Principales lugares de producción de las patologías que requieren recompresión en cámara hiperbárica / Main places of production of the pathologies that require recompression in hyperbaric chamber

INTRODUCCIÓN: Las principales patologías que requieren tratamiento en cámara hiperbárica son la enfermedad descompresiva y el embolismo arterial gaseoso. Ambas comparten la necesidad de cambios de la presión ambiental y del contenido gaseoso en el organismo. Además del buceo, existen otras situaciones que suponen cambios de presión y por tanto propician el riesgo de presentar lesiones que requieran recompresión. OBJETIVOS: Describir los principales lugares de producción de estas patologías y los mecanismos fisiopatológicos que las generan. Material y MÉTODO: Expedientes de accidentes de buceo recogidos en el Centro de Buceo de la Armada desde 1970 hasta 2017. RESULTADOS: Total 392 casos, 345 (88%) se producen en la mar, 36 (9,18%) en cámara hiperbárica, 6 (1,53%) en relación con submarinos y 4 (1,02%) en actividades hipobáricas. CONCLUSIONES: Cualquier situación que suponga un cambio de presión expone al sujeto a presentar una patología descompresiva y a necesitar un tratamiento hiperbárico. El lugar más frecuente es en la mar pero pruebas, en principio no lesivas, como un tratamiento hiperbárico, pueden predisponer a estas lesiones

INTRODUCTION: The main pathologies that require a recompression therapy are decompression sickness (DCS) and arterial gas embolism (AGE), boths can be caused by pressure-related activites and certain amount of gas (dissolved or not) in the victim's blood. Besides diving other pressure-related activities put the person in risk of this pathologies. AIM: To investigate the main place of production of these pathologies and their physiological base. METHODS: we reviewed all charts of patients with DCS and AGE from 1970-2017 at Centro de Buceo de la Armada (Cartagena). RESULTS: There were 392 cases, 345 (88%) diving related, 36 (9,18%) hyperbaric chamber-related, 6 (1,53%) submarine activities related and 4 (1,02%) hypobaric activities-related. CONCLUSIONS: Diving injuries rates are the most important but any pressure-related activity can be risky even hyperbaric chamber activity, considered the safest pressure-related activity

Compartments and organising boundaries in the Drosophila eye: the role of the homeodomain Iroquois proteins.

The Drosophila eye is patterned by a dorsal-ventral organising centre mechanistically similar to those in the fly wing and the vertebrate limb bud. Here we show how this organising centre in the eye is initiated - the first event in retinal patterning. Early in development the eye primordium is divided into dorsal and ventral compartments. The dorsally expressed homeodomain Iroquois genes are true selector genes for the dorsal compartment; their expression is regulated by Hedgehog and Wingless. The organising centre is then induced at the interface between the Iroquois-expressing and non-expressing cells at the eye midline. It was previously thought that the eye develops by a mechanism distinct from that operating in other imaginal discs, but our work establishes the importance of lineage compartments in the eye and thus supports their global role as fundamental units of patterning.

c-Irx2 expression reveals an early subdivision of the neural plate in the chick embryo.

We have cloned c-Irx2, a chick homologue of the Xiro2 and mIrx2 genes and a new member of the Iroquois family of homeodomain-containing transcription factors. Strikingly, c-Irx2 expression reveals an early subdivision of the neural plate at late primitive streak stages which later transiently resolves to a single stripe within the developing hindbrain corresponding to rhombomere 1.

The Iroquois homeodomain proteins are required to specify body wall identity in Drosophila.

The Iroquois complex (Iro-C) homeodomain proteins allow cells at the proximal part of the Drosophila imaginal wing disc to form mesothoracic body wall (notum). Cells lacking these proteins form wing hinge structures instead (tegula and axillary sclerites). Moreover, the mutant cells impose on neighboring wild-type cells more distal developmental fates, like lateral notum or wing hinge. These findings support a tergal phylogenetic origin for the most proximal part of the wing and provide evidence for a novel pattern organizing center at the border between the apposed notum (Iro-C-expressing) and hinge (Iro-C-nonexpressing) cells. This border is not a cell lineage restriction boundary.

white+ transgene insertions presenting a dorsal/ventral pattern define a single cluster of homeobox genes that is silenced by the polycomb-group proteins in Drosophila melanogaster.

We used the white gene as an enhancer trap and reporter of chromatin structure. We collected white+ transgene insertions presenting a peculiar pigmentation pattern in the eye: white expression is restricted to the dorsal half of the eye, with a clear-cut dorsal/ventral (D/V) border. This D/V pattern is stable and heritable, indicating that phenotypic expression of the white reporter reflects positional information in the developing eye. Localization of these transgenes led us to identify a unique genomic region encompassing 140 kb in 69D1-3 subject to this D/V effect. This region contains at least three closely related homeobox-containing genes that are constituents of the iroquois complex (IRO-C). IRO-C genes are coordinately regulated and implicated in similar developmental processes. Expression of these genes in the eye is regulated by the products of the Polycomb-group (Pc-G) and trithorax-group (trx-G) genes but is not modified by classical modifiers of position-effect variegation. Our results, together with the report of a Pc-G binding site in 69D, suggest that we have identified a novel cluster of target genes for the Pc-G and trx-G products. We thus propose that ventral silencing of the whole IRO-C in the eye occurs at the level of chromatin structure in a manner similar to that of the homeotic gene complexes, perhaps by local compaction of the region into a heterochromatin-like structure involving the Pc-G products.

Localization, structure and expression of the gene for translation initiation factor eIF-4E from Drosophila melanogaster.

Drosophila melanogaster contains a single copy of the gene encoding translation eukaryotic initiation factor eIF-4E, which maps in the 67A2B1 region of chromosome 3L. A genomic clone containing the entire eIF-4E gene was isolated and sequenced. Comparison of this sequence with a cDNA previously obtained in our laboratory and 5'-RACE analysis revealed the existence of three mRNAs that are generated by alternative splicing of a primary transcript. All of them have different 5' untranslated leader regions. Two of the mRNAs encode the same eIF-4E polypeptide, whose sequence has been deduced from the cDNA clone. The third mRNA species contains a new open reading frame, possibly encoding another isoform of eIF-4E, which is very similar in size to the other but has a different N-terminal sequence. Several sequences which may be involved in the regulation of transcription initiation of the eIF-4E gene, except for a consensus TATA box, were found upstream of the putative transcription initiation sites. Expression of the eIF-4E gene is spatially and temporally controlled during embryonic development. It is ubiquitously expressed during embryogenesis but transcripts preferentially accumulate in certain tissues, particularly in the pole cells, at different developmental stages.

Araucan and caupolican, two members of the novel iroquois complex, encode homeoproteins that control proneural and vein-forming genes.

In Drosophila imaginal wing discs, the achaete-scute (ac-sc) proneural genes and rhomboid (veinlet) are expressed in highly resolved patterns that prefigure the positions of sensory organs and wing veins, respectively. It is thought that these patterns are generated by a combination of factors (a prepattern) regulating these genes. We provide evidence for the existence of this prepattern by identifying two of its factors, Araucan and Caupolican. They are members of a novel family of homeoproteins, with homologs in vertebrates. Araucan and Caupolican, present in domains of the imaginal discs larger than those expressing ac-sc and rhomboid, are necessary for expression of these genes in the overlapping domains. Araucan and Caupolican appear to be positive, direct regulators of ac-sc.