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Music and the brain

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Soups for weight loss and longevity

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A 102 male senior’s secret to long life is SOUPS. What is your favorite GO TO Soup?

I always serve soups to our seniors. Soups help them with constipation and their over all health. Start your meal with soup. Add yogurt in some soups. Lemon in others. Always use ginger with chicken and fish. Do use lots of garlic and onions. You can mix fresh herbs stored in a cotton bag and removed the bag before serving.

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The Rhythm of Memory

The Rhythm of Memory

Summary: A new Nature Communications study sheds light on how the brain processes information relevant to memory.

Source: University of Freiburg.

The more we know about the billions of nerve cells in the brain, the less their interaction appears spontaneous and random. The harmony underlying the processing of memory contents has been revealed by Prof. Dr. Marlene Bartos and her team. In a study published in Nature Communications, Dr. Bartos highlights the role of inhibiting circuits in the creation of high-frequency brainwaves in the hippocampus. The study helps show how the brain processes information that is relevant to memory.

“Researchers have suspected for a long time that frequencies over 30 Hertz coordinate the synchronous cooperation of various cell networks of the brain. It’s also known that activity in this frequency range is markedly reduced in Alzheimer patients, for example,” says Bartos, summing up the underlying idea of her research.

But how do these signals, known as gamma waves, occur in several places simultaneously? And what does this mean for human memory in real terms?

As experts in the field of synaptic links, Bartos and her team intensively studied the communication between what are called interneurons in the hippocampuses of mice. Situated between two or more other neurons, an interneuron is a cell type with especially short protuberances, which can effect a transmission of inhibiting impulses to its neighboring cells quickly and efficiently.

“Similar to groups of instruments in an orchestra, there are small circuits in which inhibitory interneurons play an important part,” explains Bartos. “You could imagine their role as being like that of the conductor, who makes the horns retreat into the background at points, in order to give them full weight once more the next moment.”

The most important observation of the study was, when they are roused from rest, the surrounding cells are receptive to certain information. Then they are stimulated to develop a common potential for action, so that a signal can be transmitted to other neurons. This in turn can be measured electrophysiologically as a discharge of gamma waves.

Image shows the hippocampus.

“The interesting aspect of this is that the micro-circuits do not interfere with one another, but can store or access various information in parallel, such as the attribute form and color of an object. This allows simultaneous, parallel processing and the storage of information. We believe that this is how the initial traces of memory are laid,” says Bartos.

However, in order really to track down what makes memory, a lot more fundamental research is still required. Bartos and her team are working at top speed to make their findings usable for the treatment of neurodegenerative diseases within a few years.

ABOUT THIS NEUROSCIENCE RESEARCH ARTICLE

Funding: This research was supported by the Japan Agency for Medical Research and Development-Core Research for Evolutional Science and Technology (14532135 to S.F.), Japan Agency for Medical Research and Development (145208 and 16770835 to T.H.) and the Cell Science Foundation (K.C). The work was done by University of Freiburg in collaboration with Keio University, Kyoto University, and other institutions.

Source: Marlene Bartos – University of Freiburg
Publisher: Organized by NeuroscienceNews.com.
Image Source: NeuroscienceNews.com image is credited to Marlene Bartos.
Original Research: Full open access research for “Distance-dependent inhibition facilitates focality of gamma oscillations in the dentate gyrus” by Michael Strüber, Jonas-Frederic Sauer, Peter Jonas & Marlene Bartos in Nature Communications. Published online October 2 2017 doi:10.1038/s41467-017-00936-3

CITE THIS NEUROSCIENCENEWS.COM ARTICLE
University of Freiburg “The Rhythm of Memory.” NeuroscienceNews. NeuroscienceNews, 24 October 2017.
<http://neurosciencenews.com/memory-rhythm-7795/&gt;.

Abstract

Distance-dependent inhibition facilitates focality of gamma oscillations in the dentate gyrus

Gamma oscillations (30–150 Hz) in neuronal networks are associated with the processing and recall of information. We measured local field potentials in the dentate gyrus of freely moving mice and found that gamma activity occurs in bursts, which are highly heterogeneous in their spatial extensions, ranging from focal to global coherent events. Synaptic communication among perisomatic-inhibitory interneurons (PIIs) is thought to play an important role in the generation of hippocampal gamma patterns. However, how neuronal circuits can generate synchronous oscillations at different spatial scales is unknown. We analyzed paired recordings in dentate gyrus slices and show that synaptic signaling at interneuron-interneuron synapses is distance dependent. Synaptic strength declines whereas the duration of inhibitory signals increases with axonal distance among interconnected PIIs. Using neuronal network modeling, we show that distance-dependent inhibition generates multiple highly synchronous focal gamma bursts allowing the network to process complex inputs in parallel in flexibly organized neuronal centers.

