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John J Mcgrath - One of the best experts on this subject based on the ideXlab platform.
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maternal age and paternal age are associated with distinct childhood behavioural outcomes in a general population birth cohort
2009Co-Authors: Sukanta Saha, Adrian G Barnett, Stephen L Buka, John J McgrathAbstract:Abstract Background Recent studies show that advanced paternal age (APA) is associated with an increased risk of neurodevelopmental disorders such as autism, bipolar disorder and schizophrenia. A body of evidence also suggests that individuals who develop schizophrenia show subtle deviations in a range of behavioural domains during their childhood. The aim of the study was to examine the relationship between paternal and maternal ages and selected behavioural measures in children using a large birth cohort. Method Participants were singleton children (n = 21,753) drawn from the US Collaborative Perinatal Project. The outcome measures were assessed at 7 years. The main analyses examined the relationship between parental age and behavioural measures when adjusted for a range of potentially confounding variables, including age of the other parent, maternal race, socio-economic measures, sex, gestation length, maternal marital status, parental mental illness, and child's age-at-testing. Results Advanced paternal age was associated with a significantly increased risk of adverse ‘externalizing’ behaviours at age seven years. For every five year increase in paternal age, the odds of higher ‘externalizing’ behaviours was increased by 12% (OR = 1.12; 95% CI = 1.03, 1.21, p < 0.0001). The relationship persisted after adjusting for potential confounding factors. ‘Internalizing’ behavioural outcome was not associated with advanced paternal age. In contrast, advanced maternal age was significantly protective against adverse ‘externalizing’ behavioural outcomes, but associated with an increased risk of adverse ‘internalizing’ behavioural outcomes. Discussion The offspring of older fathers show a distinctly different pattern of behaviours compared to the offspring of older mothers. The diverse socio-cultural and biologically-mediated factors that underpin these findings remain to be clarified. In light of secular trends related to delayed parenthood, the mechanisms underlying these findings warrant closer scrutiny.
G C Perry - One of the best experts on this subject based on the ideXlab platform.
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a model for predicting the age at sexual maturity for growing pullets of layer strains given a single change in photoperiod
2002Co-Authors: P. D. Lewis, T. R. Morris, G C PerryAbstract:A model is presented which will predict mean age at first egg (AFE) for pullets of laying strains reared under non-limiting environmental conditions but exposed to a single change in photoperiod during the rearing stage. An initial analysis of 12 previously reported trials involving a wide range of genotypes showed that the response to an increase in photoperiod is not simply the inverse of the response to an equal decrease in photoperiod applied at the same age. Maximum sensitivity to a reduction in photoperiod was found shortly before onset of lay, whereas maximum sensitivity to an increment in photoperiod was observed at around 10 weeks of age. Two experiments were conducted to provide further data. The first compared the effect of 3-h increases in photoperiod from 8 h to 11 h or from 11 h to 14 h with the double increment from 8 h to 14 h and also tested a reduction from 11 h to 8 h, all imposed at 17 weeks of age. AFE was advanced to a similar extent by the changes from 8 to 11 h and from 11 to 14 h (9.8 and 10.9 days respectively). Response to the double increment was not additive: AFE on this treatment was 13.3 days earlier than for constant 8 h controls. Reduction in photoperiod from 11 to 8 h at 17 weeks delayed AFE by 18.7 days compared with constant 11-h controls. In the second experiment, pullets of two strains were transferred from 8 to 16-h photoperiods and from 16 to 8 h at 5, 7, 9, 15, 17 and 19 weeks of age. Controls were kept on constant 8 and constant 16-h days. Transfer from 8 to 16-h photoperiods at 5 weeks of age had no effect on AFE. At 7 weeks there was a bimodal response with some pullets subsequently showing advanced maturity and others not. Maximum stimulation of early maturity (31 days on average for the two genotypes) was obtained at 9 weeks of age and response to stimulation declined linearly with age thereafter. The delay in AFE resulting from a reduction in photoperiod (16 to 8 h) increased linearly between 0 and 15 weeks. At 17 and 19 weeks, the response was bimodal, with some pullets maturing at the same age as long-day controls and others showing delayed maturity. Using all this evidence and some other unpublished data, a model is developed to predict AFE as a function of mean photoperiod and change in photoperiod during the rearing phase. Elements are incorporated to allow for the insensitivity of pullets younger than 50 days to an increase in photoperiod and the effect observed late in rearing when a change in photoperiod comes too late to alter AFE for the most precocious individuals in a flock. Two coefficients are required to adjust for genotype. One describes mean AFE for the genotype when reared on constant daylength and the other defines the rate at which age effects the response to a single change in photoperiod.
