The Effects of an Infant Formula Enriched with Milk Fat Globule Membrane, Long-Chain Polyunsaturated Fatty Acids and Synbiotics on Child Behavior up to 2.5 Years Old: The COGNIS Study.

Although early life nutrition influences brain development and mental health, the long-term effects of supplemented infant formula on children´s behavior remain unclear. We analyzed the effects of a bioactive nutrients-enriched-infant formula on children's behavior up to 2.5 years, compared to a standard infant formula or breastfeeding. Current analysis involved 70 children who were fed a standard infant formula (SF, n = 29) or a bioactive compounds enriched-infant formula (EF, n = 41), during their first 18 months of life, and 33 breastfed (BF) children (reference group) participating in the COGNIS study. Behavioral problems were evaluated using the Child Behavior Checklist at 18 months and 2.5 years. Different statistical analyses were performed using SPSS. EF children aged 2.5 years presented fewer pathological affective problems than SF children. Besides, SF children were classified more frequently as bordering on internalizing problems than BF children. Rates of externalizing problems were increased in SF infants compared to EF and BF infants. Higher maternal IQ was found to have beneficial effects on internalizing and total problem rate in their offspring at 18 months of life; finally, higher maternal educational level was related with fewer ADHD problems in children at 18 months, as well as internalizing, externalizing, total and anxiety problems in children aged 2.5 years. Our analysis suggests that enriched infant formula fed infants seem to show fewer behavioral problems up to 2.5 years compared to a standard infant formula-fed infants. In addition to type of early feeding, maternal IQ and educational level seem to play a key role on children behavioral development.

Identification of dopamine- and serotonin-related genes modulated by bisphenol A in the prefrontal cortex of male rats.

There is concern that exposure of embryos and/or infants to bisphenol A (BPA) may lead to neurological and behavioral disorders with unknown prefrontal cortex (PFC) involvement. Critical PFC functions are modulated by dopamine (DA) and serotonin (5-HT) systems, whose alterations have been associated with psychopathologies that may appear in youth and/or adulthood. This study aims to determine in the PFC of male rats exposed to a low dose of BPA (10µgkg(-1)d(-1)) from gestational day 12 (GD12) to postnatal day 21 (PND21): (i) DA- and 5-HT-related genes modulated by BPA at the juvenile stage (PND21); (ii) reversible and irreversible transcriptional effects; (iii) long-term consequences (effects in adult rats, PND90). In juvenile rats, BPA altered significantly the transcription of 12 out of the 84 genes analyzed using PCR-array techniques. Interestingly, transcript levels of the neurotrophic factor Gdnf were decrease by BPA in both juvenile and adult rats. At adulthood, disruptions in genes encoding rate-limiting enzymes for DA and 5-HT synthesis emerged. Overall, the results indicate that early-life exposure to BPA has consequences on DA and 5-HT systems in both juvenile- and adult-life stages. Additionally, we reveal molecular targets that could provide the foundation for future BPA neurotoxicity studies.

Predicting Maximal Dynamic Strength From the Load-Velocity Relationship in Squat Exercise.

The aim of this study was to develop a rapid indirect method to determine an individual's maximal strength or 1 repetition maximum (RM) in untrained subjects during half-squat exercise. One hundred and five physically active young subjects (87 men and 18 women) performed a submaximal and a maximal load test during half-squat exercises on a Smith machine. In the submaximal test, subjects completed 3 repetitions with a load equivalent to body weight. The velocity and power of barbell displacement were recorded during the upward movement from 90° of knee flexion. All repetitions were performed at maximum velocity. In a subsequent 1-2RM test, the 1RM for the exercise was calculated. The variables' load and mean velocity (V(mean)) were used to construct an adjusted 1RM prediction model, which was capable of estimating the 1RM with an accuracy of 58% (F(exp) = 72.82; 2; 102 df; p ≤ 0.001). Our results indicate a good correlation between the mean displacement velocity of a load equivalent to body weight and 1RM. This relationship enables a safe and fast estimation of 1RM values in half-squat exercise (1RM = -61.93 + [121.92·V(mean)] + [1.74·load]) and provides valuable information to untrained subjects who are starting resistance training programs.

