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Monday, February 20, 2017

A new rhythm

February 20.2017


Dance benefits Parkinson's patients

Sherry Brown walks gingerly into the dance class, her right elbow anchored at her side, her hand cupped in a ball. Her balance is uneven, so she takes care in finding a seat among the circle of chairs in the light-filled room at the Stanford Neuroscience Health Center. As the slow, rhythmic keyboard music begins, her arms, stiffened by Parkinson’s disease, open in a wide, upward arc as if embracing the sky.


“You get a sense of your body and are pushing your body to do things you don’t think you can accomplish,” says Brown, who was diagnosed in 2008 with the neuro­degenerative disease. “There is something about the music and movement together that seems to help at a different level. … I come out of the class feeling energized and relaxed, all at the same time, and ready to move.”
Brown is among some 20 students who have found a welcoming community at the Dance for Parkinson’s Disease class, also known as Dance for PD. The class is not only physically therapeutic but often gives students a psychological boost. People struggling with movement and speech because of the disease say the sessions are liberating, providing a new way to express themselves.

The program, begun 15 years ago in Brooklyn, New York, and now offered in 16 countries, was introduced at Stanford last year with the opening of the new neuroscience center. It is not a traditional dance class in any sense, but rather a group artistic experience. Teachers use elements of classic and social dancing, together with imagery, poetry and live music, to inspire participants to move in creative ways. The results translate into daily life, studies show, as participants demonstrate an improvement in walking and fine-motor skills, such as tapping a finger, and feel an uplift in mood and a better sense of self that comes from gaining more physical control.
“Dancing has all the elements Parkinson’s patients can benefit from: extension and flexibility and moving with intention,” says Damara Ganley, a professional dancer and trained Dance for PD instructor. “Dancers are trained to be in their bodies in a conscious way, and Parkinson’s patients also are learning to be in their bodies in a conscious way.”
Brown, 74, gray-haired and slender, is a marriage and family therapist who
Sherry Brown says the dance classes help
her body feel more "in tune."
maintains an active social life despite her physical challenges. She says the disease crept up on her, gradually narrowing her world. Her movements became slower, more labored, and she no longer easily stood straight. She began to feel some weakness in her right hand, which would tire after writing a few words. She would easily lose her balance and began to have debilitating falls, including one in which she broke her hip and another in which she struck her head on a rock while sweeping the walk outside her home. When she was diagnosed with Parkinson’s, she says, she fell into despair.
“I definitely went through a grieving period. I felt like my life was over,” she says over a cup of tea at her dining room table. She now has a part-time personal assistant who helps around the house, though she is able to prepare the tea herself.
Parkinson’s, which affects as many as 10 million people worldwide, can cause rigid limbs, tremors, lack of muscle control and slowed movement. Patients may have impaired walking and balance and are more prone to falls. Some also suffer from depression and may experience a cognitive decline, with slowed thinking or memory problems.
Brown says daily tasks became a challenge, as she could no longer stab a piece of lettuce with a fork, handle a pair of scissors or easily get up out of a chair. She stopped accepting new referrals to her therapy practice. She no longer drove on the freeway and began to miss out on important social occasions because of disease-related fatigue.
“I spent about a year really being aware of all the losses,” she says.
Gradually, however, her life began to open up again as she came to a place of acceptance and began to improve physically with the help of new medication, physical therapy, fitness training, daily walks — and dance.

