Insulin resistance zap .
Andre Willers.
24 May 2014 .
Synopsis :
We create Protectin DX from omega-3 flaxseed via bioreactor
Psyllium-husks . A tbsp. flaxseed oil , a ¼ psyllium husk and a 2 sec microwave
nuke gives an insulin resistance zap .
Discussion :
1.Protectin DX is derived from Omega-3 fatty acids . It is
also a “cure” for diabetes type II , as it is a secretagogue for IL-6 . See appendix AA
This simply means that it reduces the insulin resistance of
muscle cells .
2. Protectin DX is not yet available outside labs , but we
can make our own .
3. We use the reactive surfaces of Psyllium husks to produce
meaningful amounts of Protectin DX.
See Appendix AA
4. See the surface of Psyllium husks :
Notice all the reactive surfaces and pockets .
This is a micro-chemical reactor .
Ideal for producing reactions from omega-3 fats .
Including Protectin DX .
5. What amount of Protectin DX is needed :
As starting point :http://en.wikipedia.org/wiki/Docosahexaenoic_acid
328.488 gm/mole
Avogrado constant number of molecules per mole = 6.022 x
10^23
Number of Muscle cells~ 20 x10^12
If we need one molecule per muscle cell , then that is
Grams of Protectin DX needed (approx.) ~ 328 x (20 x 10^12 / (6.022 x10^23))
This is about 1.093
x10^-8 gm .
Kinda small .
As a matter of fact this is the order of magnitude expected
with homoeopathic effects .
6. Let’s beef it up a little .
A tablespoon of
flaxseed oil mixed with a ¼ tsp of
psyllium husks (let stand for 10
minutes)
Should give enough Protectin DX .
Zap it in the microwave for a second or two .
Remember , chemical reactivity doubles with every 10 C
increase .
So does all those reactions in the Psyllium reaction
chambers producing Protectin DX , amongst other things .
7. A bit of overkill , but minimalism at this scale is not
called for , as Psyllium reaction chambers are involved .
8. The recipe :
A tbs(15 ml) of flaxseed oil (linseed oil) or any omega-3
oil .
About 2ml (1/2tsp) psyllium husks .
Mix well and stand for 10 minutes .
Nuke in microwave for about 2 seconds (900 W) \
Stand for about 10 minutes .
The standing is for the bioreactor pockets in the psyllium
husks to get active .
Then drink .
9. Bioreactor effects .
The psyllium surface pockets
are chemically equivalent to the succession (shaking) effects seen in homeopathic
medicines , just more effective . Especially if you give it a kick with
microwaves .
10. In other words , you can make quite effective
low-molecule count medicines by shot-gunning them with microwaves in psyllium
reactor chambers .
11. You can do this with any other medicine that is not very
effective .
12 . Boojums :
This presumes that the derivitives are benign , or not
harmful .’
However , some would be Boojums , where even a small number
of molecules will make you vanish.
Good luck !
Andre
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Appendix AA
Protectin DX
We previously demonstrated that low
biosynthesis of ω–3 fatty
acid–derived proresolution mediators, termed protectins, is associated with an
impaired global resolution capacity, inflammation and insulin resistance in
obese high-fat diet–fed mice1. These findings
prompted a more direct study of the therapeutic potential of protectins for the
treatment of metabolic disorders. Herein we show that protectin DX (PDX) exerts
an unanticipated glucoregulatory activity that is distinct from its
anti-inflammatory actions. We found that PDX selectively stimulated the release
of the prototypic myokine interleukin-6 (IL-6) from skeletal muscle and thereby
initiated a myokine-liver signaling axis, which blunted hepatic glucose
production via signal transducer and activator of transcription 3
(STAT3)-mediated transcriptional suppression of the gluconeogenic program.
These effects of PDX were abrogated in Il6-null
mice. PDX also activated AMP-activated protein kinase (AMPK); however, it did
so in an IL-6–independent manner. Notably, we demonstrated that administration
of PDX to obese diabetic db/db mice raises skeletal muscle IL-6
levels and substantially improves their insulin sensitivity without any impact
on adipose tissue inflammation. Our findings thus support the development of
PDX-based selective muscle IL-6 secretagogues as a new class of therapy for the
treatment of insulin resistance and type 2 diabetes.
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