torsdag 27. februar 2020

Corona treatment

The coronavirus has a protease which can be inhibited by nitric oxide (NO). (See link under). And since NO is produced in the sinuses, it might be feasible to dampen the coronavirus replication simply by breathing through the nose!

It might help to blow out with closed mouth while holding for the nose, so the ears feel clogged. Then highly pressured and concentrated nitric oxide reaches the lungs. Breathing in and out through the nose into a plastic bag gives a similar effect.

https://www.sciencedirect.com/science/article/pii/S1074761300800035#BIB61

Humming can increase NO concentration:
https://www.atsjournals.org/doi/full/10.1164/rccm.200202-138BC

https://www.sciencedaily.com/releases/2020/10/201002111724.htm

_________

Drugs to increase white blood cells count (immune cells) in Covid-19 infections:

To boost the number of WBCs and the immune system, amphetamine (e.g. Adderall/Ritalin/methylphenidate) can be used. One can also use Neupogen produced by Amgen.

And nicotine increases adrenaline, which again increases total immune cells count.

We will win!

Yours sincerely,

Ottar Stensvold

Molde
Norway

https://www.researchgate.net/publication/260431843_Association_of_Leukocytosis_with_Amphetamine_and_Cocaine_Use

https://www.nrk.no/norge/fa-rusmisbrukere-har-fatt-korona-_-overrasker-fagfolk-1.15108708

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4093780/

https://www.news-medical.net/amp/news/20200615/An-inverse-relationship-between-smoking-and-COVID-19.aspx

https://apjmt.mums.ac.ir/article_8472.html

https://journals.lww.com/md-journal/fulltext/2020/07020/methylphenidate_has_mild_hyperglycemic_and.72.aspx

https://www.ehealthme.com/ds/adderall/leukocytosis/

«The stimulant cohort was less likely to utilize emergency department, hospital, and intensive care services than the unmedicated cohort, and had significantly lower 30-day mortality.»
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9279163/


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tirsdag 10. november 2015

Nucleic acids as drugs

tRNA on Ribosome and how to wrap in and stop antigens with nucleic acids
Gif from http://cheminf.cmbi.ru.nl/molden/pdb.html
 Helsenotis
Regarding autoimmune MS and diabetes:
My idea is to take down the protein markers
which the T-cells home in on when they perform autoimmunity, and/or target the receptors /
surface proteins on the T-cells which they use in this task. 
In cancer, I want to target oncoproteins with oncogenes.
At GenBank and by gene sequencing we can find some of
the needed gene/protein sequences.
I try to explain my theory in this video:
http://www.youtube.com/watch?v=7834CXASQF8
I found these articles supporting my theory about amino acids` binding to their cognate codons (triplets):






Idea in biochemistry part 1-4:
PART 1
Quick web searches on the topic ribosome all show the same:
the amino acid-loaded tRNA arrives at the ribosome with its
anti-codon first. I think this is an oversimplification, which
doesn`t take notice to the probable, intuitive fact that the gene is
a blueprint for the protein, a mirror-copy made through evolution.
Say the proteins initially instructed the genes and not vice versa.
Say the food came first, and then the means to carry it.
For such a complex process as translation to proceed without many errors,
there has to be a primary mechanism of proofreading. Maybe there is a
closer link between amino acids and the mRNA than previously thought.
Maybe there is a transient key-lock binding between the amino acid and
the codon before the anticodon binds.
The bases seem to reach for the amino acids, and the first and the second
bases seem to play the greatest role. For instance, the short one-cyclic U are
in the second (midst) position in codons binding hydrophobic amino acids,
indicating the hydrophobic aa`s R-groups (side chains) will turn downwards when binding.
And hydrophilic amino acids have the longer two-cyclic A in the midst position
in their codons, indicating the R-groups will turn upwards, away from the codon,
towards the water when encountering the codons.
My point is that it should be possible to make any short gene sequence
that could match any protein, almost as an antibody. The oligonucleotides
will contract at point of binding, and they will probably work for only shorter
stretches. As far as I know it should not be too dangerous to apply in vivo,
but of course animal tests, research etc. are needed.
I read for instance in Discover Magazine and at Nature.com that eosinophilic cells
catapult mitochondrial DNA nets against parasites (malaria).It should be possible to target any protein-markers in any disease,
and hence destroy the culprits. Say, put a virus in a PCR machine and make
cheap copies of tailored antibodies! Or use the new oligo synthesis factories!
I try to explain my theory in this video:
http://www.youtube.com/watch?v=7834CXASQF8

