74 research outputs found

    Applicazioni di tecniche di telerilevamento con sistema termovisivo all'infrarosso per l'individuazione di efflussi costieri e di aree di drenaggio di corpi franosi

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    The use of camera operating in the 8-12 µm range of electromagnetic wave spectrum, prove to be satisfactory in various sectors of the engineering geology. The results of some surveyings carried out by means of fixed stations on the land have been presented. The interpretation of the thermography which have been obtained is related to the meaning which is likely to be ascribed to the temperature distribution on the surface of the investigated bodies. In fact, the system shows in the form of shades of gray or of false colour the thermal energy radiated and reflected by the observed bodies. Starting from the most traditional applications concerning the census of submarine springs, but still prerogative of the most sophisticated systems based on the use of airborne multi-spectral scanners, the easiest thermovision system, which is also likely to be used on platforms installed on small aircraft, may stretch the applications range of remote sensing techniques to various field of the engineering geology. Besides the low cost and readiness of the survey, the thermovision system, used from fixed stations, allows to obtain images in the scale of the desired detail.Examples which have been presented refer to the location of submarine springs flowing along a part of the coast near Polignano (Bari, Apulia region) and near Maratea (Potenza, Basilicata Region), the observation of a landslide near Brindisi di Montagna (Potenza, Basilicata region). In the discussion of data resulting from thermographies taken on the above said objectives one can even realize factors which may negatively affect the image interpretation such as, for instance, the disturbance caused by vegetation to the temperature distribution on the land surface

    Effects of typical and atypical antipsychotic drugs on gene expression profiles in the liver of schizophrenia subjects

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    <p>Abstract</p> <p>Background</p> <p>Although much progress has been made on antipsychotic drug development, precise mechanisms behind the action of typical and atypical antipsychotics are poorly understood.</p> <p>Methods</p> <p>We performed genome-wide expression profiling to study effects of typical antipsychotics and atypical antipsychotics in the postmortem liver of schizophrenia patients using microarrays (Affymetrix U133 plus2.0). We classified the subjects into typical antipsychotics (n = 24) or atypical antipsychotics (n = 26) based on their medication history, and compared gene expression profiles with unaffected controls (n = 34). We further analyzed individual antipsychotic effects on gene expression by sub-classifying the subjects into four major antipsychotic groups including haloperidol, phenothiazines, olanzapine and risperidone.</p> <p>Results</p> <p>Typical antipsychotics affected genes associated with nuclear protein, stress responses and phosphorylation, whereas atypical antipsychotics affected genes associated with golgi/endoplasmic reticulum and cytoplasm transport. Comparison between typical antipsychotics and atypical antipsychotics further identified genes associated with lipid metabolism and mitochondrial function. Analyses on individual antipsychotics revealed a set of genes (151 transcripts, FDR adjusted p < 0.05) that are differentially regulated by four antipsychotics, particularly by phenothiazines, in the liver of schizophrenia patients.</p> <p>Conclusion</p> <p>Typical antipsychotics and atypical antipsychotics affect different genes and biological function in the liver. Typical antipsychotic phenothiazines exert robust effects on gene expression in the liver that may lead to liver toxicity. The genes found in the current study may benefit antipsychotic drug development with better therapeutic and side effect profiles.</p

    The Concise Guide to PHARMACOLOGY 2023/24: G protein-coupled receptors.

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    The Concise Guide to PHARMACOLOGY 2023/24 is the sixth in this series of biennial publications. The Concise Guide provides concise overviews, mostly in tabular format, of the key properties of approximately 1800 drug targets, and about 6000 interactions with about 3900 ligands. There is an emphasis on selective pharmacology (where available), plus links to the open access knowledgebase source of drug targets and their ligands (https://www.guidetopharmacology.org), which provides more detailed views of target and ligand properties. Although the Concise Guide constitutes almost 500 pages, the material presented is substantially reduced compared to information and links presented on the website. It provides a permanent, citable, point-in-time record that will survive database updates. The full contents of this section can be found at http://onlinelibrary.wiley.com/doi/bph.16177. G protein-coupled receptors are one of the six major pharmacological targets into which the Guide is divided, with the others being: ion channels, nuclear hormone receptors, catalytic receptors, enzymes and transporters. These are presented with nomenclature guidance and summary information on the best available pharmacological tools, alongside key references and suggestions for further reading. The landscape format of the Concise Guide is designed to facilitate comparison of related targets from material contemporary to mid-2023, and supersedes data presented in the 2021/22, 2019/20, 2017/18, 2015/16 and 2013/14 Concise Guides and previous Guides to Receptors and Channels. It is produced in close conjunction with the Nomenclature and Standards Committee of the International Union of Basic and Clinical Pharmacology (NC-IUPHAR), therefore, providing official IUPHAR classification and nomenclature for human drug targets, where appropriate

