Study of Hematological Characteristics and Mineral Metabolism of Moscow Black Chickens in the Process of Acclimatization in the Astrakhan Region

The study of indicators characterizing the processes associated with the acclimatization of birds in new biogeochemical conditions is of interest in connection with the prospects of the poultry industry in the Astrakhan Region, where the lack of important trace elements in soils and plant feeds: Se, I, Co, is observed. In the presented study, the main hematological and biochemical parameters of blood and mineral metabolism were determined in 2 groups of chickens of the Moscow black breed: imported to the Astrakhan Region from Moscow and kept in the Moscow Region. The analyses revealed strong differences (P<0.01) in indicators of two groups. The acclimatized birds were characterized by low levels of red blood cells and hemoglobin in the blood, as well as a higher content of white blood cells than in the second group. The chickens had impaired lipid and protein metabolism. A 71.3% increase in the level of total sugar most likely indicated a stress state of birds. Compared with the chickens in the Moscow Region, the level of calcium in their blood was 32.4% lower, phosphorus – 12.9%. To a large extent, a decrease in the levels of iodine and selenium – by 5.3 and 5.2 times, respectively, was observed. Thus, in the absence of external changes, acclimatized chickens are subject to a latent form of combined I- and Se-hypomicroelementosis. At the same time, a drop in egg productivity by 19% is the recorded fact. The necessity to adapt to the new climatic conditions of the Lower Volga region for birds, combined with a lack of important trace elements, can cause increased oxidative stress in acclimatized birds. Based on the results of the study, the use of feed additives that make up for the deficiency of necessary trace elements is recommended.

Haplotypes in the GC, CYP2R1 and CYP24A1 Genes and Biomarkers of Bone Mineral Metabolism in Older Adults

Candidate gene studies have analyzed the effect of specific vitamin D pathway genes on vitamin D availability; however, it is not clear whether genetic variants also affect overall bone metabolism. This study evaluated the association between genetic polymorphisms in GC, CYP2R1 and CYP24A1 and serum levels of total 25(OH)D, iPTH and other mineral metabolism biomarkers (albumin, total calcium and phosphorus) in a sample of 273 older Spanish adults. We observed a significant difference between CYP2R1 rs10741657 codominant model and total 25(OH)D levels after adjusting them by gender (p = 0.024). In addition, the two SNPs in the GC gene (rs4588 and rs2282679) were identified significantly associated with iPTH and creatinine serum levels. In the case of phosphorus, we observed an association with GC SNPs in dominant model. We found a relationship between haplotype 2 and 25(OH)D levels, haplotype 4 and iPTH serum levels and haplotype 7 and phosphorus levels. In conclusion, genetic variants in CYP2R1 and GC could be predictive of 25(OH)D and iPTH serum levels, respectively, in older Caucasian adults. The current study confirmed the role of iPTH as one of the most sensitive biomarkers of vitamin D activity in vivo.

Hormonal biochemical monitoring at bull-producers of different breeds in the conditions of the Central Black Economic District

