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1.
Molecules ; 27(11)2022 May 31.
Article in English | MEDLINE | ID: mdl-35684493

ABSTRACT

In this study, conditions for the ultrasound-assisted extraction (UAE) of soluble polyphenols from Psidium cattleianum (PC) leaves were optimized using response surface methodology (RSM) by assessing the effect of extraction time (XET = 2, 4, and 6 min), sonication amplitude (XSA = 60, 80, and 100%), and pulse cycle (XPC = 0.4, 0.7, and 1 s). Furthermore, the optimized UAE conditions were compared with a conventional aqueous-organic extraction (AOE) method for extracting total phenolics; moreover, a phenolic profile using HPLC and antioxidant activity (DPPH, ABTS, and FRAP) were also compared. According to the RSM, the best conditions for UAE to extract the highest soluble polyphenol content and yield (158.18 mg/g dry matter [DM] and 15.81%) include a 100% sonication amplitude for 4 min at 0.6 s of pulse cycle. The optimal UAE conditions exhibited an effectiveness of 1.71 times in comparison to the AOE method for extracting total phenolics, in 96.66% less time; moreover, PC leaf extracts by UAE showed higher antioxidant values than AOE. Additionally, gallic, protocateic, chlorogenic, caffeic, coumaric, trans-cinnamic, 4-hydroxybenzoic, and syringic acids, as well as kaempferol were identified in PC leaves under UAE. PC leaf extracts are widely used for therapeutic and other industrial purposes; thus, the UAE proves to be a useful technology with which to improve the yield extraction of PC leaf phytochemicals.


Subject(s)
Psidium , Antioxidants , Phenols/chemistry , Plant Extracts/chemistry , Polyphenols
2.
Pharmaceuticals (Basel) ; 15(4)2022 Apr 12.
Article in English | MEDLINE | ID: mdl-35455462

ABSTRACT

Hibiscus sabdariffa Linn. Malvaceae (HS) is characterized by its edible calyxes. The HS calyxes are widely used for cosmetic, food, and medicinal applications. According to ethnobotanical evidence, decoction, infusion, or maceration extracts from HS calyxes have been used in folk medicine to treat many ailments. Moreover, several in vitro and in vivo studies have demonstrated the pharmacological properties and potential human health benefits of HS consumption. On the other hand, the evaluation of the physiological effects and health benefits of HS in clinical studies is most challenging. Therefore, this narrative review summarizes and discusses the physiological effects and health benefits of HS calyxes reported in clinical trials. Preparations obtained from HS calyxes (extracts, infusions, decoction, teas, beverages, capsules, and pills) are used as non-pharmacological therapies to prevent/control diverse chronic non-communicable diseases. The most-reported HS health benefits are its antihypertensive, antidyslipidemic, hypoglycemic, body fat mass reduction, nephroprotective, antianemic, antioxidant, anti-inflammatory, and anti-xerostomic activities; these effects are associated with the phytochemicals found in HS. Moreover, no adverse effects were reported during the clinical trials. However, clinical studies exhibited some limitations; thus, further studies are required to validate the clinical efficacy of HS in large-scale studies with higher doses and a good experimental design.

3.
Article in Spanish | IBECS | ID: ibc-220358

ABSTRACT

Las personas con Trastornos del Espectro Autista (TEA) representan una población heterogénea connecesidades diversas que han sido desatendidas durante la crisis provocada por el COVID-19. En este trabajose describe la intervención virtual realizada durante el confinamiento con un niño de cuatro años diagnosticadocon TEA y se hace una crítica de las carencias que el sistema sanitario tiene para proteger a este colectivo en situaciones de emergencia.(AU)


Peoplewith Autism Spectrum Disorders (ASD) represent a heterogeneous population with diverse needs that havebeen neglected during the COVID-19 crisis. This paper describes the virtual intervention carried out during theconfinement of a four-year-old boy diagnosed with ASD and criticises the shortcomings of the health system inprotecting this group in emergencies.(AU)