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a model for predicting the age at sexual maturity for growing pullets of layer strains given a single change in photoperiod
2002Co-Authors: P. D. Lewis, T. R. Morris, G C PerryAbstract:A model is presented which will predict mean age at first egg (AFE) for pullets of laying strains reared under non-limiting environmental conditions but exposed to a single change in photoperiod during the rearing stage. An initial analysis of 12 previously reported trials involving a wide range of genotypes showed that the response to an increase in photoperiod is not simply the inverse of the response to an equal decrease in photoperiod applied at the same age. Maximum sensitivity to a reduction in photoperiod was found shortly before onset of lay, whereas maximum sensitivity to an increment in photoperiod was observed at around 10 weeks of age. Two experiments were conducted to provide further data. The first compared the effect of 3-h increases in photoperiod from 8 h to 11 h or from 11 h to 14 h with the double increment from 8 h to 14 h and also tested a reduction from 11 h to 8 h, all imposed at 17 weeks of age. AFE was advanced to a similar extent by the changes from 8 to 11 h and from 11 to 14 h (9.8 and 10.9 days respectively). Response to the double increment was not additive: AFE on this treatment was 13.3 days earlier than for constant 8 h controls. Reduction in photoperiod from 11 to 8 h at 17 weeks delayed AFE by 18.7 days compared with constant 11-h controls. In the second experiment, pullets of two strains were transferred from 8 to 16-h photoperiods and from 16 to 8 h at 5, 7, 9, 15, 17 and 19 weeks of age. Controls were kept on constant 8 and constant 16-h days. Transfer from 8 to 16-h photoperiods at 5 weeks of age had no effect on AFE. At 7 weeks there was a bimodal response with some pullets subsequently showing advanced maturity and others not. Maximum stimulation of early maturity (31 days on average for the two genotypes) was obtained at 9 weeks of age and response to stimulation declined linearly with age thereafter. The delay in AFE resulting from a reduction in photoperiod (16 to 8 h) increased linearly between 0 and 15 weeks. At 17 and 19 weeks, the response was bimodal, with some pullets maturing at the same age as long-day controls and others showing delayed maturity. Using all this evidence and some other unpublished data, a model is developed to predict AFE as a function of mean photoperiod and change in photoperiod during the rearing phase. Elements are incorporated to allow for the insensitivity of pullets younger than 50 days to an increase in photoperiod and the effect observed late in rearing when a change in photoperiod comes too late to alter AFE for the most precocious individuals in a flock. Two coefficients are required to adjust for genotype. One describes mean AFE for the genotype when reared on constant daylength and the other defines the rate at which age effects the response to a single change in photoperiod.
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effect of constant and of changing photoperiods on age at first egg and related traits in pullets
1996Co-Authors: P. D. Lewis, G C Perry, T. R. MorrisAbstract:Abstract 1. The effects of constant photoperiods and of single (5 h) changes in photoperiod applied at 12 or 17 weeks of age upon age at first egg (AFE) were studied using ISA Brown and Shaver 288 pullets. 2. Birds reared from 2 d of age until after maturity on constant 10 h photoperiods matured 8 d earlier than birds reared on constant 8 h and 5 d earlier than the average for 13 or 18 h photoperiods. 3. A single increment in photoperiod from 8 to 13 h advanced AFE by 23 d (compared to 8 h constant day controls) when applied at 84 d, but by only 6 d when given at 119 d. An increase in photoperiod from 13 to 18 h advanced AFE by only 4 d, averaged across breeds and age at increase. A reduction in photoperiod from 13 to 8 h delayed AFE by 22 d when given at 84 d and by 16 d at 119 d. A similar 5 h reduction in photoperiod, but from 18 to 13 h, retarded maturity by 11 d in ISA Brown pullets, but only when given at 84 d, and delayed AFE in Shaver 288 by 12 d, but only when given at 119 d. This interaction may...
Kiyoshi Kurokawa - One of the best experts on this subject based on the ideXlab platform.
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angiotensin ii receptor antagonists and angiotensin converting enzyme inhibitors lower in vitro the formation of advanced glycation end products biochemical mechanisms
2002Co-Authors: Toshio Miyata, Charles Van Ypersele De Strihou, Yasuhiko Ueda, Kohji Ichimori, Reiko Inagi, Hiroshi Onogi, Naoyoshi Ishikawa, Masaomi Nangaku, Kiyoshi KurokawaAbstract:ABSTRACT. The implication of advanced glycation end products (AGE) in the pathogenesis of atherosclerosis and of diabetic and uremic complications has stimulated a search for AGE inhibitors. This study evaluates the AGE inhibitory potential of several well-tolerated hypotensive drugs. Olmesartan, an angiotensin II type 1 receptor (AIIR) antagonist, as well as temocaprilat, an angiotensin-converting enzyme (ACE) inhibitor, unlike nifedipine, a calcium blocker, inhibit in vitro the formation of two AGE, pentosidine and N e -carboxymethyllysine (CML), during incubation of nonuremic diabetic, nondiabetic uremic, or diabetic uremic plasma or of BSA fortified with arabinose. This effect is shared by all tested AIIR antagonists and ACE inhibitors. On an equimolar basis, they are more efficient than aminoguanidine or pyridoxamine. Unlike the latter two compounds, they do not trap reactive carbonyl precursors for AGE, but impact on the production of reactive carbonyl precursors for AGE by chelating transition metals and inhibiting various oxidative steps, including carbon-centered and hydroxyl radicals, at both the pre- and post-Amadori steps. Their effect is paralleled by a lowered production of reactive carbonyl precursors. Finally, they do not bind pyridoxal, unlike aminoguanidine. Altogether, this study demonstrates for the first time that widely used hypotensive agents, AIIR antagonists and ACE inhibitors, significantly attenuate AGE production. This study provides a new framework for the assessment of families of AGE-lowering compounds according to their mechanisms of action. E-mail: t-miyata@is.icc.u-tokai.ac.jp
Daniel L. Schacter - One of the best experts on this subject based on the ideXlab platform.