“Metabolic shift induced by systemic activation of T cells in PD-1-deficient mice perturbs brain monoamines and emotional behavior” by Michio Miyajima, Baihao Zhang, Yuki Sugiura, Kazuhiro Sonomura, Matteo M Guerrini, Yumi Tsutsui, Mikako Maruya, Alexis Vogelzang, Kenji Chamoto, Kurara Honda, Takatoshi Hikida, Satomi Ito, Hongyan Qin, Rikako Sanuki, Keiichiro Suzuki, Takahisa Furukawa, Yasushi Ishihama, Fumihiko Matsuda, Makoto Suematsu, Tasuku Honjo & Sidonia Fagarasan in Nature Immunology. Published online October 24 2017 doi:10.1038/ni.3867

Brain Structure Makes Some Resilient to Alzheimer’s

Brain Structure Makes Some Resilient to Alzheimer’s

Summary: According to researchers, the size, shape and number of dendritic spines in the brain may determine whether a person develops Alzheimer’s disease.

Source: University of Alabama at Birmingham.

The size, shape and number of dendritic spines in the brain may play a major role in whether someone gets Alzheimer’s disease, according to new research from the University of Alabama at Birmingham. Dendritic spines are sub-units of neurons that act as the connector to other neurons.

In findings published Oct. 24 in the Annals of Neurology, the research team showed, for the first time, that the presence of healthy dendritic spines conveyed a protective effect against Alzheimer’s in people whose brains had proteins associated with the disease.

“One of the precursors of Alzheimer’s is the development in the brain of proteins called amyloid and tau, which we refer to as the pathology of Alzheimer’s,” said Jeremy Herskowitz, Ph.D., assistant professor in the Department of Neurology, School of Medicine and lead author of the study. “However, about 30 percent of the aging population have amyloid and tau buildup but never develop dementia. Our study showed that these individuals had larger, more numerous dendritic spines than those with dementia, indicating that spine health plays a major role in the onset of disease.”

Neurons are constantly sending out long, thin dendritic spines in search of other neurons. When they connect, a synapse, or exchange of information between neurons, occurs. This is the basis for memory and learning.

“One obvious culprit in Alzheimer’s disease is the loss of dendritic spines and thus the loss of synapses,” said Herskowitz, who is the Patsy W. and Charles A. Collat Scholar in Neuroscience. “This would impair the ability to think, so the assumption has been that those without dementia had healthy spines and those with dementia did not. But no one had gone in to see if that was true.”

Herskowitz’s team studied brain samples from patients at memory clinics at Emory University. The control group did not have the Alzheimer’s pathology of amyloid plaques and tau tangles and never developed dementia. A second group had the Alzheimer’s pathology and progressed to the disease. The third group had the pathology, but no disease.

The researchers took thousands of microscopy images of the subject brains. Those images were then turned into 3-D images using novel, exclusive software. This allowed the team to look more fully at the shape and dimensions of each image.

“We first noted that the control group had more dendritic spines than the group with Alzheimer’s, which matched beautifully with existing historical data,” Herskowitz said. “But we also saw that the group with Alzheimer’s pathology but no disease also had more spines than the Alzheimer’s group. In fact, they had roughly the same spine density as the control group. What is even more exciting is that the ‘pathology but no disease’ group had very long spines, longer than both the control group and the disease group.”

Image shows neurons.

Herskowitz says the longer spines demonstrated great plasticity, or ability to move. This indicates that they could navigate around or through amyloid plaques or tau tangles in their efforts to connect with other neurons.

“This provides an explanation of why some people are cognitively resilient to Alzheimer’s disease, even if they possess the typical Alzheimer’s pathology,” he said.

Herskowitz says that the high plasticity and density of dendritic spines in this population could be genetic. Another theory suggests that it could be the result of healthy lifestyle behaviors, such as good diet and exercise, which are known to be protective against dementia. It may be that the reason these behaviors are protective is that they help maintain spine health, plasticity and density.

