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Wednesday, 24 July 2013
Lactate biosensor could become…
Friday, 1 August 2008
Could these drugs...
Researchers Identify Drugs that Enhance Exercise Endurance HHMI News - July 31, 2008
... Researchers have identified two drugs that mimic many of the physiological effects of exercise. The drugs increase the ability of cells to burn fat and are the first compounds that have been shown to enhance exercise endurance.
Both drugs can be given orally and work by genetically reprogramming muscle fibers so they use energy better and contract repeatedly without fatigue. In laboratory experiments, mice taking the drugs ran faster and longer than normal mice on treadmill tests. Animals that were given AICAR, one of the two drugs, ran 44 percent longer than untreated animals. The second compound, GW1516, had a more dramatic impact on endurance, but only when combined with exercise.
Ronald M. Evans, the Howard Hughes Medical Institute investigator who led the study, said drugs that mimic exercise could offer potent protection against obesity and related metabolic disorders. They could also help counter the effects of devastating muscle-wasting diseases like muscular dystrophy. Evans and his colleagues, who are at the Salk Institute for Biological Studies, published their findings on July 31, 2008, in an advance online publication in the journal Cell. ...
ZenMaster
There have been...
ZenMaster
Thursday, 29 May 2008
It's been some bad weeks again...
ZenMaster
Thursday, 17 January 2008
One Reality with CFS...
That is the reason for no post for a long time!
ZenMaster
Wednesday, 19 September 2007
This post will not be so much about CFS...
Some years ago, I noticed my hands and feet had grown and I also felt more tired and had a lot of pain everywhere. Yes, you heard right! My feet grew 4 sizes in about a year! It turned out I had a pituitary tumour that was producing growth hormone (GH), so my body in some respects started to grow as if I was in my teens again. Anyway, now two years later, my doctors have tried four different medications to stop this excessive GH production. Unfortunately, all of them have given me such bad side effects I have been forced to stop the treatments.
What I can figure out myself, these terrible side effects is post likely a result of my CFS! I get pain and even cramps in my leg muscles, much more chest pain than usual and also some disturbances in the heart rhythm and some other reactions like totally blocked out in my brain and ability to concentrate, when I take these drugs to curb this particular pituitary tumour. Most of the drugs have interfered with the dopamine system, so it’s a very complex interaction; the endocrine specialists doesn’t know or understand it themselves. It’s only because of my own knowledge and experience in cell biology I have been able to trace down some new findings and get some kind of explanation of why I have reacted this violently on the treatments.
This is not the only other medical problem I have had in the years before. But I might come back to that later some time.
I’m not complaining. I only tell my story to say it is possible to survive even when you suffer a lot constantly. I guess it is because of our intrinsic ability to adapt to what we feel in our bodies, as human beings. The ‘only’ difficulty has been how friends and even family disappear when it gets ruff... instead of staying and supporting. It could happen to anyone! It’s our biological fate.
Anyway, now after two months, I am mostly off all these side effects I have experienced this summer again. On the other hand, what is waiting is for my doctors to decide on surgery of the tumour or not instead. I am waiting for this decision this week. It is really a tiny operation, right through the nose bone and into the part of the brain where the pituitary sits, but it is a delicate procedure. I’ll just have to wait and see.
ZenMaster
Tuesday, 21 August 2007
Here are some references...
...to the original work I talked about in my previous post. If anyone is interested I can send you a more complete list. Just send me an e-mail and ask for it!
ZenMaster
References related to energy metabolism in CFS:
- Assessment of cardiac metabolic disorders with positron emission tomography.
Waldenstrom A, Langstrom B. Curr Opin Cardiol. 1991 Dec;6(6):965-71. Review. PMID: 10150067 [PubMed - indexed for MEDLINE]
- Human uterine smooth muscle exhibits a very low phosphocreatine/ATP ratio as assessed by in vitro and in vivo measurements.
Steingrimsdottir T, Ericsson A, Franck A, Waldenstrom A, Ulmsten U, Ronquist G. Eur J Clin Invest. 1997 Sep;27(9):743-9. PMID: 9352245 [PubMed - indexed for MEDLINE]
- Ionophoric action on the cellular membrane as a pathophysiological mechanism in syndrome X: myth or reality?
