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» LymeNet Flash » Questions and Discussion » Medical Questions » Any scientists or really smart people hanging around? p450 gene?

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Author Topic: Any scientists or really smart people hanging around? p450 gene?
treepatrol
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I know we are are all smart. [Big Grin]

I reposted this question from another post moved it here.

Any scientists hanging around?

Question the cytochrome p450 gene could it be ingulfed incorperated {{Mutations}} into another ?

Like this you have a tick that feeds on mice deer etc they have p450 genes. Now this tick carries lyme spirochete it gets injected into mouse or deer.
Now we know spirochetes attack phagocytes in humans. Could they or are they picking up in each cycle spirochete to mouse to deer or human the original p450 in each host??

Then there by combining mouse ,deer human p450 genes?

Could this be the reason for there ability too withstand antibiotics??

[ 22. December 2005, 09:55 AM: Message edited by: treepatrol ]

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treepatrol
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up for comments?

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Do unto others as you would have them do unto you.
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bpeck
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Hi Guys:

Substance metabolism:
The P450 system is the name for a group of enzymes in the liver which breaks down substances that pass thru the liver. Most living organisms have this system. In humans- about 50% of the drugs we take are metabolixed thru this system.
(There are other drug metabolic pathyways- but we'll stick to this one for this discussion).

In some people, there are variations of how these enzymes work- that's why some people can take some drugs without a reaction and others can't - it's just they way certain individuals systems work.

Then there's drug interactions at either inhibit for excellerate the metabolism of drugs - and even this can be affected by a persons genetic variation of the P450 system.

This is true in other organisms too.

Bacterial Variants:
A variant is a form that the bacteria can change itself into to avoid being affected by a drug - and it can change it'self back to it's original form when the threat is removed.

Bacterial mutation:
Some organisms mutate when threatened continually by a substance. A mutation stays this way, it's forever resistant to a previous drug that could kill it.


I think you may be confusing drug resistance (of bacteria) to certain medications. This is when under the pressure of antibiotics, the (bacteria) organism mutates, so that it's no longer susceptible to the antibiotic it was before the mutation.

An organism is only called pathogenic if it can infect and make someone sick.

A carrier is a person who can carry a pathogen but it does not make them sick- but if that pathogen is passed to another susceptible person it can make them sick. This is a complicate mechanism involving genetics and the immune system.

But the important thing to remember is that the P450 system is not part of our immune system- it's part of the metabolic system that breaks down and removes substances from the body. It doesn't attack per se bacteria (although some of the enzymes may be responsible for breaking down their by-products).

Hope this isn't too confusing.. and that it helps your understanding.

Barb

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Barb Peck (Elder LymeNet user). Lyme since 1975 Transfusion

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treepatrol
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quote:
Originally posted by bpeck:
Hi Guys:

Substance metabolism:
The P450 system is the name for a group of enzymes in the liver which breaks down substances that pass thru the liver. Most living organisms have this system. In humans- about 50% of the drugs we take are metabolixed thru this system.
(There are other drug metabolic pathyways- but we'll stick to this one for this discussion).

In some people, there are variations of how these enzymes work- that's why some people can take some drugs without a reaction and others can't - it's just they way certain individuals systems work.

Then there's drug interactions at either inhibit for excellerate the metabolism of drugs - and even this can be affected by a persons genetic variation of the P450 system.

This is true in other organisms too.

Bacterial Variants:
A variant is a form that the bacteria can change itself into to avoid being affected by a drug - and it can change it'self back to it's original form when the threat is removed.

Bacterial mutation:
Some organisms mutate when threatened continually by a substance. A mutation stays this way, it's forever resistant to a previous drug that could kill it.


I think you may be confusing drug resistance (of bacteria) to certain medications. This is when under the pressure of antibiotics, the (bacteria) organism mutates, so that it's no longer susceptible to the antibiotic it was before the mutation.

An organism is only called pathogenic if it can infect and make someone sick.