Les persones amb trastorns de l'espectre autista (TEA) representen una població heterogènia amb neces-sitats diverses que han estat desateses durant la crisi provocada per la COVID-19. En aquest treball es descriula intervenció virtual realitzada durant el confinament amb un nen de quatre anys diagnosticat amb TEA i es fauna crítica de les mancances que el sistema sanitari té per protegir aquest col·lectiu en situacions d'emergència.(AU)


Subject(s)
Humans , Male , Female , Child , Pandemics , Coronavirus Infections/epidemiology , Autism Spectrum Disorder , Psychotherapy , Child Health , Medical Chaperones
4.
Article in Spanish | IBECS | ID: ibc-202163

ABSTRACT

En este tra­bajo se describe el caso de una adolescente de 13 años que experimentaba conflictos relativos a la identidad de género y la orientación sexual. Desde la perspectiva psicoanalítica se exploran las variables biográficas que pudieron haber influido en la aparición de este malestar y se profundiza en la relación entre este tipo de conflic­tos durante la adolescencia y el auge de identidades que se desmarcan del binarismo heteronormativo


This paper describes the case of a 13-year-old adolescent girl who experienced conflicts related to gender identity and sexual orientation. From a psychoanalytic perspective, we explore the biographical variables that may have influenced the appea­rance of this discomfort; we examine the relationship between this type of conflict during adolescence and the rise of identities that break away from the heteronormative binarism


En aquest treball, es descriu el cas d'una adolescent de 13 anys que experimentava conflictes relatius a la identitat de gènere I l'orientació sexual. Des de la perspectiva psicoanalítica, s'exploren les variables biogràfiques que podrien ha­ver influït en l'aparició d'aquest malestar I s'aprofundeix en la relació entre aquest tipus de conflicte durant l'adolescència I l'auge d'identitats que es desmarquen del binarisme heteronormatiu


Subject(s)
Humans , Female , Adolescent , Sexual Behavior/psychology , Gender Identity , Adolescent Behavior/psychology , Psychoanalytic Therapy/methods , Psychoanalysis , Conflict, Psychological
5.
Mol Biol Rep ; 48(2): 1193-1204, 2021 Feb.
Article in English | MEDLINE | ID: mdl-33611779

ABSTRACT

The frailty syndrome is a common clinical marker of vulnerability in older adults conducive to an overall decline in inflammatory stress responsiveness; yet little is known about the genetic risk factors for frailty in elderly. Our aim was to investigate the association between the rs2476601 polymorphism in PTPN22 gene and susceptibility to frailty in Mexican older adults. Data included 630 subjects 70 and older from The Coyoacán cohort, classified as frail, pre-frail, and non-frail following Fried's criteria. Sociodemographic and clinical characteristics were compared between groups at baseline and after a multivariate analysis. The rs2476601 polymorphism was genotyped by TaqMan genotyping assay using real-time PCR and genotype frequencies were determined for each frailty phenotype in all participants and subsets by age range. Genetic association was examined using stratified and interaction analyses adjusting for age, sex and variables selected in the multivariate analysis. Disability for day-life activities, depression and cognitive impairment were associated with the risk of pre-frailty and frailty at baseline and after adjustment. Carrying the T allele increased significantly the risk of frailty in patients 76 and older (OR 5.64, 95% CI 4.112-7.165) and decreased the risk of pre-frailty under no clinical signs of depression (OR 0.53; 95% CI 0.17-1.71). The PTPN22 polymorphism, rs2476601, could be a genetic risk factor for frailty as subject to quality of life. This is the first study analyzing such relationship in Mexican older adults. Confirming these findings requires additional association studies on wider age ranges in populations of older adults with frailty syndrome.


