10 research outputs found

    Glial Cell Line-Derived Neurotrophic Factor (GDNF) as a Novel Candidate Gene of Anxiety.

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    Glial cell line-derived neurotrophic factor (GDNF) is a neurotrophic factor for dopaminergic neurons with promising therapeutic potential in Parkinson's disease. A few association analyses between GDNF gene polymorphisms and psychiatric disorders such as schizophrenia, attention deficit hyperactivity disorder and drug abuse have also been published but little is known about any effects of these polymorphisms on mood characteristics such as anxiety and depression. Here we present an association study between eight (rs1981844, rs3812047, rs3096140, rs2973041, rs2910702, rs1549250, rs2973050 and rs11111) GDNF single nucleotide polymorphisms (SNPs) and anxiety and depression scores measured by the Hospital Anxiety and Depression Scale (HADS) on 708 Caucasian young adults with no psychiatric history. Results of the allele-wise single marker association analyses provided significant effects of two single nucleotide polymorphisms on anxiety scores following the Bonferroni correction for multiple testing (p = 0.00070 and p = 0.00138 for rs3812047 and rs3096140, respectively), while no such result was obtained on depression scores. Haplotype analysis confirmed the role of these SNPs; mean anxiety scores raised according to the number of risk alleles present in the haplotypes (p = 0.00029). A significant sex-gene interaction was also observed since the effect of the rs3812047 A allele as a risk factor of anxiety was more pronounced in males. In conclusion, this is the first demonstration of a significant association between the GDNF gene and mood characteristics demonstrated by the association of two SNPs of the GDNF gene (rs3812047 and rs3096140) and individual variability of anxiety using self-report data from a non-clinical sample

    Cardiopoietic cell therapy for advanced ischemic heart failure: results at 39 weeks of the prospective, randomized, double blind, sham-controlled CHART-1 clinical trial

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    Cardiopoietic cells, produced through cardiogenic conditioning of patients' mesenchymal stem cells, have shown preliminary efficacy. The Congestive Heart Failure Cardiopoietic Regenerative Therapy (CHART-1) trial aimed to validate cardiopoiesis-based biotherapy in a larger heart failure cohort

    HÚSHASZNOSÍTÁSÚ MAGYAR TARKA TEHENEK KÜLLEMI BÍRÁLATÁNAK EREDMÉNYEI

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    Conformation scoring data of 1238 beef type Hungarian Simmental cows were evaluated between 2001 and 2011 on the database of Association of Hungarian Simmental Breeders. The aim of the study was to evaluate the effect of sire, herd, birth year and the age at scoring on type score (TIP), height at rump (FMA), width of rump (FSZ), length of rump (FHO), deep of chest (TÖM), length of body (TÖH), muscularity score (IZM), muscularity of shoulder (LIZ), muscularity of thigh (CIZ), conformation of leg (LSZ), side view of hind leg (HLO), gradient of rump (FLE), steepness of pastern (CSÜ), dug score (TGY), deep of dug (TMÉ) and conformation of teats (BIF). The database was analyzed by multifactor analysis of variance. The overall mean of the evaluated ten traits were as follows (mean±SE, point): TIP 5.54±0.04; FMA 5.78±0.07; FSZ 5.25±0.06; FHO 5.33±0.06; TÖM 5.53±0.06; TÖH 5.44±0.05; IZM 4.92±0.06; LIZ 4.83±0.06; CIZ 4.98±0.06; LSZ 5.47±0.03; HLO 5.59±0.05; FLE 5.17±0.05; CSÜ 5.82±0.08; TGY 5.90±0.06; TMÉ 6.27±0.08; BIF 5.34±0.08. The rank in phenotype of the investigated factors was as follows: 1st herd (41.65%), 2nd age at scoring (25.09%), 3rd birth year (15.90%), 4th sire (10.19%), 5th error (7.17%). In the examined period increased the deep of chest, the length of body and the type score. The points of muscularity and dug parameters and the steepness of pastern significantly decreased

    Late bedtime is associated with decreased hippocampal volume in young healthy subjects

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    Hippocampal volume loss has been described in several pathological conditions including sleep disorders. Whether differences in normal sleep are associated with differences in hippocampal volume is unknown. Here we designed a study to assess volume of the hippocampus with regard to bedtime, wake up time and sleep duration in 90 healthy university students. To assess hippocampal volumes we applied semi-automatic user-independent magnetic resonance volumetry. We found a significant association between delayed bedtime and smaller hippocampal volumes, a non-significant tendency for smaller hippocampal volumes in the late wake up time group and significantly smaller hippocampal volumes for both short and long sleepers. These results suggest the importance of adequate sleep timing and especially bedtime in determining hippocampal volume

    Image_1_17β-estradiol does not have a direct effect on the function of striatal cholinergic interneurons in adult mice in vitro.tif

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    The striatum is an essential component of the basal ganglia that is involved in motor control, action selection and motor learning. The pathophysiological changes of the striatum are present in several neurological and psychiatric disorder including Parkinson’s and Huntington’s diseases. The striatal cholinergic neurons are the main regulators of striatal microcircuitry. It has been demonstrated that estrogen exerts various effects on neuronal functions in dopaminergic and medium spiny neurons (MSN), however little is known about how the activity of cholinergic interneurons are influenced by estrogens. In this study we examined the acute effect of 17β-estradiol on the function of striatal cholinergic neurons in adult mice in vitro. We also tested the effect of estrus cycle and sex on the spontaneous activity of cholinergic interneurons in the striatum. Our RNAscope experiments showed that ERα, ERβ, and GPER1 receptor mRNAs are expressed in some striatal cholinergic neurons at a very low level. In cell-attached patch clamp experiments, we found that a high dose of 17β-estradiol (100 nM) affected the spontaneous firing rate of these neurons only in old males. Our findings did not demonstrate any acute effect of a low concentration of 17β-estradiol (100 pM) or show any association of estrus cycle or sex with the activity of striatal cholinergic neurons. Although estrogen did not induce changes in the intrinsic properties of neurons, indirect effects via modulation of the synaptic inputs of striatal cholinergic interneurons cannot be excluded.</p
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