Here are some articles supporting my theory about amino acids` binding to their cognate codons:



Sincerely,

Ottar Stensvold

PART 2
A drop of ordinary water-smear on a microscopy slide reveals a pattern:
the bacteria in the water lines up, symbolized like this:  o…..o..o…o…o
These lines are best seen at 400x magnification.
My theory / idea is that DNA from ruptured bacteria binds and absorbs proteins from its own species.
So what? If so, if a nucleic acid can bind to a protein in a coded manner,
then the aptamer technology is the tech of the future.
Say for instance the codon GUG, which codes for the amino acid valine, weakly
binds this amino acid. Symbolized like this: E-<
The codon-amino acid binding gives several combinatorial possibilities with
regard to polar interactions, mechanic fit and R-group placement.
If we can make aptamers tailored to bind specific proteins, then we can
take down any pathogen.
—-
PART 3
The amino acid sequence of the HIV surface protein GP 120
can be found at GenBank:
My plan is to try to make an array of different aptamers to hit this protein.
The approach I will use is basically to design aptamers that are based on
the amino acids` corresponding codons. In the DNA-aptamers, I will replace
U with T, and in the third wobble-position I will choose the assumed least
interfering base (T). RNA aptamers can also be used.
There is a chance that the aptamers will match directly.
The matches have to be at accessible parts of the protein`s surface.
The aptamers will be ordered (outsourced), for instance from:
or from Eurogentec in San Diego, California:
The price of the aptamers will be maybe around one tenth of comparable drugs,
i.e. monoclonal antibodies. The stock of different aptamers will be annotated at my portable computer. Then, step 2, we have to beg institutions which store HIV viruses to test the aptamers in vitro.
The results can be viewed with electron microscopes.
(One can also test aptamers on oncoproteins in stored tissue samples,
e.g. the 17 aa CD44 protein which is overexpressed on membranes on glioma cancer brain cells.)
This project needs help from media. The headlines could be:
“Burn off money to test HIV drug”
“Find miracle drug”
Press: “Will this be tested in humans? Will there be marketing? Sales?
Investing?”
Answer:  ”We will find a balanced solution, it`s fair that developed
countries pay for some of the venture.”
The task will require all communication skills and business intelligence.
It is a bit like cloud computing: once the hidden codes are found,
they have to be administered.
It is my goal to reach this goal of my life!
——————————————
PART 4
The aptamer: GGTTGGTGTGGTTGG
(or ggttggtgtggttgg)
or GGT TGG  TGT   GGT  TGG
or GGU UGG UGU GGU UGG  (in RNA) corresponds to the amino acids:
gly   trp    cys   gly   trp   abbreviations:
G      W     C      G      W
The combination “GW” occurred once in the thrombin protein,
the combination “WG” occurred twice,
the combination “WC” occurred twice
the combination “GC” occurred twice
and the combination “CG” occurred three times
The latter combination, for instance, should then bind to the aptamer-codons UGU GGU.
I did not find similar matches in the comparable plasma proteins albumin or insulin,
and I think further research will find no other similar matches either.
It is striking that the aptamer comprises the range of codons encoding the protein (aa range) it binds!
This underscores my suggestion that proteins can bind specific to their codon combinations in mRNA or (+)ssDNA.
The numbers of possibilities to get a twosome aa-combination of a pool of twenty different amino acids,
should plainly speaking be 1/20 X 1/20 = 1/400,
and this makes specific binding likely!
In the June 2009 Scientific American issue, there is an article about silent mutations (by Chamary and Hurst)
which highlights that different codons encoding the same amino acids give alterations in the proteins.
It`s thus feasible that this bias is caused by the codons` positioning of the amino acids (R-group placement in space). Hence, since nucleic acids are molds for proteins, it should be possible to use these molds as ligands for the proteins!

I think this is an area that needs further investigation.

