934 resultados para humans
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Cytokines have been shown to cause a reduction in nerve conduction when examined using animal models. Such effects, if shown in humans, could result in detrimental effects to physical function during periods heightened systemic cytokine concentrations. The study investigated the acute effects of cytokines on nerve conduction velocity (NCV) and functional measures. Measures were taken under both basal and elevated cytokine concentrations to determine any corresponding changes to NCV. A significant positive correlation was found between the cytokine IL-6 and NCV at 2 hours post-exercise (r=0.606, p=0.048). A significant negative correlation was found between IL-1ra and NCV at 24 hours post-exercise (r=-0.652, p=0.021). A significant positive correlation was also found between IL-1ra and endurance at 1 hour post-exercise (r=0.643, p=0.033). As such, it would seem that IL-6 may potentially act to enhance nerve function while other cytokines such as IL-1ra may have negative effects and reduce NCV.
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Retrotransposons, which used to be considered as junk DNA, have begun to reveal their immense value to genome evolution and human biology due to recent studies. They consist of at least ~45% of the human genome and are more or less the same in other mammalian genomes. Retrotransposon elements (REs) are known to affect the human genome through many different mechanisms, such as generating insertion mutations, genomic instability, and alteration in gene expression. Previous studies have suggested several RE subfamilies, such as Alu, L1, SVA and LTR, are currently active in the human genome, and they are an important source of genetic diversity between human and other primates, as well as among humans. Although several groups had used Retrotransposon Insertion Polymorphisms (RIPs) as markers in studying primate evolutionary history, no study specifically focused on identifying Human-Specific Retrotransposon Element (HS-RE) and their roles in human genome evolution. In this study, by computationally comparing the human genome to 4 primate genomes, we identified a total of 18,860 HS-REs, among which are 11,664 Alus, 4,887 L1s, 1,526 SVAs and 783 LTRs (222 full length entries), representing the largest and most comprehensive list of HS-REs generated to date. Together, these HS-REs contributed a total of 14.2Mb sequence increase from the inserted REs and Target Site Duplications (TSDs), 71.6Kb increase from transductions, and 268.2 Kb sequence deletion of from insertion-mediated deletion, leading to a net increase of ~14 Mb sequences to the human genome. Furthermore, we observed for the first time that Y chromosome might be a hot target for new retrotransposon insertions in general and particularly for LTRs. The data also allowed for the first time the survey of frequency of TE insertions inside other TEs in comparison with TE insertion into none-TE regions. In summary, our data suggest that retrotransposon elements have played a significant role in the evolution of Homo sapiens.
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Consumption of low-fat milk (LFM) after resistance training has been shown to have positive influences on body composition and training adaptations; however, little research has examined the effects of LFM consumption following endurance training. The purpose of the study was to look at the effects of combining additional servings of LFM following endurance exercise on body composition, bone health, and training adaptations. 40 healthy males were recruited. Individuals were randomized into 4 groups DEI (750mL LFM immediately post exercise), DEA (750mL LFM 4 hrs prior to or 6 hrs post exercise), CEI (750mL carbohydrate beverage immediately post-exercise), and CEA (750mL carbohydrate beverage immediately post-exercise). Participants took part in a 12-week endurance training intervention (1 h/day, 3 d/wk, ~60% max HR). 22 participants completed the study. Analysis showed significant increases in lean mass, spinal bone mineral content, relative VO2peak, and a decrease in Trap 5 across all groups (p < 0.05).
