3,134 publications from this institution
This comprehensive review summarizes the past, present, and future of plasmonic NP-based sensors in terms of different sensing platforms, different chemical and biological analytes, and the expected future technologies.
S.16577-16583
Several studies have shown statistically significant circadian rhythms in thromboxane and prostacyclin production, circulating platelets, platelet aggregation, clotting and fibrinolytic inhibitors, circulating angiotensin II, angiotensin sensitivity, and the inhibition of platelet aggregation produced by aspirin (ASA). Moreover, ASA exhibits a faster drug-disappearance rate when administered during the morning as compared to the evening. Despite this evidence, previous studies on the potential influence of ASA on blood pressure (BP) have not taken into consideration the chronopharmacological effects of nonsteroidal antiinflammatory drugs. This pilot study investigates the effects of ASA on BP in untreated hypertensive patients who received ASA at different times of the day according to their rest-activity cycle. We studied 78 patients with mild hypertension (36 men), 43.5±11.4 (mean±SD) years of age, divided in 3 groups: non-pharmacological hygienic-dietary recommendations (HDR); HDR and ASA (100 mg/day) on awakening; or HDR and ASA before bedtime. BP and heart rate (HR) were measured every 20 minutes during the day (07:00 to 23:00 hours) and every 30 minutes at night for 48 consecutive hours before and after 3 months of intervention. The circadian pattern of BP in each group was established by population multiple-component analysis [Fernandez & Hermida. Chronobiol Int. 1998;15:191-204]. After 3 months of non-pharmacological intervention, there was a small and non-significant reduction of BP (1.2 mm Hg for systolic BP, 1.4 mm Hg for diastolic BP; P=0.264). There was no effect of ASA on BP when given on awakening (P=0.211). A BP reduction was, however, highly significant when ASA was given before bedtime (decrease of 7.6 and 6.1 mm Hg in systolic and diastolic BP, respectively; P<0.001). There was no significant change in HR in any group. Results indicate a statistically significant administration-time dependent effect of low-dose ASA on BP in untreated patients with mild hypertension. In any trial of ASA effects, inquiries about the time when subjects took the drug are indicated and may account for discrepancies in the literature. Moreover, the influence of ASA on BP demonstrated here indicates the need to identify and control for ASA effects in patients using this drug before or during their participation in antihypertension medication trials. DGES, PM98-0106; PGICT00-PXI-32205PN; University of Vigo.
Salmonella is a leading cause of foodborne illness worldwide and is a common concern in food safety. Salmonella enterica displaying resistance to extended-spectrum cephalosporins (ESCs) and fluoroquinolone (FQs) has been deemed a high-priority pathogen by the World Health Organization. Co-resistance to ESCs and FQs has been reported in S. enterica serovar Thompson ( S . Thompson). However, the genetic context of ESCs and FQs resistance genes in S . Thompson lacks sufficient characterization. In this study, we characterized a multi-drug resistant (MDR) S . Thompson isolate recovered from a retail ready-to-eat (RTE) pork product in China. Short- and long-read sequencing (HiSeq and MinION) of the genome identified the presence of bla CMY−2 , qnrS1 , and qepA8 , along with 11 additional acquired antimicrobial resistance genes, residing on a 152,940 bp IncA/C plasmid. Specifically, the bla CMY−2 , qnrS1 , and qepA8 genes were located in insertion sequences (ISs) and integron mediated mobile genetic structure, sugE - blc - bla CMY−2 -IS Ec9 , IS 26 - orf6 - qnrS1 - orf5 -IS Kpn19 , and intl1 - qepA8 - orf10 -IS 91 - orf1 - dfrA12 - orf11 - aadA2 - qacE Δ 1 - sul1 , respectively. Each gene was identified in various bacteria species, indicating their high transfer ability. The plasmid was found to be transferable to Escherichia coli J53 by conjugation and resulted in the acquiring of multiple resistances in the transconjugants. The plasmid is closely related to plasmids from two human S . Thompson strains isolated in different regions and years in China. Moreover, core-genome Multi Locus Sequence Typing (cgMLST) and phylogenetic analysis based on global 1,868 S . Saintpaul isolates showed that the S . Thompson isolate was highly epidemiologically linked to a human isolate in China. Our findings suggest that Chinese RTE pork products are a possible source of human pathogenic ESCs and FQs co-resistant S . Thompson. Furthermore, the results underline the important role of conjugative plasmids in acquiring and transmission of ESCs and FQs resistance in S . Thompson isolates, which need continuous investigation.