Shaking Before/After DBS for Parkinson’s Treatment – Video

http://www.youtube.com/watch?v=a_4_DvquSYQ

Shaking Before/After DBS for Parkinson's Treatment
A man demonstrates the difference in his shaking or tremor before and after DBS Therapy. When medication no longer controls your Parkinson's disease symptoms as well as you would like, talk with your doctor about Medtronic DBS Therapy (deep brain stimulation). See if this FDA-approved therapy can help you return to the life and activities you enjoy. Find out more at http//www.medtronicdbs.com/info. Medtronic DBS Therapy for Parkinson's disease is not for everyone. Not everyone will receive the same results. Talk with your doctor to understand the benefits and risks of deep brain stimulation and determine if Medtronic DBS Therapy is right for you. For further information, please visit http://www.medtronicdbs.com A prescription is required. This video contains information about therapies approved for use in the United States and is intended to be viewed by residents of the United States.

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Shaking Before/After DBS for Parkinson’s Treatment – Video

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http://www.longevitymedicine.tv/shaking-beforeafter-dbs-for-parkinsons-treatment-video/

KS3:4 Science – Stem Cell Research- The Issue – Video

http://www.youtube.com/watch?v=2MVdv0o4RZQ

KS3:4 Science – Stem Cell Research- The Issue
© Crown Copyright. Provided by Arts College Limited. artsuk.org Further resources available on http Licensed to Arts College Limited. Licence information available at: artsuk.org Embryonic stem cells and the future of Parkinson's Disease. Stephen Cuff is only 39, but he suffers from Parkinson's Disease and it has turned his life upside down. He can no longer look after his two children and basic day-to-day activities like shaving, takes him a long time. Conventional drugs have not been successful for Stephen, leaving him no option but to undergo brain surgery. Stephen's operation is successful, but it doesn't cure him. One potential future cure is embryonic stem (ES) cell therapy. This is being pioneered by the likes of Professor Ian Wilmut, who became famous when he cloned Dolly the sheep. Professor Wilmut introduces us to the concept of stem cells and the science behind them, whilst presenting his opinion of the technology. Alison Davies, the chair of No Less Human, is a wheelchair user who would refuse ES cell therapy if it were available. She offers a different ethical perspective as to why the use of ES cells should not be permitted. We also hear the differing opinions of leading cell biologists at a recent stem cell conference.

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KS3:4 Science – Stem Cell Research- The Issue – Video

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http://www.longevitymedicine.tv/ks34-science-stem-cell-research-the-issue-video/

Loving Options – Assisted Living Placement Agency – Video

http://www.youtube.com/watch?v=fSw3K1Z_UVE

Loving Options – Assisted Living Placement Agency
http://www.lovingoptions.com – Assisted Living Placement Agency – 20% INSTANT REBATE first months facility fees plus FREE background check. See our Website for details. Loving Options” based in Seattle, Washington is professional placement resource for anyone that has a loved one that is considering living in Retirement Communities, Residential Care Facilities, Assisted Living Facilities, Nursing Homes, Senior Communities, Senior Care Facilities, Alzheimer's Care Facilities, Dementia Care Facilities or any other type of facility that may be requested by our valued clients. We also provide other great resources for our seniors, please visit our website for further information. Qualifiy for an “INSTANT 20% REBATE” on your first months residential fees by enrolling in one of our referred facilities, PLUS a free background check. We personally escort you on a tour of various assisted living communities, big and small. Loving Options… Because WE care! Please visit our website http://www.lovingoptions.com Or Call Us : 800-6-LOV-OPT(656-8678). We look forward to helping you.

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Loving Options – Assisted Living Placement Agency – Video

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http://www.longevitymedicine.tv/loving-options-assisted-living-placement-agency-video/

Walking Before/After DBS for Parkinson’s Treatment – Video

http://www.youtube.com/watch?v=C3i-0RJ6iFo

Walking Before/After DBS for Parkinson's Treatment
Patient shows how Parkinson's used to affect his walking, versus how he walks while receiving DBS Therapy. When medication no longer controls your Parkinson's disease symptoms as well as you would like, talk with your doctor about Medtronic DBS Therapy (deep brain stimulation). See if this FDA-approved therapy can help you return to the life and activities you enjoy. Find out more at http//www.medtronicdbs.com/info. Medtronic DBS Therapy for Parkinson's disease is not for everyone. Not everyone will receive the same results. Talk with your doctor to understand the benefits and risks of deep brain stimulation and determine if Medtronic DBS Therapy is right for you. For further information, please visit http://www.medtronicdbs.com A prescription is required. This video contains information about therapies approved for use in the United States and is intended to be viewed by residents of the United States.