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L'tre humain utilise trois systmes sensoriels distincts pour rguler le maintien de la station debout: la somesthsie, le systme vestibulaire, et le systme visuel. Le rle de la vision dans la rgulation posturale demeure peu connu, notamment sa variabilit en fonction de l'ge, du type dveloppemental, et des atteintes neurologiques. Dans notre travail, la rgulation posturale induite visuellement a t value chez des participants au dveloppement et vieillissement normaux gs de 5-85 ans, chez des individus autistes (dveloppement atypique) gs de 12-33 ans, ainsi que chez des enfants entre 9-18 ans ayant subi un TCC lger. cet effet, la ractivit posturale des participants en rponse un tunnel virtuel entirement immersif, se mouvant trois niveaux de vlocit, a t mesure; des conditions contrles, o le tunnel tait statique ou absent, ont t incluses. Les rsultats montrent que la ractivit (i.e. instabilit) posturale induite visuellement est plus leve chez les jeunes enfants; ensuite, elle s'attnue pour rejoindre des valeurs adultes vers 16-19 ans et augmente de faon linaire en fonction de l'ge aprs 45 ans jusqu' redevenir leve vers 60 ans. De plus, la plus haute vlocit du tunnel, les plus jeunes participants autistes ont manifest significativement moins de ractivit posturale comparativement leurs contrles; cette diffrence n'tait pas prsente chez des participants plus gs (16-33 ans). Enfin, les enfants ayant subi un TCC lger, et qui taient initialement modrment symptomatiques, ont montr un niveau plus lev d'instabilit posturale induite visuellement que les contrles, et ce jusqu' 12 semaines post-trauma malgr le fait que la majorit d'entre eux (89%) n'taient plus symptomatiques ce stade. En somme, cela suggre la prsence d'une importante priode de transition dans la maturation des systmes sous-tendant l'intgration sensorimotrice implique dans le contrle postural vers l'ge de 16 ans, et d'autres changements sensorimoteurs vers l'ge de 60 ans; cette sur-dpendance visuelle pour la rgulation posturale chez les enfants et les ans pourrait guider l'amnagement d'espaces et l'laboration d'activits ajusts l'ge des individus. De plus, le fait que l'hypo-ractivit posturale aux informations visuelles chez les autistes dpende des caractristiques de l'environnement visuel et de l'ge chronologique, affine notre comprhension des anomalies sensorielles propres l'autisme. Par ailleurs, le fait que les enfants ayant subi un TCC lger montrent des anomalies posturales jusqu' 3 mois post-trauma, malgr une diminution significative des symptmes rapports, pourrait tre reli une altration du traitement de l'information visuelle dynamique et pourrait avoir des implications quant la gestion clinique des patients aux prises avec un TCC lger, puisque la rsolution des symptmes est actuellement le principal critre utilis pour la prise de dcision quant au retour aux activits. Enfin, les rsultats obtenus chez une population dveloppement atypique (autisme) et une population avec atteinte neurologique dite transitoire (TCC lger), contribuent non seulement une meilleure comprhension des mcanismes d'intgration sensorimotrice sous-tendant le contrle postural mais pourraient aussi servir comme marqueurs sensibles et spcifiques de dysfonction chez ces populations. Mots-cls : posture, quilibre, vision, dveloppement/vieillissement sensorimoteur, autisme, TCC lger symptomatique, ralit virtuelle.
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Der eukaryotische Mikroorganismus Dictyostelium discoideum lebt als einzellige Ambe solange ausreichende Nahrungsressourcen zur Verfgung stehen. Sobald Nahrungsmangel eintritt, entwickeln sich die Zellen von einem einzelligen zu einem mehrzelligen Zustand, der mit einem multizellulren Fruchtkrper abschliet. Dieser Prozess wird durch eine Reihe aufeinanderfolgender Signale organisiert, die eine differentielle Genexpression regulieren. Die Gene der Discoidin I Familie gehren zu den Ersten, die im Laufe des Wachstums-Differenzierungs-bergangs (engl. GDT) aktiviert werden. Sie eignen sich daher vorzglich als Marker fr den Beginn der Entwicklung. Mit Hilfe einer REMI-Mutagenese und Discoidin I als molekularem Marker sind verschiedene Komponenten des Wachstums-Differenzierungs-bergangs in unserer Arbeitsgruppe identifiziert worden (Zeng et al., 2000 A und B; Riemann und Nellen, persnliche Mitteilung). Mit demselben Ansatz wurde in der vorliegenden Arbeit eine REMI-Mutante identifiziert, die eine Fehl-Expression von Discoidin zeigte und einen axenischen Wachstumsdefekt bei 15 C aufwies. Das Gen wurde als Homolog zum humanen Tafazzin-Gen identifiziert. Dieses Gen wurde zur Rekonstruktion des Phnotyps ber homologe Rekombination erneut disruptiert, was wie erwartet zu dem zuerst beschriebenen Phnotyp fhrte. Folgerichtig ergab eine berexpression des Gens in den Mutanten eine Komplementation des Phnotyps. Immunfluoreszenz-Experimente zeigten eine mitochondriale Lokalisation des Dictyostelium discoideum Taffazzin Proteins. Dass ein mitochondriales Protein in Zusammenhang mit dem Wachstums-Differenzierungs-bergang steht, ist ein unerwarteter Befund, der aber als Hinweis darauf gewertet werden kann, dass Mitochondrien einen direkten Einfluss auf die entwicklungsspezifische Signaltransduktion ausben. Die Taffazzin Disruptions-Mutante in Dictyostelium fhrte zu einem abnormalen Cardiolipin Metabolismus. Dieses Phospholipid ist ein charakteristischer Bestandteil der inneren Mitochondrienmembran und fr die Funktion verschiedener Enzyme erforderlich. Unsere vorlufigen Analysen des Phospholipid-Gehalts zeigten bereinstimmung mit Daten von Patienten mit Barth-Syndrom, einer humanen Erkrankung, bei der das Taffazzin-Gen Mutationen aufweist, und mit Hefe-Mutanten dieses Gens. Dies zeigt den Wert von Dictyostelium discoideum als einen weiteren Modelorganismus zur Untersuchung des Barth-Syndroms und zur Erprobung mglicher Therapieanstze.