The findings also offer a new target for slowing or preventing Alzheimer’s in the first place, Herskowitz says.

“This provides a target for drugs that would be designed to support and maintain dendritic spine health in an effort to rebuild neurons or prevent their loss,” he said. “This data suggests that rebuilding neurons is possible. And as we are better able to identify the increase of amyloid and tau early in the progression of the disease, even before symptoms arise, we might be able to one day offer a medication that can contribute to maintaining healthy dendritic spines in those with the Alzheimer’s pathology.”

ABOUT THIS NEUROSCIENCE RESEARCH ARTICLE

Funding: Herskowitz credits the innovative 3-D imaging system used in the study to groundbreaking work done by UAB science and technology honors student Benjamin Boros. Funding for the study was provided by the National Institute on Aging, part of the National Institutes of Health, and the Alzheimer’s Association.

Source: Bob Shepard – University of Alabama at Birmingham
Publisher: Organized by NeuroscienceNews.com.
Image Source: NeuroscienceNews.com image is credited to Alzheimer’s disease group.
Original Research:Abstract for “Dendritic spines provide cognitive resilience against Alzheimer’s disease” by Benjamin D. Boros, Kelsey M. Greathouse BS, Erik G. Gentry BS, Kendall A. Curtis, Elizabeth L. Birchall BS, Marla Gearing PhD, and Jeremy H. Herskowitz PhD in Annals of Neurology. Published online October 22 2017 doi:10.1002/ana.25049

CITE THIS NEUROSCIENCENEWS.COM ARTICLE
University of Alabama at Birmingham “Brain Structure Makes Some Resilient to Alzheimer’s.” NeuroscienceNews. NeuroscienceNews, 24 October 2017.
<http://neurosciencenews.com/alzheimers-brain-structure-7804/&gt;.

Abstract

Dendritic spines provide cognitive resilience against Alzheimer’s disease

Objective

Neuroimaging and other biomarker assays suggest that the pathological processes of Alzheimer’s disease (AD) begin years prior to clinical dementia onset. However, some 30 to 50% of older individuals who harbor AD pathology do not become symptomatic in their lifetime. It is hypothesized that such individuals exhibit cognitive resilience that protects against AD dementia. We hypothesized that in cases with AD pathology, structural changes in dendritic spines would distinguish individuals who had or did not have clinical dementia.

Methods

We compared dendritic spines within layer II and III pyramidal neuron dendrites in Brodmann area 46 dorsolateral prefrontal cortex using the Golgi–Cox technique in 12 age-matched pathology-free controls, 8 controls with AD pathology (CAD), and 21 AD cases. We used highly optimized methods to trace impregnated dendrites from bright-field microscopy images that enabled accurate 3-dimensional digital reconstruction of dendritic structure for morphologic analyses.

Results

Spine density was similar among control and CAD cases but was reduced significantly in AD. Thin and mushroom spines were reduced significantly in AD compared to CAD brains, whereas stubby spine density was decreased significantly in CAD and AD compared to controls. Increased spine extent distinguished CAD cases from controls and AD. Linear regression analysis of all cases indicated that spine density was not associated with neuritic plaque score but did display negative correlation with Braak staging.

Interpretation

These observations provide cellular evidence to support the hypothesis that dendritic spine plasticity is a mechanism of cognitive resilience that protects older individuals with AD pathology from developing dementia.

“Dendritic spines provide cognitive resilience against Alzheimer’s disease” by Benjamin D. Boros, Kelsey M. Greathouse BS, Erik G. Gentry BS, Kendall A. Curtis, Elizabeth L. Birchall BS, Marla Gearing PhD, and Jeremy H. Herskowitz PhD in Annals of Neurology. Published online October 22 2017 doi:10.1002/ana.25049


Connie’s comments: Motherhealth caregivers are trained to massage the head of all senior clients.

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Music and Movies Play With Our Minds By Bending Time

Music and Movies Play With Our Minds By Bending Time

Summary: Emotional processing may be linked to perception of time, especially in music and movies, a new study reports.

Source: Horizon.

Movie directors regularly manipulate the passage of time in films to entertain their audiences, but researchers are trying to unravel the effect this can have on our brains.

Little is known about how the human brain processes time or how slow motion, time lapse and even music can alter our perception of how quickly it passes, changing our emotions and cognitive abilities.