Subject(s)
Frailty/genetics , Genetic Association Studies , Genetic Predisposition to Disease , Protein Tyrosine Phosphatase, Non-Receptor Type 22/genetics , Aged , Aged, 80 and over , Alleles , Cohort Studies , Female , Frail Elderly , Frailty/physiopathology , Genotype , Humans , Male , Mexico/epidemiology , Phenotype , Polymorphism, Single Nucleotide/genetics , Quality of Life
6.
Genome Announc ; 5(11)2017 Mar 16.
Article in English | MEDLINE | ID: mdl-28302777

ABSTRACT

The whole-genome sequences of three strains of Rhizobium gallicum reported here support the concept that the distinct nodulation host ranges displayed by the symbiovars gallicum and phaseoli can be largely explained by different symbiotic plasmids.

7.
Gen Comp Endocrinol ; 234: 47-56, 2016 08 01.
Article in English | MEDLINE | ID: mdl-27174747

ABSTRACT

It is known that growth hormone (GH) and its receptor (GHR) are expressed in granulosa cells (GC) and thecal cells during the follicular development in the hen ovary, which suggests GH is involved in autocrine/paracrine actions in the female reproductive system. In this work, we show that the knockdown of local ovarian GH with a specific cGH siRNA in GC cultures significantly decreased both cGH mRNA expression and GH secretion to the media, and also reduced their proliferative rate. Thus, we analyzed the effect of ovarian GH and recombinant chicken GH (rcGH) on the proliferation of pre-hierarchical GCs in primary cultures. Incubation of GCs with either rcGH or conditioned media, containing predominantly a 15-kDa GH isoform, showed that both significantly increased proliferation as determined by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, proliferating cell nuclear antigen (PCNA) quantification and ((3)H)-thymidine incorporation ((3)H-T) assays in a dose response fashion. Both, locally produced GH and rcGH also induced the phosphorylation of Erk1/2 in GC cultures. Furthermore, GH increased IGF-I synthesis and its release into the GC culture incubation media. These results suggest that GH may act through local IGF-I to induce GC proliferation, since IGF-I immunoneutralization completely abolished the GH-induced proliferative effect. These data suggest that GH and IGF-I may play a role as autocrine/paracrine regulators during the follicular development in the hen ovary at the pre-hierarchical stage.


Subject(s)
Gonadal Hormones/metabolism , Granulosa Cells/metabolism , Growth Hormone/metabolism , Insulin-Like Growth Factor I/metabolism , Ovary/metabolism , Animals , Autocrine Communication , Cell Culture Techniques , Cell Proliferation , Chickens , Female , Paracrine Communication
8.
BMC Genet ; 17(1): 68, 2016 05 26.
Article in English | MEDLINE | ID: mdl-27230431

ABSTRACT

BACKGROUND: Genetic variations of the TCF7L2 gene are associated with the development of Type 2 diabetes (T2D). The associated mutations have demonstrated an adaptive role in some human populations, but no studies have determined the impact of evolutionary forces on genetic diversity in indigenous populations from Mexico. Here, we sequenced and analyzed the variation of the TCF7L2 gene in three Amerindian populations and compared the results with whole-exon-sequencing of Mestizo populations from Sigma and the 1000 Genomes Project to assess the roles of selection and recombination in diversity. RESULTS: The diversity in the indigenous populations was biased to intronic regions. Most of the variation was low frequency. Only mutations rs77961654 and rs61724286 were located on exon 15. We did not observe variation in intronic region 4-6 in any of the three indigenous populations. In addition, we identified peaks of selective sweeps in the mestizo samples from the Sigma Project within this region. By replicating the analysis of association with T2D between case-controls from the Sigma Project, we determined that T2D was most highly associated with the rs7903146 risk allele and to a lesser extent with the other six variants. All associated markers were located in intronic region 4-6, and their r(2) values of linkage disequilibrium were significantly higher in the Mexican population than in Africans from the 1000 Genomes Project. We observed reticulations in both the haplotypes network analysis from seven marker associates and the neighborNet tree based on 6061 markers in the TCF7L2 gene identified from all samples of the 1000 Genomes Project. Finally, we identified two recombination hotspots in the upstream region and 3' end of the TCF7L2 gene. CONCLUSIONS: The lack of diversity in intronic region 4-6 in Indigenous populations could be an effect of selective sweeps generated by the selection of neighboring rare variants at T2D-associated mutations. The survivors' variants make the intronic region 4-6 the area of the greatest population differentiation within the TCF7L2 gene. The abundance of selective peak sweeps in the downstream region of the TCF7L2 gene suggests that the TCF7L2 gene is part of a region that is in constant recombination between populations.


