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Funding Aging Research

A New Hero Has Emerged


posted on December 01, 2009

About a month ago, I met one of the most incredible persons of my life. He is only thirty years old and posses the wisdom of a street smart intellectual twice his age. He™s in top physical condition, has accumulated a small fortune and is in a healthy and happy relationship with the woman of his dreams.

Joe Polish, a long time friend of mine, introduced me to Sean Stephenson at a prestigious event about a month ago. Sean was billed as a speaker. I did not hear his speech. I was there to meet one of my partners, Joe Sugarman, and ran into Sean in the lobby. Joe Sugarman is as impressed with Sean as I am.

In fact, Sean is so impressive, that I consider him as one of my handful of heroes.

Joe Polish interviewed Sean about a week ago. It was actually a three interview series, each covering an area of Sean™s expertise. The one on Health was the one that caught my attention, and I learned enough from it to make important edits to the next edition of Life Extension Express, my book on how to achieve an open-ended youthful lifespan. I strongly suggest you listen to the interview. It™s free.

I was so transfixed with Sean™s Health interview that I also listened to the ones on Wealth and Relationships. By the time I finished, I knew Sean™s expertise was life itself. If you have even the slightest interest in improving any aspect of your life, set some quiet time aside and go to:

www.joepolish.com/sean/thanks.php

If you have anyone special in your life, invite him or her to join you. That includes your children, maybe especially your children. If I had access to this information when I was a child, I could have avoided a lot of pain and would have had an unfair advantage over other kids my age.

Listen, I know you have a full and busy life. I also know you can replace an hour here and an hour there spent on something that is not as productive¦ or as enjoyable¦as listening to these interviews. So do yourself a favor and hear at least the introduction to number one. If you™re not convinced you can profit mightily from Sean™s words, wisdom and experiences within five minutes, then you may be the most insightful and evolved person I know. If so, I want to know you better.
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LATEST HEALTHY LIFE EXTENSION HEADLINES

EXERCISE AND LEUCINE VERSUS SARCOPENIA (November 27 2009) http://www.longevitymeme.org/news/vnl.cfm?id=4485
There is good reason to believe that increased leucine in the diet and exercise can counteract some of the muscle loss characteristic to aging: "Loss of muscle mass is an unfavorable consequence of aging and many chronic diseases. The debilitating effects of muscle loss include declines in physical function and quality of life and increases in morbidity and mortality. Loss of muscle mass is the result of a decrease in muscle protein synthesis, an increase in muscle protein degradation, or a combination of both. Much research on muscle wasting has tended to focus on preventing muscle protein breakdown, and less attention has been paid to providing adequate stimulation to increase muscle protein synthesis. In this review, we present evidence to suggest that interventions aimed at increasing muscle protein synthesis represent the most effective countermeasure for preventing, delaying, or reversing the loss of skeletal muscle mass experienced in various muscle wasting conditions. Based on results from acute and chronic studies in humans in a wide variety of wasting conditions, we propose that resistance exercise training combined with appropriately timed protein (likely leucine-rich) ingestion represents a highly effective means."

EMBRYONIC STEM CELLS IN REGENERATIVE MEDICINE (November 26 2009) http://www.longevitymeme.org/news/vnl.cfm?id=4483
The New Scientist surveys current efforts to build regenerative therapies based on the pluripotency of embryonic stem cells: "Tissue grown from human embryonic stem cells, the most prized, and most controversial, cells ever grown in a lab, could at last make it into the human body. After a decade of scientific and political wrangling, several therapies are now edging towards human trials. Which will be first? The first human embryonic stem cells (hESCs) to make it into the human body could be ones that save sight. Last week, Advanced Cell Technology (ACT) of Worcester, Massachusetts, applied for permission to inject stem-cell derived retinal pigment epithelial cells (RPEs) into the eyes of 12 patients with Stargardt's macular dystrophy, a rare inherited condition which leads to blindness in middle age. Last week came the first report of human skin made from hESCs. Although the cells have so far only been tested on mice, the idea is to use skin grown from these stem cells as temporary grafts for people with burns, while they wait for a permanent graft to be grown from their own tissue."

A PROMISING CANCER VACCINE STRATEGY (November 26 2009) http://www.longevitymeme.org/news/vnl.cfm?id=4482
Via EurekAlert!: "A cancer vaccine carried into the body on a carefully engineered, fingernail-sized implant is the first to successfully eliminate tumors in mammals. The new approach [uses] plastic disks impregnated with tumor-specific antigens and implanted under the skin to reprogram the mammalian immune system to attack tumors. The new paper describes the use of such implants to eradicate melanoma tumors in mice. [This approach] redirects the immune system to target tumors, and appears both more effective and less cumbersome than other cancer vaccines. Conventional cancer vaccinations remove immune cells from the body, reprogram them to attack malignant tissues, and return them to the body. However, more than 90 percent of reinjected cells have died before having any effect in experiments. The [implants] are 8.5 millimeters in diameter and made of [a] biodegradable polymer. Ninety percent air, the disks are highly permeable to immune cells and release cytokines, powerful recruiters of immune-system messengers called dendritic cells. These cells enter an implant's pores, where they are exposed to antigens specific to the type of tumor being targeted. The dendritic cells then report to nearby lymph nodes, where they direct the immune system's T cells to hunt down and kill tumor cells."

