Contribución al estudio geobotánico de las sierras de Segura y Cazorla

Designado por la Escuela Especial de Ingenieros de Montes para desarrollar como proyecto final de carrera, el tema propuesto por el Patrimonio Forestal del Estado, sobre un estudio geobotánico de las Sierras de Segura y Casería, someto a aprobación el presente trabajo que titulo "Contribución al estudio geobotánico de las Sierras de Segura y Cazorla"

Estudio completo del aprovechamiento de las malezas de los montes "Guadahornillos" y "Vertientes del Guadalquivir" de la Sierra de Cazorla (Jaén)

La zona llamada de malezas ocupa en los montea do la Sierra de Cazorla (Jaén) una extensión considerable, no bien delimitada que - se aproxima a las 5 ó 6000 Has.

Proyecto de lucha antipaludica y saneamiento en las explotaciones forestales de Sierra Cazorla y Tranco-Cortijos Nuevos

Como huyendo de la ondulada y suave campiña, vestida de olivos, las casas de Cazorla trepen por la empinada ladera en que ésta se asienta, agazapándose bajo imponente roca, que no se sabe si protege o amenaza. Finos y gráciles álamos se alinean, mirando a la cumbre, y dibujan los arroyuelos que - hacen posible el cinturón de verdura con que se ciñe esta vieja ciudad.

Proyecto de ordenacion del grupo de montes en resinacion de la Serranía de Cazorla

Si grupo de montes en resinación de la serranía de Cazorla está formado por una parte segregada del monte de Navahondona, otra del de Guadahornillos y por el monte de Vertientes del Guadalquivir.

Proyecto de correccion del "Barranco del Herron" (Ladera de Cazorla)

El "Barranco del Herron" esta situado dentro dekl Monte "Navahondona" en el termino Municipal de Cazorla, provincia de Jaen, asi como toda su cuenca. No existen en la actualidad motivos que hagan esperar una variacion en la posicion administrativa de este barranco.

Mutations involved in Aicardi-Goutieres syndrome implicate SAMHD1 as regulator of the innate immune response

Aicardi-Goutieres syndrome is a mendelian mimic of congenital infection and also shows overlap with systemic lupus erythematosus at both a clinical and biochemical level. The recent identification of mutations in TREX1 and genes encoding the RNASEH2 complex and studies of the function of TREX1 in DNA metabolism have defined a previously unknown mechanism for the initiation of autoimmunity by interferon-stimulatory nucleic acid. Here we describe mutations in SAMHD1 as the cause of AGS at the AGS5 locus and present data to show that SAMHD1 may act as a negative regulator of the cell-intrinsic antiviral response.

Analysis of Synaptic Proteins in the Cerebrospinal Fluid as a New Tool in the Study of Inborn Errors of Neurotransmission

Abstract In a few rare diseases, specialised studies in cerebrospinal fluid (CSF) are required to identify the underlying metabolic disorder. We aimed to explore the possibility of detecting key synaptic proteins in the CSF, in particular dopaminergic and gabaergic, as new procedures that could be useful for both pathophysiological and diagnostic purposes in investigation of inherited disorders of neurotransmission. Dopamine receptor type 2 (D2R), dopamine transporter (DAT) and vesicular monoamine transporter type 2 (VMAT2) were analysed in CSF samplesfrom 30 healthy controls (11 days to 17 years) by western blot analysis. Because VMAT2 was the only protein with intracellular localisation, and in order to compare results, GABA vesicular transporter, which is another intracellular protein, was also studied. Spearman’s correlation and Student’s t tests were applied to compare optical density signals between different proteins. All these synaptic proteins could be easily detected and quantified in the CSF. DAT, D2R and GABA VT expression decrease with age, particularly in the first months of life, reflecting the expected intense synaptic activity and neuronal circuitry formation. A statistically significant relationship was found between D2R and DAT expression, reinforcing the previous evidence of DAT regulation by D2R. To our knowledge, there are no previous studies on human CSF reporting a reliable analysis of these proteins. These kinds of studies could help elucidate new causes of disturbed dopaminergic and gabaergic transmission as well as understanding different responses to L-dopa in inherited disorders affecting dopamine metabolism. Moreover, this approach to synaptic activity in vivo can be extended to different groups of proteins and diseases.

