#91: Movement Disorder Quarter, Installment #2

October 11th, 2007 Author: admin

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Steadying Guidance on Motor Disturbances

Hear these reports:

  • Gene Therapy Showed Promise for Parkinson Disease
  • NIH Examines Creatine for Parkinson’s Therapy
  • Tips for Calming Motor Fluctuations
  • Parkinson’s Drug Permax Withdrawn from Market
  • Parkinson’s Rotigotine Patch Treatment Approved
  • Safinamide Enhances Control of Parkinson’s: Combining the drug with dopamine enhanced the latter’s efficacy, which can lessen over time
  • Simvastatin Found to Reduce Parkinson’s, Alzheimer’s Risk

We also reviewed these reports from previous STAT! episodes:

  • sNNOO31 neural stem cell differentiator protein for Parkinson’s (from episode #7)
  • Stereotactic implantation of human cadaveric dopamine-producing retinal pigment epithelial cells into the striatum of Parkinson’s patients shows promise. Randomized, double-blind, placebo-controlled study underway (from episode #7)
  • Parkinson’s may improve when H. pylori infections eradicated (from episode #73)

Weblinks to:

Citations (other): Depletion of CoQ10 by Statin Drugs:

  • Langsjoen PH, Langsjoen AM. The clinical use of HMG CoA-reductase inhibitors and the associated depletion of coenzyme Q10. A review of animal and human publications. Biofactors 2003;18:101-11.
  • Jula A, Marniemi J, Huupponen R, Virtanen A, Rastas M, Ronnemaa T. Effects of diet and simvastatin on serum lipids, insulin, and antioxidants in hypercholesterolemic men: a randomized controlled trial. JAMA 2002;287:598-605.

Next week’s show: Our 4th installment of Nerve University – Education, Research And Scholarship In Neurology. We’ll continue our discussion on genetics and gene therapies - their potential for diagnosing and treating a number of neurological disorders.

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#79: Nerve University - Installment #3

July 20th, 2007 Author: admin

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Installment #2 of Nerve University - Education, Research and Scholarship in Neurology.

  • What Triggers Huntington’s Disease?
    • Listen and learn how oxidative DNA damage to the genes leads to subsequent defective enzymes, resulting in the formation and accumulation of toxic proteins.
    • This may be a model for how other neurodegenerative diseases progress - Alzheimer’s and Parkinson’s included.
    • Essentially with this information, we are treated to an exposition of how aging likely results in disease-mediated neuronal death.
    • Treatment for Huntington’s may some day be primarily gene-based (for example using ‘neurturin.’ Until then, might antioxidants like CoQ10, carotenoids, ascorbate, tocopherols, selenium, bioflavanoids be of help? Experimental data are consistent in demonstrating neuroprotection from some of the antioxidants.
  • Glial Cells Worsen ALS Pathology - through mechanism involving mutated superoxide dismutase gene:
    • In more ‘oxidation-antioxidation’ news related to neurodegeneration we learn that a defective form of this key antioxidant enzyme (SOD) in glial cells is the probable cause of amyotrophic lateral sclerosis (ALS).
    • Maybe SOD enzyme therapy, gene therapy, stem cell therapy or anti-SOD immunotherapy will someday be found helpful for treating or curing ALS.

And Last but not least: Do shifty eyes mean lies, or better learning?

Next week’s show: Our 7th installment of Defeating Dementia - Promising news and approaches for progressive brain disorders. Focus: The pros and cons of the cholinesterase inhibitors (Exelon, Aricept and Razadyne). We’ll also cover the newly validated CAIDE dementia risk score and more news on the promising Bittsburg B compound, which makes beta-amyloid in the brain visible on PET scans. It’s an exciting potential tool to assess and track Alzheimer’s progression.

Weblinks:

Other References:

  • Coenzyme Q10 enrichment decreases oxidative DNA damage in human lymphocytes: Tomasetti M., Littarru G.P., Stocker R., Alleva R.: Free Radic Biol Med. 27: 1027-1032, 1999
  • Energy metabolism defects in Huntington’s disease and effects of coenzyme Q10: Koroshetz WJ, Jenkins BG, Rosen BR, Beal MF. . Ann Neurol. 1997;41(2):160-165.
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