Guest guest Posted April 12, 2002 Report Share Posted April 12, 2002 shydrager wrote: hi bill: usually you are level headed i understand your pessimism but in the past 3 years since diagnosis of PD i have been paying attention to these sorts of announcements some of the work that Levesque does has been published see below also, growing stem cells in vitro is a new field of tissue culture growth factors, timing, new gene discoveries about development will only accelerate as results come from stem cell studies now being aproved by NIH ray strand .......................................................................... > >Message: 3 > Date: Wed, 10 Apr 2002 22:59:06 -0400 > >Subject: Re: WebMD - Self-Transplant for Parkinson's.htm > >Jerry, > >That is a news article, not a scientific paper. It also has at least >one error " It's already known that embryonic stem cell transplants can >help people with Parkinson's disease " is wrong. In truth embryonic stem > right, a report was made at a meeting with only one person undergoing the treatment there are no statistics indicating level of reproduceability we wait for more testing > >cell transplants have cured PD symptoms in mice not humans. Fetal > Jim Finn is walking ad for fetal porcine implants for PD also, not all the fetal transplants were negative in the Freed study of human fetal transplants (that paper is available free on the web) he says stem cells next, but, some way has to be devised to reduce the implant cell population if symptoms get too extreme like with controlled exposure to a rare antibiotic that they are made sensitive to > >tissue transplants did help many PD patients for periods of months up to >three years. According to this article, the patient seems to still be >taking Sinemet and the transplant seem to have helped adsorbtion >especially at 12 months. Since no one has ever reported results like >this with animals, it seems to me to be strange to experiment first on >humans, after all there is a good chance you could > kill the person by >putting it directly into the brain (and where in the brain did they put >them) > the subject of the experiment had the brain cells removed during a DBS procedure still dangerous here in Minnesota, one of the doctors (Abbott Northwestern Hospital) initially was doing brain biopsies and cites the number of successful biopies as his experience for performing DBS which is probably easier from a routine/repeatable standpoint targeting one area -- than the many of biopsies > >It took five years to develope the mouse experiments and find a way to >measure results for the pluripotent stem cells. Now these people do it >in no time and have a human experiment first???? Sounds too good to be >true. I would still like to see a reviewed scientific paper on the > I'll check PUB-MED > >experiment. AND I would like to see it duplicated on more supervised >tests (double blind). Since it is just an unverified news article - it >could be a " Pro-Life " propaganda story. How do you measure brain >dopamine in humans? I know how they do it in mice and would not what >that done to me. > dopamine activity can be assessed with PET and SPECT scans using radioactive dopamine that is how my neurogist would like to better define my " probable " MSA and distinguish it from PD but, we have to see if insurance will cover the expense my Mom (85) died last year and she had a PET scan for her lung cancer radioactive glucose was used and is metabolized faster by tumors than normal tissue and it was covered by Medicare and her private insurance all $5,000 heck I just had my second MRI at $2,000 each and it is not conclusive there has been recent discussion about " neuro protective " properties of dopamine agonists as defined in studies of progresson useing these scanners on people with Parkinsons > >Take care, Bill > .......................................................................... other references to this guy's work in news releases at archives of PARKINSN list serve next NMDA (dopamine precursor) .......................................................................... Brain 1997 Nov;120 ( Pt 11):1937-59 Human hippocampal AMPA and NMDA mRNA levels in temporal lobe epilepsy patients. Mathern GW, Pretorius JK, Kornblum HI, Mendoza D, Lozada A, Leite JP, Chimelli LM, Fried I, Sakamoto AC, Assirati JA, Levesque MF, Adelson PD, Peacock WJ. Department of Neurology, University of California, (Brain journal is freely published on the web) .......................................................................... Surg Neurol 1999 Feb;51(2):202-10 Presurgical contribution of quantitative stereotactic positron emission tomography in temporo limbic epilepsy. F, Levesque M F. Epilepsy and Brain Mapping Program, Cedars-Sinai Medical Office Towers, Los Angeles, California, USA. BACKGROUND: We quantified the interictal metabolic changes associated with temporal lobe epilepsy by using an accurate stereotactic method. METHODS: We selected 16 patients who had proven unilateral focal or regional temporal onset defined by SEEG criteria. Each patient underwent stereotactic MRI and stereotactic [18 fluoro] fluorodeoxyglucose positron emission tomography (PET). RESULTS: Asymmetries (mean, +/- SD) were found in mesio-temporal structures: amygdala (-0.033+/-0.027, p = 0.0002), hippocampus (-0.035+/-0.032, p = 0.0006), and superior temporal gyrus (-0.036+/-0.032, p = 0.0004). Four of the sixteen patients had previously had unlocalized qualitative nonstereotactic PET analysis. CONCLUSIONS: The quantitative stereotactical PET method allows a higher resolution study of mesio-temporal structures. PMID: 10029429 [PubMed - indexed for MEDLINE ................ ........................................................... Brain Res Mol Brain Res 2000 May 31;78(1-2):192-5 Fetal and adult human CNS stem cells have similar molecular characteristics and developmental potential. Palm K, Salin-Nordstrom T, Levesque MF, Neuman T. Neurofunctional Surgery Center, Department of Surgery, The CSMC Burns & Research Institute, Cedars Sinai Medical Center, UCLA School of Medicine, 8700 Beverly Boulevard, Building, Room 4018, Los Angeles, CA 90048, USA. The mammalian central nervous system (CNS) contains multipotent stem cells that develop into neurons, astrocytes and oligodendrocytes. Our current data show that fetal and adult human CNS stem cell isolates display similar proliferation kinetics, differentiate into three major cell types of the nervous system and express similar sets of regulatory genes. However, each individual CNS stem cell isolate could be distinguished by its specific gene expression and development al potential. PMID: 10891600 [PubMed - indexed for MEDLINE .......................................................................... Ray Strand Prairie Sky Design -----------------( on the Edge of the Prairie Abyss )--------------- when the sky is clear the ground is visible 50/47dx PD/40? onset http://folding.stanford.edu join MSA TEAM CURE #2508 h } Quote Link to comment Share on other sites More sharing options...
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