Exercise induction of gut microbiota modifications in obese, non-obese and hypertensive rats

Background: Obesity is a multifactor disease associated with cardiovascular disorders such as hypertension. Recently, gut microbiota was linked to obesity pathogenesisand shown to influence the host metabolism. Moreover, several factors such as host-genotype and life-style have been shown to modulate gut microbiota composition. Exercise is a well-known agent used for the treatment of numerous pathologies, such as obesity and hypertension; it has recently been demonstrated to shape gut microbiota consortia. Since exercise-altered microbiota could possibly improve the treatment of diseases related to dysfunctional microbiota, this study aimed to examine the effect of controlled exercise training on gut microbial composition in Obese rats (n = 3), non-obese Wistar rats (n = 3) and Spontaneously Hypertensive rats (n = 3). Pyrosequencing of 16S rRNA genes from fecal samples collected before and after exercise training was used for this purpose. Results: Exercise altered the composition and diversity of gut bacteria at genus level in all rat lineages. Allobaculum (Hypertensive rats), Pseudomonas and Lactobacillus (Obese rats) were shown to be enriched after exercise, while Streptococcus (Wistar rats), Aggregatibacter and Sutturella (Hypertensive rats) were more enhanced before exercise. A significant correlation was seen in the Clostridiaceae and Bacteroidaceae families and Oscillospira and Ruminococcus genera with blood lactate accumulation. Moreover, Wistar and Hypertensive rats were shown to share a similar microbiota composition, as opposed to Obese rats. Finally, Streptococcus alactolyticus, Bifidobacterium animalis, Ruminococcus gnavus, Aggregatibacter pneumotropica and Bifidobacterium pseudolongum were enriched in Obese rats. Conclusions: These data indicate that non-obese and hypertensive rats harbor a different gut microbiota from obese rats and that exercise training alters gut microbiota from an obese and hypertensive genotype background

Bone mineral density associated with physical traits and lifestyle in adolescents

INTRODUÇÃO: No Brasil, ainda são poucos os estudos que apresentam dados relevantes sobre fatores relacionados às características físicas ou estilo de vida e a densidade mineral óssea (DMO) de adolescentes do sexo feminino. OBJETIVO: Identificar e verificar a contribuição das características físicas e de estilo de vida relacionadas à DMO de adolescentes do sexo feminino. MÉTODOS: A amostra deste estudo foi composta por 329 meninas com idades entre 10 e 20 anos. Como características físicas, foram avaliados: peso corporal, estatura, índice de massa corporal, estágio de maturação sexual, raça e pigmentação cutânea. Já para o estilo de vida, os seguintes fatores foram avaliados: consumo diário de cálcio, nível de atividade física (NAF) e nível socioeconômico (NSE). A densidade mineral óssea (DMO) do corpo inteiro, da coluna lombar e do colo do fêmur foram avaliados pela densitometria óssea. As relações existentes entre variáveis dependentes e independentes foram avaliadas pela correlação de Pearson (r) e regressão múltipla Stepwise (p < 0,05). RESULTADOS: A DMO dos três sítios ósseos tende a aumentar conforme o aumento do peso corporal, estatura, IMC, idade e estágio de maturação sexual (r ≥ 0,43; p < 0,01). Por outro lado, somente o NAF (r = 0,12; p < 0,05) e o NSE (r = 0,14; p < 0,05) correlacionaram-se positivamente com a DMO. O peso corporal, estágio de maturação sexual, idade, consumo de cálcio, NSE e NAF explicaram de 48 a 68% da variação da DMO das adolescentes. CONCLUSÃO: Os resultados sugerem que a utilização de critérios como peso corporal, idade e maturação sexual sejam os mais indicados para controlar as variações da DMO de adolescentes do sexo feminino. Além disso, o NSE, o NAF e o consumo diário de cálcio possuem uma pequena participação na variação da DMO das adolescentes quando comparados com as características físicas.INTRODUCTION: Just a few studies have evaluated physical traits, lifestyle and bone mineral density (BMD) acquisition in Brazilian female adolescents. OBJECTIVE: To identify physical traits and lifestyle factors related to BMD in Brazilian female adolescents. METHODS: 329 healthy adolescent girls aged between 10 and 20 years participated in this study. The physical characteristics evaluated were: body weight, stature, body mass index, pubertal stage, self-declared ethnicity and skin color. Concerning lifestyle, the following factors were evaluated: socioeconomic status (SES), physical activity level (PAL) and daily calcium intake. Additionally, total body, lumbar spine and femoral neck bone mineral density (BMD) was assessed by bone densitometry. Pearson's coefficient of correlation (r) and stepwise regression analysis were employed to check dependent and independent variables correlation (p < 0.05). RESULTS: Total body, lumbar spine and femoral neck BMD increase as body weight, height, BMI, age and pubertal stage increase (r ≥ 0.43; p<0.01). On the other hand, only SES (r = 0.14; p<0.05) and PAL (r = 0.12; p<0.05) were correlated. After stepwise regression, body weight, pubertal stage, age, height, calcium intake, SES, and PAL explained around 48-68% for BMD variation in female adolescents. CONCLUSION: The results suggest body weight, age and pubertal stage should be used as control variables for BMD variations in female adolescents. Furthermore, SES, PAL and dialy calcium intake were less important than physical traits for BMD during adolescence