Professor Clemens Wöllner, a cognitive musicology researcher at the University of Hamburg in Germany, describes an iconic scene in the 1990s blockbuster film Forrest Gump as an example.

As the kind-hearted but hapless hero, then a child, is being chased by bullies on bikes, he runs jerkily before picking up speed and the leg braces that constrain him pop off.

‘It’s a very emotional scene — and of course it’s in slow motion,’ said Prof. Wöllner, who is the principal investigator on an EU-funded project called SloMo.

By using slow motion, usually in combination with emotionally charged music, movie directors intuitively tap into how our perception of time affects our cognition, according to Prof. Wöllner.

The way the mind perceives time is something that researchers are only beginning to study at a fundamental level, though one day the findings from such work could feed into other research on human diseases and wellbeing.

The SloMo project is aiming to explore the theory that emotional processing by the mind is linked to the perception of time.

‘The theory is that during highly emotional moments we are highly susceptible to information and take in more information,’ said Prof. Wöllner. ‘Our brain is more alert and so we have the feeling that time passes more slowly.’

The team is examining the use of slow motion in music, dance, performing arts and audiovisual media like film or sports footage.

The project, which started in April and is funded for five years through the EU’s European Research Council (ERC), comprises six main studies and an initial total of 15 experiments.

Initial findings

The researchers have already presented initial findings at the European Society for the Cognitive Sciences of Music Conference, which was held at Ghent University, Belgium, during the summer. The team showed healthy volunteers slow-motion scenes taken from movies, dance and sports footage, recording their emotional, physiological and eye-movement responses. They then recorded the same parameters in the viewers while speeding up the footage to a real-life pace.

The iconic Forrest Gump scene was one of the pieces shown. Prof. Wöllner said two key emotional dimensions, which psychologists call arousal and valence, were markedly different when people watched the original slow-motion version compared with the normal-speed version.

Arousal refers to the emotional state connected to alertness and internal activity, including physiological parameters like heart rate, while valence refers to the value of an emotion, often either as positive for feelings like happiness, or negative for feelings like anger or fear.

When subjects were shown the Forrest Gump scene in real time, their arousal state was higher, while valence was higher in the slow-motion version when music was played. The team also found that people’s eye movements differed.

‘In slow motion, the gaze behaviour of the eye was more dispersed,’ said Prof. Wöllner. ‘They looked at other things (in the scene).’ He added that in real time, viewers tended to focus more, although not exclusively, on the main character.

In other words, slow motion enabled viewers to perceive details they otherwise wouldn’t have noticed.

But other experiments within the project are also probing how music can be used to influence our perception of motion and time. Music compositions are often multi-layered with different levels of structure in both the melody and rhythm, to which listeners can synchronise.

In one experiment, the researchers are manipulating musical excerpts with different structural levels and will examine the volunteers’ judgements of duration, along with physical responses like the speed the participants tapped their fingers to the perceived pulse of the music.

From a learning point of view, slow speed is important in music practice and dance rehearsal, so the project may have implications for education. The theory is that, in slowing down, the brain’s cognitive load — or mental capacity — is reduced, making it easier to concentrate on new notes or information.

Prof. Wöllner said the project will also examine ‘time dilation’ — a phenomenon that music can also be used to alter. The idea is that repetition makes time appear to speed up, which is why time seems to go faster as we age, or why the first time we travel to a new place the journey seems long but the return leg seems faster.

Repetition is central to most musical genres and affects listeners’ expectations. Prof. Wöllner says it is possible to alter some of the musical features and study how this affects people’s perceptions of duration and behavioural responses to music.

He believes this ability to use music to change people’s perception of time could also bring benefits to their wellbeing, although he stresses that SloMo is focusing on fundamental, basic research.

Image shows a tennis ball bouncing.

‘One field certainly is how music may help in diseases with a very strong temporal component, for instance Parkinson’s,’ he said.

Mapping time

But it may be important to answer some of the basic questions about how the brain is able to encode time before looking at how this can be applied to helping treat diseases.

The EU-funded Brain in Time (BiT) project, is looking at how our brains map duration. A lot of research in recent years has focused on where in the brain time is encoded, says Professor Domenica Bueti, principal investigator on the project and head of the time perception lab at the International School for Advanced Studies (SISSA) in Trieste, Italy.

