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1.
Int. braz. j. urol ; 41(4): 773-790, July-Aug. 2015. tab, graf
Article in English | LILACS | ID: lil-763046

ABSTRACT

ABSTRACTPurpose:This study aimed to investigate the protective effects of isolated and co-administration of vitamin E (VitE) and dexamethasone (DEX) on varicocele (VCL)-induced damages in testicular tissue.Materials and Methods:Wistar rats were divided into five groups (n=6), including; control-sham, non-treated VCL-induced, VitE-treated VCL-induced (VitE, 150 mg/kg, orally), DEX-administrated VCL-induced (DEX, 0.125 mg/kg, i.p.), VitE+DEX-received VCL-induced animals. The antioxidant status analyses, histopathological examinations, hormonal assay and tissue levels of alkaline phosphatase (ALP) were analyzed. The germinal epithelium RNA damage and Leydig cells steroidogenesis were analyzed. Moreover, the Hsp70-2 protein expression was examined based on immunohistochemical and western blot analyses. The sperm parameters, DNA integrity and chromatin condensation were investigated.Results:VitE and DEX in simultaneous form of administration significantly (P<0.05) down-regulated the tissue ALP level and attenuated the VCL-decreased GSH-px, SOD and TAC levels and remarkably (P<0.05) down-regulated the testicular malondialdehyde (MDA) and nitric oxide (NO) contents. The VCL-induced histopathological alterations significantly (P<0.05) improved in VitE and DEX-administrated animals. The VitE and DEX co-administration reduced the VCL-increased RNA damage and elevated the Leydig cells steroidogenic activity. The Hsp70-2 protein level completely (P<0.05) increased in VitE and DEX alone–and-simultaneous-administrated animals. Finally, the VitE and DEX could significantly (P<0.05) improve the VCL-decreased semen quality and improved the sperm DNA integrity and chromatin condensation.Conclusion:Our data suggest that Vit E by up-regulating the antioxidant status and DEX by reducing inflammation-dependent oxidative and nitrosative stresses could improve the VCL-reduced Hsp70-2 chaperone expression and ultimately protected the testicular endocrine activities and promoted the spermatogenesis process.


Subject(s)
Animals , Male , Anti-Inflammatory Agents/administration & dosage , Antioxidants/administration & dosage , Dexamethasone/administration & dosage , /metabolism , Varicocele/drug therapy , Vitamin E/administration & dosage , Blotting, Western , Chromatin/physiology , Disease Models, Animal , DNA Damage , Drug Interactions , Glutathione Peroxidase/analysis , Immunohistochemistry , Malondialdehyde/analysis , Oxidative Stress/drug effects , Protective Agents , Rats, Wistar , Sperm Count , Sperm Motility/drug effects , Spermatozoa/drug effects , Superoxide Dismutase/analysis , Testis/drug effects , Testis/enzymology , Testis/pathology , Testosterone/blood , Varicocele/physiopathology
2.
Biol. Res ; 48: 1-8, 2015. graf
Article in English | LILACS | ID: biblio-950791

ABSTRACT

BACKGROUND: The CCCTC-binding factor (CTCF) is a highly conserved insulator protein that plays various roles in many cellular processes. CTCF is one of the main architecture proteins in higher eukaryotes, and in combination with other architecture proteins and regulators, also shapes the three-dimensional organization of a genome. Experiments show CTCF partially remains associated with chromatin during mitosis. However, the role of CTCF in the maintenance and propagation of genome architectures throughout the cell cycle remains elusive. RESULTS: We performed a comprehensive bioinformatics analysis on public datasets of Drosophila CTCF (dCTCF). We characterized dCTCF-binding sites according to their occupancy status during the cell cycle, and identified three classes: interphase-mitosis-common (IM), interphase-only (IO) and mitosis-only (MO) sites. Integrated function analysis showed dCTCF-binding sites of different classes might be involved in different biological processes, and IM sites were more conserved and more intensely bound. dCTCF-binding sites of the same class preferentially localized closer to each other, and were highly enriched at chromatin syntenic and topologically associating domains boundaries. CONCLUSIONS: Our results revealed different functions of dCTCF during the cell cycle and suggested that dCTCF might contribute to the establishment of the three-dimensional architecture of the Drosophila genome by maintaining local chromatin compartments throughout the whole cell cycle.