On the move

During a recent Friday session, Ganley, a petite woman with short-cropped hair,
Professional dancer Damara Ganley is trained
to teach Dance for PD.
opens with some gentle stretching exercises in the chair, as the keyboardist plays his own rhythmic composition, which has an ethereal quality. Participants, seated in a circle, cross their feet back and forth, then move one foot to the right while gesturing to the left. The sequence is repeated on the opposite side, requiring focused concentration.
“That tickled my brain,” Ganley says with a smile. Then she begins a sequence of movements to the lyrics “Autumn leaves are falling, falling” as the dance students join in, rolling their hands in space like leaves being tossed in the wind, then gently falling down.
The class has many interactive moments, including one in which the instructor prods the students to “say something with the body” to a neighbor in the circle, who responds in kind. The exercise is repeated with a different partner, and the results then are displayed for the entire class. “Beautiful,” Ganley says as heads nod.
On this day, the 75-minute session includes other improvisational exercises, as well as a traditional Israeli circle dance with a rather challenging series of steps. It closes with dan­cers individually calling out their names, then using a gesture to express what they are grateful for. Some blow kisses; others use a sweeping move of the arm to encompass everyone in the room. “Each of us is a living poem to be savored and acknowledged,” Ganley says.
Brown, neatly dressed in black pants and a tailored shirt, says the class has a mindful, meditative quality. “It’s totally creative and totally accepting of whatever your abilities are,” she says.
With her new medication regimen and her physical activities, she is able to do many things that weren’t possible before. For instance, in one class, she found she could again stand on her toes and keep her balance. And during a flamenco dance routine, she found herself snapping her once-rigid fingers. “It just came to me,” she says. The dance class “challenges you in ways you would not have thought possible.”
The class also has helped improve the fluidity of her movements. “I think the rhythm helps keep things more even. I feel my gait is more even. In general, my body feels more in tune — more rhythmic. It’s subtle.
“I think it has helped me a lot to appreciate what I can do — big and little things both,” she adds. “I feel that with all things I am doing — the exercise, the dance, the medications — I am definitely delaying the severe symptoms of the disease. I am pleased that I am able to have the life that I have at this point.”
'The PD dancers have told us that this type of dance restores their self-image and brings them joy.'
The program was started in 2001 by Olie Westheimer, executive director of the Brooklyn Parkinson Group, who walked into the Brooklyn studio of the Mark Morris Dance Group one day with the idea of creating a dance class for members of her group, says David Leventhal, a former Mark Morris company member who is now Dance for PD’s program director. West­heimer felt patients were spending a lot of time dwelling on the disease and shuttling to doctors’ and therapists’ offices, and she wanted them to do something positive and beneficial together. Leventhal became one of the first instructors.
“I thought it was the most enjoyable teaching experience I had ever had because people were so focused on learning and trying to absorb as much as we had to offer,” Leventhal says. “They were so engaged as students right away because for them it was not just an activity they added to their week but an essential portal for them to experience what possibilities were still available to them. It became a way of accessing their true selves — who they were as people, rather than as patients.”
Helen Bronte-Stewart helped ensure the 
neuroscience building included 
a dance studio
Helen Bronte-Stewart, MD, a Stanford professor of neurology and neurological sciences and a former professional dancer, says she has always tried to incorporate exercise, yoga and dance as part of the standard therapy for her Parkinson’s patients.
“If you improve your core strength, then the negative effects like difficulty of getting out of chairs, getting out of a car, will be better,” says Bronte-Stewart, who refers to the process of exercise and balance training as “training the machine.”
“You have to keep training that motor system — training the brain — as a way of continuing movement in a disease that otherwise limits movement, counteracting the stiffness and slowness that the brain wants to impart on the musculoskeletal system,” she says.
“As physicians, we stress the importance of physical activity, social interaction and mental stimulation to our patients with Parkinson’s disease,” she adds. “Dance for PD gives them all three. But it is much more than a possible therapy or treatment; the PD dancers have told us this type of dance restores their self-image and brings them joy.”
When the neuroscience building was in the planning stages, Bronte-Stewart says she was determined to include a dance studio and helped design the space with a flexible floor and glass walls on two sides. She and Ganley obtained a grant from the National Parkinson Foundation for the class, which is free and is open to all in the community.
“The worlds of dance and medicine have been far apart for a long time. That is why this is so exciting,” Bronte-Stewart says. “If you have a chronic debilitating disease, you begin to get an image of yourself as someone who can’t move. But you can go to this class and do something beautiful and graceful and be part of a community that accepts you. That is what we should capture, as much as whether your motor function is better.”

Backed by research


Leventhal says the program initially met with some skepticism in the medical community. “There was one neurologist who told us, ‘I think the program is great. But I can never recommend it because dancing is a frivolous activity and that would tarnish my reputation as a serious doctor,’ ” he says. “There is a lot of misconception about the amount of learning and skill and brain work and physical work that somebody has to do to execute a dance. It’s the opposite of frivolous. It directly addresses what people are struggling with. Over 15 years, people have come to recognize that.”

In fact, published studies have shown that Parkinson’s patients who do some form of dance experience measurable physical and psychological improvements. More than a dozen studies have shown that twice-weekly dance classes improve balance, motor skills, freedom of movement and endurance. One study, published in 2011 in Frontiers in Aging Neuroscience, found that even after a single class, patients were able to move their limbs more easily, tap their fingers and change their facial expressions. (Loss of facial muscle control can lead to muted expression.) The study participants also described many improvements in the quality of their lives, with one saying, “I want to fly. It gives me a swinging feeling. I feel relaxed after the dance lesson. Before, I’m always very stiff.”
Research suggests dance has benefits beyond basic exercise for these patients because it is a rich experience involving multiple senses, creative expression and social interaction. Moreover, unlike exercise classes, participants are motivated to attend, rarely missing a class and often clamoring for more, studies show.
“People tell us, ‘I always look forward to coming to class because it’s so uplifting,’ ” Bronte-Stewart says.
She says dance is a form of mental as well as physical training. “When you think of it as a neurologist, they are planning, using their executive function and they are sequencing. These are all frontal-lobe functions that can be impaired in Parkinson’s.”
Bronte-Stewart says animal studies suggest there may be a biological basis for improved neurologic function among dance participants. For instance, research shows that if animals are able to do a physical activity they enjoy, they experience less inflammation, which may help counter the disease, and are able to regenerate adult stem cells, which can help build muscle and other tissues.
“It’s not too much of a stretch to suggest that dance possibly may improve the brain’s regeneration of its own stem cells,” she says.
Juan Bulnes, center, attends with his wife, Margaret, right. Students and community members also participate in the class.