IF HDL IS GOOD, WHY NOT MAKE MORE OF IT? (November 25 2009) http://www.longevitymeme.org/news/vnl.cfm?id=4481
Here is an intriguing line of thinking: if we can identify unambiguously beneficial components of our metabolism, why not make artificial replicas and flood the body with them? "The particles that ferry cholesterol through the bloodstream are popularly known as 'bad' or 'good': bad if they deposit cholesterol on vessel walls, potentially clogging them; good if they carry the cholesterol on to the liver for excretion. Now scientists have created tiny particles in the laboratory that mimic those good carriers, scooping up the cholesterol before it can grow into dangerous deposits of plaque. The surfaces of these new particles are coated with fats and proteins so they can bind tightly with the sticky cholesterol to transport it through the bloodstream. Researchers have endowed these artificial particles with the same properties as natural particles that circulate in the blood, [called] high-density lipoproteins, or HDL. The artificial carriers can clean up sites where plaques can otherwise rupture, leading to strokes and heart attacks."

ANOTHER APPROACH VERSUS METASTASIS (November 25 2009) http://www.longevitymeme.org/news/vnl.cfm?id=4480
The real killer in cancer is its spread within the body: metastasis. A reliable method of eliminating metastasis would go a long way to making cancer just a bad, treatable condition rather than the end of life for a quarter of us. Here is one approach: researchers have "found a way to capture tumor cells in the bloodstream that could dramatically improve earlier cancer diagnosis and prevent deadly metastasis. Researchers can inject a cocktail of magnetic and gold nanoparticles with a special biological coating into the bloodstream to target circulating tumor cells. A magnet attached to the skin above peripheral blood vessels can then capture the cells. By magnetically collecting most of the tumor cells from blood circulating in vessels throughout the whole body, this new method can potentially increase specificity and sensitivity up to 1,000 times compared to existing technology. Once the tumor cells are targeted and captured by the magnet, they can either be microsurgically removed from vessels for further genetic analysis or can be noninvasively eradicated directly in blood vessels by laser irradiation through the skin that is still safe for normal blood cells."

COMPLICATING ALZHEIMER'S (November 24 2009) http://www.longevitymeme.org/news/vnl.cfm?id=4479
Much of the Alzheimer's research community is focused on removing the characteristic buildup of amyloid-beta from the brain. Amyloid and Alzheimer's are linked, so remove the amyloid. As the tools of biotechnology improve, however, matters begin to look more complicated. For example: "recent research demonstrates that amyloid-beta is also necessary to maintain proper brain functioning.  Without amyloid-beta, a normal product of cellular metabolism, one's ability to learn and remember could be profoundly damaged, so drugs currently in development to eliminate amyloid-beta could be rendered obsolete. By studying synapses in brain slices of healthy mice and in neuronal networks growing in vitro, [researchers] determined that there is an optimal amount of amyloid-beta needed to keep the neurons working well. If this precise balance is even slightly disturbed, the effectiveness of information transfer between neurons is greatly impaired. Amyloid-beta peptide, believed to be toxic, regulates the type of information that neurons transfer."

FAT AND DEMENTIA RISK (November 24 2009) http://www.longevitymeme.org/news/vnl.cfm?id=4478
Yet another study showing the risk you run by letting your body amass fat unchecked in middle age: "Women who store fat on their waist in middle age are more than twice as likely to develop dementia when they get older. Anyone carrying a lot of fat around the middle is at greater risk of dying prematurely due to a heart attack or stroke. If they nevertheless manage to live beyond 70, they run a greater risk of dementia. ... The research is based on the Prospective Population Study of Women in Gothenburg, which was started at the end of the 1960s when almost 1,500 women between the ages of 38 and 60 underwent comprehensive examinations and answered questions about their health and lifestyle. A follow-up 32 years later showed that 161 women had developed dementia, with the average age of diagnosis being 75. This study shows that women who were broader around the waist than the hips in middle age ran slightly more than twice the risk of developing dementia when they got old. However, the researchers could find no link to a high body mass index (BMI). Other studies have shown that a high BMI is also linked to dementia, but this was not the case in ours. This may be because obesity and overweight were relatively unusual among the women who took part in the Prospective Population Study."

ROOTS OF AGE-RELATED HEARING LOSS (November 23 2009) http://www.longevitymeme.org/news/vnl.cfm?id=4476

From ScienceDaily: "Age-related hearing loss is a very common symptom of aging in humans, and also is universal among mammal species, and it's one of the earliest detectable sensory changes in aging. In mice, the new study shows that the damage starts with free radicals, which are key suspects in many harmful changes of aging. Free radicals trigger a process called apoptosis, or programmed cell death, by which damaged cells 'commit suicide.' Apoptosis is often beneficial, as it eliminates cells that may be destined for cancer. Before the study, it was already clear [that] aging was associated with a major loss of hair cells and ganglion cells, so it was plausible that programmed cell death was playing a role in hearing loss. We also thought that oxidative stress - the presence of free radicals - contributes to age-related hearing loss, so we put two and two together and showed that oxidative stress does indeed induce age-related hearing loss. [Researchers] found that the suicide program was operating in hair cells and spiral ganglion neurons, and that the suicide program relied on activity in a suicide gene called bak. Activity of the bak gene [is] required for the development of age-related hearing loss. The strongest evidence for this was the fact that a strain of mice that did not have the bak gene did not show the expected hearing loss at 15 months of age."

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