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Walking Before/After DBS for Parkinson’s Treatment – Video

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http://www.longevitymedicine.tv/walking-beforeafter-dbs-for-parkinsons-treatment-video/

DBS for Parkinson’s Demo: System Off and On – Video

http://www.youtube.com/watch?v=dHcQyj9jdec

DBS for Parkinson's Demo: System Off and On
A man shows how DBS Therapy helps control movement symptoms of Parkinson's disease by temporarily turning off his DBS system. When medication no longer controls your Parkinson's disease symptoms as well as you would like, talk with your doctor about Medtronic DBS Therapy (deep brain stimulation). See if this FDA-approved therapy can help you return to the life and activities you enjoy. Find out more at http//www.medtronicdbs.com/info. Medtronic DBS Therapy for Parkinson's disease is not for everyone. Not everyone will receive the same results. Talk with your doctor to understand the benefits and risks of deep brain stimulation and determine if Medtronic DBS Therapy is right for you. For further information, please visit http://www.medtronicdbs.com A prescription is required. This video contains information about therapies approved for use in the United States and is intended to be viewed by residents of the United States.

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DBS for Parkinson’s Demo: System Off and On – Video

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http://www.longevitymedicine.tv/dbs-for-parkinsons-demo-system-off-and-on-video/

Dr Perlmutter and Parkinson’s (english) – Video

http://www.youtube.com/watch?v=C4xv2SHcA4c

Dr Perlmutter and Parkinson's (english)
Currently, Dr. Perlmutter is involved in pioneering work in the use of glutathione in fighting diseases such as Parkinson`s disease and Alzheimer`s. Dr. Perlmutter appeared on Oprah and Friends on April 3, 2009 with Dr. Oz to discuss new findings affecting Parkinson`s disease (www.oprah.com/oradio). Protandim® was proven to raise glutathione levels up to 300 percent, in a peer-reviewed study published in November 2008 in theFree Radical Biology and Medicine Journal. Dr. Perlmutter commented, “The health benefits of increased glutathione are numerous, because of its antioxidant and potential anti-aging activity factors. Protandim`s® effects on glutathione enhancement are tremendous and as a neurologist, I am keenly interested in the impact of Protandim® on brain disorders as well as a variety of medical conditions and diseases. Working with LifeVantage provides me the ability to discuss the eloquence of the science supporting this product and its profound importance in human health.” http://www.lifevantage.com/modisani

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Dr Perlmutter and Parkinson’s (english) – Video

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http://www.longevitymedicine.tv/dr-perlmutter-and-parkinsons-english-video/

The Brains of Serial Killers with Dr. James Fallon – Video

http://www.youtube.com/watch?v=mzUsaXfSQDY

The Brains of Serial Killers with Dr. James Fallon
Dr. James Fallon joins Crime Time to talk about the neuroscience that sets a psychopath's apart from other brains. He talks about the testing that is done to see the neurological patterns of serial killers, how those are distinguished from “normal” people, and what can be done with the information. GUEST BIO James Fallon, Ph.D., is a Professor Emeritus of Anatomy and Neurobiology at the University of California at Irvine School of Medicine where he is also a professor of psychiatry and human behavior. His research has delved into adult stem cells, chemical neuroanatomy and circuitry, higher brain functions, and brain imaging. He studies the neuroscience of schizophrenia, Parkinson's disease, and Alzheimer's disease. In addition, he has studied the brain activity, psychology and genetics of psychiatric patients and the brain scans of psychopathic serial killers. He is a Senior Fulbright Fellow, a National Institutes of Health Career Awardee, and sits on several corporate boards and national think tanks for science, biotechnology, the arts, and the US military. EPISODE BREAKDOWN: 00:01 Welcome to Crime Time. 01:59 The warrior gene and lack of caring. 04:14 Looking at schizophrenia compared to psycho killers. 07:51 Testing the neural responses from killers. 11:40 Identifying psychopaths in the making. 15:47 Grading psychopathy in dimensionality. 19:20 Assessing Eli Roth's brain. 20:39 The higher functions of a psychopath's brain. 21:30 Reading people's scans and assessing …