Association of serum lipid components and obesity with genetic ancestry in an admixed population of elderly women

The prevalence of metabolic disorders varies among ethnic populations and these disorders represent a critical health care issue for elderly women. This study investigated the correlation between genetic ancestry and body composition, metabolic traits and clinical status in a sample of elderly women. Clinical, nutritional and anthropometric data were collected from 176 volunteers. Genetic ancestry was estimated using 23 ancestry-informative markers. Pearsons correlation test was used to examine the relationship between continuous variables and an independent samples t-test was used to compare the means of continuous traits within categorical variables. Overall ancestry was a combination of European (57.49%), Native American (25.78%) and African (16.73%). Significant correlations were found for European ancestry with body mass index (r = 0.165; p = 0.037) and obesity (mean difference (MD) = 5.3%; p = 0.042). African ancestry showed a significant correlation with LDL (r = 0.159, p = 0.035), VLDL (r = -0.185; p = 0.014), hypertriglyceridemia (MD = 6.4%; p = 0.003) and hyperlipidemia (MD = 4.8%; p = 0.026). Amerindian ancestry showed a significant correlation with triglyceride levels (r = 0.150; p = 0.047) and hypertriglyceridemia (MD = 4.5%; p = 0.039). These findings suggest that genetic admixture may influence the etiology of lipid metabolism-related diseases and obesity in elderly women

LL-37 boosts immunosuppressive function of placenta-derived mesenchymal stromal cells

Background: Although promising for graft-versus-host disease (GvHD) treatment, MSC therapy still faces important challenges. For instance, increasing MSC migratory capacity as well as potentializing immune response suppression are of interest. For GvHD management, preventing opportunistic infections is also a valuable strategy, since immunocompromised patients are easy targets for infections. LL-37 is a host defense peptide (HDP) that has been deeply investigated due to its immunomodulatory function. In this scenario, the combination of MSC and LL-37 may result in a robust combination to be clinically used. Methods: In the present study, the effects of LL-37 upon the proliferation and migratory capacity of human placenta-derived MSCs (pMSCs) were assessed by MTT and wound scratch assays. The influence of LL-37 over the immunosuppressive function of pMSCs was then investigated using CFSE cell division kit. Flow cytometry and real-time PCR were used to investigate the molecular mechanisms involved in the effects observed. Results: LL-37 had no detrimental effects over MSC proliferation and viability, as assessed by MTT assay. Moreover, the peptide promoted increased migratory behavior of pMSCs and enhanced their immunomodulatory function over activated human PBMCs. Strikingly, our data shows that LL-37 treatment leads to increased TLR3 levels, as shown by flow cytometry, and to an increased expression of factors classically related to immunosuppression, namely IDO, IL-10, TGF-β, IL-6, and IL-1β. Conclusions: Taken together, our observations may serve as groundwork for the development of new therapeutic strategies based on the combined use of LL-37 and MSCs, which may provide patients not only with an enhanced immunosuppression regime, but also with an agent to prevent opportunistic infections

Association between the igf-2/ApaI polymorphism with the strength and muscle mass in elderly women