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mind wandering across the age gap age related differences in mind wandering are partially attributable to age related differences in motivation
2020Co-Authors: Paul Seli, Daniel Smilek, Jonathan S. A. Carriere, Roger E Beaty, Kevin Oneill, Daniel L. SchacterAbstract:Objectives A common finding in the mind-wandering literature is that older adults (OAs) tend to mind-wander less frequently than young adults (YAs). Here, we sought to determine whether this age-related difference in mind-wandering is attributable to age-related differences in motivation. Method YAs and OAs completed an attention task during which they responded to thought probes that assessed rates of mind-wandering, and they provided self-reports of task-based motivation before and after completion of the attention task. Results Age-related differences in mind-wandering are partially explained by differences in motivation, and that motivating young adults via incentive diminishes mind-wandering differences across these groups. Discussion We consider these results in the context of theories on age-related differences in mind wandering, with a specific focus on their relevance to the recently proposed motivational account of such age-related differences.
Suzelei Castro França - One of the best experts on this subject based on the ideXlab platform.
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Aqueous extracts from Uncaria tomentosa (Willd. ex Schult.) DC. reduce bronchial hyperresponsiveness and inflammation in a murine model of asthma
2018Co-Authors: Bruna Cestari Azevedo, Lucas Junqueira Freitas Morel, Fábio Carmona, Thiago Mattar Cunha, Silvia Helena Taleb Contini, Piero G. Delprete, Fernando Silva Ramalho, Eduardo Crevelin, Bianca Waléria Bertoni, Suzelei Castro FrançaAbstract:Ethnopharmacological relevance Uncaria tomentosa (Willd. Ex Schult) DC is used by indigenous tribes in the Amazonian region of Central and South America to treat inflammation, allergies and asthma. The therapeutic properties of U. tomentosa have been attributed to the presence of tetracyclic and pentacyclic oxindole alkaloids and to phenolic acids. Aims of the study To characterize aqueous bark extracts (ABE) and aqueous leaf extracts (ALE) of U. tomentosa and to compare their anti-inflammatory effects. Materials and methods Constituents of the extracts were identified by ultra performance liquid chromatography-mass spectrometry. Anti-inflammatory activities were assessed in vitro by exposing lipopolysaccharide-stimulated macrophage cells (RAW264.7-Luc) to ABE, ALE and standard mitraphylline. In vivo assays were performed using a murine model of ovalbumin (OVA)-induced asthma. OVA-sensitized animals were treated with ABE or ALE while controls received dexamethasone or saline solution. Bronchial hyperresponsiveness, production of Th1 and Th2 cytokines, total and differential counts of inflammatory cells in the bronchoalveolar lavage (BAL) and lung tissue were determined. Results Mitraphylline, isomitraphylline, chlorogenic acid and quinic acid were detected in both extracts, while isorhyncophylline and rutin were detected only in ALE. ABE, ALE and mitraphylline inhibited the transcription of nuclear factor kappa-B in cell cultures, ALE and mitraphylline reduced the production of interleukin (IL)−6, and mitraphylline reduced production of tumor necrosis factor-alpha. Treatment with ABE and ALE at 50 and 200 mg kg−1, respectively, reduced respiratory elastance and tissue damping and elastance. ABE and ALE reduced the number of eosinophils in BAL, while ALE at 200 mg kg−1 reduced the levels of IL-4 and IL-5 in the lung homogenate. Peribronchial inflammation was significantly reduced by treatment with ABE and ALE at 50 and 100 mg kg−1 respectively. Conclusion The results clarify for the first time the anti-inflammatory activity of U. tomentosa in a murine model of asthma. Although ABE and ALE exhibited distinct chemical compositions, both extracts inhibited the production of pro-inflammatory cytokines in vitro. In vivo assays revealed that ABE was more effective in treating asthmatic inflammation while ALE was more successful in controlling respiratory mechanics. Both extracts may have promising applications in the phytotherapy of allergic asthma.