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The Brains of Serial Killers with Dr. James Fallon – Video

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http://www.longevitymedicine.tv/the-brains-of-serial-killers-with-dr-james-fallon-video/

Vatican confirms Pope has pacemaker " – Video

http://www.youtube.com/watch?v=5lLttjXf_1Y

Vatican confirms Pope has pacemaker “
A day after Pope Benedict XVI announced his resignation, the Vatican acknowledges the pontiff has had a pacemaker for years. ROME mdash; A day after Pope Benedict XVI stunned Roman Catholics by announcing that he would resign at the end of the month, theVatican disclosed new details about his physical well-being on Tuesday, saying that he had been fitted with a heart pacemaker a decade ago but that the procedure had not influenced his decision to become the first pope in almost 600 years to step down. The disclosure about the device, whose existence was not widely known, came as the Vatican grappled with a series of logistical questions raised by a decision that gave Benedict just 17 days to wind up his almost eight-year papacy At a news conference, the Rev. Federico Lombardi, the Vatican spokesman, said the pacemaker was installed while the pope was still a cardinal, before his election as pope in 2005. The batteries were replaced three months ago in a routine procedure that did not influence the pope's thinking about resigning, Father Lombardi said. “This did not weigh on his decision,” Father Lombardi said. “It is more about his forces diminishing.” When he announced his resignation on Monday, the pope cited advancing years and weakness, saying his strength “has deteriorated in me to the extent that I have had to recognize my incapacity to adequately fulfill the ministry entrusted to me.” Greg Burke, the Vatican's senior communications adviser, said Benedict was fitted with …

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Vatican confirms Pope has pacemaker " – Video

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http://www.longevitymedicine.tv/vatican-confirms-pope-has-pacemaker-video/

Green Tea for Weight Loss

Green Tea Expands its Health Promoting Repertoire

German researchers find improved fat oxidation when men combine EGCG with caffeine.

From improving arthritis symptoms to preventing heart disease, heightening eye health to discouraging Alzheimer’s disease development, green tea is the libation of choice for health aficionados.  Yet as multifaceted a drink green tea is, could encouraging weight loss be added to its repertoire?  German researchers sure think so.

A team of researchers from Berlin’s University Medicine recruited 10 middle-aged men who, besides being obese, were generally healthy.  They broke the 10 men into groups of two and randomly assigned them to take an allotted amount of EGCG, some in high doses, others in low doses.  EGCG is the antioxidant compound in green tea believed to make it such a nutritional powerhouse.

One of the cooler aspects of this study is that all the men got a turn in taking a specific amount of EGCG.  In other words, instead of taking a specific amount of EGCG for the length of the study period, the men would take 300 mg of EGCG for three days, then go off for seven days, then pick up their EGCG regimen for another three days.  But instead of taking the same amount as last time, they’d take 600 milligrams.  Then go on to another group 10 days later.  So by the end of the study, all 10 men had gone through the five regimens.

(To be honest, I wish more studies were set up like this.  It makes the results of the study more reliable.)

By the end of the study, the researchers found increases in fat oxidation across the spectrum.  Compared to the time in which they took a placebo for three days, fat oxidation increased 33 percent (300 mg of EGCG daily), 20 percent (600 mg of EGCG daily), 34.5 percent (200 mg of caffeine), and 49 percent (200 mg of caffeine combined with 300 mg of EGCG).

What’s interesting is that there was greater fat oxidation when the men took the lower EGCG combination as compared to the high EGCG combination.  So apparently the Goldilocks rule applies to EGCG—not too much, not too little, but an amount that’s “just right” works for weight loss.

The question, of course, is how many drinks of green tea must one guzzle in order to see any significant weight loss?