‘What I proposed is, to go from “where” to “how” and “when”,’ she said. ‘How do brain regions encode time? What are the connections between these regions? How do they talk?’

Her project aims to test the hypothesis that there is a topography or map of time within the brain, something she refers to as a ‘chronotopy’. It will look at how the brain encodes time in the short term, at split-second level.

Prof. Bueti believes they will find that specific groups of brain cells respond selectively with different millisecond time durations.

She and her colleagues will use neuroimaging techniques, such as functional magnetic resonance imaging, to study the brains of healthy volunteers as they perform different tasks.

The team will also use a technique called transcranial magnetic stimulation to create virtual lesions within the brain while subjects are performing tasks. This can temporarily interfere with signals in the brain, allowing the researchers to study what different parts involved in time cognition do.

The project started in October 2016 with a five-year grant from the ERC.

Prof. Bueti hopes that chronomaps could provide a neurological signature of whether the brain’s time cognition system is working properly or not. This could be used to help people with conditions that have time perception problems.

People with damage to specific brain regions like the basal ganglia or cerebellum, or those with certain degenerative diseases like Parkinson’s can experience difficulties in judging time on the short scale. Understanding how the brain deals with time cognition could help develop new diagnostic tools for temporal deficiencies like these.

‘Time is so abstract,’ said Prof. Bueti. ‘Yet, it’s a fundamental dimension of everything.’

ABOUT THIS NEUROSCIENCE RESEARCH ARTICLE

Source: Horizon
Publisher: Organized by NeuroscienceNews.com.
Image Source: NeuroscienceNews.com images is credited to Josh Calabrese.

CITE THIS NEUROSCIENCENEWS.COM ARTICLE
Horizon “Music and Movies Play With Our Minds By Bending Time.” NeuroscienceNews. NeuroscienceNews, 24 October 2017.
<http://neurosciencenews.com/entertainment-time-perception-7801/&gt;.
—————-
Connie’s comments: I play the TV station JAZZTV in absence of other musical instruments in the house and it helped my Alzheimer’s patient’s mood.  All caregivers are trained to massage, dance and sing with the senior clients.
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A Little Myelin Goes A Long Way To Restore Nervous System Function

A Little Myelin Goes A Long Way To Restore Nervous System Function

Source: University of Wisconsin Madison.

In the central nervous system of humans and all other mammals, a vital insulating sheath composed of lipids and proteins around nerve fibers helps speed the electrical signals or nerve impulses that direct our bodies to walk, talk, breathe, swallow or perform any routine physical act.

But diseases of the nervous system, including multiple sclerosis (MS) in people, degrade this essential insulation known as myelin, disrupting the flow of information between the brain and the body, impairing movement, dimming vision and blunting the ability to function normally.

And while scientists have long studied myelin and understand its role in disease when it degrades, they have puzzled over how myelin repairs itself naturally and whether the thinned sheaths that are a hallmark of the healing nervous system are adequate for restoring the brain’s circuitry over the long haul.

This week (Oct. 23, 2017), in a study published in the Proceedings of the National Academy of Sciences,a team of researchers from the University of Wisconsin-Madison reports that in long-lived animals, renewed but thin myelin sheaths are enough to restore the impaired nervous system and can do so for years after the onset of disease.

The team’s findings reinforce the idea that thin myelin sheaths are a valid, persistent marker of remyelination, a hypothesis challenged by other recent research. “As the only biomarker of myelin repair available this would leave us without any means of identifying or quantifying myelin repair,” explains Ian Duncan, an expert on demyelinating diseases at the UW-Madison School of Veterinary Medicine and the senior author of the new study.

Duncan and his team looked at a unique genetic disorder that naturally afflicts Weimaraners, a breed of dog that as 12- to 14-day-old pups develop a severe tremor and loss of coordination. The condition is known to occur as the development of the myelin sheath in parts of the dog’s central nervous system is delayed. The symptoms gradually diminish and in most cases disappear altogether by 3-4 months of age.

“This is a very widespread mutation in the breed,” says Duncan, noting that myelin repair mimicking what is seen in remyelination is known to occur in these dogs as the rejuvenated nerve fibers have a thinned myelin sheath.

The new Wisconsin study was made possible as 13 years ago two Weimaraner pups, littermates, were seen as patients at the School of Veterinary Medicine and Duncan was able to maintain contact with the owners after the dogs were adopted and retrieve samples of spinal tissue after the dogs lived out their lives. As they aged, the dogs exhibited few signs of tremor and were deemed ‘neurologically normal’ up to 13 years of age.

