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1.
Environ Monit Assess ; 185(6): 4951-7, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23054280

ABSTRACT

According to Directive 2002/49, strategic noise maps and their correspondent action plans were carried out in the Autonomous Community of Navarre, Spain. Six strategic noise maps were produced for 120 km of major roads as well as a strategic noise map for the Agglomeration of the Region of Pamplona (ARP) with a population of 280,199 inhabitants. In the ARP, a total of 36,400 people (13.0 %) are exposed to Ln levels over 55 dBA and 42,300 people (15.1 %) are exposed to Lden levels over 65 dBA. With regard to major roads, a total of 3,900 people are exposed to Ln levels over 55 dBA and 2,400 people are exposed to Lden levels over 65 dBA. When designing action plans, different prioritisation criteria concerning rank-based effectiveness measures (mainly the amount of people benefitting from them) were taken into account.


Subject(s)
Environmental Monitoring , Noise , Cities/statistics & numerical data , Humans , Population Density , Spain
2.
Biochem Soc Trans ; 35(Pt 5): 1372-4, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17956354

ABSTRACT

Cell growth pathways are mediated through protein-glycan interactions including O-glycosylation. Investigation of these growth pathways can be carried out using appropriate inhibitors to identify stage-specific events. We have adopted this approach to study a group of benzyl-O-N-acetyl-D-galactosamine analogues in human colorectal cancer cell lines. Exposure to O-glycan inhibitors resulted in the induction of apoptosis, a block in proliferation, accumulation of intracellular aryl-glycans and changes in related genes as detected by gene array. Colorectal cancer cell lines susceptible to the inhibitors showed growth arrest with all compounds. However, a differential action of each inhibitor was detected in the pattern of genes affected and in the structure of aryl-glycans formed.


Subject(s)
Apoptosis , Cell Proliferation , Colorectal Neoplasms/pathology , Polysaccharides/metabolism , Cell Line, Tumor , Colorectal Neoplasms/metabolism , Glycosylation , Humans , Polysaccharides/antagonists & inhibitors , Signal Transduction
3.
Placenta ; 26(8-9): 641-53, 2005.
Article in English | MEDLINE | ID: mdl-16085043

ABSTRACT

Human equilibrative, Na(+)-independent nucleoside transport is mediated by membrane proteins sensitive (system es, hENT1) or insensitive (system ei, hENT2) to nitrobenzylthioinosine (NBMPR). Gestational diabetes and elevated extracellular concentrations of D-glucose reduce adenosine transport in human umbilical vein endothelium (HUVEC). We studied hENT2 and hENT1 expression in HUVEC, and the effect of D-glucose on their activity and expression in HUVEC preincubated with 25 mM D-glucose (24 h). hENT2 and hENT1 mRNA were quantified by real-time reverse transcription polymerase chain reaction, and their proteins were detected by Western blotting. hENT2 and hENT1 proteins are co-expressed in HUVEC and are located at the plasma membrane, however, hENT2 was mainly cytoplasmatic and perinuclear in location. D-Glucose reduced hENT1 and hENT2 mRNA expression, but only hENT1 protein abundance at the plasma membrane. Adenosine transport was inhibited by D-glucose and NMBPR (1 microM) in intact cells and membrane vesicles. Hypoxanthine inhibited adenosine transport in the absence or in the presence of 1 microM NBMPR. D-Glucose reduced NBMPR maximal binding in intact cells, membrane vesicles, and plasma membrane fractions. In conclusion, the present study demonstrates that hENT2 and hENT1 are co-expressed in HUVEC, and even when adenosine transport is also mediated by hENT2, the hENT2-mediated transport activity is not involved in the d-glucose-induced down-regulation of total adenosine transport.


Subject(s)
Adenosine/metabolism , Endothelium, Vascular/metabolism , Equilibrative Nucleoside Transporter 1/metabolism , Equilibrative-Nucleoside Transporter 2/metabolism , Hypoglycemia/metabolism , Cells, Cultured , Dose-Response Relationship, Drug , Down-Regulation , Drug Combinations , Endothelium, Vascular/cytology , Endothelium, Vascular/drug effects , Equilibrative Nucleoside Transporter 1/genetics , Equilibrative-Nucleoside Transporter 2/genetics , Glucose/pharmacology , Humans , Hypoxanthine/pharmacology , Nucleoside Transport Proteins/metabolism , RNA, Messenger/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Thioinosine/analogs & derivatives , Thioinosine/pharmacology , Umbilical Veins
4.
J Comp Physiol B ; 175(3): 185-92, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15731922

ABSTRACT

Adaptation of eurythermal fish to naturally varying environmental conditions involves modulation of expressions of various factors in the hypothalamo-hypophyseal axis. Here we used three complementary approaches to assess the seasonal variation of growth hormone (GH) protein and mRNA levels in pituitary glands of acclimatized carp fish. First, a polyclonal antibody raised against an oligopeptide derived from the carp GH sequence was used for immunohistochemistry; second, oligonucleotides specific for GH transcripts were used for in situ hybridization. Specific immunodetection of GH coincides with visualization of GH mRNA in the proximal pars distalis, the specific location of somatotroph cells in carp pituitary gland. Finally, competitive RT-PCR analyses confirmed that GH expression exhibits seasonal cyclical reprogramming with higher levels in summer- than in winter-adapted fish. The expression pattern suggests an important role for GH in the molecular mechanisms underlying the acclimatization process. In parallel, amplification of sequences from the fourth intron and adjacent sites from exons IV and V demonstrates the existence of a new GH gene previously undescribed. The detection of transcripts corresponding to each gene suggests that both GH gene copies are active in the duplicated carp genome and that they are similarly affected by seasonal adaptation.


Subject(s)
Acclimatization/physiology , Carps/genetics , Fish Proteins/genetics , Growth Hormone/genetics , Pituitary Gland/physiology , RNA, Messenger/metabolism , Seasons , Animals , Base Sequence , Carps/metabolism , Fish Proteins/biosynthesis , Gene Expression Regulation , Growth Hormone/biosynthesis , Growth Hormone/immunology , Immunohistochemistry , Introns , Male , Molecular Sequence Data , Nucleic Acid Hybridization , Reverse Transcriptase Polymerase Chain Reaction , Sequence Alignment
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