Researchers say it may be as few as three drinks or as many as 10 drinks…per day!  Now, as much as I like to drink tea, I don’t have the time, nor the inclination to drink that amount of green tea every day!

But that as it may, the very fact that I could lose weight by drinking that amount of green tea every day illustrates just how amazing a drink green tea is.

The study is published in the European Journal of Clinical Nutrition.

Sources:
nutraingredients.com

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Are Old Stem Cells Less Useful?

Researchers are gathering evidence to suggest that stem cells from the old are less useful when transplanted - which means that some form of repair or other manipulations may need to be included in future stem cell therapies for the degenerative conditions of aging: "Clinical trials of cardiac cell therapy have indicated limited benefits in aging patients, even though preclinical studies using young animals consistently reported significant improvements. Animal studies have demonstrated reduced efficacy of donor cells isolated from older individuals. Here, we evaluated the effects of donor age on the function of human mesenchymal stem cells (hMSCs) in the context of cell therapy for ischemic cardiomyopathy. ... The regenerative capacity of hMSCs was significantly influenced by age. Transplanting young hMSCs improved functional outcomes after an MI by preventing matrix degradation and promoting angiogenesis. The clinical implication is that aged patients require an optimized source of stem cells for treatment."

View the Article Under Discussion: http://www.ncbi.nlm.nih.gov/pubmed/20583954

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The Full Reality of Living With Parkinson’s Disease Profiled – Video

http://www.youtube.com/watch?v=emd6r9IKHlM

The Full Reality of Living With Parkinson's Disease Profiled
Parkinson's Patient and Advocate, Jo-Ann G, Talks about Why She Is Sharing Her Story Consider this: In the time it takes you to sift through 30 minutes' worth of email, at least 3 people will learn they have Parkinson's disease (PD). And many are unprepared for their new reality. While most people recognize PD symptoms that impact movement, like slowness and tremors or stiffness, the disease also involves a range of non-motor symptoms that can significantly impact the lives of those affected. For the full story, go to

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The Full Reality of Living With Parkinson’s Disease Profiled – Video

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Parkinson’s Disease as Localized Garbage Catastrophe

Alpha-synuclein is associated with Parkinson’s disease (PD), and is believed to play a central role in the mechanisms that cause the destruction of dopamine-generating neurons, and thus the pathology of the condition. Here, researchers dig deeper into the processes involved:

Overexpression of a protein called alpha-synuclein appears to disrupt vital recycling processes in neurons, starting with the terminal extensions of neurons and working its way back to the cells’ center, with the potential consequence of progressive degeneration and eventual cell death. “This is an important new insight. I don’t think anybody realized just how big a role alpha-synuclein played in managing the retrieval of worn-out proteins from synapses and the role of alterations in this process in development of PD.”

Using a variety of leading-edge imaging technologies, including a new fluorescent tagging technique developed for electron microscopy, [the] scientists created three-dimensional maps of alpha-synuclein distribution both in cultured neurons and in the neurons of mice engineered to over-express the human protein. They found that excess levels of alpha-synuclein accumulated in the presynaptic terminal – part of the junction where axons and dendrites of brain cells meet to exchange chemical signals.

“The over-expression of alpha-synuclein caused hypertrophy in these terminals. The terminals were enlarged, filled with structures we normally don’t see.” [As] alpha-synuclein accumulates in the terminals, it appears to hinder normal degradation and recycling processes in neurons. This would progressively impair the release of neurotransmitters. In time, the neurons might simply stop functioning and die.

Link: http://www.sciencedaily.com/releases/2013/02/130207141402.htm

Source:
http://www.fightaging.org/archives/2013/02/parkinsons-disease-as-localized-garbage-catastrophe.php

Source:
http://www.longevitymedicine.tv/parkinsons-disease-as-localized-garbage-catastrophe/

An Interview With Judith Campisi

Scientific American interviews Judith Campisi, a member of the SENS Research Foundation’s scientific advisory board and a noted figure in the aging research community. You’ll note that her views are fairly conservative, much closer to the mainstream of longevity science than to SENS, however:

[SciAm]: Why is it so hard to figure out what causes aging?