Subject(s)
Ethnicity/genetics , Introns/genetics , Polymorphism, Genetic , Transcription Factor 7-Like 2 Protein/genetics , Diabetes Mellitus, Type 2/genetics , Exons/genetics , Humans , Mexico/ethnology , Mutation , Recombination, Genetic
9.
Aging Male ; 19(1): 58-63, 2016.
Article in English | MEDLINE | ID: mdl-26555196

ABSTRACT

OBJECTIVE: Since vitamin D is an important regulator of muscle function, the effect of vitamin D deficiency on frailty syndrome has been recently studied. This cross-sectional study aimed to determine the association between 25(OH)-vitamin D levels and frailty status in Mexican community-dwelling elderly. METHODS: Sample of 331 community-dwelling elderly aged 70 or older, a subset of those included in the "Coyoacán cohort" were included. 25(OH)-vitamin D assay and frailty status were measured. RESULTS: Mean age was 79.3 years and 54.1% were women. Those classified as frail were more likely to have lower Mini-Mental State Examination score (p = 0.015), more disability for instrumental activities of daily living (p < 0.001) and for activities of daily living (p < 0.001). Serum 25(OH)-vitamin D levels were lower in the frail subgroup when compared with the non-frail one (p < 0.001). Multivariate logistic regression analyses showed a significant association between intermediate tertile [odds ratios (OR) = 4.13; 95% confidence intervals (CI) 2.00-8.56] or insufficient tertile (OR = 8.95; 95% CI 2.41-33.30) of vitamin D levels and frailty even after adjusting for potential confounders. CONCLUSION: These results suggest that older adults with low 25(OH)-vitamin D levels are associated with the probability to being frail compared with those with sufficient vitamin D levels.


Subject(s)
Frail Elderly/statistics & numerical data , Vitamin D Deficiency/complications , Vitamin D/analogs & derivatives , Activities of Daily Living , Aged , Cross-Sectional Studies , Female , Humans , Independent Living/statistics & numerical data , Male , Mexico/epidemiology , Risk Factors , Vitamin D/blood , Vitamin D Deficiency/blood
10.
Aging Clin Exp Res ; 28(5): 823-32, 2016 Oct.
Article in English | MEDLINE | ID: mdl-26646252

ABSTRACT

Inflammation is a key event that is closely associated with the pathophysiology of frailty. The relationship of genetic polymorphisms into inflammatory cytokines with frailty remains poorly understood. The aim of this study was to investigate the association between VNTR polymorphisms of the IL-4 and IL-1RN genes with the risk of frailty. We included a sample of 630 community-dwelling elderly aged 70 and older. Both IL-4 and IL-1RN VNTR polymorphisms were genotyped by the polymerase chain reaction (PCR) method. Mean age was 77.7 years (SD = 6.0) and 52.5 % were women. The participants classified as frail were more likely to be older, had lower MMSE score (p < 0.001), and had more disability for IADL (p < 0.001) and ADL (p < 0.001). Genotypic and allelic frequencies for the IL-4 VNTR polymorphism did not show significant differences between study groups (p > 0.05). However, we just observed a significant difference in the allelic frequencies for the A2 allele of the IL-1RN VNTR polymorphism between frail and nonfrail groups (OR 1.84, 95 % CI 1.08-3.12, p = 0.02). In addition, we analyzed the combined effect of the IL-4 and IL-1RN VNTR polymorphisms and their possible association with frailty, where the combined IL-4 (low) -IL-1Ra (high) genotype was identified as a marker of risk to frailty syndrome (OR 7.86, 95 % CI 1.83-33.69, p = 0.006). Our results suggest that both A2 allele and the combined IL-4 (low) -IL-1Ra (high) genotype might be genetic markers of susceptibility to frailty in Mexican elderly.