Image shows myelin.

The purpose of the study, says Duncan, was to confirm that thin myelin sheaths persisted and supported normal neurologic function.

To expand on the results, Duncan also looked at a condition in cats, another long-lived species that has been shown to fully recover nervous system function after demyelination. In particular, Duncan’s team was interested in remyelination of the optic nerves.

That element of the study, looking at remyelination two years after the onset of the condition, Duncan notes, is an example of “true demyelination and remyelination. We found that nearly every optic nerve fiber was remyelinated with a thin myelin sheath, which is important for understanding human disease because in multiple sclerosis, the optic nerve is often the first to be demyelinated.”

The new findings confirm that the gold standard for evaluating remyelination is the long-term persistence of thin myelin sheaths, which support nerve fiber function and survival, Duncan notes. The results are important for diseases like MS as it means that new therapies designed to promote myelin repair can be safely evaluated and quantified based on the presence of thin myelin sheaths.

ABOUT THIS NEUROSCIENCE RESEARCH ARTICLE

Funding: These studies were supported in part by NMSS grant RG-1501-02876 and by a prior grant from the MS Hope for a Cure Foundation.

Source: Ian Duncan – University of Wisconsin Madison
Publisher: Organized by NeuroscienceNews.com.
Image Source: NeuroscienceNews.com image is credited to the researchers.
Original Research:Abstract for “Thin myelin sheaths as the hallmark of remyelination persist over time and preserve axon function” by Ian D. Duncan, Rachel L. Marik, Aimee T. Broman, and Moones Heidari in PNAS. Published online October 24 2017 doi:10.1073/pnas.1714183114

CITE THIS NEUROSCIENCENEWS.COM ARTICLE
University of Wisconsin Madison “A Little Myelin Goes A Long Way To Restore Nervous System Function.” NeuroscienceNews. NeuroscienceNews, 24 October 2017.
<http://neurosciencenews.com/myelin-nervous-system-7802/&gt;.

Abstract

Thin myelin sheaths as the hallmark of remyelination persist over time and preserve axon function

The presence of thin myelin sheaths in the adult CNS is recognized as a marker of remyelination, although the reason there is not a recovery from demyelination to normal myelin sheath thickness remains unknown. Remyelination is the default pathway after myelin loss in all mammalian species, in both naturally occurring and experimental disease. However, there remains uncertainty about whether these thin sheaths thicken with time and whether they remain viable for extended periods. We provide two lines of evidence here that thin myelin sheaths may persist indefinitely in long-lived animal models. In the first, we have followed thin myelin sheaths in a model of delayed myelination during a period of 13 years that we propose results in the same myelin sheath deficiencies as seen in remyelination; that is, thin myelin sheaths and short internodes. We show that the myelin sheaths remain thin and stable on many axons throughout this period with no detrimental effects on axons. In a second model system, in which there is widespread demyelination of the spinal cord and optic nerves, we also show that thinly remyelinated axons with short internodes persist for over the course of 2 y. These studies confirm the persistence and longevity of thin myelin sheaths and the importance of remyelination to the long-term health and function of the CNS.

“Thin myelin sheaths as the hallmark of remyelination persist over time and preserve axon function” by Ian D. Duncan, Rachel L. Marik, Aimee T. Broman, and Moones Heidari in PNAS. Published online October 24 2017 doi:10.1073/pnas.1714183114


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Support for Populist Ideologies Linked to National Narcissism and Feelings of Disadvantage

Support for Populist Ideologies Linked to National Narcissism and Feelings of Disadvantage

Summary: University of Kent researchers report people who believe they are disadvantaged are more likely to have an unrealistic belief in the greatness of their country and support populist ideologies.

Source: University of Kent.

People who perceive they are part of a disadvantaged group are more likely to have an unrealistic belief in the greatness of their nation and support populist ideologies.

A team of psychologists and political scientists from the universities of Kent (UK), Warsaw (Poland) and Maryland (USA) found in three studies that national collective narcissism was linked to support for populism. In the UK, collective narcissism predicted support for Brexit, in the US it predicted support for Donald Trump, and in Poland it predicted support for the populist Law and Justice party.