[Judith Campisi]: In many ways we already know what causes aging. We just don’t know what causes aging in the kind of molecular detail that would allow us to intervene in large meaningful ways. It’s not even clear that once we solve those mysteries we will be able to intervene in aging or dramatically extend longevity.

I started my career studying cancer. Look at all the things we have learned since the 1970s about how cancers form in the body. And yet, still the best cures we have for most cancers are sledgehammers. Biology is complex – and this is a reality that the public has to come to grips with and our legislators have to come to grips with.

I predict aging will follow the same trajectory as cancer research. Why is aging so difficult to figure out? It’s because it’s a really tough problem. I think it’s tougher than cancer. The time has come to really wallow in the complexities.

[SciAm]: What would you say is one of the biggest mysteries of aging research?

[Judith Campisi]: Why do organisms with remarkable genetic similarity have sometimes remarkable differences in life span? We know that for the most part, many of the processes that go on in the human body also go on in yeast and mice. Yet, yeast live a few days, a mouse lives about three years, and people live for decades. We really do not know what evolution has done to take basically the same genes and produce different life spans.

[SciAm]: Is that where the naked mole rat comes in?

[Judith Campisi]: Yes. The mystery shows up even in species that are mouselike. The naked mole rat is more related to the mouse than to us – it looks like a mouse. And yet it lives for 30 years, or 10 times longer than a regular mouse. On top of all that, it has signs of oxidative damage that exceeds that of the mouse.

Now there are three ideas that scientists have come up with to try to explain why naked mole rats live so long: Maybe oxidative damage doesn’t cause aging. Maybe naked mole rats are evolutionary oddities. And then my personal favorite, maybe it’s not oxidative damage that is the problem but how the cell responds to the damage. But that’s all speculative.

Link: http://www.scientificamerican.com/article.cfm?id=aging-ask-the-experts-can-aging-be-controlled

Source:
http://www.fightaging.org/archives/2013/02/an-interview-with-judith-campisi.php

Source:
http://www.longevitymedicine.tv/an-interview-with-judith-campisi/

Final Complexity is Less Relevant than that of Root Causes

I think we can all agree that, separately, each of aging, cancer, and Alzheimer’s disease is a complicated phenomenon. Is cancer more or less complicated than aging, however? Are the likely several different disease processes leading to a similar end presently lumped under the heading of Alzheimer’s disease more or less complex than either cancer or aging? I think that arguments could be made for any ordering of the three, though not all of them are good arguments, and anything that fits in this short blog post is going to involve a fair amount of hand-waving. We could compare the funding and researcher man-years devoted to understanding each, for example, or papers published, or some other similar research metric. I suspect that cancer wins by those measures, if we airily assume that greater amounts of funding are led by the fact that there is much more to catalog at the level of genes, proteins, and cellular mechanisms. I don’t think that this is a safe assumption.

If we look at the SENS vision of aging, or indeed any damage-based model of how and why we age, we might say that aging is more simple than Alzheimer’s, or more simple than any age-related condition. Aging stems from simple root causes, which expand out into massively complex and varied failure modes as damage interacts with damage and systems flail and fail in any number of ways. To draw an analogy, the rust that eats iron structures is a very simple, homogenous thing – a trivial set of a few chemical reactions, easily described, easily prevented. Yet a structure can fail in countless ways due to rust, as the progression and damage caused is stochastic. Which girder or support will be eaten to breaking point first? Similar structures might fail in similar ways more often, perhaps because they allow moisture to linger in the same places.

But you get the point: from simple causes great complexity can arise. The more complex the structure, the greater the number of failure modes that simple forms of damage can cause. We humans are tremendous complex, vast, interlinked arrays of molecular machinery, and in most modern theories of aging the few rusts we are theorized to suffer (some with much more evidence than others) are pretty simple at root. Thus any age-related condition must be more complex than its cause, aging, by virtue of being an end result rather than the cause of that end result. That is one way of looking at it. Another is to view the end state of aging as a whole and measure that complexity – which is obviously also much more complex than the simple processes that gave rise to it.

