As I was writing the message below describing how
Cystic Fibrosis patients take A LOT of supplements,
minerals, and so on I realised I'm not quite sure
about..
Are there any foods, drinks, etc. that decrease the
effectiveness of the CS? Some interactions??
Thanks,

Maia


--- Maja Hristozova <majahristoz...@yahoo.com> wrote:
> Hello Duncan
> Yes, selenium is well known and taken by most Cystic
> Fibrosis people that I know. They also take
> additional
> antioxidants, almost all vitamins (C + all the fat
> solable), Calcium, Magnesium (which play a major
> role
> in many processes in the body), DHA, CoEnzymeQ10 and
> some antioxidant herbs and essential oils. The list
> of
> daily supplements is really long. 
> As for the GSH - taking it orally is not.. clear. I
> mean there are pros and cons, something to do with
> the
> fact that when taken orally it doesn't go into the
> cells but stays outside (which for some reason is
> not
> good for CF). There are CF people that use it orally
> with success, but others are sceptical. Not many
> papers on that. There is a group of researchers
> though
> that investigated GSH inhalations. This is 'on the
> age' research, very new, not established but so far
> successful. 
> 
> As someone pointed though all these things do not
> change the genetical disorder - the CFTR channel is
> still staffed up and so far there is no cure for
> that.
> 
> 
> And there are other issues - mixing and interaction
> between all these supplements. The more they become
> the more you get confused what causes what. You get
> bounded by all the timing and dossages ...
> Just recently MannaRelief started a study on the
> effect of their products (mainly Aloe Vera based) on
> CF patients. So now some take these gluconutriens as
> well. 
> 
> I'll update later today how is Kamellia going with
> the
> Colloidal Silver. 
> 
> Maia
> 
> --- Duncan Crow <duncanc...@shaw.ca> wrote:
> > Did the cystic fibrosis treatement program address
> > the control of 
> > oxidative stress?  I ask because there are
> hundreds
> > of articles pointing 
> > out the culprit in lung disorders as being chronic
> > oxidative stress 
> > (lipid peroxidation). This can be stopped cold
> with
> > cold-processed whey 
> > and selenium, and an antioxidant program.
> >
> http://members.shaw.ca/duncancrow/medline_links.html
> > Here's just one study chosen at random so you'll
> see
> > what I mean.
> > 
> > The mucus and inflammation and most of the scar
> > tissue is produced by 
> > irritation from whatever sourse and propagated by
> > free radical damage. 
> > Glutathione increase (requires selenium) stops all
> > that and also reduces 
> > the Th2 inflammatory cell count on favour of
> > non-inflammatory, reduced 
> > damage, Th1. But since all the antioxidants work
> > together I recommend a 
> > program of them to my clients.
> > 
> > __________________________
> > Monaldi Arch Chest Dis 2002 Jun-Aug;57(3-4):173-6
> > Related Articles, Links 
> >  
> > Role of oxidative stress in pulmonary fibrosis.
> > 
> > Mastruzzo C, Crimi N, Vancheri C.
> > 
> > Dipartimento di Medicina Interna e Medicina
> > Specialistica, Sezione di 
> > Malattie Respiratorie, Universita di Catania, via
> > Passo Gravina 187, I-
> > 95125 Catania, Italy.
> > 
> > Pulmonary fibrosis can be observed as an end state
> > in a number of chronic 
> > inflammatory pulmonary diseases. Although the
> > mechanisms by which lung 
> > fibrosis develops are not fully ascertained,
> recent
> > findings suggest that 
> > oxidative stress may play an important role in the
> > pathogenesis of tissue 
> > fibrosis affecting apoptosis of both structural
> and
> > inflammatory cells 
> > and altering the cytokine microenvironment
> balance.
> > Damage and alteration 
> > of alveolar epithelial cells is one of the
> hallmarks
> > of interstitial lung 
> > fibrosis. Recently, it has been demonstrated that
> > the presence of 
> > oxidative stress may lead to the damage,
> activation
> > and/or apoptosis of 
> > alveolar epithelial cells either directly, through
> > an imbalanced 
> > intracellular redox equilibrium, or indirectly, by
> > activating redox-
> > sensitive effector pathways, such as transcription
> > factors and 
> > angiotensin converting enzyme, increasing the
> > conversion of 
> > angiotensinogen into angiotensin II that can be
> > considered a mediator of 
> > oxidative stress, capable of inducing apoptosis.
> > Furthermore, it has been 
> > demonstrated that angiotensin II acts as a
> > proinflammatory cytokine and 
> > is effective in activating fibroblasts through the
> > release of 
> > transforming growth factor (TGF-beta). As well as
> > activation, 
> > differentiation, proliferation and apoptosis of
> > fibroblasts seem related 
> > to the oxidant/antioxidant balance, and the
> > maintenance of a high 
> > intracellular level of reduced glutathione (GSH)
> is
> > considered crucial in 
> > providing a reducing environment within the cell,
> > able to protect against 
> > oxidative stress. In those conditions where
> > oxidants, either inhaled or 
> > produced by inflammatory cell, increase, the ratio
> > between GSH and 
> > oxidized glutathione (GSSH) may lower, influencing
> a
> > variety of cellular 
> > redox-sensitive signaling processes such as the
> > activation of nuclear 
> > factor-kB (NF-kB) and activator protein-1 (AP-1)
> > that lead to a 
> > transcriptional up-regulation of a number of genes
> > involved in 
> > inflammation and/or fibrogenesis, including
> > cytokines [interleukin (IL)-
> > 1,, tumor necrosis factor (TNF-alpha), IL-6]
> > chemokines (IL-8), adhesion 
> > molecules (VCAM-1, ICAM-1) and growth factors
> > (GM-CSF). In addition, 
> > several studies have shown that oxidative stress
> may
> > also affect the 
> > immune response by inducing an up-regulation of
> > HLA-DR as well as the 
> > expression of two costimulatory molecules such as
> > CD40 and CD86, 
> > determining a persistent state of immune
> activation,
> > and affecting the 
> > Th1/Th2 balance, modulating the T-cell effector
> > response towards the Th2 
> > phenotype. It is clear that a better understanding
> > of the precise 
> > sequence of events that make the difference
> between
> > normal tissue repair 
> > and fibrosis, including the role played by
> oxidative
> > stress, will 
> > certainly improve our therapeutic approach to
> > pulmonary fibrosis.
> > ___________________________
> > > You would be surprised.... Cystic Fibrosis
> people
> > have
> > > tried many things...
> > > One mother tried DMSO on the sputum of her
> Cystic
> > > Fibrosis son. It tickens the mucus though and
> she
> > > never tried using with on the son. Tick mucus is
> > > killing for them. I assume it's because their
> > mucus
> > > has a different structure. They have much more
> > salt in
> > > the sweat, etc. 
> > 
> > 
> > --
> > The silver-list is a moderated forum for
> discussion
> 
=== message truncated ===


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