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1.
Environ Res ; 156: 644-651, 2017 07.
Article in English | MEDLINE | ID: mdl-28463823

ABSTRACT

The association between the consumption of seafood and its benefits on cardiovascular (CVD) risk can be challenged by its heavy metal (HM) content. This study aimed to explore the association of seafood consumption and its estimated HM contents with the lipid profile and lipid oxidation biomarkers in adults from a Spanish Mediterranean area who do not present risk factors for CVD. In this cross-sectional study, the clinical history, three-day dietary record, lipid profile (LDLc, HDLc, APOB/A, and triglyceride levels), plasma oxidised LDL (oxLDL) and 8-isoprostane levels of 81 adults without risk factors for CVD [43% men, with a mean age of 43.6 years (95%CI: 40.1-47.1)] were assessed. The HM [arsenic (As), cadmium (Cd), mercury (Hg), and lead (Pb)] contents of seafood were estimated according to data from analyses of marine species in the same Mediterranean area. Moderate adherence to the Mediterranean diet (score: 4.6 of 9) with a mean seafood consumption of 74.9g/day (95%CI: 59.9-89.9), including 22.7g of shellfish per day (95%CI: 13.5-31.9), was observed. The estimated HM contents were lower than the provisional tolerable weekly intakes (PTWIs): 21.12µg/kg/week As, 0.57µg/kg/week InAs, 0.15µg/kg/week Cd, 1.11µg/kg/week Hg and 0.28µg/kg/week Pb. After adjusting by confounder variables, an increase in shellfish consumption was associated with increases in the levels of LDLc (P=0.013), non-HDLc (P=0.015), APOB/A (P=0.02) and plasma oxLDL (P=0.002). Moreover, an increase in the estimated As and Hg levels in shellfish was associated with an increase in LDLc (P=0.015 and P=0.018, respectively), non-HDLc (P<0.008 and P<0.008, respectively), APOB/A ratio (P=0.008 and P=0.009, respectively), and oxLDL (P≤0.001 and P≤0.001, respectively) levels. In conclusion, in adults without risk factors for CVD, increasing shellfish consumption, even by a moderate amount, could favour a pro-atherogenic lipid profile and a higher level of oxidised LDL. These associations are likely influenced by the estimated exposure to As and Hg from shellfish despite these values are lower than the PTWIs.


Subject(s)
Arsenic/analysis , Food Contamination/analysis , Lipids/blood , Metals, Heavy/analysis , Seafood/analysis , Water Pollutants, Chemical/analysis , Adult , Cross-Sectional Studies , Diet , Exercise , Female , Humans , Male , Middle Aged , Oxidative Stress , Spain
2.
J Pharm Biomed Anal ; 51(2): 382-90, 2010 Jan 20.
Article in English | MEDLINE | ID: mdl-19410411

ABSTRACT

The use of high throughput techniques to find differences in gene expression profiles between related samples (transcriptomics) that underlie changes in physiological states can be applied in medicine, drug development and nutrition. Transcriptomics can be used to provide novel biomarkers of a future pathologic state and to study how bioactive food compounds or drugs can modulate them in the early stages. In this study, we examine the expression pattern in order to determine the effect of the pathological-inflammatory state on the RAW 264.7 cell model and to ascertain how isoflavones and their active functional metabolites alleviate the inflammatory burst and the extent of gene modulation due to the presence of polyphenols. Results demonstrated that genistein (20 microM) and equol (10 microM) significantly inhibited the overproduction of NO and PGE(2) induced by LPS plus INF-gamma when a pre-treatment was performed or when administered during activation. Daidzein, however, did not exert similar effects. Moreover, both isoflavone treatments regulated gene transcription of cytokines and inflammatory markers, among others. The transcriptomic changes provide clues firstly into defining a differential expression profile in inflammation in order to select putative biomarkers of the inflammatory process, and secondly into understanding the isoflavone action mechanism at the transcriptional level. In conclusion, isoflavone modulates the inflammatory response in activated macrophages by inhibiting NO and PGE(2) and by modulating the expression of key genes defined by transcriptomic profiling.


Subject(s)
Gene Expression Profiling , Inflammation , Isoflavones , Macrophages/drug effects , Macrophages/metabolism , Animals , Biomarkers/metabolism , Cell Line , Cell Survival/drug effects , Dinoprostone/analysis , Dinoprostone/metabolism , Dose-Response Relationship, Drug , Gene Expression/drug effects , Inflammation/genetics , Inflammation/immunology , Inflammation/metabolism , Interferon-gamma/pharmacology , Isoflavones/genetics , Isoflavones/immunology , Isoflavones/pharmacology , Lipopolysaccharides/pharmacology , Macrophage Activation/drug effects , Macrophages/immunology , Mice , Molecular Structure , Nitrites/analysis , Nitrites/metabolism , Time Factors
3.
FEMS Microbiol Lett ; 135(2-3): 327-32, 1996 Jan 15.
Article in English | MEDLINE | ID: mdl-8595874

ABSTRACT

High hexokinase activity was not related to glucose repression in Candida utilis IGC 3092. The addition of Cibacron Blue 3G-A to growing cells in batch culture led to a permanent in vivo hexokinase inactivation, decreased growth rate and inhibited alcohol dehydrogenase. Hexokinase inactivation up to 90% did not alleviate glucose repression of alpha-glucosidase, as has been described for Saccharomyces cerevisiae and other yeasts. Moreover, when cells were physiologically derepressed by growing them in a chemostat at low glucose concentrations, the highest hexokinase activity was shown by the derepressed cells, and decreased as repression increased. Thus, in our strain of C. utilis, hexokinase activity was inversely proportional to glucose repression.