Cerebrospinal Fluid Synaptic Proteins as Useful Biomarkers in Tyrosine Hydroxylase Deficiency

Tyrosine hydroxylase (TH) deficiency is an inborn error of dopamine biosynthesis and a cause of early parkinsonism. Two clinical phenotypes have been described. Type “B”: early onset severe encephalopathy; type “A”: later onset, less severe and better response to L-dopa. We aimed to study the expression of several key dopaminergic and gabaergic synaptic proteins in the cerebrospinal fluid (CSF) of a series of patients with TH deficiency and their possible relation with the clinical phenotype and response to L-DOPA. Dopamine transporter (DAT), D2-receptor and vesicularmonoamine transporter (VMAT2)weremeasured in the CSF of 10 subjectswith THdeficiency byWestern blot analysis. In 3 patients, data of pre- and post-treatmentwith L-DOPA were available, and in one of them, GABA vesicular transporter was determined. Results were compared to an age-matched control population. The concentration of D2-receptors in CSFwas significantly higher in patients with TH deficiency than in controls. Similarly, DAT and vesicular monoamine transporter type 2 were up-regulated. Studies performed before LDOPA, and on L-DOPA therapy showed a paradoxical response with D2 receptor expression increase as L-Dopa doses and homovanillic concentration gradually raised in a B phenotype patient. The opposite results were found in two patients with A phenotype. However, this is a very small sample, and further studies are needed to conclude robust differences between phenotypes. Synaptic proteins are detectable in the CSF and their quantification can be useful for understanding the pathophysiology of neurotransmitter defects and potentially to adjust and personalize treatments in the future.

Undetectable Levels of CSF Amyloid-β Peptide in a Patient with 17β-Hydroxysteroid Dehydrogenase Deficiency

17β-hydroxysteroid dehydrogenase 10 (HSD10) deficiency is a rare X-linked inborn error of isoleucine catabolism. Although this protein has been genetically implicated in Alzheimer's disease pathogenesis, studies of amyloid-β peptide (Aβ) in patients with HSD10 deficiency have not been previously reported. We found, in a severely affected child with HSD10 deficiency, undetectable levels of Aβ in the cerebrospinal fluid, together with low expression of brain-derived neurotrophic factor, α-synuclein, and serotonin metabolites. Confirmation of these findings in other patients would help elucidating mechanisms of synaptic dysfunction in this disease, and highlight the role of Aβ in both early and late periods of life.

Studies on Trypanosoma rangeli Tejera, 1920: IX. Course of infection in different stages of Rhodnius prolixus

Frequent individual observations od different stages of Rhodnius prolixus exposed to Trypanosoma rangeli, revealed a higher susceptibility to infection in the bugs exposed during the two first instars. The mortality rate in infected bugs was significantly higher than in controls, indicating that the parasite was responsible for the majority of deaths. An analysis of the mortality distribution, per instar, is presented. Statistical analysis of deaths among the different infected instars, showed that T. rangeli produces its pathological effect in any stage of R. prolixus independently of its susceptibility to the parasite. The survival to adult decreased in all the infected instar bugs. A significant longer time to reach the adult stage was observed in the infected bugs when compared with controls, excepting for specimens exposed in the third instar. The epidemiological significance of the present results is discussed.

Epidemiologia de la leishmaniasis tegumentaria en merida, Venezuela. I. Diversidade y dispersion de especies flebotominas en tres pisos altitudinales y su possible rôle en la transmission de enfermedad

Como parte de un estudio epidemiológico sobre leishmaniasis en el Estado Mérida, Venezuela, se presenta la diversidad y dispersión de las especies flebotominas identificadas en 15 localidades ubicadas en 3 pisos altitudinales entre los 175 y los 1.960 m.s.n.m. De 7.126 espécimes capturados (5.132 hombres y 1.994 femenino) se registran 24 especies de Lutzomyia, reconociéndose 10 de las llmadas antropofílicas. Se detalla la distribución de las especies en cada piso altitudinal y en el domicilio humano, el peridomicilio y el ambiente silvestre. Se discute el posible papel que juegan las diferentes especies en la transmisión de la leishmaniasis tegumentaria en cada piso altitudinal en particular y en la región andino-venezolana, en general.