Dance classes may also counter some of the cognitive and mood issues that affect patients, who may withdraw and suffer social isolation and poor self-esteem. The classes provide a social setting where everyone is accepted, regardless of their limitations, and studies show participants feel their mood lighten and their anxiety decline. In a 2015 study published in Journal of Neural Transmission by Westheimer and colleagues from four universities, participants reported feeling less helpless, grateful for the companionship and a general sense of improved health.
Albert Cohen, one of the Stanford dance students, says he appreciates the sense of camaraderie and caring among the students. “The attitude there is positive and receptive, which is worth a lot,” says Cohen, 87. “I’m not sitting in a room doing nothing. So it’s very beneficial.”
A musicologist and former chair of Stanford’s Department of Music, Cohen suffered a major fall in the summer that fractured his hip and pelvis. When he and his wife, Betty, returned after a two-month hiatus, class members embraced them with hugs and good wishes. Betty Cohen says the gathering is the highlight of her week.
“You’re getting out. You’re with other people. You are exposed to music, which helps the brain. There is rhythm and movement. I think all of this is helpful,” she says. “It really is more than the dance and the music. It’s greater than the sum of its parts. Something emanates from the heart and soul. It helps me emotionally accept everything that I’m finding hard to accept.”
Caregivers are encouraged to attend the classes to support their partners and to share a positive experience. “I think the class allows care partners to see their loved ones and companions in a different light and enjoy an hour together when they are not dealing with the struggle of daily life but see each other as dance partners and as co-learners. That’s very important,” Leventhal says. Stanford medical students and undergraduates also participate in the class through specially designed coursework.
"There is something about the music and movement together that seems to help at a different level.'
Juan Bulnes, who was diagnosed with Parkinson’s in 2008, regularly attends class with his wife, Margaret. He often does the movements in his chair, as he is shaky on his feet and afraid he will fall, he says.
“There is joy in the dancing class,” says Bulnes, a 74-year-old computer scientist. “We do some of the same movements as in other classes, like tai chi or physical therapy, and here we do them with an added, special flair that comes from conscious dance movements, such as gracefully waving your hands to imitate falling leaves, rain, wind or reaching for the stars. Integrating physical exercise, rhythm, music and ima­gination makes dancing a very liberating experience.”

Making it more accessible

Leventhal, who gave up performing five years ago to devote all of his time to the project, has been making the program more widely available and providing opportunities for practice between classes. The flagship Dance for PD program in New York has developed three DVDs, which have been distributed to 4,000 people worldwide, and last year began live streaming classes from Brooklyn and Toronto.
Mark Morris Dance Group, together with the New York creative agency SS+K, has also created Moving Through Glass, custom software for use on the Google Glass platform to help Parkinson’s patients navigate the world outside the dance studio. The application enables users wearing the device — a head-mounted display in the form of a pair of eyeglasses — to play modules in which Mark Morris dancers give prompts, taking them through home exercises to help with specific problems, like regaining balance or unfreezing the limbs. The app is being evaluated at three locations around the country, including Stanford, where Bronte-​Stewart has recruited dance class participants to try it out.
Dance for PD, meanwhile, is becoming a widely accepted form of Parkinson’s therapy. Stanford recently added a second class that meets on Monday afternoons.
Sherry Brown attends both the Monday and Friday sessions, as she is determined to do what she can to forestall any further physical decline. “I do have fears about the future and there’s nothing I can do about that. I like to stay in the present as much as I can,” she says.
The dance class helps set aside her fears, at least for the moment. “It has helped me adjust to the future. It becomes a little less scary about the unknown, seeing other people go through it,” she says. “It focuses you on the present, and the rest of your worries fade into the distance. You are focused on the here and now.”
http://stanmed.stanford.edu/2017winter/dance-for-parkinsons-disease-at-the-stanford-neuroscience-health-center.html

HomeFeatured Discovery of Genetic Switch Could Help Prevent Parkinson’s Symptoms

NEUROSCIENCE NEWS
Summary: A new study reveals a critical gene network involved in Parkinson’s disease.


Source: University of Leicester.

By discovering the gene networks that orchestrate this process, the researchers have singled out new therapeutic targets that could prevent neuron loss. NeuroscienceNews.com image is for illustrative purposes only.

“Studying the roles of genes such as ATF4 in human neurons could lead to tailored interventions that could one day prevent or delay the neuronal loss seen in Parkinson’s” – Dr Miguel Martins, MRC Toxicology Unit, University of Leicester.

A genetic ‘switch’ has been discovered by MRC researchers at the University of Leicester which could help to prevent or delay the symptoms of Parkinson’s disease.
In a paper published in the journal Cell Death and Differentiation, the team discovered that a gene called ATF4 plays a key role in Parkinson’s disease, acting as a ‘switch’ for genes that control mitochondrial metabolism for neuron health.

Dr Miguel Martins from the MRC Toxicology Unit at the University of Leicester, who led the research, explained: “When the expression of ATF4 is reduced in flies, expression of these mitochondrial genes drops. This drop results in dramatic locomotor defects, decreased lifespan, and dysfunctional mitochondria in the brain.

“Interestingly, when we overexpressed these mitochondrial genes in fly models of Parkinson’s, mitochondrial function was reestablished, and neuron loss was avoided.”
By discovering the gene networks that orchestrate this process, the researchers have singled out new therapeutic targets that could prevent neuron loss.

Some forms of Parkinson’s are caused by mutations in the genes PINK1 and PARKIN, which are instrumental in mitochondrial quality control.

Fruit flies with mutations in these genes accumulate defective mitochondria and exhibit Parkinson’s-like changes, including loss of neurons.
The researchers used PINK1 and PARKIN mutant flies to search for other critical Parkinson’s genes — and using a bioinformatics approach discovered that the ATF4 gene plays a key role.