Sincerely,

Ottar Stensvold

Molde
Norway
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torsdag 15. januar 2015

The Red Bull effect


The Red Bull effect
Caffeine and glucose (also called grape sugar or dextrose) has each a well-known effect.
Caffeine acts particularly in the brain by blocking the receptor(s) for the inhibitory neurotransmitter adenosine.
The adenosine level increases by physical efforts and by the time we are awake.
The caffeine molecule resembles the adenosine molecule.
Maybe the effect of caffeine can be enhanced by the creation of a stuff that resembles adenosine more
than caffeine alone does, in a reaction between caffeine and glucose.
The Red Bull drink contains both caffeine and glucose, and the reason why this drink works so well could be a chemical reaction between these two molecules.
Chemically it is fully feasible that there will be created a compound which resembles adenosine more than caffeine alone does.
Thus there will be a stronger effect, ie a better blockage of the receptor(s).
See picture attachment - at right it shows the common formation of a glycosidic bond between caffeine and glucose,
where nitrogen attaches to the anomeric carbon in a nucleophilic substitution reaction. Acidic pH, pressure and heat will catalyze this reaction.
I have not tried to blend caffeine and glucose. I don`t know the health risks, not even for the legal Red Bull drink.
Please be responsible.

Sincerely,

Ottar Stensvold

Molde 
Norway
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onsdag 3. desember 2014

Booster Sports Drops




I present here the nutrient I have developed, for general info in the first place.

I think there is a great opportunity in applying energy to the immune system. The stuff described here under (polyacetylated carbohydrates / sugar derivatives found in plants) will as all nutrients first encounter the immune cells when taken up to blood. It will even directly fuel the immune cells by diffusion into the mucous membranes in the lymphatic tissue in and around the tonsils.

It thus implies great opportunities not only by means of nutritional energy supply, but also by means of worldwide distribution and sales. 

"and the leaves of the tree were for the healing of the nations" - Revelation 22:2

________________________________________________
Booster Sports Drops Rum is made of sugar, vinegar and rum aroma.

Colour may vary. Store cold and dry.


the booster sports drops 
natural nutraceutical boooooster

Ladies and gentlemen, let me introduce the world-class nutraceutical: The Booster Sports Drops. It`s an invention based on the precious experience made by the sugar plantation slaves. During their suffering in the heat of the day, they drank / ate raw cane sugar and experienced an enduring stream of energy. This made them capable to bear inhuman burdens of work. The secret lay in the acetylated sugar compounds in the canes. I will honor the memory of these good people and prevent slavery and unfair treatment from happening again. Therefore, I invented The Booster Sports Drops. I discovered this kind of sugar compound that can access the cells in the body without the help of insulin. Insulin is a hormone that in a complex receptor-ligand-cascade chain lets the cells express glucose transporters as GLUT-4 (and other transporter / receptor proteins like for instance LDL-receptors) in their membranes, e.g. muscle cells. This sugar compound is less polar and more branched than ordinary glucose, and it thus more easily bind to the unpolar cell membrane (softens it). At the interface of the cell membranes, it also solutes glucose. The cells will simply engulf this by endocytosis. Other nutrients, as for example cholesterol (in LDL) will also be taken up in the process. This scavenges the blood, lowering the glucose rate and the cholesterol rate in the blood, - key factors for a healthy life! It thus functions as a generic insulin / glucose transporter, and might help diabetics among others. The sugar compound in the Booster Sports Drops promotes endocytosis. Once taken up by the cells, the complex carbohydrates (in endosomes) will be attached by lysosomes in the cytoplasm. The acidic (low pH) lysosome vesicles contain acid hydrolases. These enzymes hydrolyse the sugar compounds and release new functional molecules, namely acetic acids which otherwise can`t enter cells in such packages. In a normal human cell, there are around 2000 mitochondria (more in muscle cells). The mitochondria are the energy factories of the body. Acetic acid enters the mitochondria and goes directly into the citric acid cycle and a high yield, O2-consuming energy production. This process ignites the whole body, and keeps the metabolism, the burning of nutrients - "the wheel of life" - in motion. Since the sugar in the Booster Sports Drops are evenly distributed and don`t discriminate between cells, it restores a physiological balance. Acetylation increases bioavailability and crossing of the blood-brain barrier. Luckily, it let the most healthy cells utilize, thrive and work. One can for instance assume that cancer cells, which have an insufficient respiratory chain, and mainly survive by the incomplete, anaerobic glycolysis (breakdown of glucose) which occurs in the cytoplasm, get suppressed when other healthy nearby cells thrive by respiration (i.e. immune cells). And maybe the cancer cells lack the efficient lysosomal machinery to avoid engorgement / molecule overload / sensitivity for metabolism. The same can be true for other diseases as well (e.g. bacterial cells). And consider treatment of diseases which occur because of too strong immune reactions: overactive autoimmune phagocytes can be kept busy by the drug (complex sugar derivatives) instead of destroying surrounding tissue for food / debris (e.g. arthritis and allergy / asthma). Triggering of naive regulatory T cells is another possibility. There are other benefits as well: it makes the endothel of the circulatory system more resilient, and can decrease blood pressure by ca. 5%. And maybe deployment in membranes of erythrocytes and neurons will increase flexibility and give a more rapid exchange of CO2 / O2 and neurotransmitters. Actually, the nervous system use one-third of the body`s energy and should benefit from any good sugar-supply! The Booster Sports Drops is the ideal drops for any high-performer, whether it`s the brain worker, the athlete or the creative artist. It lights the fire! The way these nutraceutical carbohydrate compounds act in the body have always been naturally occurring. There are also drugs, like auranofin (Ridaura) or aspirin that contains ester-bonded acetic acid, and which mechanism of action has not been fully revealed yet. Along with the slaves, it`s also appropriate to mention Jesus who got the strengthening vinegar when suffering at the cross (John 19). The healing energy source is now revealed, elucidated and fortified! The Booster Sports Drops does not contain alcohol, but it has a wonderful blended taste of Jamaica rum and caramel. And the flavour? - It`s like dew beside a river in the Norwegian spring forest. 