Subject(s)
Animals , Repressor Proteins/physiology , Chromatin/physiology , Drosophila Proteins/physiology , Drosophila melanogaster/chemistry , Genome, Insect/genetics , Mitosis/physiology , Binding Sites , Base Sequence , Cell Cycle/physiology , Conserved Sequence , Computational Biology , Synteny , Chromatin Assembly and Disassembly/physiology , Molecular Sequence Annotation , Datasets as Topic , CCCTC-Binding Factor , Interphase/physiology
3.
Braz. j. vet. res. anim. sci ; 50(6): 474-481, 2013. ilus, tab
Article in Portuguese | LILACS | ID: lil-789908

ABSTRACT

In canine specie, oocyte maturation rates are low and the percentage of oocytes that remain in the stage of germinal vesicle (GV) regardless of culture conditions is high. During maturation oocyte undergoes modification and the GV chromatin remodeling manifested by changes in the configuration and positioning. The objective of this work is to evaluate the configuration and positioning of chromatin of oocytes in GV stage during anestrus and diestrus bitches. The ovaries of 33 females (20 bitches in anestrous and 13 in diestrus) were isolated, sliced and only cumulus-oocyte complexes (COCs) grade 1 were subjected to solution of 0.2% hyaluronidase for release in cumulus cells. After this process, the selected oocytes were stained and evaluated. From a total of 920 oocytes, 566 were classified as grade 1 and the stages of chromatin configuration identified as GV-1, GV-2, GV-3 and GV-4. The observed changes in chromatin configuration been characterized as a transition dispersed chromatin (GV-1, GV-2) for partially condensed (GV-3) until it reaches a fully condensed stage (GV-4). The data analyzed from the chromatin configuration showed a significant difference between the stages with a higher proportion of GV-1 and GV-2 for the anoestrus and GV-3 and GV-4 during diestrus. There is need for further studies to be able to have a proper understanding of the influence of chromatin configuration of oocytes in GV stage in resumption of meiosis and consequently in oocyte meiotic competence...


Na espécie canina as taxas de maturação oocitária são baixas e a porcentagem de oócitos que permanecem em estagio de vesícula germinativa (VG), independente das condições de cultivo, e alta. Durante a maturação oocitária, a VG sofre modificação e remodelamento da cromatina, que se manifesta por alterações na sua configuração e posicionamento. Assim, o objetivo deste trabalho e avaliar a configuração e o posicionamento da cromatina de oócitos em estagio de VG durante o anestro e diestro de cadelas. Os ovários de 33 fêmeas (20 cadelas em anestro e 13 em diestro) foram isolados, fatiados e os complexos cumulus-oócitos (COCs) foram submetidos à solução de hialuronidase 0,2% para a liberação das células do cumulus. Apos esse processo, os oócitos selecionados foram corados, avaliados e apenas COCs grau 1 foram utilizados. De um total de 920 oócitos, 566 foram classificados como grau 1 e os estágios de configuração da cromatina identificados como VG-1, VG-2, VG-3 e VG-4. As alterações observadas na configuração da cromatina foram caracterizadas como transição de uma cromatina dispersa (VG-1, VG-2) para parcialmente condensada (VG-3) ate atingir um estagio totalmente condensado (VG-4). Os dados analisados da configuração da cromatina mostraram uma diferença significativa entre as fases de anestro e diestro, com maior proporção de VG-1 e VG-2 durante o anestro e de VG-3 e VG-4 durante o diestro. Ha necessidade de novos estudos para uma compreensão adequada da influencia da configuração da cromatina de oócitos no estagio de VG na retomada da meiose e na competência meiótica do oócito...