Dr Martins added: “Studying the roles of these genes in human neurons could lead to tailored interventions that could one day prevent or delay the neuronal loss seen in Parkinson’s.”
The findings build upon recent research by the University of Leicester team, which recently discovered several genes that protect neurons in Parkinson’s disease, creating possibilities for new treatment options.
Two of the genes — PINK1 and PARKIN — affect how mitochondria break down amino acids to generate nucleotides – the metabolism of these molecules generates the energy that cells need to live.
ABOUT THIS GENETICS RESEARCH ARTICLE
Dysfunctional mitochondrial metabolism has been linked to Parkinson’s and the team of researchers previously showed that boosting this metabolism with nucleotides can protect neurons.
Funding: The study was supported by Medical Research Council.
Source: Miguel Martins – University of Leicester 
Image Source: NeuroscienceNews.com image is in the public domain.
Video Source: The video is credited to Research Square.
Original Research: Full open access research for “dATF4 regulation of mitochondrial folate-mediated one-carbon metabolism is neuroprotective” by Ivana Celardo, Susann Lehmann, Ana C Costa, Samantha HY Loh & L Miguel Martins in Cell Death and Differentiation. Published online February 17 2017 doi:10.1038/cdd.2016.158


Abstract

dATF4 regulation of mitochondrial folate-mediated one-carbon metabolism is neuroprotective
Neurons rely on mitochondria as their preferred source of energy. Mutations in PINK1 and PARKIN cause neuronal death in early-onset Parkinson’s disease (PD), thought to be due to mitochondrial dysfunction. In Drosophila pink1 and parkin mutants, mitochondrial defects lead to the compensatory upregulation of the mitochondrial one-carbon cycle metabolism genes by an unknown mechanism. Here we uncover that this branch is triggered by the activating transcription factor 4 (ATF4). We show that ATF4 regulates the expression of one-carbon metabolism genes SHMT2 and NMDMC as a protective response to mitochondrial toxicity. Suppressing Shmt2 or Nmdmc caused motor impairment and mitochondrial defects in flies. Epistatic analyses showed that suppressing the upregulation of Shmt2 or Nmdmc deteriorates the phenotype of pink1 or parkin mutants. Conversely, the genetic enhancement of these one-carbon metabolism genes in pink1 or parkin mutants was neuroprotective. We conclude that mitochondrial dysfunction caused by mutations in the Pink1/Parkin pathway engages ATF4-dependent activation of one-carbon metabolism as a protective response. Our findings show a central contribution of ATF4 signalling to PD that may represent a new therapeutic strategy.

“dATF4 regulation of mitochondrial folate-mediated one-carbon metabolism is neuroprotective” by Ivana Celardo, Susann Lehmann, Ana C Costa, Samantha HY Loh & L Miguel Martins in Cell Death and Differentiation. Published online February 17 2017 doi:10.1038/cdd.2016.158

http://neurosciencenews.com/parkinsons-genetics-neurology-6128/

Alzheimer’s, Parkinson’s linked to body’s mishandling of ‘garbage’

February 20, 2017


A new study…may help explain how diseases like Alzheimer’s and Parkinson’s spread in the brain. Sometimes when neurons dispose of toxic waste, neighboring cells get sick.
“Normally the process of throwing out this trash would be a good thing,” says Monica Driscoll, professor of molecular biology and biochemistry at Rutgers University. “But we think with neurodegenerative diseases like Alzheimer’s and Parkinson’s, there might be a mismanagement of this very important process that is supposed to protect neurons but, instead, is doing harm to neighbor cells.”
“What we found out could be compared to a person collecting trash and putting it outside for garbage day,” says Driscoll. “They actively select and sort the trash from the good stuff, but if it’s not picked up, the garbage can cause real problems.”
The roundworms engineered to produce human disease proteins associated with Huntington’s disease and Alzheimer’s threw out more trash consisting of these neurodegenerative toxic materials. While neighboring cells degraded some of the material, more distant cells scavenged other portions of the diseased proteins.
“These findings are significant,” Driscoll says. “The work in the little worm may open the door to much needed new approaches to addressing neurodegeneration and diseases like Alzheimer’s and Parkinson’s.”
https://www.geneticliteracyproject.org/2017/02/20/alzheimers-parkinsons-linked-to-bodys-mishandling-of-garbage/

Holly Robinson Peete - Brings Real Life Glamour to the AGTA Spectrum Awards™

DALLAS, Feb. 18, 2017



Being glamorous and leading a 'real' life might seem like contradictory concepts, but it's all a day in the life for actress Holly Robinson Peete. The multi-talented actress, entrepreneur, author and philanthropist is currently shooting the second season of her family docu-series "For Peete's Sake" with her husband, former NFL quarterback Rodney Peete, their four children and her mother, Dolores. The show gives a positive spin to reality TV by sharing their lives, everyday challenges and their journey with son RJ, who has autism. 

Being a mom, career woman and shooting a docu-series can be demanding, but Robinson Peete juggles her multi-faceted life in style. The actress recently launched a namesake clothing line, HRP by Holly Robinson Peete, exclusively available at EVINE Live. The collection, which she wears on her show, reflects her funky everyday "casual couture" look. 

Featured in the photo: Holly Robinson Peete Necklace: Jewelsmith, Inc.; Ring #1: Wendy Brandes Jewelry; Ring #2: T. Foster & Co, Fine Jewelers; Bracelet: ARYA ESHA; Earrings: llyn strong fine art jewelry; Photographer: Andrew MacPherson; Stylist and Producer: Tod Hallman In a photo shoot for the American Gem Trade Association (AGTA), Robinson Peete, who starred in the hit feature film "21 Jump Street," and television series "Chicago Fire," looked stunning in the spectacular jewelry designed by the 2016 Summer AGTA Spectrum Award winners. Robinson Peete wears simple jewelry such as gold and silver hoops as her "go to" daytime look, but glamorous jewelry and gemstones are very much a part of her lifestyle. 

