Fatigue Therapy
Research results from University of Kentucky, Department of Physiology
update understanding of fatigue therapy
March 30th, 2008
(NewsRx.com) -- Current study results from the report, 'Free radicals
and muscle fatigue: Of ROS, canaries, and the IOC,' have been
published.
According to a study from the United States, "Skeletal muscle fibers
continually generate reactive oxygen species (ROS) at a slow rate that
increases during muscle contraction.
This activity-dependent increase in ROS production contributes to
fatigue of skeletal muscle during strenuous exercise."
"Existing data suggest that muscle-derived ROS primarily act on
myofibrillar proteins to inhibit calcium sensitivity and depress
force.
Decrements in calcium sensitivity and force are acutely reversible by
dithiothreitol, a thiol-selective reducing agent.
These observations suggest that thiol modifications on one or more
regulatory proteins are responsible for oxidant-induced losses during
fatigue.
More intense ROS exposure leads to losses in calcium regulation that
mimic pathologic changes and are not reversible.
Studies in humans, quadrupeds, and isolated muscle preparations
indicate that antioxidant pretreatment can delay muscle fatigue.
In humans, this phenomenon is best defined for N-acetylcysteine (NAC),
a reduced thiol donor that supports glutathione resynthesis. NAC has
been shown to inhibit fatigue in healthy adults during electrical
muscle activation, inspiratory resistive loading, handgrip exercise,
and intense cycling," wrote M.B Reid and colleagues, University of
Kentucky, Department of Physiology.
The researchers concluded: "These findings identify ROS as endogenous
mediators of muscle fatigue and highlight the importance of future
research to (a) define the cellular mechanism of ROS action and (b)
develop antioxidants as novel therapeutic interventions for treating
fatigue."
Reid and colleagues published their study in Free Radical Biology &
Medicine (Free radicals and muscle fatigue: Of ROS, canaries, and the
IOC. Free Radical Biology & Medicine, 2008;44(2):169-79).
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http://tinyurl.com/ynpdhm
"Iron-chelating agents, N-acetyl-L-cysteine (NAC), apocynin,probucol,
and edaravone, are useful in preventing cardiovascular injury and
diseases."
Recent Patents on Anti-Infective Drug Discovery, 2006, 1,
17-31171574-891X/06 $100.00+.00(c) 2006 Bentham Science Publishers
Ltd.Recent Progress in Pharmacological Research of Antioxidants
inPathological Conditions: Cardiovascular Health
Who loves ya.
Tom
Jesus Was A Vegetarian!
http://tinyurl.com/2r2nkh
Man Is A Herbivore!
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DEAD PEOPLE WALKING
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Taka - 25 Mar 2008 02:23 GMT
> Fatigue Therapy
> Research results from University of Kentucky, Department of Physiology
[quoted text clipped - 60 lines]
>
> DEAD PEOPLE WALKINGhttp://tinyurl.com/zk9fk
Yeah, give them antioxidants before exercise and you never grow
muscles ... No pain no gain - without the oxidative damage you cannot
stimulate muscle growth. You do need ROS and possibly AA metabolites
such as PGF/PGE2 to improve your physique. That's how it works and
why herbivores can never be successful athletes ...
Taka
ironjustice - 25 Mar 2008 18:55 GMT
On Mar 24, 6:23 pm, Taka <taka0...@gmail.com> wrote:You do need ROS
and possibly AA metabolites
such as PGF/PGE2 to improve your physique. <<
"With the AA metabolites, the tissue may be permanently stuck
in the original destructive phase of inflammation"
You can have it both ways .. taka .. ?
Must be nice ..
http://tinyurl.com/2bjotq
Who loves ya.
Tom
Jesus Was A Vegetarian!
http://tinyurl.com/2r2nkh
Man Is A Herbivore!
http://tinyurl.com/a3cc3
DEAD PEOPLE WALKING
http://tinyurl.com/zk9fk
> > Fatigue Therapy
> > Research results from University of Kentucky, Department of Physiology
[quoted text clipped - 70 lines]
>
> - Show quoted text -
Taka - 26 Mar 2008 15:40 GMT
> On Mar 24, 6:23 pm, Taka <taka0...@gmail.com> wrote:You do need ROS
> and possibly AA metabolites
[quoted text clipped - 4 lines]
>
> You can have it both ways .. taka .. ?
Fortunately yes, if you think quantitatively and not only
qualitatively. Also there are tissues which are better off without AA
such as stem cells but highly differentiated and specialized cells may
(notice the MAY) require it for optimal functioning. Also optimal
function in short term doesn't equal preservation of the function for
the longest time possible. I do believe we need prostaglandins
(isolated from PROSTAte) for reproduction, childhood growth and muscle
growth in sports. But there is an important threshold for the AA
content in cells beyond which you may have rather destructive than
constructive inflammatory response. The AA metabolites called
leukotrienes are responsible for the destructive phase and this is
what you get when you are messing with Omega-3 to inhibit the
prostaglandin production. If you are unfortunate to be overloaded
with AA, as most westerners are, the antioxidants specifically
inhibiting 5-LOX (making the leukotrienes) like AKBA may be useful
together with exercise which will help you to burn the excessive AA
stores. Go to check this holly plant called Boswellia serrata but
don't come back telling me all it does is reducing the iron ...
Taka
ironjustice - 26 Mar 2008 16:34 GMT
On Mar 26, 7:40 am, Taka <taka0...@gmail.com> wrote: don't come back
telling me all it does is reducing the iron <<
Why exactly iyho would it be registered as .. "not compatible with
copper or iron" .. ?
There are only a few reasons for that kind of precautionary ..
labling ..
Who loves ya.
Tom
Jesus Was A Vegetarian!
http://tinyurl.com/2r2nkh
Man Is A Herbivore!
http://tinyurl.com/a3cc3
DEAD PEOPLE WALKING
http://tinyurl.com/zk9fk
> > On Mar 24, 6:23 pm, Taka <taka0...@gmail.com> wrote:You do need ROS
> > and possibly AA metabolites
[quoted text clipped - 25 lines]
>
> Taka