Subject(s)
Animals , Female , Dogs , Anestrus , Chromatin/physiology , Diestrus , Oocytes/growth & development , Reproductive Techniques/veterinary
4.
Clinics ; 68(supl.1): 5-14, 2013.
Article in English | LILACS | ID: lil-668033

ABSTRACT

The integrity of the sperm genome and epigenome are critical for normal embryonic development. The advent of assisted reproductive technology has led to an increased understanding of the role of sperm in fertilization and embryogenesis. During fertilization, the sperm transmits not only nuclear DNA to the oocyte but also activation factor, centrosomes, and a host of messenger RNA and microRNAs. This complex complement of microRNAs and other non-coding RNAs is believed to modify important post-fertilization events. Thus, the health of the sperm genome and epigenome is critical for improving assisted conception rates and the birth of healthy offspring.


Subject(s)
Female , Humans , Male , Epigenomics , Embryonic Development/genetics , Fertilization/genetics , Spermatozoa/physiology , Chromatin/physiology , Embryonic Development/physiology , MicroRNAs/physiology , Oocytes/physiology , RNA
5.
Biol. Res ; 45(4): 381-386, 2012. ilus
Article in English | LILACS | ID: lil-668690

ABSTRACT

The aim of this study was to investigate the effect of boar age on quality traits and fertility of liquid-stored semen. Boars were allocated into 3 age groups: 7-10 months (young), 18-33 months (mature), 51-61 months (old). Ejaculates of > 200x10(6) sperm/ml and 85% total motile sperm were extended to 30x10(6) sperm/ml, stored at 17-18 °C and used within 12-24 h for artificial insemination (AI) of 2062 multiparous sows. After 24 h of storage, aliquots of diluted semen were assessed for sperm progressive motility (SPM), incidence of sperm chromatin instability (SCI), proportion of live morphologically normal sperm (LMNS) and head morphometry of LMNS. The results showed that young boars had higher percentages of SCI and lower proportions of LMNS than those of the mature (p < 0.05) and old (p < 0.001) boars, respectively. Sperm head dimensions of young and old boars were greater (p < 0.03-0.001) than those of mature boars. The farrowing rate of young boars (65%) was significantly lower (p < 0.001; χ2= 30-61) than those of the mature (87.2%) and old (84.7%) boars. The relationship between sperm head dimensions and boar fertility was non-significant. In conclusion, boar age is an important physiological factor contributing to the success of swine AI.


Subject(s)
Animals , Female , Male , Pregnancy , Fertility/physiology , Insemination, Artificial/veterinary , Semen/physiology , Sperm Motility/physiology , Spermatozoa/physiology , Age Factors , Chromatin/physiology , Pregnancy Rate , Swine
6.
Neotrop. ichthyol ; 5(4): 457-470, Oct.-Dec. 2007. ilus
Article in English | LILACS | ID: lil-471977

ABSTRACT

Spermiogenesis and sperm ultrastructure were analyzed in two species of characids with different modes of fertilization: externally fertilizing Hemigrammus erythrozonus and inseminating Corynopoma riisei. Spermiogenesis in H. erythrozonus is characterized by lateral development of the flagellum, nuclear rotation, formation of a shallow nuclear fossa, condensation of the chromatin by elimination of the electron-lucent area from the peripheral region of the nucleus, and renewal of the nuclear membrane. Multilammelated membrane and multivesicular bodies were also observed during elimination of the excess cytoplasm. The spermatozoon exhibits characters typical of "aquasperm," i.e. a spherical head containing a spherical nucleus with highly condensed chromatin, several small mitochondria located at the base of the nucleus within a cytoplasmic collar that extends into a long cytoplasmic sleeve surrounding the anterior part of the single flagellum, which is contained within a cytoplasmic canal. The flagellum lacks fins. The proximal and distal centrioles are nearly parallel to one another, with the anterior tips of both located within shallow nuclear fossae. Spermiogenesis in C. riisei is characterized by nuclear elongation alongside the forming flagellum, formation of an elongate cytoplasmic canal, displacement and elongation of the mitochondria, and uniform condensation of chromatin throughout the nucleus through enlargement of the diameter of the chromatin granules. The spermatozoon has an elongate nucleus with two elongate mitochondria localized to one side. Mitochondria are also located posterior to the nucleus forming a mitochondrial region. The single flagellum, which lacks fins, is lateral to the nucleus and initially contained within the greatly elongate cytoplasmic canal before exiting the canal at its posterior terminus. The spermatozoon of C. riisei exhibits several characters typical of "introsperm," such as an elongate nucleus...