    Finding New Genes for Non-Syndromic Hearing Loss through an In Silico Prioritization Study

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    At present, 51 genes are already known to be responsible for Non-Syndromic hereditary Hearing Loss (NSHL), but the knowledge of 121 NSHL-linked chromosomal regions brings to the hypothesis that a number of disease genes have still to be uncovered. To help scientists to find new NSHL genes, we built a gene-scoring system, integrating Gene Ontology, NCBI Gene and Map Viewer databases, which prioritizes the candidate genes according to their probability to cause NSHL. We defined a set of candidates and measured their functional similarity with respect to the disease gene set, computing a score () that relies on the assumption that functionally related genes might contribute to the same (disease) phenotype. A Kolmogorov-Smirnov test, comparing the pair-wise distribution on the disease gene set with the distribution on the remaining human genes, provided a statistical assessment of this assumption. We found at a p-value that the former pair-wise is greater than the latter, justifying a prioritization strategy based on the functional similarity of candidate genes respect to the disease gene set. A cross-validation test measured to what extent the ranking for NSHL is different from a random ordering: adding 15% of the disease genes to the candidate gene set, the ranking of the disease genes in the first eight positions resulted statistically different from a hypergeometric distribution with a p-value and a power. The twenty top-scored genes were finally examined to evaluate their possible involvement in NSHL. We found that half of them are known to be expressed in human inner ear or cochlea and are mainly involved in remodeling and organization of actin formation and maintenance of the cilia and the endocochlear potential. These findings strongly indicate that our metric was able to suggest excellent NSHL candidates to be screened in patients and controls for causative mutations

    The Concise Guide to PHARMACOLOGY 2023/24: G protein-coupled receptors.

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    peer reviewedThe Concise Guide to PHARMACOLOGY 2023/24 is the sixth in this series of biennial publications. The Concise Guide provides concise overviews, mostly in tabular format, of the key properties of approximately 1800 drug targets, and about 6000 interactions with about 3900 ligands. There is an emphasis on selective pharmacology (where available), plus links to the open access knowledgebase source of drug targets and their ligands (https://www.guidetopharmacology.org), which provides more detailed views of target and ligand properties. Although the Concise Guide constitutes almost 500 pages, the material presented is substantially reduced compared to information and links presented on the website. It provides a permanent, citable, point-in-time record that will survive database updates. The full contents of this section can be found at http://onlinelibrary.wiley.com/doi/bph.16177. G protein-coupled receptors are one of the six major pharmacological targets into which the Guide is divided, with the others being: ion channels, nuclear hormone receptors, catalytic receptors, enzymes and transporters. These are presented with nomenclature guidance and summary information on the best available pharmacological tools, alongside key references and suggestions for further reading. The landscape format of the Concise Guide is designed to facilitate comparison of related targets from material contemporary to mid-2023, and supersedes data presented in the 2021/22, 2019/20, 2017/18, 2015/16 and 2013/14 Concise Guides and previous Guides to Receptors and Channels. It is produced in close conjunction with the Nomenclature and Standards Committee of the International Union of Basic and Clinical Pharmacology (NC-IUPHAR), therefore, providing official IUPHAR classification and nomenclature for human drug targets, where appropriate

    THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: G protein-coupled receptors.