Please search the web for explanatory videos and pictures of cell membranes, endocytosis, auranofin molecule, aspirin molecule, glucose molecule etc. 

- see this 35-second video about endocytosis: 
http://www.youtube.com/watch?v=4gLtk8Yc1Zc 

A three-cyclic sugar / carbohydrate compound, with acetic acid attached, is probably present in the Booster Sports Drops. (Picture shown in frontpage heading) 

Ac=Acetate=CH3CO2- get dynamically released in the cytoplasm by the help of acid hydrolases (esterases). 

Polyphenols, like for instance resveratrol (found in red wine) or curcumin (found in turmeric), or quercetin - a flavonoid in fruits / apples and other polyphenols (e.g in green tea), can maybe act upon cell membranes in a similar fashion as the polycyclic molecule in the Booster Sports Drops. Please search the web for info about resveratrol, curcumin, quercetin and polyphenols / flavonoids / antioxidants. See also cinnamaldehyde / cinnamon in this regard.

Picture of polyacetylated a complex carbohydrate molecule are shown in frontpage heading. Similar molecules are probably present in the Booster Sports Drops.

Loosely bound acetic acid is ready to be released in cells!

Please search the internet for info about glucose transporters.
The sugar derivative in the Booster Sports Drops can interact with / substitute / supplement the glucose transporters. Note that there are also other isoforms of glucose transporters which are not dependent upon insulin for their expression (e.g. in brain cells). 

Regarding sugar cane plantation slaves, see picture: 
http://www.movinghere.org.uk/galleries/roots/caribbean/images/S0001575.jpg

Mitochondrion - see picture: 
http://www.mda.org/publications/images/pamphlet_mitochondria_diag.jpg
The end product adenosine triphosphate (ATP) in mitochondria is an energy carrier molecule which play a key role in cell communication and activity. The Booster Sports Drops is quickly converted into ATP. The oxidative phosphorylation to form ATP occurs in the electron transport chain where oxygen (1/2 O2) is reduced to form water, H2O, by the joining of two protons (2H+) and two electrons (2e-). Please search the web for info about the citric acid cycle! The pivotal citric acid cycle takes place in mitochondria. The quick, initiating, igniting, efficient fuel in this cycle is acetate or acetyl (CH3CO): Acetate + Coenzyme A (CoA-SH) + ATP => Acetyl-CoA + ADP. The stuff (free acetate) bypasses both glycolysis and the extremely complicated pyruvate dehydrogenase complex by the help of the enzyme Acetyl-CoA Synthetase to become Acetyl-CoA!

Written by / invented by Ottar Stensvold
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fredag 10. oktober 2014

Therapeutic HIV vaccine - RNA viruses - Ebola


Enzymatic cleavage of viral genomes: hydrolysis interchangeable with ammonolysis in a kind of nitrogen fixation.

