cognitive-function
Recent Research Papers on
cognitive-function
Author: M.S. Westerterp-Plantenga
The global prevalence of obesity has increased considerably in the last decade. Tools for obesity management including caffeine, and green tea have been proposed as strategies for weight loss and weight maintenance. These ingredients may increase energy expenditure and have been proposed to counteract the decrease in metabolic rate that is present during weight loss. Positive effects on body-weight management have been shown using green tea mixtures. Green tea, by containing both tea catechins and caffeine, may act through inhibition of catechol O-methyl-transferase, and inhibition of phosphodiesterase. Here the mechanisms may also operate synergistically. A green tea–caffeine mixture improves weight maintenance, through thermogenesis, fat oxidation, and sparing fat free mass. The sympathetic nervous system is involved in the regulation of lipolysis, and the sympathetic innervation of white adipose tissue may play an important role in the regulation of total body fat in general. Taken together, these functional ingredients have the potential to produce significant effects on metabolic targets such as thermogenesis, and fat oxidation. An ethnic or genetic effect, and habitual caffeine or green tea catechin intake may act as confounders; this remains to be revealed.
Author: Laurent Bazinet and Monica Araya-Farias and Alain Doyen and Dominique Trudel and Bernard Têtu
Due to the increasing market for functional foods and the chemopreventive action of (−)-epigallocatechin gallate (EGCG), manufacturers produce ready-to-drink green tea infusions enriched or not in EGCG. However, the maintenance of green tea catechins stability in drinks is always a challenge. In this context, the objectives of this study were (1) to assess the catechin stability in tea drink during a 6-month storage, (2) to evaluate the impact of process unit operations on catechin stability and (3) to compare the catechin and caffeine contents of commercially available tea drinks. It appeared that the stability of catechins during long-term storage was optimum at low temperature (4 °C) and acidic pH (pH 4.0). During the processing of the EGCG-enriched green tea drink, all the process unit operations, except heat-treatment, had no impact on catechin concentrations. In addition, in commercially available tea drinks, except enriched green tea drinks, their catechin contents are very low to provide health benefits.
Author: Stéphane Bastianetto and Slavica Krantic and Rémi Quirion
Background: It has been suggested that accumulation of amyloid-beta (Aß) peptides into senile plaques plays a pivotal role in neuronal cell death occuring in Alzheimer's disease (AD). Aß produces two major types of programmed cell death (PCD) in vitro which requires the activation of effectors of caspase-dependent and -independent cell death pathways, namely caspase-3 and apoptosis inducing factor (AIF). Published data comparing the expression of AIF in post-mortem brains from AD patients and neurologically normal subjects in the course of aging suggest the relevance of AIF in the pathogenesis of AD Reix et al, Neurobiol Aging 28:351, 2007; Yu et al., Am. J. Path., in press). Recent epidemiological studies have reported that elderly people have a lower risk (up to 50%) to develop AD if they regularly eat fruits and vegetables and drink a moderate amount of tea and red wine. Numerous studies indicate that polyphenols derived from these foods and beverages account for the observed neuroprotective effects. In particular, polyphenols extracted from green tea (i.e. epigallocatechin gallate or EGCG) or red wine (i.e. resveratrol) blocked hippocampal cell death against Aß-induced toxicity (Bastianetto et al, Eur J Neurosci 23:55, 2006; Han et al, Br J Pharmacol 141:997, 2004). Our main objective is to determine whether concurrent inactivation of both main types of PCD may have additive therapeutic benefit in AD. Methods: Mixed hippocampal cell cultures were prepared from E19 fetuses obtained from Sprague-Dawley rats. They were grown in D-MEM high glucose containing 10% (v/v) fetal bovine serum. Experiments were performed in 6-day-old cultures. Results: The 24-hour exposure of cultured hippocampal cells to Aß1-42 (15 μM) alone or in combination with either resveratrol (20 μM) or EGCG (10 μM) reduced Aß1-42-mediated increased expression of the 57 kDa death-inducing form of AIF. Moreover, EGCG completely inhibited the activation of the key apoptotic executioner, caspase-3, and reduce the number of apoptotic cells, whereas resveratrol was less effective. Conclusions: Our findings show that these polyphenols do not share the same mechanism of action, suggesting that a combination of EGCG and resveratrol might provide additional neuroprotection against Aß-associated cell death.