Foram analisadas a espermiogênese e ultraestrutura dos espermatozóides de dois caracídeos com modos de fertilização distintos: fertilização externa em Hemigrammus erythrozonus e inseminação em Corynopoma riisei. A espermiogênese em H. erythrozonus é caracterizada pelo desenvolvimento lateral do flagelo, rotação nuclear, formação de uma fossa nuclear rasa, condensação de cromatina por eliminação da área elétron-lúcida na região periférica do núcleo e renovação da membrana nuclear. Membrana multilamelada e corpos multivesiculares foram observados durante a eliminação do excesso de citoplasma. O espermatozóide exibe os caracteres típicos do "aquaespermatozóide," com uma cabeça esférica que contem um núcleo esférico com cromatina muito condensada, várias mitocôndrias pequenas localizadas na base do núcleo e dentro de um colar citoplasmático, extedendo-se em uma bainha citoplasmática longa que rodeia a parte anterior do único flagelo, que está contido dentro de um canal citoplasmático. O flagelo carece de aletas. Os centríolos proximais e distais são quase paralelos, com as partes anteriores dos dois localizadas dentro de fossas nucleares pouco profundas. A espermiogênese em C. riisei é caracterizada pelo alongamento nuclear ao longo do flagelo, a formação de um canal citoplasmático longo, deslocamento e alongamento das mitocôndrias e uma condensação uniforme da cromatina por todo o núcleo por meio do aumento do diâmetro dos grânulos de cromatina. O espermatozóide tem um núcleo alongado com duas mitocôndrias alongadas dispostas em um lado. Algumas mitocôndrias localizam-se posteriormente ao núcleo formando uma região mitocondrial. O único flagelo, que carece de aletas, é lateral ao núcleo, posicionado anteriormente dentro de um canal citoplasmático muito alongado. O espermatozóide de C. riisei exibe vários caracteres típicos de "introespermatozóides" tais como um núcleo alongado e parte média alongada (região mitocondrial). A cromatina nuclear...


Subject(s)
Animals , Chromatin/physiology , Spermatogenesis/physiology , Spermatozoa/cytology , Fertilization/physiology , Fishes/genetics
7.
Experimental & Molecular Medicine ; : 247-254, 2007.
Article in English | WPRIM | ID: wpr-201430

ABSTRACT

The largest subunit of eukaryotic RNA polymerase II contains a unique domain at its carboxy-terminus, which is referred to as the carboxy-terminal domain (CTD). The CTD is made up of an evolutionarily conserved heptapeptide repeat (YSPTSPS). Over the past decade, there has been increasing attention on the role of the CTD in transcription regulation in the view of mRNA processing and chromatin remodeling. This paper provides a brief overview of the recent progress in the dynamic changes in CTD phosphorylation and its role in integrating multiple nuclear events.


Subject(s)
Animals , Humans , Amino Acid Motifs , Amino Acid Sequence , Chromatin/physiology , Chromatin Assembly and Disassembly , Conserved Sequence , Histones/metabolism , Isomerism , Phosphorylation , Protein Structure, Tertiary , RNA Polymerase II/chemistry , RNA, Messenger/metabolism , Transcription, Genetic
8.
Braz. j. vet. res. anim. sci ; 43(4): 554-560, 2006. ilus
Article in Portuguese | LILACS | ID: lil-461491