This could also be relevant for Ebola, which also is a single-stranded RNA virus:

Therapeutic HIV vaccine

The body's initial "vaccine-reaction" against HIV could be prolonged if the viruses were inactivated. In comparison, the poliovirus can be inactivated by cleavage of its RNA by ammonia. Hopefully, the same can be true for HIV. Both viruses contain single-stranded RNA and hydrolytic proteases. Perhaps the proteases perform (catalyse) ammonolysis of the phosphodiester bonds in RNA, and so cut the strands. HIV has even RNase H which is specialized in breaking RNA strands. I guess there are proteins with nuclease activity also in the Ebola viruses, e.g. the nucleoprotein (NP). Maybe even coiled, viral RNA can work on itself as an ammonolytic ribozyme. The phosphorus/phosphate (PO4-) in RNA repels water more than it repels ammonia, and is thus favoring ammonolysis over hydrolysis. (NH3 is a stronger nucleophile and a slightly lighter molecule than H2O).
The tight encapsulation/packing of RNA in the viruses will promote the ammonolysis process. It brings the 2' hydroxyl group close to the phosphorus, catalysing breakage of the phosphodiester bonds. There is high inward osmotic pressure in viruses. The hydrophobic cores in the ribonucleoproteins will attract ammonia.
(The Ebola viruses are extra prone to breakage during mechanical stress in vivo because of their long, rod-shaped forms).
And the host cells use RNases to hydrolyse foreign RNA. Maybe the RNases switch to ammonolysis when ammonia is available, and thereby speed up this defense.
In this regard, inhalation of ammonia could be a way to destroy HIV and other RNA viruses in blood and tissue.

Written by:

Ottar Stensvold

Molde 
Norway

Principle of hydrolysis:

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fredag 22. august 2014

Cholesterol might ease Ebola infections


Picture of Ebola virus entry into cell from 
http://www.einstein.yu.edu/faculty/10768/kartik-chandran/
Picture from http://www.nature.com/nrm/journal/v2/n9/fig_tab/nrm0901_657a_F2.html
If you flip-flop cholesterol (top), you can see it resembles benzylpiperazine adamantane diamide, a known NPC1 inhibitor (bottom)


I suggest Gogel Mogel could be beneficial for Ebola patients, simply by blocking Niemann–Pick C1 (NPC1), a cholesterol transporter protein, by cholesterol. The Ebola virus uses NPC1 for cell entry, and when cholesterol blocks this protein the viruses' entry into the cytoplasm will be impeded. Then there will be an increased virus accumulation and degradation in lysosomes. Raw eggs in Gogel Mogel will deliver much free, easy-absorbable cholesterol, and in addition they will deliver free amino acids, which are essential for quick synthesis of antibodies. 


See excerpts from Wikipedia below. 

Sincerely, 

Ottar Stensvold 

Molde
Norway

 Gogel Mogel:
__________________________
Preparation

The dish consists of raw egg yolks and sugar, beaten and ground until they form a creamy texture, with no discernible grains of sugar. In modern kitchens, it is often mixed in a blender until it changes color and becomes thick. A classic single Gogl-Mogl portion is made from two egg yolks and three teaspoons of sugar beaten into a cream-like dish. Variations can be made by adding chocolate, vodka, rum, honey, vanilla, lemon juice, raisins, whipped cream, or a number of other ingredients based on one's own taste preferences. A Polish variation includes the addition of orange juice, creating a taste similar to an Orange Julius.

Uses

Gogel Mogel is often prepared as a transition food for babies moving from a cereal diet to one that includes eggs and other soft foods. It is also a folk medicine used for treating colds or flu, particularly chest colds and laryngitis. Gogle-mogle is ranked highly among other traditional cold remedies such as Grandma's chicken soup. The baby transition recipe includes raw eggs and sugar which in spite of its widespread use in Russia, is a health risk to young children due to possible contraction of Salmonella.
The traditional usage of Gogle Mogle as a home remedy for treating a sore throat is supported by research done in Israel.[5][6] The simplest form of preparation as a remedy is with no egg, but only honey added to warm milk. More commonly, a single raw egg is added to a cup of warm milk and mixed with a tablespoon of honey.