Author: Marco Assunção and Maria J. Santos-Marques and Félix Carvalho and José P. Andrade
We previously found that prolonged consumption of green tea (GT), a rich source of antioxidant polyphenols, protected proteins and lipids against oxidation and reduced lipofuscin deposition in the rat hippocampal formation as well as improving spatial memory during aging. In this work, we sought to investigate whether GT treatment could interfere with age-related changes in redox status and cellular signaling systems related to oxidative stress and survival in the same brain region. To address this issue, five male Wistar rats were fed with GT from 12 to 19 months of age and results were compared to those obtained from controls age 19 months (C-19 M). A third group of rats was evaluated at 12 months of age to provide baseline data. At completion of the specified time points, the glutathione levels and antioxidant enzyme activities, the activation of the transcription factors cyclic AMP response element-binding (CREB) and nuclear factor-κB (NF-κB, p50 and p65 subunits), and the levels of brain-derived neurotrophic factor (BDNF) and B-cell lymphoma-2 (Bcl-2) were measured in hippocampal formations. GT-treated rats presented higher reduced and lower oxidized glutathione levels and displayed favorable alterations in antioxidant enzyme activities compared to C-19 M animals. In addition, GT increased CREB activation and the levels of BDNF and Bcl-2, but had no effect on activation of NF-κB subunits, relative to age-matched controls. We conclude that long-term GT ingestion improves antioxidant systems and activates CREB in the aging rat hippocampal formation, leading to neuroprotection mediated by downstream upregulation of BDNF and Bcl-2.
Author: Yan Xu and Jun-jian Zhang and Li Xiong and Lei Zhang and Dong Sun and Hui Liu
Responses to oxidative stress contribute to damage caused by chronic cerebral hypoperfusion, which is characteristic of certain neurodegenerative diseases. We used a rat model of chronic cerebral hypoperfusion to determine whether green tea polyphenols, which are potent antioxidants and free radical scavengers, can reduce vascular cognitive impairment and to investigate their underlying mechanisms of action. Different doses of green tea polyphenols were administered orally to model rats from 4 to 8 weeks after experimentally induced cerebral hypoperfusion, and spatial learning and memory were assessed using the Morris water maze. Following behavioral testing, oxygen free radical levels and antioxidative capability in the cortex and hippocampus were measured biochemically. The levels of lipid peroxidation and oxidative DNA damage were assessed by immunohistochemical staining for 4-hydroxynonenal and 8-hydroxy-2′-deoxyguanosine, respectively. Rats that received green tea polyphenols 400 mg/kg per day had better spatial learning and memory than saline-treated rats. Green tea polyphenols 400 mg/kg per day were found to scavenge oxygen free radicals, enhance antioxidant potential, decrease lipid peroxide production and reduce oxidative DNA damage. However, green tea polyphenols 100 mg/kg per day had no significant effects, particularly in the cortex. This study suggests that green tea polyphenols 400 mg/kg per day improve spatial cognitive abilities following chronic cerebral hypoperfusion and that these effects may be related to the antioxidant effects of these compounds.
Author: Quansheng Chen and Jiewen Zhao and Zhiming Guo and Xinyu Wang
Taste sensor technique with multivariate calibration was attempted to determine the contents of catechins (EGCG, EGC and ECG) and caffeine in green tea in this work. The system of data acquisitions based on taste sensor was developed in the experiment. Two multivariate calibrations, which were partial least square (PLS) and artificial neural network with principal component analysis (PCA-ANN), were applied to build forecasting models, respectively. Some parameters were optimized by cross-validation in building model. The performance of the final model was evaluated according to root mean square error of prediction (RMSEP) and correlation coefficient (R) in the prediction set. Experimental results showed that the PCA-ANN model is superior to the PLS model, and the results of each optimal model were obtained by PCA-ANN as follows: RMSEP (%) = 0.2399, R = 0.9037 for Caffeine model; RMSEP (%) = 0.3101, R = 0.8204 for ECG model; RMSEP (%) = 0.4113, R = 0.8384 for EGC model; RMSEP (%) = 0.6065, R = 0.9473 for EGCG model. This work demonstrated that taste sensor technique with multivariate calibration can be successfully employed to determine main catechins and caffeine contents in green tea.
