect of ruminal fluid pH depression on biochemical indices of blood, urine, feces, and milk, and to determine which of them may be helpful as a marker for the diagnosis of subacute ruminal acidosis (SARA). Ruminal fluid samples were obtained by rumenocentesis from 305 cows representing 13 commercial dairy herds. The herds were selected based on percentages of cows with an assigned value of ruminal fluid pH segregated into three groups as: SARA-positive herd, if at least 25% of the ruminal fluid samples indicated a pH < 5.6; SARA-risk herd, if less than 25% of ruminal fluid samples indicated a pH < 5.6, but at least 33% showed a pH ≤ 5.8; and SARA-negative herd, if less than 25% of the ruminal fluid samples indicated a pH < 5.6, but less than 33% exhibited a pH = 5.8. Moreover, the dairy cows were divided according to the ruminal fluid pH into three groups as follows: healthy cows (HC, pH>5.80, n = 196), risk cows (RC, pH 5.8 – 5.6, n = 51), and acidotic cows (AC, pH < 5.6, n = 58). Almost 19% (58/305) of the cows were classified as acidotic (pH < 5.6) and 46.2% of the herds as SARA-positive. In the AC group, higher concentrations of insulin-like growth factor-I (IGF-I), non-esterified fatty acids (NEFA), rectal temperature and lower blood pH, compared with those of the HC group, were recorded. Moreover, in the SARA-positive herds, higher concentrations of IGF-I and the lowest blood pH, compared with SARA-negative herds, were observed. The lowering of ruminal fluid pH increased the blood IGF-I and NEFA concentrations and the rectal temperature and decreased the blood pH. These measures are indicators of the physiological changes that occur as part of the pathogenesis of the condition and may be helpful for the diagnosis of the SARA syndrome when serial measurements are conducted.
The swine RYR1 (ryanodine receptor 1) gene is a major gene for meatiness, but its effect on the fatness and location of fat deposition is less known. A known mutation in this gene is responsible for a drastic deterioration of meat quality. We provide evidence that the mutation (c.1843T) alters FAT distribution between back fat and abdominal fat, which are of different value in meat processing.The study included 486 gilts representing the Polish Landrace, PL (n=242) and synthetic line L990 (n=244). All gilts were classified into 3 clusters according to their predisposition to fat distribution between visceral and subcutaneous tissues. We found a relationship between this classification and RYR1. The mutation c.1843C>T changed the distribution of body fat between these tissues in PL and L990 (P=0.0384), and in L990 separately (P=0.0277). No evidence for such an effect was observed when PL was analyzed separately. Compared to the CC homozygotes the T allele was associated with a lower abdominal fat deposition and heterozygous gilts tended to allocate adipose tissue in back fat;however, the effect on fat distribution was independent of general fatness of a pig.
The aim of this study was to assess the variation in levels of glucose and selected peptide hormones (insulin, leptin and ghrelin) in blood serum of young adults, depending on their nutritional status. Investigations were conducted with the participation of 18 persons, which were divided into three groups characterised by different nutritional status – BMI: <20 kg/m2, 20–25 kg/m2 and >25 kg/m2. Blood samples were collected from each examined person before they have eaten and next blood serum levels were determined for glucose, insulin, leptin, active and total ghrelin. Significant (p<0.05) inter-group differences were shown in leptin concentration, with the highest values of this parameter shown in the group of overweight persons (31.68±23.29 ng/cm3), while the lowest for individuals with BMI<20 kg/m2 (5.81±4.57 ng/cm3). Statistically significant correlations were found between BMI and leptin level (r=0.56, p<0.05), the share of fat mass and levels of insulin (r=0.52, p<0.05) and leptin (r=0.81, p<0.001), as well as the mean skinfolds thickness and the concentration of insulin (r=0.47, p<0.05) and leptin (r=0.63, p<0.01).
Ghrelin is a hormone mainly produced in the stomach and its first discovered action was connected with regulating growth hormone secretion. It was found that ghrelin injection increases growth hormone release and that this action is dose-dependent. Ghrelin may influence growth hormone secretion both by central and peripheral action. Ghrelin acts via its receptors named growth hormone secretagogue receptors (GHSR). Ghrelin receptors were found in almost all tissues including the central nervous system. Besides influence on growth hormone secretion, ghrelin also regulates food intake and energy metabolism centrally as well as peripherally. In our study, active ghrelin and growth hormone levels in serum were measured. We also investigated gene expression of proghrelin, growth hormone releasing hormone (GHRH) and growth hormone receptor (GH-R) in the hypothalamus and the active form of ghrelin receptor (GHSR-1a) in hypothalamus and pituitary. Expression of growth hormone and growth hormone releasing hormone receptor (GHRH-R) in the pituitary were also measured. The results of our study indicate that active ghrelin and growth hormone levels in serum increased during pregnancy. Expression of ghrelin in hypothalamus and its receptor also increased in hypothalamus and pituitary during pregnancy. We also observed that growth hormone gene expression rose in pituitary, while its receptor mRNA level in hypothalamus decreased. Additionaly, growth hormone expression in placenta decreased during pregnancy. Moreover, GHRH in hypothalamus and its receptor in pituitary showed reduced levels during pregnancy. Our results may indicate that ghrelin is a important factor influencing growth hormone release during pregnancy.
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