Subject(s)
Frail Elderly/statistics & numerical data , Interleukin 1 Receptor Antagonist Protein/genetics , Interleukin-4/genetics , Minisatellite Repeats/genetics , Aged , Aged, 80 and over , Alleles , Disability Evaluation , Female , Genetic Markers , Genetic Predisposition to Disease , Genotype , Geriatric Assessment/methods , Humans , Independent Living/statistics & numerical data , Male , Mexico/epidemiology , Polymorphism, Genetic
11.
Gen Comp Endocrinol ; 224: 148-59, 2015 Dec 01.
Article in English | MEDLINE | ID: mdl-26231908

ABSTRACT

Growth hormone (GH) is expressed in several extra-pituitary tissues, including the primary and secondary lymphoid organs of the immune system. In birds, GH mRNA and protein expression show a specific developmental distribution pattern in the bursa of Fabricius (BF), particularly in epithelial and B cells. Changes in the bursal concentration and distribution of locally produced GH during ontogeny suggest it is involved in B cell differentiation and maturation, as well as in a functional survival role in this organ, which may be mediated by paracrine/autocrine mechanisms. Here, we analyzed the anti-apoptotic effect of GH in BF and the intracellular signaling pathways involved in this activity. Also, we studied if this effect was exerted directly by GH or mediated indirectly by IGF-I. Bursal cell cultures showed an important loss of their viability after 4h of incubation and a significant increase in apoptosis. However, treatment with 10nM GH or 40 nM IGF-I significantly increased B cell viability (16.7 ± 0.67% and 13.4 ± 1.12%, respectively) when compared with the untreated controls. In addition, the presence of apoptotic bodies (TUNEL) dramatically decreased (5.5-fold) after GH and IGF-I treatments, whereas co-incubation with anti-GH or anti-IGF-I, respectively, blocked their anti-apoptotic effect. Likewise, both GH and IGF-I significantly inhibited caspase-3 activity (by 40 ± 2.0%) in these cultures. However, the use of anti-IGF-I could not reverse the GH anti-apoptotic effects, thus indicating that these were exerted directly. The addition of 100 nM wortmannin (a PI3K/Akt inhibitor) blocked the GH protective effects. Also, GH stimulated (3-fold) the phosphorylation of Akt in bursal cells, and adding wortmannin or an anti-GH antibody inhibited this effect. Furthermore, GH was capable to stimulate (7-fold) the expression of Bcl-2. Taken together, these results indicate that the direct anti-apoptotic activity of GH observed in the chicken bursal B cell cultures might be mediated through the PI3K/Akt pathway.


Subject(s)
Apoptosis/drug effects , Bursa of Fabricius/metabolism , Growth Hormone/pharmacology , Insulin-Like Growth Factor I/metabolism , Phosphatidylinositol 3-Kinases/metabolism , Animals , B-Lymphocytes/cytology , B-Lymphocytes/drug effects , B-Lymphocytes/metabolism , Blotting, Western , Bursa of Fabricius/cytology , Bursa of Fabricius/drug effects , Caspase 3/metabolism , Cells, Cultured , Chickens/metabolism , Enzyme-Linked Immunosorbent Assay , Immunoenzyme Techniques , In Situ Nick-End Labeling , Male , Phosphorylation/drug effects , Signal Transduction/drug effects
12.
Gen Comp Endocrinol ; 190: 182-7, 2013 Sep 01.
Article in English | MEDLINE | ID: mdl-23684966