Does the complexity of the end state of aging matter, however? Or for that matter, the end state of cancer or Alzheimer’s disease? This is not an idle question, as it points to the consequences that result from different core philosophies or approaches in medicine and medical research. Do we fix a problem by working to understand its end states and then try to clean up after or block every branching failure mode, or do we aim to remove the root causes and then let our biology try to restore itself?

That is not a question with a correct answer for all times and places: sometimes it isn’t enough just to remove a root cause, sometimes the root cause is unknown. It is clear, however, that when it comes to age-related conditions a great deal of modern medicine runs along the lines of being an ever more sophisticated means of sticking a finger into the rapidly eroding hole in the dam, rather than repairing the hole in a way that will last. Consider the widespread efforts to safely remove amyloid beta in Alzheimer’s disease, for example: it seems likely that this is not a case of treating root causes, which remain poorly understood at this time, but rather cleaning up the most evident of the biological signatures.

The regulatory structure for medicine and medical research in the US and Europe biases researchers towards the goal of producing what are ultimately less effective treatments for end causes. The system is so set up that the path of least resistance is to research some part of the complex pathology of a late-stage disease, where there is more room to carve out something that can be patented, and then build what are essentially palliative medicines for people who are very sick, having long suffered their particular named condition. Prevention and root causes don’t yet get anywhere near as much attention. When it comes to aging itself, it isn’t even legal in the US to try to produce and commercialize a clinical therapy that might do some good.

But prevention and root causes are exactly where the attention should be when it comes to aging and age-related diseases. Root causes are simple, end stages are complex: that is reflected in the cost and time required to produce therapies. The way to harness the complexity of our self-repairing biology rather than fight against it is to look to removing causes rather than cleaning up after the spreading tree of secondary and tertiary consequences. This has long been understood by the public and researchers alike when it comes vaccination, poisons, and all sorts of other areas of medicine. Somehow it has gone a little astray in the matter of aging and age-related disease. That must change.

Source:
http://www.fightaging.org/archives/2013/02/final-complexity-is-less-relevant-than-that-of-root-causes.php

Source:
http://www.longevitymedicine.tv/final-complexity-is-less-relevant-than-that-of-root-causes/

An Actuarial Overview on Human Longevity and Mortality

When you look at the vast sums of money involved, one might argue that the actuarial community has a greater incentive to understand aging than the aging research establishment does – billions of dollars rest on the degree to which predictions of future human longevity match up to reality. Unfortunately for the actuaries (and the rest of us) that future is very uncertain. We stand at a cusp in biomedical research, an era of rapid progress in fundamental biotechnology, and one in which great leaps forward in application may or may not happen at any time.

Producing true rejuvenation in laboratory mammals is a matter of a billion dollars and ten years or so at this point in time, and the vagaries of human organization that lead up to sufficient interest and funding to start on that goal are essentially random: perhaps we manage to talk the world around to it five years from now, perhaps fifteen, perhaps longer. Who knows – it’s a people and persuasion issue, and those are hard to pin to a timeline.

Here is an interesting PDF that tours some of the present thinking on human longevity by the actuarial community:

Longevity is an important issue: the implication of increasing longevity has far-reaching effects for our social programs; and for our financial security as we grow into old age. It is also a trend which actuaries are well suited to analyze: we have unique training and experience that allows us to distill large volumes of data into key elements that can inform predictions of future events. As we partner with other experts, we are helping to shape the discussion on the implications of increasing longevity.

First, around the globe people are living longer. While there is evidence that the rate of improvement is different between men and women, and between people of different races, geographies and social statuses, the evidence remains that we are all living longer.

Secondly, our understanding of what factors have a material effect on our expected lifetime is growing, but it is not complete. In particular, our understanding of older age mortality is limited, in part because the data at older ages is sparse and of varying quality. There are open questions related both to the rate of improvement and the ultimate age at which it is appropriate to assume a mortality table should end.

