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1.
Data Brief ; 47: 108908, 2023 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-36761405

RESUMO

Flash droughts are characterized by rapid development and intensification, which makes early warning and monitoring difficult. Flash drought monitor (FDM) is a near-real time monitoring system for Spain (https://flash-drought.csic.es) based on the Standardized Precipitation Evapotranspiration Index (SPEI). Flash drought identification was based on rapid and anomalous declines in SPEI at a short time scale (1-month). Thus, FDM enables operational tracking of flash drought conditions in Spain at high spatial resolution (1.1 × 1.1 km) and high temporal frequency (weekly). Likewise, to put flash drought monitoring into a temporal context, the FDM also provides weekly flash drought conditions recorded in Spain from 1961 to the present. The FDM is a useful tool for preparedness and mitigation of flash droughts in Spain. Furthermore, the data provided by the FDM could be useful to develop future studies in relation to the flash drought in Spain.

6.
Actas Dermosifiliogr ; 113(2): 187-188, 2022 Feb.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-35244563
17.
J Colloid Interface Sci ; 358(1): 167-74, 2011 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-21420687

RESUMO

Thrombospondin-1 (TSP-1) is a protein involved in angiogenesis and tumor metastasis. In a previous study, a tridecapeptide sequence of TSP-1B [KRFKQDGGWSHWG] was synthesized and its biological activity was determined as well as the activity of three related sequences TSPB-(E), TSPB-(S), and TSPB-(Abu)(6). These peptides were tested for activity on the cell growth of three human carcinoma cells lines and only TSPB-(Abu)(6) increased proliferation of MCF7 and HT-29. The main aim of this study was to perform physicochemical measurements, in a comparative way, to determine if the differences in activity could be related to physicochemical properties. Peptides were characterised by HPLC capacity factors, UV, fluorescence, and CD spectra (either in buffer solution or in the presence of lipid vesicles), surface activity, and aggregation. Moreover, the interaction of these peptides with phospholipids was determined through their penetration in monolayers of DPPC, PG, or PS as well as their miscibility in mixed monolayers. Besides, using liposomes as model membranes, the affinity of these peptides for phosphatidylcholine was measured with vesicles labeled with fluorescent markers (TMA-DPH, laurdan, pyrene). Results show that these molecules are highly hydrophilic and their surface activity is low. Mixed monolayers indicate that there is almost no miscibility. Besides, its presence does not modify noticeably the microviscosity of bilayers. Moreover, UV and fluorescence spectra of peptides were not affected by the presence of lipids in the media but CD spectra recorded in TFE/water (1/1) resulted in small changes for TSPB, TSPB-(E), and TSPB-(S) peptides. On the contrary CD spectra of TSPB-(Abu)(6) derivatives were clearly much more sensitive to the polarity of the environment. According to these data the biological activity of peptide with a cyclic aspartimide moiety at position 6 could be related to a specific conformational change in the peptide chain promoted by a hydrophobic membrane-like environment.


Assuntos
Peptídeos/química , Trombospondina 1/química , Sequência de Aminoácidos , Dicroísmo Circular , Humanos , Lipossomos/química , Dados de Sequência Molecular , Fosfolipídeos/química , Estrutura Secundária de Proteína , Espectrometria de Fluorescência
18.
J Pept Sci ; 16(7): 315-21, 2010 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20552567

RESUMO

New therapies in cancer treatment are focusing on multifaceted approaches to starve and kill tumors utilizing both antiangiogenic and chemotherapeutic compounds. In this work, we searched for a peptide vector that would home liposomes both to endothelial and tumor cells. [Abu6]TSPB and [Abu6]TSPA, aspartimide analogs of natural sequences of TSP-1 and TSP-2, respectively, were tested for adhesion of tumor and endothelial cells, in vivo and in vitro antiangiogenic effects, and in vivo antitumor action. Both peptides support the adhesion of both types of cells, but only [Abu6]TSPA inhibits the angiogenesis in vivo, and [Abu6]TSPA-targeted L-DOX decreases by 58% (P < 0.008) the HT29 tumor growth in nude mice. The improvement in the doxorubicin antitumor effect should be attributed to the antiangiogenic effect of [Abu6]TSPA, since [Abu6]TSPB, despite being a good ligand for both cell types, had no effect on tumor growth.


Assuntos
Doxorrubicina/administração & dosagem , Doxorrubicina/farmacocinética , Portadores de Fármacos/química , Sistemas de Liberação de Medicamentos/métodos , Lipossomos/uso terapêutico , Trombospondinas/farmacologia , Inibidores da Angiogênese/farmacologia , Animais , Adesão Celular/efeitos dos fármacos , Linhagem Celular Tumoral , Células Endoteliais , Humanos , Camundongos , Camundongos Nus , Mimetismo Molecular , Neovascularização Patológica/tratamento farmacológico , Trombospondinas/uso terapêutico , Ensaios Antitumorais Modelo de Xenoenxerto
19.
Colloids Surf B Biointerfaces ; 57(2): 243-9, 2007 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-17383163

RESUMO

Three hydrophobic derivatives of GHK peptide containing either N-terminal hexanoyl, decanoyl or myristoyl acyl moieties were synthesized. The binding of these peptidolipids to phospholipid bilayers as well as their hemolytic activity were determined. Moreover, the influence of these peptidolipids on several physicochemical properties of liposomes was studied. Binding experiments indicate a high affinity of these peptidolipids for lipids ordered in liposomes. Nevertheless, this interaction does not promote the release of entrapped carboxyfluorescein. Experiments carried out by the asymmetric membrane method (NBD-PE/dithionite) and quenching studies (PC-pyrene/KI) indicate that this association has a protective effect suggesting that the hydrophobic moiety inserts in the external part of the bilayer and the peptide chain remains protruding from the surface hindering the entrance or the approach of reactants to it. The microviscosity of DPPC bilayers determined using TMA-DPH as fluorescent marker was not affected by the presence of peptidolipids. Besides, results indicate that myristoyl-GHK produces total hemolysis at 2.5x10(-4)M but decanoyl and hexanoyl derivatives at 5x10(-4)M induce only 10% of hemolysis.


Assuntos
Bicamadas Lipídicas , Oligopeptídeos/química , Fosfolipídeos/química , Cromatografia Líquida de Alta Pressão , Polarização de Fluorescência , Espectrometria de Massas , Viscosidade
20.
Anal Bioanal Chem ; 385(8): 1552-61, 2006 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16850293

RESUMO

A solid-state electrochemical application of the H-point standard addition method to the quantification of two depositable metals A and B, which produce strongly overlapped stripping peaks, is described. The method is based on the mechanical transference of mixtures of the solid sample plus a selected compound, of a reference depositable metal R, and of known amounts of a reference material containing A or B, to paraffin-impregnated graphite electrodes. After a reductive deposition step, voltammograms recorded for those modified electrodes immersed into a suitable electrolyte produce stripping peaks for the oxidation of all of the metals deposited. Measurement of the currents at selected potentials in overlapping peaks corresponding to the stripping of A and B permits the quantitation of these metals in the solid sample, while avoiding matrix effects. The method was applied to the simultaneous determination of Pb and Sn in archaeological glazes using PbCO(3) and SnO(2) as standards and ZnO as a reference material.

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