ABSTRACT

Growth hormone (GH) has several effects on the immune system. Our group has shown that GH is produced in the chicken bursa of Fabricius (BF) where it may act as an autocrine/paracrine modulator that participates in B-cell differentiation and maturation. The time course of GH mRNA and protein expression in the BF suggests that GH may be involved in development and involution of the BF, since GH is known to be present mainly in B lymphocytes and epithelial cells. In addition, as GH is anti-apoptotic in other tissues, we assessed the possibility that GH promotes cell survival in the BF. This work focused on determining the mechanism by which GH can inhibit apoptosis of B cells and if the PI3K/Akt pathway is activated. Bursal cell cultures were treated with a range of GH concentrations (0.1-100nM). The addition of 10nM GH significantly increased viability (16.7±0.6%) compared with the control and decreased caspase-3 activity to 40.6±6.5% of the control. Together, these data indicate that GH is produced locally in the BF and that the presence of exogenous GH in B cell cultures has antiapoptotic effects and increases B cell survival, probably through the PI3k/Akt pathway.


Subject(s)
Growth Hormone/metabolism , Animals , B-Lymphocytes/metabolism , Bursa of Fabricius/metabolism , Chickens , Immune System/metabolism , Phosphatidylinositol 3-Kinases/metabolism , Proto-Oncogene Proteins c-akt/metabolism
13.
Gen Comp Endocrinol ; 183: 17-31, 2013 Mar 01.
Article in English | MEDLINE | ID: mdl-23262274

ABSTRACT

Neuroprotection is a mechanism within the central nervous system (CNS) that protects neurons from damage as a result of a severe insult. It is known that growth hormone (GH) is involved in cell survival and may inhibit apoptosis in several cell types, including those of the CNS. Both GH and GH-receptor (GHR) genes are expressed in the cerebellum. Thus, we investigated the possible neuroprotective role of GH in this organ, which is very sensitive to hypoxic/ischemic conditions. Endogenous GH levels increased in the brain and cerebellum (30% and 74%, respectively) of 15-day-old chicken embryos exposed to hypoxia during 24h compared to normoxia. In primary embryonic cerebellar neuron cultures treated under hypoxia (0.5% O(2)) and low glucose (1g/L) conditions (HLG) for 1h, GH levels increased 1.16-fold compared to the control. The addition of 1nM recombinant chicken GH (rcGH) to cultures during HLG increased cell viability (1.7-fold) and the expression of Bcl-2 (1.67-fold); in contrast the caspase-3 activity and the proportion of apoptotic cells decreased (37% and 54.2%, respectively) compared to HLG. rcGH activated the PI3K/Akt pathway both under normoxic and HLG conditions, increasing the proportion of phosphorylated Akt (1.7- and 1.4-fold, respectively). These effects were abolished by wortmannin and by immunoneutralization, indicating that GH acts through this signaling pathway. Furthermore, the 15-kDa GH variant (10nM) significantly increased cell viability and decreased caspase-3 activity during HLG condition. Thus GH may act as a paracrine/autocrine neuroprotective factor that preserves cellular viability and inhibits apoptotic cell death.


Subject(s)
Cerebellum/drug effects , Growth Hormone/pharmacology , Hypoxia-Ischemia, Brain/veterinary , Neuroprotective Agents/pharmacology , Androstadienes/pharmacology , Animals , Apoptosis/drug effects , Cell Survival/drug effects , Cells, Cultured , Cerebellum/metabolism , Cerebellum/pathology , Chick Embryo , Gene Expression Regulation, Developmental/drug effects , Genes, bcl-2/drug effects , Growth Hormone/metabolism , Growth Hormone/physiology , Hypoxia-Ischemia, Brain/drug therapy , Hypoxia-Ischemia, Brain/pathology , Phosphoinositide-3 Kinase Inhibitors , Wortmannin
14.
Syst Appl Microbiol ; 35(6): 353-8, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22858268