"It's funny because my line [HRP] is really about the casual mom, but listen, I'm on red carpets," she said. "It's really important to me to accessorize," explained Robinson Peete who loves to dress up and wear dramatic gowns when she steps out in Hollywood. "When I step it up, I try to go all the way," she said. "I've been in this business for 30 years so I've seen all different types of jewelry and Diamonds, but what is so unique about the gemstones is that there's a story behind everything and the colors are so bright and brilliant and different - and I get off on color," said Robinson Peete. "When I did this photo shoot, every time they would hand me something else to put on, it was like each item gave you a certain feeling and put you in a certain mood. I loved them all." 

During the shoot, Robinson Peete wore a spectacular platinum pendant featuring a 13.44mm golden South Sea cultured Pearl accented with Diamonds by Judy Evans, Oliver & Espig Gallery of Fine Arts, which won the "Best Use of Pearls" title at the AGTA Spectrum Awards. The piece was complimented by other winning jewelry including Ricardo Basta, E. Eichberg, Inc.'s stunning "Honey" ring which features a Helodor accented with Sapphires and Diamonds and won in the "Business/Day Wear" category. "You know jewelry is spectacular when you want to plan an outfit around it," said Peete. "Rarely do you build around jewelry, but these gemstones are so spectacular and so fun," explained the actress who highlighted Citrines and Sapphires as two of her favorite stones. 

During the photo shoot, she wore a royal blue Caroline Herrera gown which was accented with jewelry from the AGTA Spectrum Awards "Evening Wear" category - a black Opal ring with Sapphires and Diamonds by Phillip Dismuke, Jewelsmith, Inc.that took second place honors and a stunning pendant by Robert Pelliccia, J.R. Dunn Jewelers featuring a boulder Opal accented with blue and pink Sapphires and Diamonds on a black Diamond bead necklace that captured third place in the category. 

While Robinson Peete has a wonderful family and many achievements, her life has not been without challenges. When her father was diagnosed with Parkinson's disease, her world changed. "My dad [has] been gone for 14 years now, but his struggle with Parkinson's led us to a life of service," said Robinson Peete. Inspired to help those affected by Parkinson's, she and Rodney founded the HollyRod Foundation in 1997. After their son, RJ, was diagnosed with autism they expanded the mission of HollyRod to also provide support and resources to families affected by autism. To help raise funds for the foundation, every year they hold events such as DesignCare - and fashion and entertainment are very much on the agenda. 

While fashion is a highlight of DesignCare, HollyRod, most importantly, has been able to help many people thanks to the support of dedicated friends and sponsors. "We're really blessed to have great partners," said Robinson Peete. "One in 68 kids are affected by autism spectrum disorder. It's on the rise and what happens is a lot of these children have no access to therapy services or any compassionate care and the same with Parkinson's," she said. "It's really rewarding to give back." she said. "We've been really blessed to be able to pay it forward." For more information about DesignCare and the HollyRod Foundation visit www.hollyrod.org. 

ByN. Jayne Seward 
For further information regarding the AGTA Spectrum Awards, contactMegan Whitmireat (800) 972-1162 or visit the AGTA website atwww.agta.org. 
The American Gem Trade Association is a not-for-profit Association serving the natural colored gemstone and cultured pearl industry since 1981. Headquartered inDallas, Texas, The AGTA serves the industry as "The Authority in Color." 

To view the original version on PR Newswire, visit:http://www.prnewswire.com/news-releases/holly-robinson-peete--brings-real-life-glamour-to-the-agta-spectrum-awards-300409742.html 
SOURCE American Gem Trade Association
MENAFN1902201700701241ID1095254353

http://menafn.com/1095254353/Holly-Robinson-Peete---Brings-Real-Life-Glamour-to-the-AGTA-Spectrum-Awards™

“May May” Ali stars at Paulie Ayala’s Punching Out Parkinson’s Fundraiser

February 20, 2017

By Jeff Zimmerman
Photos: Robert Hughes


It was not shocking that Maryum “May May” Ali packed the house last night as the featured guest at “Meet The Champs V” at The Fort Worth Club in downtown Fort Worth, Texas for former 2x world champion Paulie Ayala’s Punching Out Parkinson’s annual fundraiser. After all, her dad, “The Greatest” Muhammad Ali, loved being around people so being an Ali and big crowds is just par for the course. Ayala’s Punching Out Parkinson’s was created to help those inflicted with the dreadful disease of Parkinson’s that has no cure where he leverages non-contact boxing drills to help with such things as balance, hand eye coordination, mental focus and muscle memory.

The star of the night was May May as she is affectionately known and definitely got her dad’s gift of gab. She shared very honest and personal stories of his fight against Parkinson’s, both the ups and the downs.

She also talked about some of the possible contributing factors to her dad’s disease such as the pesticide that was sprayed on the log cabins at her dad’s training camp in Deer Lake, Pennsylvania where he spent much of his time. Also Ali’s dad, Cassius Clay Sr. was a great sign painter in Louisville, KY painting markets, liquor stores and much more. The cans of lead paint were kept in the back of the house where Ali and his brother grew up and the fumes were extremely powerful. May May only found this out a year ago that her dad inhaled these fumes as a child. 

She suggested that perhaps the boxing and all the head trauma brought out the Parkinson’s a little sooner, but the inhaling of the paint and pesticides could have a played a bigger role as Ali did not inherit the Parkinson’s gene.