Purpose: To conduct a comprehensive monitoring of bulls of different breeds in the summer in a comparative perspective to the study of protein-lipid and mineral metabolism, as well as to determine hormonal status on the content of endogenous hormones: testosterone, estradiol, cortisol and serum thyroxine per day taking seed.Materials and methods. For the first time in a Chernozem region of the Russian Federation (Voronezh region) was carried out comprehensive monitoring of bulls of red-motley Holstein (n = 16), Red-and-White (n = 8) and Simmental (n = 6) rocks in the same time of year (summer) of the protein-lipid and mineral metabolism, as well as the level of endogenous hormone (testosterone, estradiol, cortisol, thyroxine) and their cholesterol precursor in comparative aspect, immediately after taking the seed. Age range bulls ranged from 2 to 11 years. General monitoring was conducted on 23 indices of blood serum 3 rocks. The studies were conducted by modern methods, using modern equipment and reagents.Results. At Red Pied Holsteins an increase of total protein 100.45 g / L versus 92 g / l in normal (above the norm of 9.2%, as compared with red and White breed at the level of 11.3%). A similar increase in concentration in the blood of Holstein bulls red-White breed recorded on globulins, 68.87 g / l to 63 g / l in normal (above the norm of 9.3%), and with respect to the red-and-White breed 17, 6%. Also notes the high content of AST bulls red-motley Holstein against the red-and-White 18%, but within the reference range. Condition protein and lipid metabolism in sires only differed in content of creatinine, which amounted to 165.04 micromol / l against 163 mmol / l in normal, 1.6% higher as compared to the red and white breed this index was higher 18.7%. According to the content of testosterone highest rate was observed in bulls red-White breed 54.73 ± 9.51 nmol / l, is 10.2% more than in bulls red checkered-Holstein and 12.45% compared with Simmental breed. Similarly, in terms of serum cortisol - 355.60 ± 39.2 nmol / l in the red-bulls White breed that more than 2-fold compared with bulls Red Pied Holstein and Simmental. The difference is statistically significant at P ≤ 0,01. According to the content of estradiol relatively low levels recorded in the bulls of red-motley breed - 0.265 nmol / L vs. 0.301 nmol / L in red bulls-motley Holstein, and 0.332 nmol / L - Simmental, is lower by 13.6% and 25 , 3%, respectively.Conclusion. It was found that substantially all of the studied parameters in bulls 3 breeds are at reference values, and this gives grounds to assume that all of these breeds are well adapted to the conditions of Black Soil.

Association between bone mineral metabolism and vascular calcification in end-stage renal disease

Background Development of vascular calcification is accelerated in patients with end-stage renal disease. In addition to traditional risk factors of cardiovascular disease (CVD) abnormal bone and mineral metabolism together with many other factors contribute to the excess cardiovascular burden in patients on dialysis. Aortic calcification score and coronary calcification score are predictive of CVD and mortality. The aim of this study was to evaluate the possible relationship between arterial calcification and bone metabolism. Methods Thirty two patients on dialysis were included. All patients underwent a bone biopsy to assess bone histomorphometry and a 18F-NaF PET scan. Fluoride activity was measured in the lumbar spine (L1 – L4) and at the anterior iliac crest. Arterial calcification scores were assessed by computerized tomography for quantification of coronary artery calcification score and lateral lumbar radiography for aortic calcification score. Results This study group showed high prevalence of arterial calcification and 59% had verified CVD. Both CAC and AAC were significantly higher in patients with verified CVD. Only 22% had low turnover bone disease. There was a weak association between fluoride activity, which reflects bone turnover, measured in the lumbar spine, and CAC and between PTH and CAC. There was also a weak association between erosion surfaces and AAC. No significant association was found between calcification score and any other parameter measured. Conclusions The results in this study highlight the complexity, when evaluating the link between bone remodeling and vascular calcification in patients with multiple comorbidities and extensive atherosclerosis. Several studies suggest an impact of bone turnover on development of arterial calcification and there is some evidence of reduced progression of vascular calcification with improvement in bone status. The present study indicates an association between vascular calcification and bone turnover, even though many parameters of bone turnover failed to show significance. In the presence of multiple other factors contributing to the development of calcification, the impact of bone remodeling might be diminished. Trial registration The study is registered in ClinicalTrials.gov protocol registration and result system, ID is NCT02967042. Date of registration is 17/11/2016.

