Remarks by Dr. Rowe

March 28, 2011
 

THE CASE FOR A DEBATE WITH ROBERT ZUBRIN

Joe 

  An additional point raised by your question relates to the problems involved in using human subjects but clearly human studies will always play a vital role. I meant to bring up another extremely important issue but I was side-tracked in response to questions and because of time constraints i.e. another nail in the coffin regarding atrophy of the heart with prolonged space missions. When I presented my first Space –related paper at a NASA meeting in Toulouse, France in 1995 I defended my position regarding elevations of adrenaline with space flight  after my presentation – based on the Russian studies cited by Atkov and Bednenko, Hypokinesia and Weightlessness : Clinical and Physiologic Aspects, 1992, pp 32-34.  Also after relatively brief Space missions experimental animal studies showed: “in the cardiac muscle pronounced atrophic  changes ( atrophy due to non-use ) ----“. Furthermore “synthesis of myocardial (cardiac) proteins is suppressed and renewal of its structure is inhibited.”

After months of prolonged exploration on Mars in search of evidence of water, involving traveling long distances, and after return at least 20 months later, how can the atrophied heart withstand high G forces during reentry? What is the risk of congestive heart failure as experienced by Irwin on reentry in just 2 weeks after Apollo 15 and which might be fatal? This is a complication of hypokinesia (decreased movement) and contributes to the complications of microgravity but is clearly a separate issue; duplicating 1 G. might not prevent this complication. This pertains to a similar problem which I used in my last SPACE SHOW regarding the Charles Darwin analogy i.e. Darwin's traveling by "submarine" through blood vessels, in confined quarters to skeletal muscles and all the while triggering oxidative stress. 

It is illogical to head straight for Mars without first determining Man's tolerance to withstanding a very prolonged period in a hostile dusty environment and also to determine the tolerance to the increased G forces during reentry : Don't forsake the Moon for Mars. 
 
 

I would love to debate such issues as this on a Space Show with Dr. Robert Zubrin but I am certain he would never consent nor could any host be found who would consent to handling the storm which might erupt.                                                                                       
                                                                                                                                                William J. Rowe M.D. FBIS

  

March 31, 2011

Regarding the recent E mail request for further clarification as to the vascular mechanisms for insulin resistance, with loss of capillaries triggered by oxidative stress, space flight – related invariable elevations of adrenaline and vicious cycles with significant magnesium ion reductions, can contribute to the loss of capillaries; this results in an augmented diffusion distance from capillaries to skeletal muscle and in turn insulin resistance.                     
                                                                                                                                              
William J. Rowe M.D. FBIS

March 31, 2011

I have received an E mail requesting a more detailed explanation regarding the mechanisms for insulin resistance and the reactions of glucose uptake in the skeletal muscles using the analogy of Charles Darwin. I used this analogy to explain that by oxidative stress mechanisms –triggered by obesity related release of cytokines(small peptides) which signal/trigger oxidative stress, there would be, in turn, progressive injuries to the lining of the capillaries with a progressive loss of some capillaries; if this occurred in the vicinity of the uptake of glucose by insulin in the skeletal muscles (Galapagos Islands) after long travel by the ” submarine” (on my home page) through the capillaries there would be insulin resistance. I emphasized that a decrease in the number of capillaries (destroyed by oxidative stress) may impair the action of insulin and alter the uptake of glucose in the skeletal muscles. The mechanism is related to the increase in the diffusion distance of insulin. I hope this clarifies the analogy.  A very recent publication: Molecules in motion: influences of diffusion on metabolic structure and function in skeletal muscle. Kinsey ST, Locke BR, Dillaman RM , J of Experimental Biology; 214: 263-274, 2011.)                                                                                                        
                                                                                                                                                
William J. Rowe M.D. FBIS

  

March 30, 2011

There are a couple of other points which need to be addressed in response to Joe’s question and statements. The peer review system in science has its share of detractors but its still the best method of insuring progress in science with cautious supervision by one’s peers. Also some may raise the issue that in order to avoid the hazards of potential congestive heart failure during reentry after at least a 20 month mission to Mars– conducive to atrophy of the heart muscle, an adequate exercise program can prevent this. But I have emphasized that both too much and too little exercise can injure a normal heart and that with the increase in body heat in microgravity there is the risk of intensifying the significant magnesium deficiencies which already exist with space flight.                         
                                                                                                                                                
William J. Rowe M.D. FBIS

  March 29, 2011

In response to Andy Hill’s questions I had not considered the use of artificial light on the ISS as a partial solution to the vitamin D deficiency problem which is unfortunately common both on earth and in space. Since however there is invariable malabsorption vitamin D will have to be given subcutaneously but as I have pointed out, at this time, there is no replenishable silicon subcutaneous device to administer it. Similarly pharmaceuticals cannot be administered through the nasal route because the circulation of the nasal passages might be impaired eventually through mechanisms similar to those I have published regarding the impairment in fingertip circulation in reference to my Apollo 15 Space Syndrome. I mentioned that the replacement of vitamin D deficiencies on earth would require a dose of 800-1000 I.U. / day but studies will have to be conducted to determine the proper subcutaneous dose and also determine which pharmaceuticals, minerals, and vitamins deteriorate in space and when. Finally I emphasized in one of my interviews that there are few if any subcutaneous pharmaceuticals; the companies are at this time not interested in developing them because there is very little demand with the exception of insulin.                                                                                                          
                                                                                                                                               
 William J. Rowe M.D.  FBIS