112 research outputs found

    Fish milt quality and major factors influencing the milt quality parameters: A review

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    In commercial fish production, the evaluation of milt quality is essential in order to increase the efficiency of artificial fertilization. Numerous studies have demonstrated that qualitative parameters of milt (i.e. seminal fluid composition, spermatozoa motility and sperm production) could be influence by several factors including biological characteristics of brooders (age, weight and length), rearing conditions of brooders (temperature, photoperiod, nourishment, undesirable components and animal welfare and health), artificial induction of spawning, spawning season (repeated milt collection and spermiation time) and post stripping factors (chemical properties of diluents and short-term and long-term storage of milt). In the present paper, we review the roles of these factors on quality of milt fish. On the whole understanding of the factors that affect milt quality could be useful for adjustment and efficient management of these factors in order to obtain good milt for fertilization.Keywords: Fish production, milt quality, artificial fertilizatio

    Compensatory growth assessment by plasma IGF-I hormone measurement and growth performance in rainbow trout (Oncorhynchus mykiss)

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    This study aimed to show the difference in compensatory growth (CG) with different starvation and feeding periods replications, depending on the IGF-I hormone level in the blood. There were 4 treatments in 3 replications. Other indexes like food coefficient ratio (FCR), specific growth rate (SGR) and daily food intake were also examined during the experiment. Fish were fed twice a day ad libitum as follows during the 65 days. Treatment A (TA): control treatment, continues feeding. Treatment B (TB): 4 weeks of starvation and 5 weeks of re-feeding. Treatment C (TC): 3 weeks of starvation and 5 weeks of re-feeding. Treatment D (TD): 2 weeks of starvation and 5 weeks of re-feeding. Each tank contained 23fishes in each unit with an initial mean weight (SD) of 47.19 ± 0.42 (g). Blood was sampled in IGF-I hormone concentration at the beginning of the experiment, at the end of the starvation period and every 12 days in re-feeding periods. There was no significant difference between the treatments in FCR (P > 0.05). TB and TC had significant difference (P < 0.01) in comparison with other treatments in SGR, but no significant difference was observed among them (P > 0.05). IGF-I concentrations came down in comparison with control treatment at the end of the starvation period (Day 29) (P < 0.001), but no significant difference was observed among the treatments at the end of the re-feeding period (P > 0.05). According to the results, TB and TC showed more indexes of CG in comparison with TA and TD. Still IGF-I cannot show the quality of CG alone and other growth relating physiological elements in different feeding diets and regimes will be evaluated in future studies

    Effects of storage duration and storage temperature on viability of stored ova of kutum (Rutilus frisii kutum) in ovarian fluid

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    Effects of post-stripping oocyte ageing and temperature on egg viability rates were studied in kutum (Rutilus frisii kutum). Eggs were retained outside the ovarian cavity (in vitro storage) with ovarian fluid at various temperatures of 4, 10, 12 and 26°C. Stored ova of six female kutum were fertilized separately after 0 (control eggs fertilized prior to storage), 2, 4, 6, and 8 h post-stripping (HPS) using fresh and pooled sperm obtained from five males. Eyeing, hatching and eyed egg mortality rates were recorded as an index of egg viability. The results indicated that the maximum eyeing (87%) and hatching (75%) rates of eggs took place at 0 HPS followed by 8 HPS (> 80 and > 70%, respectively) at 4°C. As storage temperature increased, egg viability decreased to 80, 70 and 50% viable at 8 HPS at 4, 10 and 12°C, respectively. The eggs stored at 26°C lost their viability almost completely after 4 HPS. Eyed-egg mortality increased from 13% at 0 HPS to 48.2% and at 4 HPS, at 26°C. This study demonstrated that the in vitro storage method is an applicable effective fertilization technique that can be used for restocking programs of kutum within 8 h at temperatures ranging from 4 to 12°C.Key words: Rutilus frisii kutum, egg storage, temperature, ovarian fluid

    Identification of the Schistosoma mansoni TNF-Alpha Receptor Gene and the Effect of Human TNF-Alpha on the Parasite Gene Expression Profile