Thirdly, in many regions, there is no broad consensus on the appropriate base mortality rates and improvement factors that should be used to value life-contingent liabilities, or on the models that should be used to forecast those rates into the future. This creates challenges for practitioners who must develop their own projections; inefficiencies as the use of different data, assumptions and models leads to different mortality forecasts; and inconsistencies across disciplines – for example, between the pension and insurance communities – as each develops its own independent view of future mortality. Having said this, the actuarial community has dealt with issues of this magnitude in the past: We need to begin to hone in on techniques that will allow us to become comfortable with the wide variances that can be produced by our projection models. As evidenced by the material presented in the body of this report, there are techniques – stress testing, scenario testing, risk heat maps, screening systems – that we can use to give us insight into what base mortality rates and improvement factors could be.

Link: http://www.soa.org/files/research/projects/research-2013-soa-living-100.pdf

Source:
http://www.fightaging.org/archives/2013/02/an-actuarial-overview-on-human-longevity-and-mortality.php

Source:
http://www.longevitymedicine.tv/an-actuarial-overview-on-human-longevity-and-mortality/

Reforging the Brain, One Small Piece at a Time

The repair of aging in the human brain will have to proceed one small step at a time. Either the rejuvenation biotechnologies of the SENS program will prove sufficient to remove every aggregate and process that stops an old brain maintaining itself like a young brain does, or there must be an even more patchwork quilt of therapies, each one fixing some form of damage. The former is a much more efficient path towards meaningful healthy life extension than the latter, but the vast majority of laboratory research and related funding goes towards progress on the harder, slower road.

So reforging the brain: if we’re not thinking about picking out the fundamental forms of cellular and molecular damage that cause aging and then letting the body repair itself, then the list of repairs is a long one. There is myelin to be restored where it wears away; the matter of diminished stem cell activity and so ever fewer new neurons created to replace losses; the failure of structures like the choroid plexus that remove unwanted metabolic byproducts from cerebral fluids; the malfunctioning of the brain’s complex complement of immune cells; and so on for many, many more items.

Here are a couple of research releases, each looking at one small aspect of the brain’s fine structure, and giving some insight into means of repair.

Cells Forged from Human Skin Show Promise in Treating Multiple Sclerosis, Myelin Disorders

The source of the myelin cells in the brain and spinal cord is cell type called the oligodendrocyte. Oligodendrocytes are, in turn, the offspring of another cell called the oligodendrocyte progenitor cell, or OPC. Myelin disorders have long been considered a potential target for cell-based therapies. Scientists have theorized that if healthy OPCs could be successfully transplanted into the diseased or injured brain, then these cells might be able to produce new oligodendrocytes capable of restoring lost myelin, thereby reversing the damage caused by these diseases.

It took [researchers] four years to establish the exact chemical signaling required to [transform human induced pluripotent stem cells, or hiPSCs, into] OPCs in sufficient quantities for transplantation and each preparation required almost six months to go from skin cell to a transplantable population of myelin-producing cells.

They found that the OPCs spread throughout the brain and began to produce myelin. They observed that hiPSC-derived cells did this even more quickly, efficiently, and effectively than cells created using tissue-derived OPCs. The animals were also free of any tumors, a dangerous potential side effect of some stem cell therapies, and survived significantly longer than untreated mice. “The new population of OPCs and oligodendrocytes was dense, abundant, and complete. In fact, the re-myelination process appeared more rapid and efficient than with other cell sources.”

Dickkopf makes fountain of youth in the brain run dry

Cognitive decline in old age is linked to decreasing production of new neurons. [Scientists] have discovered in mice that significantly more neurons are generated in the brains of older animals if a signaling molecule called Dickkopf-1 is turned off. In tests for spatial orientation and memory, mice in advanced adult age whose Dickkopf gene had been silenced reached an equal mental performance as young animals.

Neural stem cells in the hippocampus are responsible for continuous supply of new neurons. Specific molecules in the immediate environment of these stem cells determine their fate: They may remain dormant, renew themselves, or differentiate into one of two types of specialized brain cells, astrocytes or neurons. One of these factors is the Wnt signaling molecule, which promotes the formation of young neurons. However, its molecular counterpart, called Dickkopf-1, can prevent this.

Stem cells in the hippocampus of Dickkopf knockout mice renew themselves more often and generate significantly more young neurons. The difference was particularly obvious in two-year old mice: In the knockout mice of this age, the researchers counted 80 percent more young neurons than in control animals of the same age. Moreover, the newly formed cells in the adult Dickkopf-1 mutant mice matured into potent neurons with multiple branches. In contrast, neurons in control animals of the same age were found to be more rudimentary already.