One of the highlights of her speech was about the book she wrote about her dad, “I Shook Up the World: The Incredible Life of Muhammad Ali,” which would go for $2,000 in the live auction. May May threw in an autographed picture of her dad as a bonus to the highest bidder. She wrote the book for kids as a way to tell her dad’s history but also make it appealing with pictures based off the many poems he told, for example, where he says “I’ve wrestled with alligators” prior to his fight with George Foreman in the Rumble in the Jungle, the book illustrates Ali wrestling with an alligator.

She recalled the painful fights with Larry Holmes and Trevor Berbick at the end of his career when the family knew he was slowing down and was slurring his speech. The family wanted him to lose against Berbick so he would stop fighting, which turned out to be his last fight and he lost. May May described going to school after that fight was like going to a morgue.

She talked about her dad as this independent, alpha male and his denial phase where he didn’t want to take his medication or do the speech therapy. He would hide his meds as he didn’t like the way they made him feel. On one occasion, the news showed a story how the medication he was taking could be harmful, so he went a whole year defiantly not taking them.

Ali lost a lot of trust in his doctors as they now said his Parkinson’s was going to progress more after 11 years of telling him differently. It was a period of 3 or 4 years where it was difficult to get her dad to do what he was supposed to do.
Ali was an optimist by nature, a glass half full person and he had nothing to compare himself too as he didn’t know anyone with the disease. So he just kept moving and kept the faith he always had.

She recounted the lighting of the torch at the 1996 Olympics in Atlanta as a turning point for her dad. She was worried that his shaking would get worse if he was nervous and she jokingly said, “daddy don’t burn the whole stadium down, don’t drop the torch, daddy don’t drop it.” It was a huge moment for Ali seeing all the love and support as he had been away from the spotlight for some time.

She went into detail on how her family learned to cope with his disease and rotated visits with her siblings so her stepmom could have time to rest too. May May also shared how her dad got an impulsive control disorder, punding, caused from the dopamine medication. He loved pretty things in magazines and would rip the pages out and put them on the floor, he could do this for hours. If you tried to intervene he would get upset, so instead, they would bring him magazines and spend time with him.

On one occasion, they went to a party at a mansion Ali had once owned 15 years earlier and had big table books. Due to the punding, he wanted to rip the pages out of the books, but the family left early to avoid anything happening.

She discussed how exercise helped her dad immensely after first not wanting to do it. He was a boxer, so he had a gym built at his house. He loved magic. He boxed and did his magic. She recalled the wide eyes he got when the family celebrated his 74th and last birthday with a magician.

In addition to the exercise, her dad chose prayer and his faith saved him. He was a spiritual person who believed in the higher power and never questioned Parkinson’s and why he got it. He said others had leukemia and cancer and were in pain, Ali was not in pain.

Ali was a proud man and made others stronger too on how he handled himself. May May described a time after the Atlanta Olympics, when a lady approached her shaking and said she never went out because people would stare at her and she felt lonely and isolated. But after seeing Ali, she went out to the coffee shop and to the grocery store with her daughters and when someone would stare, she would say, “I have what Muhammad Ali has, what are you looking at,” which drew a roar from everyone.

In closing, May May shared a touching poem she wrote about her dad, called PEARL, paralleling his life with and without Parkinson’s.
Deborah Hawkins of the WBC was also on hand to present May May and the Ali family a plaque for their efforts towards Parkinson’s disease research and in the support of Paulie Ayala’s Punching Out Parkinson’s program. Local ESPN radio personality and longtime boxing announcer Mark Elfenbein participated in the live auction portion of the program that included the “I Shook Up the World: The Incredible Life of Muhammad Ali” book and a 10 person trip to Destin, Florida that went for $4,000. The event included several other auction items that were available for bid and a sit down dinner.

Past keynote speakers have included Rich Clifford, former NASA Astronaut who had a secret battle with Parkinson’s during his space travels, former 4X Boxing World Champion and Hall of Famer Terry Norris and CIA’s Chief of Disguise, Tony and Jonna Mendez.

For more information on the program or to make a donation visit www.punchingoutparkinsons.org.

Follow Jeff on Twitter @jazboxing

http://www.fightnews.com/Boxing/may-may-ali-stars-paulie-ayalas-punching-parkinsons-fundraiser-394774

Repetitive head injuries may not cause movement problems for former NFL players

February 19, 2017




Former NFL players who had repeated head injuries may not have significant problems with motor functions later in life, according to a preliminary study released today that will be presented at the American Academy of Neurology's 69th Annual Meeting in Boston, April 22 to 28, 2017.


Motor functions are complex movements where the muscles and nerves work together, like walking, kicking and writing.
Repeated head injuries have been shown to lead to chronic traumatic encephalopathy (CTE), a  that causes thinking, behavior, and mood problems. Problems with motor functions have also been documented among former boxers who had repeated head injuries and were later confirmed to have CTE. Researchers wanted to know if former NFL players experience similar motor function problems from repeated head injuries.
"We found that while the motor functions of former NFL players were not as good as other men their age, they were still within normal range and not related to repeated head injury," said study author Samuel Frank, MD, of Harvard Medical School in Boston, Mass., and member of the American Academy of Neurology.
For the study, researchers compared 95 former NFL players, ages 40-69, to 25 men of the same age who had no history of playing contact sports or having a head injury. They were evaluated with a test that measures  like speech, writing, eating, gait, and posture. Their balance and dexterity was also evaluated. They also were examined with tests of cognitive functioning and brain imaging. The study, referred to as DETECT, was conducted at Boston University School of Medicine.
Scores on the motor tests were low and overall in the normal range for both the NFL players and the control group. Higher scores indicate a greater impact of movement disorder symptoms. But the former NFL player group did have significantly higher scores than the control group with an average score of five compared to an average score of two. People with Parkinson's disease may have scores in the 10- to 60-point range.
Those with worse motor scores were also more likely to have worse scores on tests of thinking skills and executive function, which involves planning and problem solving.
The researchers found no relationship between an estimate of cumulative head impacts and motor scores.
"Our findings could signify that head trauma in football may have less impact on regions of the brain that control motor function than head trauma in boxing," said Frank. "This research adds to what we already know about repeated  and how they affect athletes. Larger studies are now needed to further test this hypothesis."