Waldenstrom A, Ronquist G. J Intern Med. 1995 Sep;238(3):187-9. No abstract available. PMID: 7673847 [PubMed - indexed for MEDLINE]
- Disturbed energy balance in skeletal muscle of patients with untreated primary hypertension.
Ronquist G, Soussi B, Frithz G, Schersten T, Waldenstrom A. J Intern Med. 1995 Aug;238(2):167-74. PMID: 7629485 [PubMed - indexed for MEDLINE]
- Coxsackie B3 myocarditis induces a decrease in energy charge and accumulation of hyaluronan in the mouse heart.
Waldenstrom A, Fohlman J, Ilback NG, Ronquist G, Hallgren R, Gerdin B. Eur J Clin Invest. 1993 May;23(5):277-82. PMID: 8394817 [PubMed - indexed for MEDLINE]
- Phosphocreatine turnover and pH balance in forearm muscle of patients wit syndrome X.
Soussi B, Schersten T, Waldenstrom A, Ronquist G. Lancet. 1993 Mar 27;341(8848):829-30. No abstract available. PMID: 8096030 [PubMed - indexed for MEDLINE]
- Angina pectoris patients with normal coronary angiograms but abnormal thallium perfusion scan exhibit low myocardial and skeletal muscle energy charge.
Waldenstrom A, Ronquist G, Lagerqvist B. J Intern Med. 1992 Apr;231(4):327-31. PMID: 1588255 [PubMed - indexed for MEDLINE]
- Low energy charge in human uterine muscle.
Wedenberg K, Ronquist G, Waldenstrom A, Ulmsten U. Biochim Biophys Acta. 1990 Jan 29;1033(1):31-4. PMID: 2137351 [PubMed - indexed for MEDLINE]
Saturday, 11 August 2007
Now comes the big news...
In the late 1980-ies and early 1990, my cardiologist together with a biochemist at the hospital designed and performed a series of experimental investigations that really turned out to give some new results on what is wrong when you have CFS.
In short, something is wrong with the energy consumption, or as we cell biologists say the ATP metabolism. ATP is the prime energy molecule in cells, and most of it is produced in the mitochondria of cells. It was not that there is too little ATP, on the contrary the synthesis in my heart or skeletal muscle cells were 3-5 times the normal when tested on biopsies. Still, after only a few minutes work, the ATP levels could drop to only 10 or 20 percent of the normal values, while in normal people it only decrease 10 or 15 percent in total, during the same conditions. Furthermore, it took more than an hour of rest to regain the ATP levels I should have, while the control persons got their ATP back within a few minutes.
Another observation from these experiments was that the acidity, or pH value, inside the muscle cells dropped dramatically, from the normal 7.2 down to 6.0. This was so extreme that no one had seen before, and was believed the cells shouldn’t survive, but obviously I did – well my muscle cells was live and had no ultrastructural damages seen in many other conditions. When this result was repeated at several occasions, and with different techniques, we had to believe they were correct. The low pH was also related to production and release of large amount of lactic acid in the blood.
All these experimental data fits so well with the clinical picture! I can move around, but slowly in order to not ware out totally. However, when exercised in some way – like walking for a while slowly – it can take more than a day, even two days before I am back to my “normal” level of strength. And I still feel – always – as I have been running a marathon in my legs. That is a lot of lactate all the time, giving me muscle ache.
Later, I will try to tell more about the specific tests that were done – give more technical details – because I think this is a very important finding they did, not only on me but on a small group of people with CFS here where I live. However, it was never noticed at other research places, even though most of these results were published in scientific journals. One explanation could have been it was rather difficult and complex experiments to perform, but I really don’t know why.
Well, so much for my story today. No treatment came out of this, and I still suffering the same way, untreated. And the reason for this metabolic disturbance, the original cause, is still of course obscured.
But if you want, go ask your doctor about these things! Maybe there are someone that will be able to take up this again, and come a little further!
ZenMaster