A sarcopenia diminui a capacidade funcional do idoso. O gene candidato Fator de Crescimento semelhante à Insulina-2 (IGF-2) tem influência na sarcopenia. Este estudo objetivou investigar a associação entre o polimorfismo ApaI do gene IGF-2 e os fenótipos força e massa muscular. Participaram deste estudo 252 voluntárias (66,94 ± 5,59 anos), as quais tiveram a força muscular mensurada em aparelho isocinético, a composição corporal analisada pelo DEXA e o nível de atividade física determinado pelo IPAQ. O DNA foi extraído e genotipado para o polimorfismo ApaI do gene IGF-2. Foi utilizada uma Anova e uma Ancova para comparar as variáveis (p>0,05). Não houve diferença significante entre as variáveis: idade, massa corporal, estatura, IMC e o percentual de gordura nos três grupos genotípicos. A análise de covariância demonstrou que não ocorreram diferenças significantes entre os grupos com os fenótipos analisados. Portanto, não houve associações significativas entre o polimorfismo ApaI do IGF-2 com a força muscular isocinética e a massa livre de gordura.Sarcopenia reduces functional capacity in elderly people. The candidate gene Insulin Growth Factor (IGF-2) has been suggested to influence on sarcopenia. This study aimed to investigate the association between the IGF-2 / ApaI polymorphism and the phenotypes muscle mass and strength. The study involved 252 subjects (66.94 ± 5.59 years), who underwent muscle strength measurements using an isokinetic dynamometer, and fat-free mass (FFM) assessment using DEXA. Volunteers also answered the IPAQ questionnaire to determine physical activity levels. Statistical procedures included ANOVA and ANCOVA to compare variables (p< 0.05). No significant difference was detected between age, weight, height, BMI and body fat percentage in the three genotype groups. The analysis of covariance evidenced no significant difference between groups regarding the evaluated muscle-related phenotypes. Therefore, there was no significant association between IGF-2 / ApaI polymorphism with isokinetic muscle strength and FFM in this population

Self-Selected Pacing During a World Record Attempt in 40 Ironman-Distance Triathlons in 40 Days

The present case study analyzed performance, pacing, and potential predictors in a self-paced world record attempt of a professional triathlete to finish 40 Ironman-distance triathlons within 40 days. Split times (i.e., swimming, cycling, running) and overall times, body weight, daily highest temperature, wind speed, energy expenditure, mean heart rate, and sleeping time were recorded. Non-linear regressions were applied to investigate changes in split and overall times across days. Multivariate regression analyses were performed to test which variables showed the greatest influence on the dependent variables cycling, running and overall time. The athlete completed the 40×Ironman distances in a total time of 444:22 h:min. He spent 50:26 h:min in swimming, 245:37 h:min in cycling, 137:17 h:min in running and 11:02 h:min in transition times. Swimming and cycling times became slower across days, whereas running times got faster until the 20th day and, thereafter, became slower until the 40th day. Overall times got slower until the 15th day, became faster to 31st, and started then to get slower until the end. Wind speed, previous day's race time and average heart race during cycling were significant independent variables influencing cycling time. Body weight and average heart rate during running were significant independent variables influencing running performance. Cycling performance, running performance, and body weight were significant independent variables influencing overall time. In summary, running time was influenced by body weight, cycling by wind speed, and overall time by both running and cycling performances

Screening fetal losses for monosomy X with a simple PCR-based procedure

To screen for monosomy X in spontaneous fetal losses we explored a simple molecular strategy based on loss of heterozygosity at highly polymorphic X-linked loci. We developed a multiplex fluorescent procedure that allows the simultaneous amplification of five dinucleotide repeat polymorphisms in a large low-recombination region in the long arm of the X chromosome. Analysis was performed by computer-assisted laser densitometry. We did not find any instances of homozygosity at all five loci in 30 normal females tested, nor among 37 women whose typing data were retrieved from the Fondation Jean Dausset - CEPH genotype database. In addition, all cases of monosomy X previously diagnosed by conventional cytogenetics presented the anticipated loss of heterozygosity at all loci. We studied 19 spontaneously aborted female fetuses and we found four samples homozygous for the five loci (21%), in good agreement with the expected rate of monosomy X in first trimester spontaneous abortions. We conclude that the loci have high diversity and high efficiency in PCR-amplification and that our multiplex procedure constitutes a simple and useful molecular screening test for monosomy X in abortions and stillbirths