Modes and Mechanisms of Pacific Decadal-Scale Variability.

The modes of Pacific decadal-scale variability (PDV), traditionally defined as statistical patterns of variance, reflect to first order the ocean's integration (i.e., reddening) of atmospheric forcing that arises from both a shift and a change in strength of the climatological (time-mean) atmospheric circulation. While these patterns concisely describe PDV, they do not distinguish among the key dynamical processes driving the evolution of PDV anomalies, including atmospheric and ocean teleconnections and coupled feedbacks with similar spatial structures that operate on different timescales. In this review, we synthesize past analysis using an empirical dynamical model constructed from monthly ocean surface anomalies drawn from several reanalysis products, showing that the PDV modes of variance result from two fundamental low-frequency dynamical eigenmodes: the North Pacific-central Pacific (NP-CP) and Kuroshio-Oyashio Extension (KOE) modes. Both eigenmodes highlight how two-way tropical-extratropical teleconnection dynamics are the primary mechanisms energizing and synchronizing the basin-scale footprint of PDV. While the NP-CP mode captures interannual- to decadal-scale variability, the KOE mode is linked to the basin-scale expression of PDV on decadal to multidecadal timescales, including contributions from the South Pacific.

Effect of live Eimeria vaccination or salinomycin on growth and immune status in broiler chickens receiving in-feed inclusion of gelatin and vitamin E.

This experiment determined if 2% of gelatin, to improve the levels of proline and glycine in the diet, and 70 mg/kg of vitamin E supplementation would relieve the impaired performance of male Cobb broilers vaccinated for coccidiosis. Half of the chicks were vaccinated via water (live oocysts), while the other half received medication (salinomycin) in the feed until 35 d of age. The effects of coccidiosis vaccine on performance and mRNA levels of genes involved in mucin synthesis, cytokines, trefoil family factor-2 (TFF2), and metabolic processes (CD36) in the jejunum of broilers were measured. Vaccination negatively affected performance in the first 21 d; however, the inclusion of gelatin and vitamin E reduced this negative response. Additionally, supplementation with these nutrients led to an improvement in broilers receiving the coccidiostat (P < 0.05). From 21 to 35 d, birds treated with gelatin and coccidiosis vaccine experienced better body weight gain than birds without gelatin and vitamin E (P < 0.05). Vaccinated chickens had decreased body weight and decreased anti-inflammatory cytokine expression. Furthermore, they had increased inflammatory cytokine expression, mucin 2 expression, and TFF2 compared to salinomycin-fed broilers (P < 0.05). Transcripts for IL-1B, IFN-y, MUC2, TFF2 were decreased while mRNAs for IL-4 and IL-10 increased in salinomycin-fed broilers compared to vaccinated broilers (P < 0.05). In conclusion, broilers vaccinated against coccidiosis increase their pro-inflammatory immune status and mucin expression compared to broilers receiving salinomycin. These events may contribute to lower performance in vaccinated broiler chicks. Moreover, vitamin E and gelatin can minimize the vaccine's negative immune effects and promote better performance.

Análise de medicamentos antiinflamatórios não esteroidais manipulados empregando espectroscopia de reflexão difusa no infravermelho com transformada de Fourier (DRIFTS) / Analysis of nonsteroidal antiinflammatory drugs in compounded medicines by diffuse-reflectance infrared Fourier transform spectroscopy (DRIFTS)

A análise de dois fármacos diferentes, mas estruturalmente semelhantes, foi realizada, empregando espectros de reflexão difusa no infravermelho médio com transformada de Fourier (DRIFTS), em associação com a técnica de análise por agrupamentos hierárquicos (AAH). Amostras de 3 diferentes farmácias de manipulação, contendo diclofenaco de sódio 50mg, diclofenaco de potássio 50mg e seus respectivos excipientes, foram analisadas em duplicata por dois analistas. Para a análise multivariada foi empregado o aplicativo Pirouette R 2.7 da Infometrix, selecionando-se o conjunto de regiões dos espectros com maior número de informações. Os dendogramas foram construídos com os dados auto-escalados e correção do espalhamento de luz (MSC), utilizando três tipos de construções: simples, flexível e incremental. Com a aplicação da AAH, constatou-se a formação de diferentes grupos obedecendo à discriminação de cada princípio ativo, indicando seus fornecedores e, em separado, outro grupo. Estes resultados demonstram que a técnica DRIFTS, em conjunto com ferramentas quimioterápicas, constitui uma excelente opção para a caracterização de fármacos, gerando uma inovadora metodologia para auxiliar no controle da qualidade de processos industriais de produção de medicamentos

Constructive genetic algorithm for clustering problems.

Genetic algorithms (GAs) have recently been accepted as powerful approaches to solving optimization problems. It is also well-accepted that building block construction (schemata formation and conservation) has a positive influence on GA behavior. Schemata are usually indirectly evaluated through a derived structure. We introduce a new approach called the Constructive Genetic Algorithm (CGA), which allows for schemata evaluation and the provision of other new features to the GA. Problems are modeled as bi-objective optimization problems that consider the evaluation of two fitness functions. This double fitness process, called fg-fitness, evaluates schemata and structures in a common basis. Evolution is conducted considering an adaptive rejection threshold that contemplates both objectives and attributes a rank to each individual in population. The population is dynamic in size and composed of schemata and structures. Recombination preserves good schemata, and mutation is applied to structures to get population diversification. The CGA is applied to two clustering problems in graphs. Representation of schemata and structures use a binary digit alphabet and are based on assignment (greedy) heuristics that provide a clearly distinguished representation for the problems. The clustering problems studied are the classical p-median and the capacitated p-median. Good results are shown for problem instances taken from the literature.

