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Moiseeva, V.

Publications and source records attributed to Moiseeva, V..

4 recordsLinked to original sources

Reward impulsivity is linked to addictive-like behaviors towards sweet food and sugary drinks but not fatty food

Overconsumption of hyperpalatable food is a worldwide problem. Although many previous studies have shown the link between monetary delay discounting and propensity to overconsume food, the studies did not focus on the link between delay discounting and various subcategories of palatable food. In the present study, we investigate the link between the individual propensity to choose smaller immediate rather than larger delayed reward and the degree of problematic eating behavior for five types of palatable food (sweets, sugary drinks, fatty food, salty snacks, and starchy food). The delay discounting task was used to measure propensity to choose immediate rather than delayed rewards, while the degree of addictive-like behavior was measured using the modified Yale food addiction scale (mYFAS) for each food category. Both model-free and model-based analysis showed that there is a significant correlation between the addiction score for sweet food and the tendency to choose smaller immediate rather than larger delayed rewards. A model-based analysis showed the same significant correlation for sugary drinks. However, no such correlation was observed for other food categories (fatty, salty, or starchy food), suggesting that reward impulsivity may play different roles in addictive-like behavior towards various food categories.

neuroscience↗

Network-community analysis of cellular senescence

Most cellular phenotypes are genetically complex. Identifying the set of genes that are most closely associated with a specific cellular state is still an open question in many cases. Here we study the transcriptional profile of cellular senescence using a combination of network-based approaches, which include eigenvector centrality feature selection and community detection. We apply our method to cell-type-resolved RNA sequencing data obtained from injured muscle tissue in mice. The analysis identifies some genetic markers consistent with previous findings, and other previously unidentified ones, which are validated with previously published single-cell RNA sequencing data in a different type of tissue. The key identified genes, both those previously known and the newly identified ones, are transcriptional targets of factors known to be associated with established hallmarks of senescence, and can thus be interpreted as molecular correlates of such hallmarks. The method proposed here could be applied to any complex cellular phenotype even when only bulk RNA sequencing is available, provided the data is resolved by cell type.

systems biology↗

The influence of learning on robustness of working memory to distractors

Inhibition of irrelevant information is a crucial process within the working memory (WM) system. In the present study, we explored how inhibition of distractors is learned within a Sternberg-like WM task and how this learning process affects readout performance. We introduced distractors of varying strength as well as novel stimuli to a classic Sternberg task. Our findings show that the length of the training period affected obstructiveness of distractors as well as differences between WM loads. Significant differences between conditions observed early on in accuracy became void after general ceiling performance was reached. Moreover, accuracy and reaction times, which are commonly used as readouts of WM performance, were affected differently by training. While both improved significantly, only accuracy exhibited differential dependency of experimental conditions on training. It is essential to consider these dynamics when introducing a WM task which requires a long training period.

neuroscience↗

Characterizing the middle-age neurophysiology using EEG/MEG

Middle adulthood - the period of life between 40 and 60 years of age - is accompanied by important physical and emotional changes, as well as cognitive and neuronal ones. Nevertheless, middle age is often overlooked in neuroscience under the assumption that this is a time of relative stability, although cognitive decline, as well as changes in brain structure and function are well-established by the age of 60. Here we characterized the middle-aged brain in the context of healthy younger and older adults by assessing resting-state electrophysiological and neuromagnetic activity in two different samples (N = 179, 631). Alpha and beta oscillations - two key ageing signatures - were analyzed in terms of spectral power and burst events. While posterior alpha power and burst rate features changed linearly with age, similarly to behavioral measures, sensorimotor beta power and burst rate properties varied non-linearly, with inflection points during middle age. The findings suggest that ageing is characterized by distinct spatial and temporal brain dynamics, some critically arising in middle age.

neuroscience↗