Subject(s)
Candida/enzymology , Glucose/metabolism , Hexokinase/antagonists & inhibitors , Candida/metabolism , Enzyme Induction , Enzyme Inhibitors/pharmacology , Enzyme Repression , Glucosidases/metabolism , Hexokinase/biosynthesis , Maltose/metabolism , Oxygen Consumption , Triazines/pharmacology
5.
Ann Hum Genet ; 58(3): 265-73, 1994 07.
Article in English | MEDLINE | ID: mdl-7872649

ABSTRACT

The absence in South American aboriginals of an Asian-specific marker, a 9-bp deletion between the genes for the second subunit of cytochrome oxidase II and lysine transfer RNA in region V, has been interpreted as a bottlenecking effect at the Isthmus of Panama during the peopling of the Americas. We screened mitochondrial DNA (mtDNA) for this 9-bp tandem repeat and for polymorphisms in specific regions of the mtDNA in 2 ancient and 31 contemporary samples from South American aboriginals. We found additional (mtDNA) diversity in South American aboriginals in three ways. First, an Asian-specific marker not previously reported in South American aboriginals was identified by a sequencing analysis in both the contemporary Andean and Amazonian aboriginal peoples. Second, two new haplotypes so far unique to South American aboriginals were found. Additionally, we show that South American aboriginals fall into discrete populations. These results suggest that the prehistoric colonization of South America is the outcome of multiple migrations; the data do not support a bottlenecking effect at the Isthmus of Panama.


Subject(s)
Asian People/genetics , DNA, Mitochondrial/genetics , Indians, South American/genetics , Adult , Base Sequence , Biological Evolution , Bolivia , Child , Colombia , Female , Genetic Markers , Haplotypes , Humans , Male , Molecular Sequence Data , Mummies , Peru , Polymorphism, Restriction Fragment Length , Repetitive Sequences, Nucleic Acid
7.
Rev. bras. genét ; 10(2): 247-51, jun. 1987. tab
Article in English | LILACS | ID: lil-42138

ABSTRACT

As prevalências dos alelos dos sistemas da glicose-6-fosfato desidrogenase (G6PD), hemoglobina (Hb), ABO, Rh e haptoglobina (Hb) foram investigadas em duas populaçöes colombianas miscigenadas de origem predominantemente indígena (da tribo Noanama) e africana. Entre os negróides os marcadores para G6PD, Rh e Hp mostraram as freqüências esperadas, mas os valores relativamente altos encontrados para Hb*C (0,057) e ABO*O (0,853), assim como o baixo para ABO*B (0,046), devem ser enfatizados. Os resultados relativos à hemoglobina podem ser explicados por imigraçäo de pessoas de áreas com altas prevalências de Hb*C na Africa, ou sobrevivência diferencial de portadores deste gene na Colombia; enquanto os achados no ABO podem refletir mistura com Ameríndios. A presença de um indivíduo deficiente para G6PD, assim como a ocorrência de Hb*C (0,106), ABO*A (0,260) e ABO*B (0,027) entre aqueles classificados como Ameríndios sugere nível alto de mistura, mas a ausência de Rh (-) entre eles está de acordo com o esperado. O número de tipagens para haptoglobina realizadas neste grupo foi baixo; a freqüência observada de Hp*1 (0,700) é similar à encontrada em índios sul-americanos em geral, mas difere da prevalência observada em um estudo prévio de índios Noanama


Subject(s)
Humans , Glucosephosphate Dehydrogenase/genetics , Hemoglobins/genetics , Indians, South American , Polymorphism, Genetic , ABO Blood-Group System/genetics , Colombia
8.
Theor Appl Genet ; 61(2): 183-91, 1982 Jun.
Article in English | MEDLINE | ID: mdl-24270342

ABSTRACT

Through a series of genetic load studies made on 1) samples of Drosophila willistoni from two sites in Mesitas, Colombia, it was found that the relative contributions to the total, subvital and lethal loads reflect lethal equivalences (B/A) ratios which support more the balancing theory of population structure than the neutralist theory. Moreover, measurements of population size have revealed the existance of very small demes in local populations. Under such conditions we have calculated extremely small lethal equivalence ratios in demes where probably a great deal of consanguinity takes place. We are aware that under these conditions B/A ratios cannot be very good monitors of random load measurements and, therefore, suggest a change in the mathematical formulation that take into consideration the existance of small populations.Furthermore, it appears plausible that the degree of penetrance in the heterozygous condition changes as the population structure changes. We speculate that natural populations may have unknown selective mechanisms capable of guiding unknown dominance modifiers according to the intensity of selection.

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