Dopamine-glutamate interactions in the striatum: behaviourally relevant modification of excitotoxicity by dopamine receptor-mediated mechanisms.

The two most important afferent projections to the striatum contain glutamate and dopamine, respectively. Excitotoxic damage resulting from excessive stimulation of the N-methyl-D-aspartate subtype of glutamate receptor has been implicated in pathophysiology of ischaemic stroke, hypoglycaemic brain damage and Huntington's disease. We studied the ability of the dopamine system to modify the anatomical, neurochemical and behavioural consequences of glutamatergic toxicity in the striatum. In a first set of experiments, the specific N-methyl-D-aspartate receptor agonist quinolinate was injected unilaterally into the striatum of rats pretreated with one of (i) intraperitoneal (i.p.) saline (controls); (ii) i.p. haloperidol, a D2 dopamine receptor agonist; or (iii) 6-hydroxydopamine lesion of the ipsilateral nigrostriatal tract. Quinolinate-induced striatal damage, as assessed by morphometric and neurochemical criteria, was significantly attenuated in the animals with 6-hydroxydopamine lesions and in those pretreated with haloperidol, compared with saline-pretreated controls. There were no significant differences between the 6-OHDA and haloperidol groups. In a second set of experiments, animals received (i) bilateral intrastriatal quinolinate plus perioperative i.p. saline; (ii) bilateral intrastriatal quinolinate plus i.p. haloperidol; or (iii) bilateral intrastriatal saline. Again, the quinolinate-lesioned animals treated with perioperative haloperidol had significantly less striatal damage than the bilateral quinolinate rats. Behavioural assessment in the Morris Water Maze showed the bilateral quinolinate+haloperidol group to be significantly less impaired on a spatial acquisition task than the bilateral quinolinate animals. Measures of spontaneous daytime motor activity showed significant differences in average speed and rest time between the bilateral quinolinate+haloperidol rats and the bilateral quinolinate group. The performance of the bilateral quinolinate+haloperidol group was not significantly different from that of controls on any of the behavioural tasks. These results indicate an important role for D2 dopamine receptor-mediated mechanisms in striatal excitotoxicity. Since the excitotoxic process involves the same fundamental signalling mechanism that is involved in normal glutamatergic transmission, these findings imply an ability of D2 receptor blockade to modify glutamate signalling in the striatum. These results may have implications for treatment strategies in ischaemic stroke, hypoglycaemic brain damage and schizophrenia.

Behavioral characterization of quinolinate-induced lesions of the medial striatum: relevance for Huntington's disease.

Huntington's disease (HD) in an inherited neurodegenerative disorder in which the striatum undergoes marked atrophic changes. Patients with HD typically have impaired cognitive function, including deficient visuospatial skills, lack of cognitive flexibility and poor recall of memories. The relationship between these cognitive abnormalities and the striatal degeneration of HD is incompletely understood. In order to explore this issue, we studied the behavior of rats with histologically confirmed bilateral quinolinate (QUIN)-induced lesions of the medial striatum. In a series of Morris Water Maze (MWM) experiments and Delayed Alternation (DA) tests, QUIN-lesioned animals exhibited: (i) impaired acquisition of visuospatial skills; (ii) impaired "transfer of learning"; (iii) preseverative behavior; (iv) deficient retrieval or retention of stored memories. The lesioned rats were unimpaired with swimming to a visible platform, while moving spontaneously in behavior boxes, and when performing various specialized tests of motor function. These results indicate that QUIN-induced lesions of the medial striatum can produce impairments of visuospatial skills, cognitive flexibility, and recall. These are the categories of cognitive function that are disturbed in HD. This suggests that the striatal degeneration of HD could be a sufficient explanation for the cognitive abnormalities associated with the illness.

Concurrent language and motor performance in bilinguals: a test of the age of acquisition hypothesis.

The objective of the present study was to test the hypothesis that the age at which a second language is acquired influences the pattern of cerebral lateralization associated with that language. Subjects who differed in terms of the age at which they had acquired their second language (English or French) were tested on a concurrent task paradigm involving motor and language performance. Hemispheric processing was inferred from the pattern of lateralized and generalized interference between the tasks. No support was found for the age-of-acquisition hypothesis. Instead, the data indicated a language-specific effect. Regardless of age of acquisition and of whether the first language was English or French, bilingual subjects showed lateralized interference effects consistent with left-hemisphere processing when reading in English and translating from French into English, but no lateralized interference when reading in French and translating from English into French. Whether this effect reflects characteristics of the two languages or the influence of social factors in subject-experimenter interaction is considered.

MPTP-induced neurotoxicity and the quest for a preventative therapy for Parkinson's disease.

Less than 10 years have passed since the discovery that 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) is capable of producing parkinsonism in both humans and non-human primates. In that time, there has been considerable interest in the possibility that the pathogenesis of idiopathic Parkinson's disease (PD) might involve a process analogous to that of MPTP toxicity. One hypothesis holds that PD might arise, at least in part, from exposure to an MPTP-like environmental toxin. Rapid progress has been made towards elucidating the precise mechanism by which MPTP exerts toxicity, and clarifying the relationship of MPTP toxicity to idiopathic PD. The goal of these efforts is to develop a therapy that inhibits the underlying disease process in PD.