ABSTRACT

The taxonomic position of Phaseolus vulgaris rhizobial strains with available sequenced genomes was examined. Phylogenetic analyses with concatenated conserved genomic fragments accounting for over half of each genome showed that Rhizobium strains CIAT 652, Ch24-10 (newly reported genome) and CNPAF 512 constituted a well-supported group independent from Rhizobium etli CFN 42(T). DNA-DNA hybridization results indicated that CIAT 652, Ch24-10 and CNPAF 512 could correspond to R. etli, although the hybridization values were at the borderline that distinguishes different species. In contrast, experimental hybridization results were higher (over 80%) with Rhizobium phaseoli type strain ATCC 14482(T) in congruence to phylogenetic and ANIm analyses. The latter criterion allowed the reclassification of R. etli strains 8C-3 and Brasil5 as R. phaseoli. It was therefore concluded, based on all the evidence, that the CIAT 652, Ch24-10, and CNPAF 512 strains should be reclassified as R. phaseoli in spite of several common features linking them to R. etli. The R. phaseoli and R. etli speciation process seems to be a more recent event than the speciation that has occurred among other sister species, such as R. leguminosarum-R. etli or R. rhizogenes-R. tropici.


Subject(s)
Genome, Bacterial , Rhizobium etli/classification , Rhizobium etli/genetics , DNA, Bacterial/genetics , Databases, Genetic , Genomics/methods , Nucleic Acid Hybridization , Phaseolus/microbiology , Phylogeny
15.
Plasmid ; 68(3): 149-58, 2012 Nov.
Article in English | MEDLINE | ID: mdl-22813963

ABSTRACT

In bacteria, niche adaptation may be determined by mobile extrachromosomal elements. A remarkable characteristic of Rhizobium and Ensifer (Sinorhizobium) but also of Agrobacterium species is that almost half of the genome is contained in several large extrachromosomal replicons (ERs). They encode a plethora of functions, some of them required for bacterial survival, niche adaptation, plasmid transfer or stability. In spite of this, plasmid loss is common in rhizobia upon subculturing. Rhizobial gene-expression studies in plant rhizospheres with novel results from transcriptomic analysis of Rhizobium phaseoli in maize and Phaseolus vulgaris roots highlight the role of ERs in natural niches and allowed the identification of common extrachromosomal genes expressed in association with plant rootlets and the replicons involved.


Subject(s)
Plant Roots/genetics , Plasmids , Rhizobium , Agrobacterium/genetics , Agrobacterium/metabolism , Extrachromosomal Inheritance , Gene Expression Regulation, Bacterial , Molecular Sequence Data , Phaseolus/microbiology , Plasmids/genetics , Plasmids/metabolism , RNA, Ribosomal, 16S , Replicon , Rhizobium/genetics , Rhizobium/metabolism , Rhizosphere , Sequence Analysis, DNA , Sinorhizobium/genetics , Sinorhizobium/metabolism , Zea mays/microbiology
16.
Ginecol Obstet Mex ; 76(6): 319-26, 2008 Jun.
Article in Spanish | MEDLINE | ID: mdl-18800588

ABSTRACT

BACKGROUND: Oxidative stress has been related to several conditions during pregnancy (preeclampsia, abortions and premature rupture of membranes); it causes higher sensitivity of the endothelial blood vessel constriction and aggravates the endothelium dependent vasodilatación. OBJECTIVE: To determine the oxidative stress level and histological changes in preeclamptic women's placenta. PATIENTS AND METHOD: Longitudinal and comparative study. There were included 25 patients referred from second level health units (IMSS, ISSSTE and Hospital General de Zacatecas). To evaluate oxidative stress level, a sample of blood and placenta were obtained during delivery and a second sample was taken during mediate puerperium (10 days). RESULTS: In control group, total lipidic peroxide levels in serum were 135.6 +/- 7.3 nmol of MDA/mL of serum, compared with the group of moderate hypertension, which registered 222.0 +/- 35.15 nmol MDA/mL. Total lipidic peroxides in serum during puerperium for control group were 150.4 +/- 30.8 and 183.3 +/- 18.51 nmol MDA/mL for the group of moderate hypertension. Placental lipoperoxidation for control group was 0.40 +/- 0.03 microg MDNg, and of 0.32 +/- 0.03 microg MDN/g for the group of mild hypertension. Patients of moderate hypertension group showed an increase at 34% on placental lipoperoxidation over control group. Placental histological alterations where characterized by vascular remodeling loss, deposits of proteinaceous material and macrophagic process. CONCLUSION: Total lipidic peroxide levels in serum increases during preeclampsia. Histological changes refer uterus-placental ischemia that, probably, induces the oxidative stress.