ABSTRACT

O espermograma é um dos principais métodos de avaliação da fertilidade em mamíferos, contudo, algumas alterações do sêmen como a compactação da cromatina dos espermatozóides, não são identificadas nessa rotina, podendo interferir significativamente na fertilidade de reprodutores. Na avicultura, geralmente a avaliação de reprodutores é feita por amostragem e os parâmetros avaliados são em menor número que em mamíferos, sendo que a compactação da cromatina dos espermatozóides de galo nunca foi explorada. Este trabalho teve como objetivo verificar através da microscopia eletrônica de transmissão, se existe diferentes intensidades de compactação de cromatina em espermatozóides de galo. Para isto, foram coletadas 20 amostras de sêmen de galo, que foram fixadas por 48 horas em glutaraldeído 4% tamponado em cacodilato de sódio 0,1M a pH 7,2, após centrifugado e lavado em tampão cacodilato o sêmen foi pós-fixados em tetróxido de ósmio a 1% mais ferrocianeto de potássio a 1,25%. O sedimento foi incluído, cortado e posteriormente contrastado. Os cortes foram examinados e documentados em microscópio eletrônico Zeiss EM-109. Geralmente, os espermatozóides de galo possuem acrossoma com material homogêneo ou levemente granular e de densidade moderada, o núcleo com cromatina densa e levemente granular, varia as tonalidades de cinza, ou seja, os graus de compactação. Observou-se também o “perforatorium”, estrutura que une o núcleo ao acrossoma. A inserção da cauda é por meio de dois centríolos, sendo um transversal e o outro longitudinal ao eixo. A peça intermediária possui axonema típico envolto por mitocôndrias aparentemente dispostas longitudinalmente. A transição entre as peças intermediária e principal da cauda é marcada pela ausência das mitocôndrias. A peça principal é formada pelo axonema envolto por uma camada de citoplasma granular. Na avaliação das patologias morfológicas observaram-se cabeças arredondadas, dobradas, envoltas por conteúdo da peça intermediária...


The spermiogram is one of the principal methods of evaluation of the fertility in mammals; however some semen modifications as the spermatozoa chromatin condensation, are not identified in this routine, and can expressively interfere in the fertility of reproducers. In poultry breeding, generally the evaluation of reproducers is made by sampling and the evaluated parameters are in fewer quantities than in mammals, considering the spermatozoa chromatin condensation of the fowl has never been exploited. The objective of this work is verifying through the transmission electron microscopy, whether there are different intensities of spermatozoa chromatin condensation of fowl. So that, have been collected 20 samples of fowl semen, which were placed in 4% glutaraldehyde buffered in 0.1M sodium cacodilate to pH 7.2 for 48 hours, after being centrifugated and rinsed in cacodilate tampon, the semen was post-fixed in 1 % osmium tetroxide plus 1.25% potassium ferrocyanide. The sediment was embedded, cut and contrasted. The thin sections were examined and documented in transmission electronic microscopy Zeiss EM -109. Generally the fowl spermatozoon has acrosome with homogenic or slightly granular and of moderate density material, the nucleus with dense or slightly granular chromatin, varies the gray scales, that is, the grades of condensation. It was also observed the "perforatorium", structure that links the nucleus to the acrosome. The insertion of the tail is made through two cetriules, being one transversal and the other longitudinal to the axle. The intermediate piece has typical axoneme involved by mitochondrias, apparently displayed longitudinally. The transition between the principal and the intermediate pieces of the tail is marked by the absence of the mitochondrias. The principal piece is formed by axoneme involved by a granular cytoplasm layer. In the evaluation of the morphological pathologies, it was observed rounded heads, folded, involved by the...


Subject(s)
Animals , Male , Chromatin/physiology , Spermatozoa/ultrastructure , Fertility/physiology , Chickens/physiology , Microscopy, Electron, Transmission , Semen Analysis , Sperm Count/methods
9.
Biocell ; 27(3): 353-362, Dec. 2003.
Article in English | LILACS | ID: lil-384235

ABSTRACT

Spermatogenesis, with emphasis on spermiogenesis, is described for the lizard, Tropidurus itambere, using light microscopy, phase contrast and epifluorescence, as well as scanning and transmission electron microscopy. Cellular differentiation involves events of chromatin condensation, nuclear elongation and the formation of structural complexes, such as the acrosomal and axonemal ones. Other new characteristics, exclusive for this species, include various aspects of the subacrosomal granule, the insertion of the pro-acrosomal vesicle and the development of these structures to participate in the acrosomal complex. Radial projections occurjust above the nuclear shoulders, which have been recognized already from the beginning of cellular elongation. The development of the midpiece, the dense bodies, formation of the flagellum and elimination of residual cytoplasm result in the final characterization of the mature spermatozoon. Comparisons between Tropiduridae and other lizard families are made.