Provided by: American Academy of Neurology 

https://medicalxpress.com/news/2017-02-repetitive-injuries-movement-problems-nfl.html

Research sheds light on mechanisms underlying aging

February 16, 2017



Aric Rogers, Ph.D., of the MDI Biological Laboratory in Bar Harbor, Maine, studies the molecular mechanisms underlying aging in the roundworm, C. elegans. Credit: MDI Biological Laboratory


Scientists have known for decades that drastically restricting certain nutrients without causing malnutrition prolongs health and lifespan in a wide range of species, but the molecular mechanisms underlying this effect have remained a mystery.


In a paper recently published in the journal Aging Cell, MDI Biological Laboratory scientist Aric Rogers, Ph.D., sheds light on an important genetic pathway underlying this process, raising the possibility that therapies can be developed that prolong the healthy years without having to suffering the consequences of a severely restricted diet.
"It's tantalizing to think that we might be able to activate a protective response to enhance our own health without resorting to extreme dietary regimes," Rogers said.
Rogers studies mechanisms important to the positive effects of dietary restriction in an intact organism—the tiny roundworm, C. elegans—as opposed to cells in a petri dish. C. elegans is an important model in aging research because it shares nearly half of its genes with humans and because of its short lifespan—it lives for only two to three weeks—which allows scientists to study many generations over a short period of time.
"Aric's identification of a molecular mechanism governing the life-prolonging effects of dietary restriction is a validation of our unique approach to research in aging and regenerative biology," said Kevin Strange, Ph.D., president of the MDI Biological Laboratory. "Our use of whole organisms as research models provides greater insight into the many factors controlling physiological processes than the use of cells alone."
Rogers studies the  underlying aging at the MDI Biological Laboratory's Kathryn W. Davis Center for Regenerative Biology and Medicine. The laboratory is an independent, non-profit biomedical research institution located in Bar Harbor, Maine, focused on increasing healthy lifespan and increasing the body's natural ability to repair and regenerate tissues damaged by injury or disease.
The life-prolonging effects of , also known as DR or CR (calorie restriction), occur in just about every animal tested. They are thought to be an evolutionary adaptation to harsh environmental conditions. In the absence of enough food to eat, evolution has programmed organisms to switch from a growth mode to a survival mode so they can live long enough to reproduce when conditions improve.
Scientists have known for decades that drastically restricting certain nutrients without causing malnutrition prolongs health and lifespan in a wide range of species, but the molecular mechanisms underlying this effect have remained a mystery.In a paper recently published in the journal Aging Cell, MDI Biological Laboratory scientist Aric Rogers, Ph.D., sheds light on an important genetic pathway underlying this process, raising the possibility that therapies can be developed to prolong healthy human lifespan. Credit: MDI Biological Laboratory


Journal reference: Aging Cell
https://medicalxpress.com/news/2017-02-mechanisms-underlying-aging.html
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Discovery of novel autophagy regulators for treatment of neurodegenerative diseases

February 17, 2017

Synthesised curcumin analog C1 specifically binds to TFEB and promotes its nuclear translocation, and then activates autophagy and lysosome biogenesis to degrade alpha-synuclein. Credit: Hong Kong Baptist University



A research team led by Professor Li Min, Director of the Teaching and Research Division (CMTR), and Director of the Mr and Mrs Ko Chi Ming Centre for Parkinson's Disease Research under the School of Chinese Medicine (SCM) of Hong Kong Baptist University (HKBU), discovered a novel autophagy regulator for the treatment of neurodegenerative disorders such as Alzheimer's and Parkinson's disease. The research team was granted a US patent for the study, and related findings were published in the prestigious academic journal Autophagy. The team will explore further collaboration with a potential biotechnology company in the hope of applying such knowledge in new drug development.

Autophagy – how your body detoxifies and repairs itself – is a lysosome degradation pathway for material and energy metabolism and recycling, and plays vital roles in the growth, development and homeostasis of cells. It is essential to the functioning of human cells not only because it facilitates cell renewal and delays ageing, such a mechanism can also help protect the human body by killing bacteria and viruses when a person is infected. In addition, it can sustain the body's functioning by recycling material and energy under adverse conditions like starvation. 
Dysregulation of autophagy has been linked to the pathogenesis of a number of diseases, such as , cancers and diabetes. Japanese biologist Professor Yoshinori Ohsumi was awarded the 2016 Nobel Prize in Medicine for his discovery of autophagy mechanisms. Such a discovery not only helps identify the causes of diseases and develop effective medication therapies, but also implies that there is a great potential for the development of small molecule autophagy regulators in treating different human diseases.. 
Professor Li Min and Dr Song Juxian, Research Assistant Professor of CMTR have been actively engaged in identifying and developing novel autophagy regulators derived from Chinese medicines for the prevention and treatment of neurodegenerative diseases, including Parkinson's disease and Alzheimer's disease. By screening a series of synthesised curcumin derivatives, they found a compound that directly binds to and activates the transcription factor EB (TFEB), a master regulator of autophagy and lysosome biogenesis. According to the research findings, this TFEB activator potently degrades the neurotoxic protein aggregates including the amyloid precursor protein and Tau in Alzheimer's disease and alpha-synuclein in Parkinson's disease in neuronal cells and animal models by inducing autophagy.
Professor Li Min said: "The development of natural autophagy regulators will further help develop new drugs for the treatment of related neurodegenerative diseases. Many researchers in the field of  are interested in this compound since it directly targets TFEB without inhibiting the mammalian target of rapamycin pathway. It will not affect the normal functioning of cells during the eliminating process of the neurotoxic protein aggregates. In addition, this small molecule is orally effective and can be easily synthesised."
More information: Ju-Xian Song et al. A novel curcumin analog binds to and activates TFEB in vitro and in vivo independent of MTOR inhibition, Autophagy (2016). DOI: 10.1080/15548627.2016.1179404