Subject(s)
Oxidative Stress , Placenta/pathology , Pre-Eclampsia/metabolism , Pre-Eclampsia/pathology , Adult , Female , Humans , Longitudinal Studies , Pregnancy
18.
Rev. urug. cardiol ; 18(1/3): 20-30, nov. 2003. tab, graf
Article in Spanish | LILACS | ID: lil-364887

ABSTRACT

El rol del sistema nervioso autónomo en la fisiopatología del síncope mediado neurológicamente es trascendental. La respuesta autonómica durante la prueba de inclinación puede ser estudiada con la variabilidad de la frecuencia cardíaca buscando explicar los cambios autonómicos previos al síncope. Objetivos: estudiar la variabilidad de la frecuencia cardíaca en pacientes con síncope recurrente sometidos a una prueba de inclinación. Material y método: analizamos 19 pacientes consecutivos. Se midieron los intervalos RR de los últimos 5 minutos a 0° y a 75° en los pacientes negativos y en los 5 minutos previos al síncope en los positivos. Los intervalos RR se analizaron en el dominio temporal y espectral. También estudiamos el promedio y el desvío estándar de la presión arterial sistólica y diastólica a 75°. Resultados: la edad media fue 26,8±7 años, 78 por ciento eran mujeres. Diez pacientes (grupo 1) tuvieron una respuesta positiva a los 12±5 minutos de iniciada la prueba. Nueve pacientes (grupo 2) no desarrollaron síncope. En ambos grupos se observó un incremento significativo de la frecuencia cardíaca. El desvío estándar de los intervalos RR normales (SDNN) a 75° aumentó significativamente en el grupo l. El desvío estándar de la presión arterial durante la inclinación fue significativamente mayor en los positivos. No encontramos otras diferencias significativas. Conclusiones: los pacientes con síncope mediado neurológicamente mostraron variaciones en el tono autonómico y desarrollaron síncope cuando se incrementó el SDNN. El análisis de la variabilidad de la frecuencia cárdiaca permite conocer en mayor profundidad los cambios autonómicos que ocurren previo al síncope.


Subject(s)
Humans , Adolescent , Adult , Tilt-Table Test , Heart Rate/physiology , Syncope, Vasovagal/physiopathology
19.
Rev. urug. cardiol ; 17(1/3): 50-53, nov. 2002. ilus
Article in Spanish | LILACS | ID: lil-364868

ABSTRACT

La intoxicación digitálica es proarrítmica, pudiendo provocar gran variedad de arritmias. En este trabajo presentamos una arritmia poco común, secundaria a intoxicación digitálica pero con un patrón electrocardiográfico típico, conocida como taquicardia ventricular bidireccional.


Subject(s)
Humans , Female , Aged , Arrhythmias, Cardiac , Tachycardia, Ventricular , Digoxin
20.
Rev. méd. Urug ; 16(2): 160-164, set. 2000. ilus, tab, graf
Article in Spanish | LILACS | ID: lil-301314

ABSTRACT

El cisapride es el fármaco de elección en casos de reflujo gastroesofágico. Dentro de sus efectos colaterales se detalla la prolongación del intervalo QTU. En este artículo describimos un caso de prolongación del QTU probablemente asociado a esta medicación. El uso del cisapride debe ser vigilado, particularmente en grupos de alto riesgo, por lo que se recomienda realizar electrocardiogramas seriados. También deben recordarse los otros fármacos que prolongan el QT que no deben asociarse al cisapride y tampoco combinarse entre sí


Subject(s)
Humans , Female , Aged , Cisapride , Long QT Syndrome/chemically induced , Torsades de Pointes , Drug Monitoring
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