RESUMEN
The modification of achira starch a thermoplastic biopolymer is shown. Glycerol and sorbitol, common plasticizers, were used in the molten state with organic acids such as oleic acid and lactic acid obtaining thermodynamically more stable products. The proportion of starch:plasticizer was 70:30, and the acid agent was added in portions from 3%, 6%, and 9% by weight. These mixtures were obtained in a torque rheometer for 10 min at 130 °C. The lactic acid managed to efficiently promote the gelatinization process by increasing the available polar sites towards the surface of the material; as a result, there were lower values in the contact angle, these results were corroborated with the analysis performed by differential scanning calorimetry and X-ray diffraction. The results derived from oscillatory rheological analysis had a viscous behavior in the thermoplastic starch samples and with the presence of acids; this behavior favors the transitions from viscous to elastic. The mixture of sorbitol or glycerol with lactic acid promoted lower values of the loss module, the storage module, and the complex viscosity, which means lower residual energy in the transition of the viscous state to the elastic state; this allows the compounds to be scaled to conventional polymer transformation processes.
Asunto(s)
Ácido Láctico/química , Ácido Oléico/química , Plásticos/química , Reología , Almidón/química , Temperatura , Rastreo Diferencial de Calorimetría , Módulo de Elasticidad , Espectrofotometría Ultravioleta , Almidón/ultraestructura , Termogravimetría , Torque , Viscosidad , Difracción de Rayos XRESUMEN
Tryptophan is an essential amino acid precursor of neurotransmitter serotonin and triptamine. During its metabolism, indole-3-acetic acid (IAA) is generated; this substance presents both antioxidant and prooxidant effects in different biological systems in addition to hipoglicemic effects. To date, electroencephalography (EEG) has been used to evaluate the temporal effect of several substances in neurotransmission. The goal of this study was to characterize the effect of IAA in the brain by analysing the EEG signal and evaluate the oxidative status by means of biochemical parameters. The EEG was acquired by using a noninvasive method, and the brain electric signal was analysed by advanced digital signal processing techniques to determinate the energy signal filtered in different band frequencies. Furthermore, the oxidative status of the brain was investigated by measuring the activity of antioxidant enzymes and lipid peroxidation as well as blood glucose rates of the animals treated with different doses of IAA. Our results showed the relationship of IAA administration with changes in EEG signals. The oxidative status of the brain was modified by IAA after 14 days of treatment.
Asunto(s)
Encéfalo/metabolismo , Ácidos Indolacéticos/metabolismo , Triptófano/metabolismo , Animales , Glucemia/metabolismo , Encéfalo/efectos de los fármacos , Catalasa/metabolismo , Electroencefalografía , Glutatión Reductasa/metabolismo , Ácidos Indolacéticos/farmacología , Peroxidación de Lípido , Masculino , Malondialdehído/metabolismo , Oxidación-Reducción , Ratas Wistar , Superóxido Dismutasa/metabolismoRESUMEN
Heavy alcohol consumption is a known risk factor for various forms of dementia and the development of Alzheimer's disease (AD). In this work, we investigated how intragastric alcohol feeding may alter the liver-to-brain axis to induce and/or promote AD pathology. Four weeks of intragastric alcohol feeding to mice, which causes significant fatty liver (steatosis) and liver injury, caused no changes in AD pathology markers in the brain [amyloid precursor protein (APP), presenilin], except for a decrease in microglial cell number in the cortex of the brain. Interestingly, the decline in microglial numbers correlated with serum alanine transaminase (ALT) levels, suggesting a potential link between liver injury and microglial loss in the brain. Intragastric alcohol feeding significantly affected two hepatic proteins important in amyloid-beta (Aß) processing by the liver: 1) alcohol feeding downregulated lipoprotein receptor-related protein 1 (LRP1, â¼46%), the major receptor in the liver that removes Aß from blood and peripheral organs, and 2) alcohol significantly upregulated APP (â¼2-fold), a potentially important source of Aß in the periphery and brain. The decrease in hepatic LRP1 and increase in hepatic APP likely switches the liver from being a remover or low producer of Aß to an important source of Aß in the periphery, which can impact the brain. The downregulation of LRP1 and upregulation of APP in the liver was observed in the first week of intragastric alcohol feeding, and also occurred in other alcohol feeding models (NIAAA binge alcohol model and intragastric alcohol feeding to rats). Modulation of hepatic LRP1 and APP does not seem alcohol-specific, as ob/ob mice with significant steatosis also had declines in LRP1 and increases in APP expression in the liver. These findings suggest that liver steatosis rather than alcohol-induced liver injury is likely responsible for regulation of hepatic LRP1 and APP. Both obesity and alcohol intake have been linked to AD and our data suggests that liver steatosis associated with these two conditions modulates hepatic LRP1 and APP to disrupt Aß processing by the liver to promote AD.