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Understanding how the human visual system recognizes objects is one of the key challenges in neuroscience. Inspired by a large body of physiological evidence (Felleman and Van Essen, 1991; Hubel and Wiesel, 1962; Livingstone and Hubel, 1988; Tso et al., 2001; Zeki, 1993), a general class of recognition models has emerged which is based on a hierarchical organization of visual processing, with succeeding stages being sensitive to image features of increasing complexity (Hummel and Biederman, 1992; Riesenhuber and Poggio, 1999; Selfridge, 1959). However, these models appear to be incompatible with some well-known psychophysical results. Prominent among these are experiments investigating recognition impairments caused by vertical inversion of images, especially those of faces. It has been reported that faces that differ "featurally" are much easier to distinguish when inverted than those that differ "configurally" (Freire et al., 2000; Le Grand et al., 2001; Mondloch et al., 2002) ??finding that is difficult to reconcile with the aforementioned models. Here we show that after controlling for subjects' expectations, there is no difference between "featurally" and "configurally" transformed faces in terms of inversion effect. This result reinforces the plausibility of simple hierarchical models of object representation and recognition in cortex.
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Educaci per a la ciutadania i drets humans (ECDH) s una rea que neix amb la LOE, aprovada per les Corts espanyoles l'abril de 2006
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Aquest document s un text-guia destinat als alumnes de l'assignatura de Sociologia de l'Empresa dels estudis de Diplomatura en Cincies Empresarials, dissenyat per facilitar el seguiment i l'estudi de la matria tant pel sistema presencial com semipresencial. Els autors pertanyen al Departament: DOGEDP, i imparteixen classes en assignatures de Sociologia de l'empresa i Direcci de Recursos Humans
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Aquest document s un text-guia destinat als alumnes de l'assignatura de Sociologia de l'Empresa dels estudis de Diplomatura en Cincies Empresarials, dissenyat per facilitar el seguiment i l'estudi de la matria tant pel sistema presencial com semipresencial. Els autors pertanyen al Departament: DOGEDP, i imparteixen classes en assignatures de Sociologia de l'empresa i Direcci de Recursos Humans
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Resumen tomado parcialmente de la publicaci??n
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El resumen es traduccin del publicado con el artculo
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Resumen tomado de la propia publicaci??n. Volumen especial dedicado a filosof??a y ciencias de la educaci??n
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El resumen es copia de la presentacin del libro
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The signaling pathway of phosphatidylinositol 3-kinase (PI3K) is critical in many aspects of growth and cell survival. The path of PI3K is stimulated physiologically as a result of many growth factors and regulatory factors. Several genetic alterations such as amplification, mutation and chromosomal arrangements may compromise the PI3K pathway, generating permanent activation in different cancer types have found evidence of these deleterious genetic modifications. Abnormal activation of the PI3K pathway results in alteration of the control mechanisms of growth and cell survival, which favors the competitive growth, and frequently metastatic capacity, greater resistance to treatment. The aim of this paper is to review matters relating to the operation of the PI3K/Akt signaling pathway and its role in the process of carcinogenesis in humans.
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Resumen de la revista en cataln