44 research outputs found

    ADVERSE EFFECTS OF WET DISTILLERS GRAINS WITH SOLUBLES (WDGS) IN THE DIET OF DAIRY COWS

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    Corn wet distillers grains with solubles (WDGS) included up to 25% in the diet of 16 Simmental dairy cows, 27 to 72 months old, during three weeks, negatively affected rumen function monitored by non-invasive parameters, such as fecal consistency, and also influenced milk quality by reducing milk fat content. Dry distillers' grains with solubles (DDGS) are currently the most attractive by-product of the bioethanol industry due to the possibility of application in the diet of various animal species, whereas WDGS is often more locally available and financially affordable; however, there is little data in the literature indicating potential negative consequences of its use. Therefore, this report aims to point out, based on a practical example, the possible problems of its application in the diet of dairy cows as the most metabolically sensitive category, as well as to demonstrate steps to prevent and/or mitigate eventual errors

    Synthesis, structure and thermogravimetric analysis of alpha,omega-telechelic polydimethylsiloxanes of low molecular weight

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    A series of alpha,omega-telechelic polydimethylsiloxanes (PDMS), with predetermined molecular weights of about 2500 g mol(-1), was synthesized by siloxane equilibration reaction. Syntheses were performed using octamethylcyclotetrasiloxane (D-4) and various disiloxanes: hexamethyldisiloxane (HMDS), 1,1,3,3-tetramethyldisiloxane (TMDS), 1,3-divinyltetramethyldisiloxane (DVTMDS), 1,3-bis(3-carboxypropyl) tetramethyldisiloxane (DCPTMDS) and 1,3-bis(3-aminopropyl) tetramethyldisiloxane (DAPTMDS). The role of the disiloxane was to introduce terminal functional groups at the end of the polymer chains and to control the molecular weight of the polymers. Polymers with trimethyl, hydrido, vinyl, carboxypropyl and aminopropyl end-groups were obtained in this way. The structure of the alpha,omega-telechelic PDMSs was confirmed by NMR and IR spectroscopy. The molecular weights of the polymers were determined by H-1-NMR, gel permeation chromatography (GPC) and dilute solution viscometry. Thermogravimetric analysis (TGA) under nitrogen and air showed that the type of the terminal groups significantly influenced the thermal and thermo-oxidative stability, as well as the degradation mechanism of the alpha,omega-telechelic PDMSs

    IGF1R Gene Alterations in Small for Gestational Age (SGA) Children

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    BACKGROUND: Small for gestational age children (SGA) is born on term with BW and or BL of -2.0 standard deviation score (SDS). SGA children have an increased risk of being short, developing DM, and cardiovascular and cerebrovascular disease. Often defects of IGF1R are the cause of SGA. Most frequently affected part of the IGF1R gene is the exon 2.AIM: To investigate whether the exon 2 of the IGF1R gene is affected in the SGA children.PATIENTS AND METHODS: A cohort of 100 SGA children born in term was evaluated for alterations in IG1R gene. Their anthropometric parameters, IGF1 serum concentrations and IGF1 SDS values were analysed. The molecular analysis of IGF1R gene was performed by PCR restriction-site analysis and followed by direct sequencing of conspicuous fragments.RESULTS: Within our cohort, 64 SGA children were with short stature (height SDS -3.25 ± 0.90 SDS), and 36 were with normal height for their age and sex, (H SDS was 0.20 ± 1.1 SDS). None of these children had microcephaly (occipitofrontal circumference -0.70 ± 1.01 SDS vs 0.06 ± 0.56 SDS in SGA children with normal height) or dysmorphic features. The IGF1 serum concentrations and IGF1 SDS values of all children were within normal range. Only one child had lower normal serum IGF1 concentration. No alterations in exon 2 of IGF1R gene were detected.CONCLUSIONS: The genetic analysis of the exon 2 of the IGF1R gene did not detect any gene defects in the analysed patients. The putative genetic defect in those children affects other parts of the IGF1R gene or another gene (s), or yet unidentified factors