Osteoarthrosis and Combined Pathology: Features of Pathogenesis (Literature Review)

The purpose of the study. Identification of key links in the pathogenesis, which will improve the diagnostic and treatment approaches in such patients. Materials and methods. Analytical and bibliosemantic methods were used in the research. Results. Modern scientists are actively discussing the problems of providing medical care to patients who, in addition to the underlying disease, have an aggravating effect of concomitant, combined pathology. Interestingly, in the publications of domestic literature we find the terms "combined", "concomitant", "combined" pathology. The English-speaking scientific community uses the terms - "comorbidity" when it comes to damage to 2 organs or systems and "multimorbidity" when more than 3 diseases. The problem of combined pathologies is one of the key in modern medicine. Osteoarthritis is one of the most common diseases in Ukraine and around the world. Exhausting degenerative-dystrophic pathology, which is combined with high personal and socio-economic burden. According to the European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO) and the International Society for the Study of Osteoarthritis (OARSI), it is known that a middle-aged patient with osteoarthritis has 4 combined pathologies, including In addition to osteoarthritis, up to 8 other chronic diseases are diagnosed in old age. In clinical practice, a combination of this disease with hypertension and type 2 diabetes is often observed. However, there are still many differences in the opinion of scientists about the pathogenesis of osteoarthritis with combined pathologies. Conclusions. Scientific research in the modern world is aimed at studying the complex relationships between diseases that are often found in combination in the same patient. During the research the data of modern domestic and foreign literature were reviewed and analyzed and data on new ideas of common links in the pathogenesis of osteoarthritis, arterial hypertension and type 2 diabetes mellitus, which combines disorders in the system of oxidant-antioxidant, protease-antiprotease imbalance, proteolytic and fibrinolytic activities of blood plasma, changes in endothelial function, impaired mineral metabolism, the impact of vitamin D deficiency on the further development of chronic inflammation with the activation of cytokine synthesis. The information presented in the review is a reason to assume that the combined pathologies show the potential for complicating each other, complicating the diagnosis and treatment tactics

Multicenter Retro-Prospective Observational Study on Chronic Hypoparathyroidism and rhPTH (1-84) Treatment

The use of recombinant human PTH (1-84) [rhPTH(1-84)] is approved as hormonal replacement therapy in patients with hypoparathyroidism not adequately controlled with conventional therapy. The objective of this study was to investigate the effects of 12 months of rhPTH (1-84) treatment in a cohort of patients selected according to the indications of recent hypoparathyroidism guidelines. It is a multicenter, observational, retro-prospective, open label study. Eleven Italian Endocrinological centers were involved. Fourteen adult subjects with chronic hypoparathyroidism treated with rhPTH (1-84) for 12 months were enrolled. Main outcome measures included serum and urinary parameters of mineral metabolism, renal function, oral calcium and vitamin D doses, and clinical manifestations. At 12 months, 61.5% of patients discontinued calcium supplement and 69.2% calcitriol. Mean serum calcium levels quickly normalized after initiation of rhPTH (1-84) treatment compared to baseline (p=0.009). Rare hypo-hypercalcemia episodes were reported. Renal function was maintained normal and no renal complications were reported. Serum and urinary phosphate and urinary calcium were maintained in the normal range. Mean phosphatemia levels linearly decreased from 3 months up to 12 months compared to baseline (p= 0.014). No severe adverse events were described. In conclusion, this study confirm the efficacy and safety of rhPTH (1-84) therapy.

Hepatic transcriptome analysis identifies genes, polymorphisms and pathways involved in the fatty acids metabolism in sheep