Source:
http://www.fightaging.org/archives/2013/02/reforging-the-brain-one-small-piece-at-a-time.php

Source:
http://www.longevitymedicine.tv/reforging-the-brain-one-small-piece-at-a-time/

Pre and Post Rehab Personal Trainer in Chinatown DC (202) 506-5390 Ultimate Results – Video

http://www.youtube.com/watch?v=9-E1h2cFqnI

Pre and Post Rehab Personal Trainer in Chinatown DC (202) 506-5390 Ultimate Results
Pre and Post Rehab Personal Trainer in Arlington VA (703) 678-8500 Ultimate Results Post-Rehab Exercise Specialist and Personal Trainer myur.com We provides the skills and knowledge necessary to Post Rehabilitation Exercise services to clients and receive the recognition for being on the forefront of health care to our clients. Our Medical Exercise Specialist develops safe and effective post rehabilitative fitness programs for clients with various limitations that are recovering from a variety of injuries, disease and treatments. With proper personal training you can take the next step toward having a normal and healthier lives. a higher hourly income, as well as becoming the potential training company or facility for post rehab patients/clients from area hospitals, physical therapist clinics and Sport and Senior Rehab Centers. The Post Rehabilitative Certified Exercise Specialist trainer is trained to help you with Prescribe exercise programming and testing for clients, especially those coping with multiple conditions Apply exercise programming in your day-to-day practice, Parlay specific symptoms of a disease or disability into an effective exercise testing or programming prescription, Stay current on the latest drugs used to treat chronic diseases and disabilities, Emphasize practical application rather than scientific theory Post Rehabilitative Exercise Specialist Certification Course Learning Objectives: bull; Describe the framework for determining functional capacity …

By: Mustafa Nazary<span style="color: #666666; font-size: 11px;"

Read the original:
Pre and Post Rehab Personal Trainer in Chinatown DC (202) 506-5390 Ultimate Results – Video

Source:
http://www.longevitymedicine.tv/pre-and-post-rehab-personal-trainer-in-chinatown-dc-202-506-5390-ultimate-results-video/

Pre and Post Rehab Personal Trainer in Foggy Bottom DC (202) 506-5390 Ultimate Results – Video

http://www.youtube.com/watch?v=xx-1E3pogU0

Pre and Post Rehab Personal Trainer in Foggy Bottom DC (202) 506-5390 Ultimate Results
Pre and Post Rehab Personal Trainer in Foggy Bottom DC (202) 506-5390 Post-Rehab Exercise Specialist and Personal Trainer myur.com We provides the skills and knowledge necessary to Post Rehabilitation Exercise services to clients and receive the recognition for being on the forefront of health care to our clients. Our Medical Exercise Specialist develops safe and effective post rehabilitative fitness programs for clients with various limitations that are recovering from a variety of injuries, disease and treatments. With proper personal training you can take the next step toward having a normal and healthier lives. a higher hourly income, as well as becoming the potential training company or facility for post rehab patients/clients from area hospitals, physical therapist clinics and Sport and Senior Rehab Centers. The Post Rehabilitative Certified Exercise Specialist trainer is trained to help you with Prescribe exercise programming and testing for clients, especially those coping with multiple conditions Apply exercise programming in your day-to-day practice, Parlay specific symptoms of a disease or disability into an effective exercise testing or programming prescription, Stay current on the latest drugs used to treat chronic diseases and disabilities, Emphasize practical application rather than scientific theory Post Rehabilitative Exercise Specialist Certification Course Learning Objectives: bull; Describe the framework for determining functional capacity. bull; Develop …

By: Mustafa Nazary<span style="color: #666666; font-size: 11px;"

Originally posted here:
Pre and Post Rehab Personal Trainer in Foggy Bottom DC (202) 506-5390 Ultimate Results – Video

Source:
http://www.longevitymedicine.tv/pre-and-post-rehab-personal-trainer-in-foggy-bottom-dc-202-506-5390-ultimate-results-video/