Subject(s)
Humans , Male , Spermatogenesis/physiology , Spermatozoa/ultrastructure , Lizards/anatomy & histology , Testis/ultrastructure , Acrosome/physiology , Acrosome/ultrastructure , Sertoli Cells/physiology , Sertoli Cells/ultrastructure , Chromatin/physiology , Chromatin/ultrastructure , Spermatogonia/physiology , Spermatogonia/ultrastructure , Spermatozoa/physiology , Flagella/physiology , Flagella/ultrastructure , Lizards/physiology , Microscopy, Electron , Microscopy, Electron, Scanning , Cell Nucleus/physiology , Cell Nucleus/ultrastructure , Testis/physiology , Seminiferous Tubules/physiology , Seminiferous Tubules/ultrastructure
10.
Biocell ; 27(3): 329-346, Dec. 2003.
Article in English | LILACS | ID: lil-384237

ABSTRACT

The fine structure of the binucleate, parasitic protist Giardia lamblia during interphase and divisional stages was studied by serial thin sectioning and three-dimensional reconstructions. The earlier sign of nuclear division is the development of a few peripheral areas of densely packed chromatin directly attached to the inner nuclear envelope. An intracytoplasmic sheet of ventral disk components grows from the cell periphery towards one of the nuclei, apparently constricting this nucleus, which becomes located at a ventral bulge. After the basal bodies become duplicated, a full nuclear division occurs in trophozoites, giving two pairs of parent-daughter nuclei. This full division occurs in a dorsal-ventral direction, with the resulting nuclear pairs located at the sides of the two sets of basal bodies. A new ventral disk is formed from the disk-derived sheets in the cell harboring the four nuclei. Cytokinesis is polymorphic, but at early stages is dorsal-to-dorsal. Encysting trophozoites show the development of Golgi cisternae stacks and dense, specific secretory granules. 3-D reconstructions show that cysts contain a single pair of incompletely strangled nuclei. The dividing Giardia lacks a typical, microtubular spindle either inside or outside the nuclei. The nuclear envelope seems to be the only structure involved in the final division of the parent-daughter nuclei.


Subject(s)
Giardia lamblia/ultrastructure , Nuclear Envelope , Cell Nucleus/ultrastructure , Golgi Apparatus/physiology , Golgi Apparatus/ultrastructure , Cytoplasm/physiology , Cytoplasm/ultrastructure , Chromatin/physiology , Chromatin/ultrastructure , Cell Division/physiology , Giardia lamblia/physiology , Microscopy, Electron , Nuclear Envelope , Cell Nucleus/physiology , Organelles/physiology , Organelles/ultrastructure , Secretory Vesicles/physiology , Secretory Vesicles/ultrastructure
11.
Southeast Asian J Trop Med Public Health ; 1997 ; 28 Suppl 3(): 46-57
Article in English | IMSEAR | ID: sea-34629

ABSTRACT

Genomic imprinting is a new concept proposed to explain unusual observations in early mammalian development, the occurrence of certain genetic diseases, genetic anticipation or incomplete penetrance, and tumorigenesis. The basic mechanism of the imprinting has remained obscure, although DNA-methylation, chromatin structure, and/or DNA replication may have a role. Genomic imprinting is a biological phenomenon determined by an evolutionally acquired, underlying system that may control harmonious development and growth in mammals. It is also relevant to the occurrence of some genetic disorders in man.


Subject(s)
Angelman Syndrome/genetics , Animals , Beckwith-Wiedemann Syndrome/genetics , Chromatin/physiology , DNA Methylation , Genetic Diseases, Inborn/genetics , Genomic Imprinting/genetics , Humans , Kidney Neoplasms/genetics , Mice , Phenotype , Prader-Willi Syndrome/genetics , Wilms Tumor/genetics
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