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    The Concise Guide to PHARMACOLOGY 2021/22 is the fifth in this series of biennial publications. The Concise Guide provides concise overviews, mostly in tabular format, of the key properties of nearly 1900 human drug targets with an emphasis on selective pharmacology (where available), plus links to the open access knowledgebase source of drug targets and their ligands (www.guidetopharmacology.org), which provides more detailed views of target and ligand properties. Although the Concise Guide constitutes over 500 pages, the material presented is substantially reduced compared to information and links presented on the website. It provides a permanent, citable, point-in-time record that will survive database updates. The full contents of this section can be found at http://onlinelibrary.wiley.com/doi/bph.15538. G protein-coupled receptors are one of the six major pharmacological targets into which the Guide is divided, with the others being: ion channels, nuclear hormone receptors, catalytic receptors, enzymes and transporters. These are presented with nomenclature guidance and summary information on the best available pharmacological tools, alongside key references and suggestions for further reading. The landscape format of the Concise Guide is designed to facilitate comparison of related targets from material contemporary to mid-2021, and supersedes data presented in the 2019/20, 2017/18, 2015/16 and 2013/14 Concise Guides and previous Guides to Receptors and Channels. It is produced in close conjunction with the Nomenclature and Standards Committee of the International Union of Basic and Clinical Pharmacology (NC-IUPHAR), therefore, providing official IUPHAR classification and nomenclature for human drug targets, where appropriate

    Integrative neurobiology of metabolic diseases, neuroinflammation, and neurodegeneration

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    Alzheimer’s disease (AD) is a complex, multifactorial disease with a number of leading mechanisms, including neuroinflammation, processing of amyloid precursor protein (APP) to amyloid β peptide, tau protein hyperphosphorylation, relocalization and deposition. These mechanisms are propagated by obesity, the metabolic syndrome and type-2 diabetes mellitus. Stress, sedentariness, dietary overconsumption of saturated fat and refined sugars, and circadian derangements/disturbed sleep contribute to obesity and related metabolic diseases, but also accelerate age-related damage and senescence that all feed the risk of developing AD too. The complex and interacting mechanisms are not yet completely understood and will require further analysis. Instead of investigating AD as a mono- or oligocausal disease we should address the disease by understanding the multiple underlying mechanisms and how these interact. Future research therefore might concentrate on integrating these by systems biology approaches, but also to regard them from an evolutionary medicine point of view. The current review addresses several of these interacting mechanisms in animal models and compares them with clinical data giving an overview about our current knowledge and puts them into an integrated framework

    GROUNDWATER PROTECTION IN KARST ENVIRONMENT

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    Protection of karstic groundwater quality can be successful only if it is based on reliable reconstructions of conceptual models of the karstic aquifers, which are normally of high complexity: this requires the integration of classical hydrogeological information with that obtainable by using natural tracers, according to multi-tracing methods. The definition of the conceptual model includes elements as the identification of recharge areas, their connection with discharge areas, the sequence of physical – chemical processes acting into the aquifer and the transport mechanisms. With reference to the identification of recharge areas, two casestudies are illustrated. The first deals with a continental karstic aquifer (Monti Simbruini, Central Italy) discharging through springs used for drinking purposes: it has been studied by using the stable deuterium and oxygen-18 isotopes according to the “mass-center” method coupled with the “inverse hydrogeological budget” method. The second regards a platform karstic aquifer (Murgia, Southern Italy), discharging through coastal brackish springs, which is exploited by wells for both drinking and agricultural purposes: for recognizing some elements of the conceptual model a multi-tracing approach has been adopted, which uses the crossverification of information coming from the interpretation of isotopic, chemical and physical tracers. Moreover, with the aim of outlining the factors that control the pollutant transport in karstic aquifers, two case-studies related to Murgia aquifer illustrate a first method for defining the hazard due to direct injection of effluents from treatment plants and a second approach for defining, through monitoring data, the transport mechanisms of pollutant released at land surface

    Karstic aspects in the assessment of groundwater vulnerability of Maiella, Italy

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    This paper concerns the vulnerability of the Maiella karstic aquifer, by applying two important and specific methods for this type of aquifer. The Maiella carbonate massif, situated in Central Italy, more exactly in the Abruzzi Apennines, covers a surface of 416 square km. It represents an important groundwater basin in Italy, with the particular and distinctive features of a karst aquifer. The unique framework of a karst aquifer derives from its special properties such as the existence of swallowholes, the absence of surface drainage, the presence of karstic dissolution networks, large springs, the dual nature of recharge (concentrated and point) and the duality of the permeability. Therefore, assessment of vulnerability of a karst area is complex because it is fundamental to take into consideration the overall effects of the previously mentioned factors. Because of their special structure, karst aquifers are particularly vulnerable to pollution. In particular, this study focuses on peculiar karstic features influencing vulnerability of Maiella site. Carrying on the research, vulnerability maps have been prepared by using a geographic information system. Lastly the results obtained by applying the two mentioned methods are compared , trying to identify and outline the more sensitive area
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