Fatty acids (FA) in ruminants, especially unsaturated FA (USFA) have important impact in meat quality, nutritional value, and flavour quality of meat, and on consumer’s health. Identification of the genetic factors controlling the FA composition and metabolism is pivotal to select sheep that produce higher USFA and lower saturated (SFA) for the benefit of sheep industry and consumers. Therefore, this study was aimed to investigate the transcriptome profiling in the liver tissues collected from sheep with divergent USFA content in longissimus muscle using RNA deep-sequencing. From sheep (n = 100) population, liver tissues with higher (n = 3) and lower (n = 3) USFA content were analysed using Illumina HiSeq 2500. The total number of reads produced for each liver sample were ranged from 21.28 to 28.51 million with a median of 23.90 million. Approximately, 198 genes were differentially regulated with significance level of p-adjusted value <0.05. Among them, 100 genes were up-regulated, and 98 were down-regulated (p<0.01, FC>1.5) in the higher USFA group. A large proportion of key genes involved in FA biosynthesis, adipogenesis, fat deposition, and lipid metabolism were identified, such as APOA5, SLC25A30, GFPT1, LEPR, TGFBR2, FABP7, GSTCD, and CYP17A. Pathway analysis revealed that glycosaminoglycan biosynthesis- keratan sulfate, adipokine signaling, galactose metabolism, endocrine and other factors-regulating calcium metabolism, mineral metabolism, and PPAR signaling pathway were playing important regulatory roles in FA metabolism. Importantly, polymorphism and association analyses showed that mutation in APOA5, CFHR5, TGFBR2 and LEPR genes could be potential markers for the FA composition in sheep. These polymorphisms and transcriptome networks controlling the FA variation could be used as genetic markers for FA composition-related traits improvement. However, functional validation is required to confirm the effect of these SNPs in other sheep population in order to incorporate them in the sheep breeding program.

Overview: prevalence and structure of metabolic diseases of laying chickens, their influence on egg quality and condition of young chickens

The article analyzes and presents statistics on the number of laying hens in Ukraine, production, consumption and import of eggs for the last 5 years, the spread of metabolic diseases of laying hens on the basis of a review of literature sources. Metabolic disorders are the largest group of poultry diseases classified as metabolic diseases and cause significant economic losses. Hepatitis, hepatodystrophy, cirrhosis, liver abscesses, cholecystitis, and gallstone disease are diagnosed in laying hens as a result of impaired carbohydrate, lipid, protein, and mineral metabolism. With a lack or imbalance of calcium and phosphorus or D-hypovitaminosis, in chickens develop diseases such as osteoporosis and hypocalcemia, which reduce egg-laying, quality of hatching eggs and young poultry, and can lead to the death of embryos and adults. Hypovitaminosis (A, D, E) and microelementosis (Co, Cu, Zn, J) in poultry cause decreased immunity, disorders of hormonal system, growth, reproductive functions, egg production, dysfunction of internal organs and nervous system, contribute to the formation of defective eggs, development in embryo of alimentary diseases, which affects the hatchability and quality of young poultry. In view of this, the norms of feeding and keeping poultry are constantly being improved based on an in-depth study of these processes. The subject of this work was a comparative review of the results obtained by various authors on the most common metabolic diseases of laying hens, their impact on productive traits (laying), quality characteristics of eggs, embryogenesis, quality of young laying hens of modern high-yielding crosses. This review of literature sources can serve as a tool for determining the future direction of research, as well as an indicator of its practical application.

Polymorphism of the genetic determinants of bone mineral metabolism in various groups of the Komi people

