New to the Huntington's Disease Lighthouse?
 Welcome to the HDlighthouse!
 Getting started.
 
Home \ Research \ General Research \ Updates
  HD Lighthouse Editor's Comment: P53 is for short hand for cancer tumor related protein number 53. Cancer research has developed mice that do not make any P53. The P53 null mice get a lot of tumors.

The mutated Huntington's disease gene protects carriers from many forms of cancer. Some researchers have suggested that P53 may have something to do with HD. The results of crossing HD mice with P53 null mice could be enlightening. Would these mice develop cancer tumors or HD symptoms?

The new drugs being investigated by researcher Matson are P53 suppressors. P53 suppressors are exciting new candidates for HD mice trials. --Jerry

Posted to HDLighthouse: 27-Sep-2002
HDL Update: New Drugs Protect Nerve Cells In Parkinson Mice


P53 Inhibitors Protect Mouse Brains
"...these new drugs are remarkably effective in the animal studies, and appear to be well-tolerated", says Mark Mattson, Ph.D., chief of the NIA’s Laboratory of Neurosciences.

Two experimental drugs appear to prevent Parkinson’s disease-like brain damage and motor dysfunction in mice, according to investigators at the National Institute on Aging (NIA) Gerontology Research Center. The finding identifies a new approach for slowing or halting the progression of Parkinson’s disease that may one day help treat people who have it.

“Although one must be cautiously optimistic when moving drugs from animals to humans, as the results are not always the same, these new drugs are remarkably effective in the animal studies, and appear to be well-tolerated”, says Mark Mattson, Ph.D., chief of the NIA’s Laboratory of Neurosciences.

In the study, dopamine-producing nerve cells in mice treated with pifithrin-alpha (PFT), an experimental cancer treatment, and Z-1-117, a modified version of PFT, were more resistant to being killed by environmental toxins and pesticides, such as MPTP, iron, and rotenone. These toxins are suspected of increasing the risk of Parkinson’s disease in humans and can induce symptoms of the disease in rats and mice. The drugs also helped preserve motor function in mice exposed to these compounds. The investigators suspect the drugs work because they block the action of p53, a protein that may promote the death of dopamine-producing nerve cells.

The NIA team found that p53 kills these nerve cells by causing an increase in the permeability of the membranes surrounding mitochondria, the organelles in the cell that produce energy. This increased permeability causes the release of chemicals from mitochondria that destroy the cell. The same alterations in mitochondria are believed to occur in dying nerve cells in Alzheimer’s disease and in people who have had strokes. However, PFT and Z-1-117 prevented these mitochondrial alterations.

“Not only do these findings reveal a new avenue for treating people who have Parkinson’s disease, but they provide the opportunity to better understand how p53 kills nerve cells and whether this might also occur in other neurological diseases,” Dr. Mattson said. His lab is currently determining whether the p53 inhibitors might be effective in mouse models of Alzheimer’s disease and has found that PFT and Z-1-117 are effective in reducing nerve cell damage and improving functional recovery following a stroke in mice. If additional studies confirm that these drugs are safe and effective in animals, then they will likely be tested in humans.

Parkinson's disease occurs when nerve cells in a brain region called the substania nigra die or become impaired and can no longer produce dopamine. Without dopamine, individuals can develop tremor or trembling in hands, arms, legs, jaw, and face; rigidity or stiffness of the limbs and trunk; bradykinesia, or slowness of movement; and postural instability or impaired balance and coordination. Patients may also have difficulty walking, talking, or completing other simple tasks. The disease is both chronic and progressive. Parkinson's is not usually inherited, but incidence of the disease increases with age, with an average onset at about 60 years. It afflicts about 50,000 Americans annually.

The NIA leads the Federal effort supporting and conducting biomedical, clinical, social, and behavioral research on aging. This effort includes research into the causes and treatment of Alzheimer’s disease, Parkinson’s disease, stroke and other neurodegenerative disorders associated with age. Press releases, fact sheets, and other materials about aging and aging research can be viewed at the NIA’s general information Web site, www.nia.nih.gov.

# # #

Source: NIH/National Institute On Aging 25-Sep-2002
Read the HDAC/HDLighthouse Forum. Post your comments
   

 

Peptide May Treat Huntington Disease
A first clinical sign of the mutant huntingtin gene is decreased blood flow. Researchers at USF have discovered a ...
Jerry Lampson
Posted to HDL: 13 Feb 2004

Toxin 3NPA and Huntington's Disease
HD researcher Mark Mattson recently invited Edward Calabrese to visit his lab to discuss the possibility of experiments that would ...
Jerry Lampson
Posted to HDL: 12 Dec 2003

Mosaicism In Huntington's Disease
This is the single most important follow up after the discovery of the mutant gene in 1993. If the expansion ...
Jerry Lampson
Posted to HDL: 16 Nov 2003

Organ Regeneration Sparks Huntington Hope
Massachusetts General Hospital researchers have harnessed newly discovered cells from an unexpected source, the spleen, to cure juvenile diabetes in ...
Jerry Lampson
Posted to HDL: 14 Nov 2003

Laser To Aid Huntington's Disease Research
Sandia nanolaser may help extend life-spans by rapidly analyzing possible neuroprotectant drugs. Preventing mitochondria from turning ugly may postpone Alzheimer’s, ...
Jerry Lampson
Posted to HDL: 23 Sep 2003

Small Molecules May Treat Huntington's Disease
Reata seeks to discover small molecules that will cross the blood brain barrier and disable the mutant hutingtin protein. ...
Jerry Lampson
Posted to HDL: 16 Sep 2003

Huntington's Misfolding Folding Protein
It is thought that the mutant Huntington's disease gene produces a protein that folds differently. Knowing just how the mutant ...
Jerry Lampson
Posted to HDL: 30 Aug 2003

ALS Protein Found in Huntington's Disease
The researchers have discovered the mutant SOD1 protein is also found in Parkinson's disease, Huntington's disease and Alzheimer's disease. ...
Jerry Lampson
Posted to HDL: 28 Aug 2003

Lab To Find Cure For Huntington's Disease
The new lab is part of a larger set of labs in the Health Profession Building that is scheduled to ...
Jerry Lampson
Posted to HDL: 21 Aug 2003

Researchers Discover Cause For Aging
Amazingly, if we perturb insulin/IGF-1 signaling and reproductive cells in the same animal, we end up with animals that live ...
Jerry Lampson
Posted to HDL: 16 May 2003
[an error occurred while processing this directive]

Disclaimer & Privacy Policy | Welcome | Site Feedback Marsha@HDLighthouse.org