Provided by: Hong Kong Baptist University

https://medicalxpress.com/news/2017-02-discovery-autophagy-treatment-neurodegenerative-diseases.html

Parkinson's: 'Genetic switch' may play key role in preserving brain cells

Published: 

The researchers used fruit flies carrying mutant forms of PINK1 and PARKIN genes to search for other genes involved in Parkinson's disease.
Image credit: Miguel Martins, University of Leicester

So conclude researchers at the University of Leicester in the United Kingdom, who led a new study published in the journal Cell Death and Differentiation.
Worldwide, more than 10 million people are living with Parkinson's disease, a progressive brainwasting disorder that affects movement.
Parkinson's disease gives rise to symptoms that include: muscle rigidity; impaired gait, balance, and posture; tremors in the limbs, hands, face, and jaw; and problems with speech.


The disease primarily impacts a part of the brain called the substantia nigra, where it gradually destroys vital brain cells, or neurons, that produce dopamine - a chemical messenger that is essential for controlling movement.
The loss of dopamine-producing cells can happen for a number of reasons, but in some hereditary cases of Parkinson's disease, it can result from unhealthy mitochondria - tiny compartments inside cells that provide them with energy to function and stay alive.

Genetic switch controls mitochondrial health

Some hereditary forms of Parkinson's disease are caused by mutations in the genes PINK1 and PARKIN, which play an important role in maintaining the quality and integrity of mitochondria.?

For their study, the team used fruit flies because they offer a good model for investigating the genetic and molecular processes of human diseases. The insects carry around 75 percentof the genes that cause human disease.
For example, fruit flies with mutations in PINK1 and PARKIN also show hallmarks of Parkinson's disease - they have weak muscles, struggle to fly, move slowly, and lose dopamine cells in their brains. They also accumulate defective mitochondria.
The researchers used fruit flies carrying mutant forms of PINK1 and PARKIN genes in order to search for other genes involved in Parkinson's disease.
Using an approach called bioinformatics, they discovered that a gene called ATF4 is vital for mitochondrial health; it acts as a switch for increasing or decreasing the activity of PINK1 and PARKIN.
Study leader Dr. Miguel Martins, of the MRC Toxicology Unit at Leicester, explains that when ATF4 expression was reduced in the fruit flies, it also reduced expression of PINK1 and PARKIN, leading to "dramatic locomotor defects, decreased lifespan, and dysfunctional mitochondria in the brain."
The team also found that overexpression of these mitochondrial genes in fruit fly models of Parkinson's disease re-established mitochondrial function and averted loss of brain cells.
By finding the gene networks that orchestrate the mitochondrial processes that keep brain cells healthy, the team believes that they have identified a number of new targets for the treatment of Parkinson's disease.
"Studying the roles of these genes in human neurons could lead to tailored interventions that could one day prevent or delay the neuronal loss seen in Parkinson's."
Dr. Miguel Martins
http://www.medicalnewstoday.com/articles/315909.php
 

VIRTUAL REALITY AIDS PARKINSON'S DISEASE


18th February 2017 - New research 



Virtual reality (VR) technology has been proposed as a new means of rehabilitating people with Parkinson's Disease that has added value over that of physiotherapy. It potentially optimises motor learning in a safe environment, and by replicating real-life scenarios could help improve functional activities of daily living.

Virtual reality (VR) means experiencing things through computers that don't really exist. It is a believable, and interactive 3D computer-created world that you can explore so that you feel you really are there, both mentally and physically. 

For more information go to : http://www.explainthatstuff.com/virtualreality.html 


Most of the studies intended to improve motor function using commercially available devices were compared with the use of physiotherapy. The interventions lasted for between 4 and 12 weeks. In comparison to physiotherapy, Virtual Reality may lead to a moderate improvement in step and stride length. Virtual Reality and physiotherapy may have similar effects on gait, balance, and quality of life. However, the authors concluded that there was low-quality evidence of a positive effect of short-term Virtual Reality exercise on step and stride length.

Reference : The Cochrane Database of Systematic Reviews [2016] 12 : CD010760 (K.Dock, E.M.Bekkers, V.Van den Bergh, P.Ginis, L.Rochester, J.M.Hausdorff, A.Mirelman, A. Nieuwboer) Complete abstract : http://www.ncbi.nlm.nih.gov/pubmed/28000926

http://www.viartis.net/parkinsons.disease/news/170218.pdf mail@viartis.net

©2017 Viartis 

http://www.viartis.net/parkinsons.disease/news/170218.pdf