    Canine Dirofilaria Infections in Two Uninvestigated Areas of Serbia: Epidemiological and Genetic Aspects

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    In 2009 canine filarial infections were investigated in two northern areas of Serbia (Pancevo and Veliko Gradiste), applying morphometry, biochemical staining, and immunological kit to detect Dirofilaria immitis antigens, and two home-made ELISAs to detect antibodies to D. repens and D. immitis somatic/metabolic polyproteins. Moreover, molecular tools were applied to analyze the phylogenetic relationships of the isolates. The microfilariae detected in 21/122 dogs (17.2%) were identified as D. repens (n = 21) and D. immitis (n = 2). D. immitis antigens were found in another 13 animals with occult infection. All of the 15 heartworm-positive dogs also had antibodies to this parasite, which were detected in another 13 subjects, indicating an overall D. immitis seroprevalence rate of 22.9%. Serology for D. repens revealed evidence of antibodies in 42.6% of the dogs, but was negative for 4 microfilaremic dogs. As for the two different areas, the prevalence of microfilariae and/or D. immitis antigens, mainly due to D. repens microfilaremic animals, was not significantly higher in Veliko Gradiste (33.3%) than in Pancevo (22%). However, serology showed a different epidemiological picture. Heartworm infection occurred more often in both areas, and antibodies to dirofilarial nematodes were detected in 72.9% of dogs living in Pancevo, a rate higher than in those living in Veliko Gradiste (57.1%). No risk factors for infection were found, confirming the uselessness of prophylactic drugs against D. repens, and suggesting the presence in these areas of sunrise- or sunset-biting mosquitoes as important vectors. The results indicate the need for both appropriate entomological studies and further research on the intra-species variability shown by D. repens

    Metabolomic Profiling of Bipolar Disorder by 1H-NMR in Serbian Patients

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    Bipolar disorder (BD) is a brain disorder that causes changes in a person’s mood, energy, and ability to function. It has a prevalence of 60 million people worldwide, and it is among the top 20 diseases with the highest global burden. The complexity of this disease, including diverse genetic, environmental, and biochemical factors, and diagnoses based on the subjective recognition of symptoms without any clinical test of biomarker identification create significant difficulties in understanding and diagnosing BD. A 1H-NMR-based metabolomic study applying chemometrics of serum samples of Serbian patients with BD (33) and healthy controls (39) was explored, providing the identification of 22 metabolites for this disease. A biomarker set including threonine, aspartate, gamma-aminobutyric acid, 2-hydroxybutyric acid, serine, and mannose was established for the first time in BD serum samples by an NMR-based metabolomics study. Six identified metabolites (3-hydroxybutyric acid, arginine, lysine, tyrosine, phenylalanine, and glycerol) are in agreement with the previously determined NMR-based sets of serum biomarkers in Brazilian and/or Chinese patient samples. The same established metabolites (lactate, alanine, valine, leucine, isoleucine, glutamine, glutamate, glucose, and choline) in three different ethnic and geographic origins (Serbia, Brazil, and China) might have a crucial role in the realization of a universal set of NMR biomarkers for BD

    Accumulation of 17 organochlorine pesticides in muscle of pikeperch (Sander lucioperca) from Garaši reservoir (Serbia)

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    Samples of pikeperch (20 in total) were caught at Garaši reservoir during the summer of 2017. The objectives of this research was to analyse the concentrations of 17 organochlorine pesticides (aldrin, α-HCH, β-HCH, γ-HCH, δ-HCH, 4,4’-DDD, 4,4’-DDE, 4,4’-DDT, dieldrin, endosulfan I, endosulfan II, endosulfan sulfate, endrin, endrin aldehyde, heptachlor, heptachlor epoxide, and metoxychlor) in fish muscle by gas chromatography with mass spectrometric (GC-MS) detection. QuEChERS method was used for extraction and clean-up of pesticide residues from muscle tissue. Three phenyl phosphate (TPP) was used as an internal standard. Concentrations of 4,4’-DDD, 4,4’-DDE, 4,4’-DDT, heptachlor and heptachlor epoxide in fish muscle were compared with the maximum allowed concentrations (MAC) in fish meat set by the national legislation of Serbia. This reservoir is used as a drinking water source. Therefore, the hypothesis was that it was exposed to low organic pollution. The concentrations of all analyzed pesticides were below the detection limits. In conclusion, there is no health risk for consumption of pikeperch from Garaši reservoir