The subject of the study is autochthonous population of the Northern and Middle Cis-Urals: Komi-Permyaks, Komi (Zyryans), and Komi-Izhems. The aim of the study is to compare the population frequencies of the LCT (rs4988235) and VDR (FokI rs2228570 and BsmI rs1544410) genes and to consider the contribution of environ-mental and cultural factors to the formation of differences in the genetic determinants of bone tissue metabolism. In total, 181 Komi-Permyak, 223 Komi, and 200 Komi-Izhem subjects were tested clinically and genetically. The evaluation consisted of the determination of polymorphic loci of VDR and LCT genes variants and assessment of clinical and laboratory lactase activity. The information on traditional diet and food composition was obtained from ethnographic materials. The study group of Komi-Izhems differs by a high proportion of C*LCT carriers (0.85) from the other two groups (p < 0.05). The prevalence of hypolactasia, i.e., limited lactase production, is also higher (p < 0.05) in Komi-Izhems (0.64) than in Komi-Permyaks (0.47) and Zyryans (0.41). The T*BsmI allele frequency is higher in Komi-Izems (0.493) in hetero- CT* (0.463) and homozygote TT* (0.261) genotypes, as compared to Zyryans (p < 0.05, where the frequencies are 0.377, 0.329 and 0.212, respectively). The values of BsmI allele and genotype frequencies in Komi-Permyaks are intermediate and do not differ significantly from those in Komi-Izhems and Zyryans. The concentration of T*FokI is highest in Komi-Permyaks (0.528). They are followed by Zyryans (the difference is insignificant, p > 0.05). Komi-Izhems have the smallest proportion of T*FokI allele carriers (0.400) and significantly differ from Komi-Permyaks (p = 0.01). The genotype distributions in FokI locus of VDR in the groups of Komi-Permyaks and Zyryans do not differ, but both show higher CT*FokI genotype frequencies than Komi-Izhems (0.549 and 0.569 against 0.288; p < 0.001). Poor livestock production and a lack of milk in the traditional subsistence economy of the Komi-Permyaks weakened the selection in favor of T*LCT allele and lactase persistence. The low intake of calcium with milk was compensated by an increase in the sensitivity of the target organs to calciferol, the regulator of mineral metabolism, by maintaining the high frequency of carriers of T*BsmI and T*FokI alleles of VDR gene in the population. The more productive dairy farming of Zyryans stimulated selection in favor of lactase persistence. The possibility of continuous consumption of calcium from milk eased the selection pressure on VDR loci. The regulation by T*FokI produced a physiologically sufficient effect and T*BsmI carriership remained low. The diet of the Komi-Izhems, who were accustomed to high-latitude regions, comprised low-lactose dairy products. The population preserved a high carriage of C*LCT and the phenotype of hypolactasia. Moderately intensive selection for vitamin D receptor sensitivity showed up in the increase of VDR T*BsmI frequency only. The high D-vitamin status of the Izhem people was leveraged by the traditional diet with a considerable intake of ergocalciferol-rich venison and fish. The Komi-Permyaks, Komi (Zyryans) and Komi-Izhems occupied different ecological niches and the groups found different ways to adapt to the unfavorable bone-homeorhesis conditions. The flexible responses to the pressure of the environmental factors were imple-mented by the selection of variants of LCT, VDR FokI and VDR BsmI genes, which are located in different chro-mosomes and determine different stages of mineral metabolism. We contend that modern interpopulation differences in distribution of the genotypes and alleles are the manifestations of different strategies of ecological adaptation of anthropologically related groups.

Environmental Factors That Affect Parathyroid Hormone and Calcitonin Levels

Calciotropic hormones, parathyroid hormone (PTH) and calcitonin are involved in the regulation of bone mineral metabolism and maintenance of calcium and phosphate homeostasis in the body. Therefore, an understanding of environmental and genetic factors influencing PTH and calcitonin levels is crucial. Genetic factors are estimated to account for 60% of variations in PTH levels, while the genetic background of interindividual calcitonin variations has not yet been studied. In this review, we analyzed the literature discussing the influence of environmental factors (lifestyle factors and pollutants) on PTH and calcitonin levels. Among lifestyle factors, smoking, body mass index (BMI), diet, alcohol, and exercise were analyzed; among pollutants, heavy metals and chemicals were analyzed. Lifestyle factors that showed the clearest association with PTH levels were smoking, BMI, exercise, and micronutrients taken from the diet (vitamin D and calcium). Smoking, vitamin D, and calcium intake led to a decrease in PTH levels, while higher BMI and exercise led to an increase in PTH levels. In terms of pollutants, exposure to cadmium led to a decrease in PTH levels, while exposure to lead increased PTH levels. Several studies have investigated the effect of chemicals on PTH levels in humans. Compared to PTH studies, a smaller number of studies analyzed the influence of environmental factors on calcitonin levels, which gives great variability in results. Only a few studies have analyzed the influence of pollutants on calcitonin levels in humans. The lifestyle factor with the clearest relationship with calcitonin was smoking (smokers had increased calcitonin levels). Given the importance of PTH and calcitonin in maintaining calcium and phosphate homeostasis and bone mineral metabolism, additional studies on the influence of environmental factors that could affect PTH and calcitonin levels are crucial.