TELOMERES 

and Possible Regeneration using our

Pinealstim generator or   Hunza Water antioxidant

A major thrust of Biophysica's research since 1992, originally supported by a grant from the National Research Council of Canada, is in possible regeneration of Pineal, Pituitary and Telomeres using electromagnetic energy, signals and frequencies emitted by the Pinealstim generator.  We now have  Trans-Cerebral and whole body stimulation devices which emit longitudinal Scalar EM waves.  This new technology  might possibly be promising in protecting and regenerating telomeres and we invite interested research investors. 

The Pinealstim Cellular Regenerator emits a constant magnetic field, pulsed light pulses and repetitive high voltage pulses each of duration 3 microseconds and containing within each pulse, high frequency information and Scalar Waves using a Caduceus Coil.  Repetition rate is scanned and controlled by feedback circuitry.  The energy is powerful and palpable and can penetrate deeply into cellular structures.  We are developing a portable model for applying to limbs, abdomen etc.

Telomeres are specialized DNA-protein complex at ends of linear chromosomes. They are essential for proper maintenace of chromosomes, and play a major role in aging and cancer. Telomerases are specialized reverse transcriptases that are involved in synthesis of telomeres in most organisms. They are very interesting DNA polymerases in that they carry RNA template within them.

T he excitement over telomerase continues to mount as evidence accumulates that makes the connection between telomere length and cell lifespan likely to be more than a coincidence. The most recent findings show that the age span of cultured cells, normally limited to around 50 to 90 cell doublings--the so-called Hayflick limit, named for the scientist who first observed that the lifespan of cultured cells was finite--can be more than doubled by transfecting them with telomerase genes (A.G. Bodnar et al., Science, 279:349-52, 1998). These findings come on the heels of a series of observations correlating the loss of telomerase activity and/or the shortening of the ends of chromosomes (telomeres) with the loss of proliferative capacity, an observation that holds true in a number of situations: somatic (limited proliferative capacity) as compared to germ cells (larger proliferative capacity); normal tissue (limited) versus malignant tumors (unlimited); and normal T cells versus HIV-infected T cells, whose telomeres resemble those of aged individuals.

Telomere & Telomerase in the News
Scientific American
Turning Back the Strands of Time by Kristin Leutwyler (February 2, 1998)
Telomeres, Telomerase and Cancer by Carol W. Greider & Elizabeth H. Blackburn (February, 1996)
The Scientist
Telomere Without End, Amen by Laura DeFrancesco (March 30, 1998)
Telomere Findings May Yield Tips For Treating Cancer, Geriatric Disorders by Ricki Lewis (Feb. 19, 1996)
CNN Interactive
Scientists discover cellular 'fountain of youth' (January 13, 1998)
Researchers seek biological key to 'fountain of youth' (November 4, 1996)
TIME
An Attack on Aging by Christine Gornan (Jan. 26, 1998 Vol. 151 No. 3)
The Immortality Enzyme by J. Madeleine Nash (Sept. 1, 1997 Vol. 150 N0. 9)
U.S. News Online
New technique resets the biological clock by Rita Rubin (January 26, 1998)
What causes aging? by Nancy Shute (August 18, 1997)
 

Telomere & Telomerase Research Information at http://resolution.colorado.edu/~nakamut/telomere/telomere.html

Old Cells Can Be Young Again (telomeres can be repaired) from www.alsearsmd.com/


When you get sick, your immune system makes copies of its disease-fighting white blood cells called T-cells. These cells divide over and over again to fight off the bacteria or virus that’s invading your body.

The more often these cells reproduce, the shorter their telomeres become until they stop copying. The older you get, the fewer active T-cells you have because they’ve fought off as much sickness as they can. The bottom line is that when your telomeres are short, your immune system looks and acts old.

This makes your risk for infection and disease much higher. One study looked at about 150 people from 60-75 years old. The ones who had shorter telomeres were three times more likely to die from heart disease. And they were eight times more likely to die from an infectious disease.

Shortened telomeres also appear to be the mechanism for many chronic diseases like:

Diabetes. When you eat too many carbohydrates, your pancreas is asked to create more insulin than it’s supposed to. And to get the job done, the pancreas has to create more of a factory to create the insulin it needs by making more cells. If the pancreas is continually challenged to produce more and more insulin, the cells have to continue to divide. When their telomeres are too short, they can’t reproduce anymore. And your body can’t make the insulin you need. This is what causes diabetes.4


Atherosclerosis. One study I read looked at men with high blood pressure. Those with shorter telomeres in their white blood cells were more likely to get heart disease.5


Alzheimer’s disease. Alzheimer’s patients’ glial cells, the maintenance cells to the brain, have short telomeres. Some kind of toxic environmental hazard caused those cells to replicate to defend themselves.6
But you don’t have to let your immune system grow old. When telomerase is activated, you strengthen your cells by keeping the telomeres long, strong and young. And the younger your cells are, the more powerful they are at fighting sickness and disease.

In fact, for most of the people in a brand new study, telomerase activation therapy reduced the percentage of immune cells with short telomeres by 10-50 percent. And the amount of older immune cells decreased by 10-20 percent.7 This represents an “apparent age reversal of 5-20 years!”8

Grow Younger Naturally

Tons of research is going on every day and you’ll be reading more and more about telomerase in the coming months. But in the meantime, you can help slow the aging of your cells with nutrients.

One of the best nutrients for activating your telomerase is trusty omega-3. A new study in the Journal of the American Medical Association followed about 600 people over a full five years. They found that daily supplements of omega-3 significantly increased telomerase activity.9

References:

1 Cong, Yusheng, Shay, Jerry W., "Actions of human telomerase beyond telomeres," Cell Research June 2008; 18:725-732
2 Simon, R., Chan, W. L., Blackburn, Elizabeth H., "Telomeres and telomerase," Phil. Trans. R. Soc. Lond. B 2004; 359, 109-121
3 Cawthon, R.M., Smith, K.R., O’Brien, E., et al, “Association between telomere length in food and mortality in people aged 60 years or older,” Lancet 2003; 361(9355): 393-395
4 Sampson, M., Winterbone, M., et al, “Monocyte Telomere Shortening and Oxidative DNA Damage in Type 2 Diabetes,” Diabetes Care 2006
5 Benetos, A., Gardner, J., et al, “Short Telomeres are Associated with Increased Carotid Atherosclerosis in Hypertensive Subjects,” Hypertension 2004
6 Farfara, D., Lifshitz, V., et al, “Neuroprotective and neurotoxic properties of glial cells in the pathogenesis of Alzheimer's disease,” Journal of Cellular and Molecular Medicine 2008
7 Harley, C., Weimin, L., et al, “A Natural Product Telomerase Activator as Part of a Health Maintenance Program,” Rejuvenation Research 2010
8 Ibid.
9 Ramin Farzaneh-Far, M.D., "Association of Marine Omega-3 Fatty Acid Levels with Telomeric Aging in Patients with Coronary Heart Disease,” JAMA 2010; 303(3):250-257
10 Xu, Qun, Parks, Christine G., DeRoo, Lisa A., et al, “Multivitamin use and telomere length in women," Am J Clin Nutr March 2009; 89: 1857-1863, 2009
11 Richards, J Brent, et al, "Higher serum vitamin D concentrations are associated with longer leukocyte telomere length in women," Journal of Clinical Nutrition Nov. 2007; Vol. 86, No. 5, 1420-1425



 

This page last updated October 4, 2010

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