RESUMEN
Complexity measurement using Lempel and Ziv algorithm (LZ) has been used to analyze physiological data. This work shows that the Lempel and Ziv complexity measurement of EEG signals using wavelets transforms is independent of electrode position and dependent on cognitive tasks and brain activity. EEG database with 122 subjects from the public EEG dataset was used in this study. This database have spontaneous EEG and evoked potential (EP) data from a 64-multielectrode array under a variety of conditions collected at several centers in the United States, sponsored by the National Institute on Alcohol Abuse and Alcoholism (NIAAA) project. Two experiments were performed with this database. The first experiment was to test the dependency of electrode positions into LZ complexity measures and the second experiment was to analyze if the LZ complexity was sensitive to the EEG acquired from control and alcoholic subjects. The results show that the complexity measurement is dependent on the changes of the pattern of brain dynamics and not dependent on electrode position.
Asunto(s)
Algoritmos , Electrodos , Electroencefalografía/instrumentación , Potenciales Evocados , HumanosRESUMEN
This research presents a noninvasive method for the acquisition of brain electrical signal in rat. Was used an electroencephalography (EEG) system developed for bovine and adapted to rats. The bipolar electrode system (needle electrodes) was glued on the surface of the head of the animal without surgical procedures and the other electrode was glued to the tail, as ground. The EEG activity was sampled at 120Hz for an hour. The accuracy and precision of the EEG measurement was performed using Fourier analysis and signal energy. For this, the digital signal was divided into sections successive of 3 seconds and was decomposed into four frequency bands: delta (0.3 to 4Hz), theta (4-8Hz), alpha (8-12Hz) and beta (12-30Hz) and energy (µV²) of the series of time filtered were calculated. The method allowed the acquisition of non-invasive electrical brain signals in conscious rats and their frequency patterns were in agreement with previous studies that used surgical procedures to acquire EEG in rats. This system showed accuracy and precision and will allow further studies on behavior and to investigate the action of drugs on the central nervous system in rats without surgical procedures.
Este trabalho apresenta um método não invasivo para a aquisição de sinal elétrico cerebral em ratos. Utilizou-se um sistema de eletroencefalografia EEG desenvolvido para bovino e adaptado para ratos. O sistema bipolar de eléctrodos (eléctrodos de agulha) foi colado na superfície da cabeça do animal, sem procedimentos cirúrgicos e outro eletrodo foi colado na cauda, como terra. A atividade do EEG foi amostrada em 120Hz durante uma hora. Foi calculada a exatidão e a precisão da medida de EEG usando análise de Fourier e energia do sinal. Para isso, o sinal digital foi dividido em trechos sucessivos de 3 segundos, decomposto em quatro faixas de frequência: delta (0,3-4Hz), teta (4-8Hz), alfa (8-12Hz) e beta (12-30Hz) e a energia (µV²) das séries de tempo filtradas foram calculadas. O método não invasivo permitiu adquirir sinais elétricos cerebrais em ratos conscientes e seus padrões de frequências foram de acordo com trabalhos anteriores, que utilizaram procedimentos cirúrgicos para adquirir EEG em ratos. Esse sistema apresentou exatidão e precisão e permitirá novos estudos sobre comportamento e para investigar a ação de drogas no sistema nervoso central sem procedimentos cirúrgicos em ratos.