Author: Yoon Woo Koh and Eun Chang Choi and Sung Un Kang and Hye Sook Hwang and Mi Hye Lee and JungHee Pyun and RaeHee Park and YoungDon Lee and Chul-Ho Kim
Hepatocyte growth factor (HGF) and c-Met have recently attracted a great deal of attention as prognostic indicators of patient outcome, and they are important in the control of tumor growth and invasion. Epigallocatechin-3-gallate (EGCG) has been shown to modulate multiple signal pathways in a manner that controls the unwanted proliferation and invasion of cells, thereby imparting cancer chemopreventive and therapeutic effects. In this study, we investigated the effects of EGCG in inhibiting HGF-induced tumor growth and invasion of oral cancer in vitro and in vivo. We examined the effects of EGCG on HGF-induced cell proliferation, migration, invasion, induction of apoptosis and modulation of HGF/c-Met signaling pathway in the KB oral cancer cell line. We investigated the antitumor effect and inhibition of c-Met expression by EGCG in a syngeneic mouse model (C3H/HeJ mice, SCC VII/SF cell line). HGF promoted cell proliferation, migration, invasion and induction of MMP (matrix metalloproteinase)-2 and MMP-9 in KB cells. EGCG significantly inhibited HGF-induced phosphorylation of Met and cell growth, invasion and expression of MMP-2 and MMP-9. EGCG blocked HGF-induced phosphorylation of c-Met and that of the downstream kinases AKT and ERK, and inhibition of p-AKT and p-ERK by EGCG was associated with marked increases in the phosphorylation of p38, JNK, cleaved caspase-3 and poly-ADP-ribose polymerase. In C3H/HeJ syngeneic mice, as an in vivo model, tumor growth was suppressed and apoptosis was increased by EGCG. Our results suggest that EGCG may be a potential therapeutic agent to inhibit HGF-induced tumor growth and invasion in oral cancer.
Author: Atsuo Miyagishima and Sadahiro Fujiki and Aya Okimura and Sakae Arahata and Shinsuke Inagaki and Yasunori Iwao and Shigeru Itai
We have recently succeeded in manufacturing low-caffeine tea (LCT) by employing a special picking method in the 3rd leaf period and shortening the leaf-rolling process. In the present study, the effect of this special method on the content of other physiologically active substances, such as catechins, theanine, and vitamin C, as well as the mechanism of reduction of caffeine content in the LCT were investigated using capillary electrophoresis. By comparing the various components of tea leaves at different picking periods with or without shortening of the rolling process, it was found that the delayed leaf picking period and shortening of the rolling process used in the manufacture of LCT selectively reduced the caffeine content while retaining catechins, theanine, and vitamin C at a sufficient level. Therefore, our study demonstrated that this modified method may be useful in the manufacture of decaffeinated green tea.
Author: E.J. Okello and G.J. McDougall and S. Kumar and C.J. Seal
There is mounting evidence that the deposition and aggregation of β-amyloid peptides (Aβ) in the brain play a significant role in the development and pathogenesis of Alzheimer's disease. There is further evidence that free radical species such as hydrogen peroxide (H2O2) mediate Aβ induced toxicity. Previous studies have demonstrated that green tea polyphenols possess neuroprotective properties through their ability to ameliorate oxidative stress induced by free radical species. Green tea polyphenols have also been shown to enhance cognition in various animal models of induced cognitive impairment. Upon ingestion, green tea polyphenols are metabolised and undergo bio-transformation which affects their bioavailability and therefore efficacy. In this study, a green tea extract was subjected to a simulated gastrointestinal digestion and a ‘colon-available’ extract (CAGTE) prepared and assessed for its potential protective effects against H2O2 and Aβ(1–42) induced cytotoxicity using differentiated PC12 cells (dPC12) as a model for neuronal cells. CAGTE represents green tea phytochemicals potentially available after upper gastrointestinal digestion. CAGTE which was depleted in flavan-3-ols, as shown by LC–MS analysis, protected dPC12 cells at concentration ranges of 0.3–10 μg/ml and 0.03–0.125 μg/ml for H2O2 and Aβ(1–42), induced cytotoxicity, respectively. At high concentrations, CAGTE exhibited direct anti-proliferative effects, in line with the reputed anti-cancer properties of green tea polyphenols. These results demonstrate that potentially bioavailable green tea metabolites are able to ameliorate both H2O2 and Aβ(1–42) induced cytotoxicity.
Author: Li Guo and Qin Liang and Xianfeng Du
Tea polysaccharide (TPS) is attracting more attention gradually in many fields due to its particular biological properties. To further elucidate the functions of TPS to starch-based foods, experiments were carried out using mixed amylose/amylopectin/TPS system as a model. The effects of TPS in green tea on the glass transition temperatures (Tgs) of the mixtures with different amylose/amylopectin ratios at low water contents were investigated using high-speed differential scanning calorimetry (Hyper-DSC). The results showed that the Tgs of amylose, amylopectin and their mixtures decrease with increasing concentration of TPS. It is suggested that the addition of TPS has plasticizing effects on the structures of amylose and amylopectin on the molecular level. Based on the molecular characteristics of TPS, the results in this study indicated that TPS is a homogeneous and spherical polymer with branch in solution, which can increase free volume and molecular movement of amylose and amylopectin chains. TPS can also produce greater electrostatic repulsion and decrease association among macromolecules, thereby resulting in the decrease of the Tgs of amylose, amylopectin and their mixtures.