Ebola:
_________________________
Entry

There are two candidates for host cell entry proteins. The first is the host-encoded Niemann–Pick C1 (NPC1), a cholesterol transporter protein, which appears to be essential for entry of Ebola virions into the host cell, and for its ultimate replication.[11][12] In one study, mice that were heterozygous for NPC1 were shown to be protected from lethal challenge with mouse-adapted Ebola virus.[11] In another study, small molecules were shown to inhibit Ebola virus infection by preventing viral envelope glycoprotein (GP) from binding to NPC1.[12][13] Hence, NPC1 was shown to be critical to entry of this filovirus, because it mediates infection by binding directly to viral GP.
When cells from Niemann Pick Type C patients lacking this transporter were exposed to Ebola virus in the laboratory, the cells survived and appeared impervious to the virus, further indicating that Ebola relies on NPC1 to enter cells; [citation needed] mutations in the NPC1 gene in humans were conjectured as a possible mode to make some individuals resistant to this deadly viral disease. [citation needed][speculation?] The same studies described similar results regarding NPC1's role in virus entry for Marburg virus, a related filovirus. A further study has also presented evidence that NPC1 is critical receptor mediating Ebola infection via its direct binding to the viral GP, and that it is the second "lysosomal" domain of NPC1 that mediates this binding.[14]
The second candidate is TIM-1 (aka HAVCR1).[15] TIM-1 was shown to bind to the receptor binding domain of the EBOV glycoprotein, to increase the receptivity of Vero cells. Silencing its effect with siRNA prevented infection of Vero cells. TIM1 is expressed in tissues known to be seriously impacted by EBOV lysis (trachea, cornea, and conjunctiva). A monoclonal antibody against the IgV domain of TIM-1, ARD5, blocked EBOV binding and infection.
Together, these studies suggest NPC1 and TIM-1 may be potential therapeutic targets for an Ebola anti-viral drug and as a basis for a rapid field diagnostic assay. [citation needed]
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torsdag 30. september 2010

Disintegration of cancer cells


SHEPHERDS

Why didn`t the shepherds get cancer?
- a proposed explanation.

The best known shepherds are they who went to find the newborn Son of God, Jesus Christ. Their journey changed the course of history. They found what was to become the centre and the goal; the heavenly communion with Christ. Shepherds seemed to be the chosen ones from an early stage. In the jews` exodus from Egypt, they played a crucial role, and both Moses and King David were shepherds before they got chosen as leaders.
In this society, cancer was rare. Why? In accordance to the immune surveillance theory, I will try to give an explanation. (I see ammonia as a counterpart to nitrogen oxide - a known immune response mediator).
In cancer, the genome goes “wild”. In the highly proliferating cancer cells, it is in vast abundance and scattered around. The rapidly dividing cells` genome lies open for transcription and replication, and is an easy target.
Now and then such cellular changes occur. To ward them off, one need a stuff that chops up the cancer genome. One such stuff could be ammonia. It`s a gaseous by-product in the bacterial breakdown of urine, especially sheep`s urine. Its odor is well-known. And the shepherds breathe in a lot. Ammonia‘s reaction with water is basic:
NH3 + H2O = NH4+ + HO-
The interior of cancer cells tends to be alkaline due to accumulation of lactate, ion channel efflux of H+, and due to consumption of H+ in excessive fatty acid synthesis. Less H+ gives more HO- and this drives the equilibrium to the left.
Ammonia diffuses directly through cell membranes and soakes the whole tissue. The body wards off this molecule by aminotransferases and by the urea cycle in the liver. DNA, with its densely stacked nitrogenous bases G + C and A + T, is somehow condensed and possesses hydrogen bonding between the bases (between N, O and H atoms).
My assumption is that DNA is vulnerable for ammonia, especially in alkaline cancer cells. NH3 will disturb (break) the hydrogen bonding between the nitrogenous bases and unzip the DNA strands. (Like dissolves like; the related molecule urea is used in laboratories to split dsDNA). Hence, the fragile cancer cells in mitosis will be the first to be destroyed when systemic ammonia is present. This could be an explanation for the low cancer incidence among the shepherds. Although NH3 is a toxic molecule, to breathe in a sheepfold, or over an open bottle of household ammonia, for that matter, is not that hazardous. This seems strange, but for God is nothing impossible, and he can use the strangest ways to fully elaborate his love for humankind.

Written by:

Ottar Stensvold

Molde
Norway


PS! See these links about ammonia`s selective destruction of the cancerous Jurkat cells and the cancerous HeLa cells:

http://www.ncbi.nlm.nih.gov/pubmed/18642273

http://www.springerlink.com/content/p055268176kk0547/

Nasser G Haghighat, Monica M Oblinger and D W McCandless:
"When C6-glioma cells were exposed to 15 mM ammonium chloride, we observed major cell death (only 32% cell survival relative to control) within 72 h."
https://www.researchgate.net/publication/8504569_Cytoprotective_Effect_of_Estrogen_on_Ammonium_Chloride-Treated_C6-Glioma_Cells
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