    Untargeted Lipidomics Study of Bipolar Disorder Patients in Serbia

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    The Lipidomic profiles of serum samples from patients with bipolar disorder (BD) and healthy controls (C) were explored and compared. The sample cohort included 31 BD patients and 31 control individuals. An untargeted lipidomics study applying liquid chromatography (LC) coupled with high-resolution mass spectrometry (HRMS) was conducted to achieve the lipid profiles. Multivariate statistical analyses (principal component analysis and partial least squares discriminant analysis) were performed, and fifty-six differential lipids were confirmed in BD and controls. Our results pointed to alterations in lipid metabolism, including pathways of glycerophospholipids, sphingolipids, glycerolipids, and sterol lipids, in BD patient sera. This study emphasized the role of lipid pathways in BD, and comprehensive research using the LC-HRMS platform is necessary for future application in the diagnosis and improvement of BD treatments

    Structural, optical and photocatalytic properties of BiFeO3 nanoparticles

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    BiFeO3 (BFO) precursor powder was synthesized by ultrasound asissted sol–gel route at relatively low temperature, starting from Bi-nitrate, Fe-nitrate, and ethylene glycol. Structural, optical, and photocatalytic properties of the obtained powder were investigated. X-ray diffraction analysis confirmed that thermal treatment of precursor powder at 500 °C led to formation of pure phase BiFeO3. BFO is p-type semiconductor where determined band gap was 2.20 eV, indicating its potential application as visible-light-response photocatalyst. Mott-Schottky measurements were performed to determine flat band potential and position of valence and conduction bands. Obtained BFO powder is used for photocatalytic degradation of typical organic azo dye Mordant Blue 9 in concentration of 50 mg/l. Measurements were performed for different times of irradiation and pH of the dye solution. Photodegradation products were analyzied by HPLC technique, and mechanism of photocatalytic degradation of organic dye was proposed

    IGF1R Gene Alterations in Children Born Small for Gestitional Age (SGA)

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    BACKGROUND: Small for gestational age (SGA)-born children are a heterogeneous group with few genetic causes reported. Genetic alterations in the IGF1 receptor (IGF1R) are found in some SGA children. AIM: To investigate whether alterations in IGF1R gene are present in SGA born children. PATIENTS AND METHODS: We analysed 64 children born SGA who stayed short (mean -3.25 ± 0.9 SDS) within the first 4 years of age, and 36 SGA children who caught up growth (0.20 ± 1.1 SDS). PCR products of all coding IGF1R exons were screened by dHPLC followed by direct sequencing of conspicuous fragments to identify small nucleotide variants. The presence of IGF1R gene copy number alterations was determined by Multiplex Ligation-dependent Probe Amplification (MLPA). RESULTS: The cohort of short SGA born children revealed a heterozygous, synonymous variant c.3453C > T in one patient and a novel heterozygous 3 bp in-frame deletion (c.3234_3236delCAT) resulting in one amino acid deletion (p.Ile1078del) in another patient. The first patient had normal serum levels of IGF1. The second patient had unusually low IGF1 serum concentrations (-1.57 SD), which contrasts previously published data where IGF1 levels rarely are found below the age-adjusted mean. CONCLUSIONS: IGF1R gene alterations were present in 2 of 64 short SGA children. The patients did not have any dysmorphic features or developmental delay. It is remarkable that one of them had significantly decreased serum concentrations of IGF1. Growth response to GH treatment in one of the patients was favourable, while the second one discontinued the treatment, but with catch-up growth
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