HLA class I & II alleles in multiple sclerosis patients from Puerto Rico.

Multiple Sclerosis (MS) is a complex disease where genetic and environmental factors have been implicated. The onset of symptoms occurs in individuals from twenty to fifty years of age, producing a progressive impairment of motor, sensory and cognitive functions. MS is more frequent in females than in males with a ratio of 4:1. The prevalence of the MS varies among ethnics groups such as Europeans, Africans and Caucasians. The estimated prevalence of MS in Puerto Rico is 42 for each 100,000 habitants, which is more than the prevalence reported for Central America and the Caribbean. In spite of this prevalence, the genetic component of MS has not been explored in order to know the alleles' expression of Puerto Rican MS patients and compare it with the allele expression in other ethnic groups. Thirty-five patients and 31 control subjects were genotyped. The allele frequencies expressed in this sample were similar to those expressed for Puerto Ricans in the National Marrow Donor Program Registry (n = 3,149). The most prevalent alleles for MS patients were HLA-DRB1*01 and *03. HLA-DQB1*04 was the most frequent in the control group and HLA-A*30, in MS patients. These findings are in agreement with published data. HLA-DQB1*04 was a marginal protector in this sample and this role has not been described before. The accuracy of the results is limited due to the sample size. After performing a statistical power analysis it showed that by increasing the sample the values would be significant.

The effect of acute moderate hypoxia on accumulated oxygen deficit during intermittent exercise in nonacclimatized men.

The objective of this study was to determine the effect of acute moderate hypoxia and rest duration on performance and on the accumulated oxygen deficit (AOD) in high-intensity intermittent efforts. After preliminary tests, 2 groups of nonacclimatized men (resident at 690 m above sea level) carried out 3 randomized protocols of effort (EXP1, EXP2, and EXP5) on 3 different days. These tests were performed at acute moderate altitude (2,320 m) by the hypoxia group (H) and in normoxia by the normoxia group (N). During EXP1 the subjects ran a maximum of five 400-m sprints (90% intensity) on a treadmill, with a pause between efforts of 1 minute. In EXP2 and EXP5 the same protocol was repeated, increasing the rest period between sprints to 2 and 5 minutes, respectively. Lactate accumulation and exhaled gases were measured during the tests. Accumulated oxygen deficit was calculated for each sprint. The total AOD (SigmaAOD) for each type of protocol was determined to be the sum of the corresponding accumulated deficits. The AODs were influenced by the length of rest period (p < 0.05) but not by H. The increase in recovery time between sprints increased the SigmaAOD (7,843 +/- 4,435 vs. 7,137 +/- 2,117 ml; 11,013 +/- 4,616 vs. 9,931 +/- 2,731 ml; 12,611 +/- 4,594 vs. 12,907 +/- 3,085 ml for H and N in EXP1, EXP2, and EXP5, respectively). The AOD increased in value when the same sprint was compared from EXP1 to EXP5 (p < 0.05). The results obtained show that exposure to acute moderate altitude does not affect the anaerobic pathway contribution in intermittent high-intensity exercises. Performance during this type of repeated effort is not altered during acute exposure to moderate altitude, which should be taken into account when an acclimatizing period is not possible.

Production of monoclonal antibodies to Sp 2/0-AG14 myeloma cells

La técnica de hibridomas, desarrollada por Kohler y Milstein, permite la obtención de anticuerpos de especificidad única (p.e. anticuerpos monoclonales). Esta metododlogía fue introducida en el Laboratorio de Immunología del Departamento de Microbiología de la Escuela de Medicina, Recinto de Ciencias Médicas, UPR en 1986. La producción de anticuerpos monoclonales contra Sp2/0-Ag 14 que aquí se reporta, describe la metodología utilizada y es de importancia porque constituye el primer trabajo sobre anticuerpos monoclonales realizado en el Recinto de Ciencias Médicas y en Puerto Rico