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    Schistosoma mansoni is the major causative agent of schistosomiasis in the Americas. This parasite takes advantage of host signaling molecules such as cytokines and hormones to complete its development inside the host. Tumor necrosis factor-alpha (TNF-α) is one of the most important host cytokines involved in the inflammatory response. When cercariae, the infective stage, penetrates the human skin the release of TNF-α is started. In this work the authors describe the complete sequence of a possible TNF-α receptor in S. mansoni and detect that the receptor is most highly expressed in cercariae among all life cycle stages. Aiming to mimic the situation at the site of skin penetration, cercariae were mechanically transformed in vitro into schistosomula and exposed to human TNF-α. Exposure of early-developing schistosomula to the human hormone caused a large-scale change in the expression of parasite genes. Exposure of adult worms to human TNF-α caused gene expression changes as well, and the set of parasite altered genes in the adult parasite was different from that of schistosomula. This work increases the number of known signaling pathways of the parasite, and opens new perspectives into understanding the molecular components of TNF-α response as well as into possibly interfering with parasite–host interaction

    Disruption of Mitochondrial DNA Replication in Drosophila Increases Mitochondrial Fast Axonal Transport In Vivo

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    Mutations in mitochondrial DNA polymerase (pol γ) cause several progressive human diseases including Parkinson's disease, Alper's syndrome, and progressive external ophthalmoplegia. At the cellular level, disruption of pol γ leads to depletion of mtDNA, disrupts the mitochondrial respiratory chain, and increases susceptibility to oxidative stress. Although recent studies have intensified focus on the role of mtDNA in neuronal diseases, the changes that take place in mitochondrial biogenesis and mitochondrial axonal transport when mtDNA replication is disrupted are unknown. Using high-speed confocal microscopy, electron microscopy and biochemical approaches, we report that mutations in pol γ deplete mtDNA levels and lead to an increase in mitochondrial density in Drosophila proximal nerves and muscles, without a noticeable increase in mitochondrial fragmentation. Furthermore, there is a rise in flux of bidirectional mitochondrial axonal transport, albeit with slower kinesin-based anterograde transport. In contrast, flux of synaptic vesicle precursors was modestly decreased in pol γ−α mutants. Our data indicate that disruption of mtDNA replication does not hinder mitochondrial biogenesis, increases mitochondrial axonal transport, and raises the question of whether high levels of circulating mtDNA-deficient mitochondria are beneficial or deleterious in mtDNA diseases

    Modeling risk factors and confounding effects in stroke

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    Long non-coding RNAs and cancer: a new frontier of translational research?

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    Author manuscriptTiling array and novel sequencing technologies have made available the transcription profile of the entire human genome. However, the extent of transcription and the function of genetic elements that occur outside of protein-coding genes, particularly those involved in disease, are still a matter of debate. In this review, we focus on long non-coding RNAs (lncRNAs) that are involved in cancer. We define lncRNAs and present a cancer-oriented list of lncRNAs, list some tools (for example, public databases) that classify lncRNAs or that scan genome spans of interest to find whether known lncRNAs reside there, and describe some of the functions of lncRNAs and the possible genetic mechanisms that underlie lncRNA expression changes in cancer, as well as current and potential future applications of lncRNA research in the treatment of cancer.RS is supported as a fellow of the TALENTS Programme (7th R&D Framework Programme, Specific Programme: PEOPLE—Marie Curie Actions—COFUND). MIA is supported as a PhD fellow of the FCT (Fundação para a Ciência e Tecnologia), Portugal. GAC is supported as a fellow by The University of Texas MD Anderson Cancer Center Research Trust, as a research scholar by The University of Texas System Regents, and by the Chronic Lymphocytic Leukemia Global Research Foundation. Work in GAC’s laboratory is supported in part by the NIH/ NCI (CA135444); a Department of Defense Breast Cancer Idea Award; Developmental Research Awards from the Breast Cancer, Ovarian Cancer, Brain Cancer, Multiple Myeloma and Leukemia Specialized Programs of Research Excellence (SPORE) grants from the National Institutes of Health; a 2009 Seena Magowitz–Pancreatic Cancer Action Network AACR Pilot Grant; the Laura and John Arnold Foundation and the RGK Foundation

    Recent developments in genetics and medically assisted reproduction : from research to clinical applications

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    Two leading European professional societies, the European Society of Human Genetics and the European Society for Human Reproduction and Embryology, have worked together since 2004 to evaluate the impact of fast research advances at the interface of assisted reproduction and genetics, including their application into clinical practice. In September 2016, the expert panel met for the third time. The topics discussed highlighted important issues covering the impacts of expanded carrier screening, direct-to-consumer genetic testing, voiding of the presumed anonymity of gamete donors by advanced genetic testing, advances in the research of genetic causes underlying male and female infertility, utilisation of massively parallel sequencing in preimplantation genetic testing and non-invasive prenatal screening, mitochondrial replacement in human oocytes, and additionally, issues related to cross-generational epigenetic inheritance following IVF and germline genome editing. The resulting paper represents a consensus of both professional societies involved.Peer reviewe
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