The study found that collective narcissism, i.e. an unrealistic belief in the greatness of the nation, increased in response to group feelings of being disadvantaged, especially when this was long lasting.

The researchers suggest that the narrative of relative disadvantage, fuelled by populist leaders, might reinforce a ‘defensive and destructive’ national perspective. Narcissistic beliefs about the in-group greatness are a way to compensate for feelings of being worse off than other groups.

One of the team, Dr Aleksandra Cichocka of the University of Kent’s School of Psychology, said that the results might partially explain why populism is often linked to prejudicial attitudes and behaviours.

Image shows a group of people.

In the first study, data from Poland in 2014 was used to examine the relationship between national collective narcissism versus conventional national identification and support for the populist Law and Justice party and its leader. The researchers found that collective narcissism, rather than mere strength of national identification, was a significant predictor of support for this party.

Study two was conducted around the EU Referendum in the UK. Researchers found that a perception of long-term group disadvantage resulted in a higher willingness to adopt populist views reflected in Brexit support. They found that this link was driven by national collective narcissism.

Study three examined support for Donald Trump. Researchers found that feelings that Americans were being disadvantaged relative to immigrants was associated with national collective narcissism, which in turn predicted preference for Trump.

ABOUT THIS NEUROSCIENCE RESEARCH ARTICLE

Source: Martin Herrema – University of Kent
Publisher: Organized by NeuroscienceNews.com.
Image Source: NeuroscienceNews.com image is in the public domain.
Original Research: Abstract for “Populism as Identity Politics: Perceived In-Group Disadvantage, Collective Narcissism, and Support for Populism” by Marta Marchlewska, Aleksandra Cichocka, Orestis Panayiotou, Kevin Castellanos, and Jude Batayneh in Social Psychological and Personality Science. Published online October 4 2017 doi:10.1177/1948550617732393

CITE THIS NEUROSCIENCENEWS.COM ARTICLE
University of Kent “Support for Populist Ideologies Linked to National Narcissism and Feelings of Disadvantage.” NeuroscienceNews. NeuroscienceNews, 24 October 2017.
<http://neurosciencenews.com/populism-national-narcissism-7803/&gt;.

Abstract

Populism as Identity Politics: Perceived In-Group Disadvantage, Collective Narcissism, and Support for Populism

Self-esteem is shaped by the appraisals we receive from others. Here, we Populists combine anti-elitism with a conviction that they hold a superior vision of what it means to be a true citizen of their nation. We expected support for populism to be associated with national collective narcissism—an unrealistic belief in the greatness of the national group, which should increase in response to perceived in-group disadvantage. In Study 1 (Polish participants; n = 1,007), national collective narcissism predicted support for the populist Law and Justice party.

In the experimental Study 2 (British participants; n = 497), perceived long-term in-group disadvantage led to greater support for Brexit and this relationship was accounted for by national collective narcissism. In Study 3 (American participants; n = 403), group relative deprivation predicted support for Donald Trump and this relationship was accounted for by national collective narcissism. These associations were present even when we controlled for conventional national identification. We discuss implications of the link between collective narcissism and support for populism.

“Populism as Identity Politics: Perceived In-Group Disadvantage, Collective Narcissism, and Support for Populism” by Marta Marchlewska, Aleksandra Cichocka, Orestis Panayiotou, Kevin Castellanos, and Jude Batayneh in Social Psychological and Personality Science. Published online October 4 2017 doi:10.1177/1948550617732393


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Residential care options for Alzheimer’s

As Alzheimer’s disease progresses, you may no longer be able to care for the person at home. When that happens, you may want to look for a long-term care facility for the person.

Residential care options

Continuing care retirement communities (CCRCs)—a home, apartment, or room in a retirement community where people with Alzheimer’s can live and get care. Residents may move from one level of care to another—for example, from independent living to more supervised care.
Assisted living facilities—a facility with rooms or apartments for people who may need some help with daily tasks. Some assisted living facilities have special Alzheimer’s units.
Group homes—a home where several people who can’t care for themselves and two or more staff members live. At least one caregiver is on site at all times.

Nursing homes—a place for people who can’t care for themselves anymore. Some nursing homes have special Alzheimer’s disease care units.

Your own house

Your own house with hospital bed, pole (connected from floor to ceiling) to hang on to when transferring from bed to wheelchair and senior safe your  house with guide rails and other measures. And employ a private caregiver or home helper.

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