A carrier is a person who can carry a pathogen but it does not make them sick- but if that pathogen is passed to another susceptible person it can make them sick. This is a complicate mechanism involving genetics and the immune system.

But the important thing to remember is that the P450 system is not part of our immune system- it's part of the metabolic system that breaks down and removes substances from the body. It doesn't attack per se bacteria (although some of the enzymes may be responsible for breaking down their by-products).

Hope this isn't too confusing.. and that it helps your understanding.

Barb

I understand that what Iam saying if {Homo sapiens =57 or Mus musculus mouse = 102} {cytochrome p450 is a gene}
Then if through {spirochete has these too CYP's}
They absorb mutate this in the ability to process
Like you said part of the metabolic system that breaks down and removes substances from the body.it thus has a way to deal with problem of why the Bb spirochete has so much more dna than other bacteria.

Also if it can process abx chemicals so that it can metabolise them well there you go.

Components of P450-containing systems

putidaredoxin reductase = PdR

Borrelia burgdorferi - - - - 2 - - - - -
Treponema pallidum - - - 1 2 1 - - - -
Mycobacterium tb 20 - 2 - 8 3 - 1 2 1
Pseudomonas A 3 2 5 - 10 1 1 6 - -
Pseudomonas aeruginosa = Pseudomonas A

Its strange how some of the more virulent bacteria all contain this one PdR at high numbers.

Borrelia burgdorferi 2
Treponema pallidum 2
Mycobacterium tb 8
Pseudomonas aeruginosa 10


Interesting read
Evolution of bioinorganic motifs in P450-containing systems

[ 23. December 2005, 11:46 AM: Message edited by: treepatrol ]

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Do unto others as you would have them do unto you.
Remember Iam not a Doctor Just someone struggling like you with Tick Borne Diseases.

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treepatrol
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While I was jumpin around foud this interesting look at the one at the bottom.
Of the taxonomy tree.

Borrelia afzelii
Borrelia andersonii
Borrelia bissettii
Borrelia burgdorferi
Borrelia garinii
Borrelia japonica
Borrelia lusitaniae
Borrelia sp. AA4Pool
Borrelia sp. AI-1
Borrelia sp. B31
Borrelia sp. BC-1
Borrelia sp. CA1133
Borrelia sp. CA1176
Borrelia sp. CA128
Borrelia sp. CA13
Borrelia sp. CA134
Borrelia sp. CA142
Borrelia sp. CA20
Borrelia sp. CA22
Borrelia sp. CA27
Borrelia sp. CA28
Borrelia sp. CA29
Borrelia sp. CA31
Borrelia sp. CA33
Borrelia sp. CA370
Borrelia sp. CA372
Borrelia sp. CA378
Borrelia sp. CA388
Borrelia sp. CA393
Borrelia sp. CA394
Borrelia sp. CA395
Borrelia sp. CA399
Borrelia sp. CA400
Borrelia sp. CA401
Borrelia sp. CA402
Borrelia sp. CA404
Borrelia sp. CA411
Borrelia sp. CA426
Borrelia sp. CA443
Borrelia sp. CA446
Borrelia sp. CA448
Borrelia sp. CA462
Borrelia sp. CA468
Borrelia sp. CA502
Borrelia sp. CA504
Borrelia sp. CA507
Borrelia sp. CA547
Borrelia sp. CA552
Borrelia sp. CA8
Borrelia sp. D22
Borrelia sp. D35
Borrelia sp. FD-1
Borrelia sp. FL18
Borrelia sp. FL27
Borrelia sp. FL35
Borrelia sp. FL42
Borrelia sp. HN6
Borrelia sp. HN7
Borrelia sp. HN8
Borrelia sp. HNM13
Borrelia sp. HNM14
Borrelia sp. HNM19
Borrelia sp. IA1
Borrelia sp. Ir-3519
Borrelia sp. Ir-4721
Borrelia sp. Ir-4812
Borrelia sp. Ir-5215
Borrelia sp. LV5
Borrelia sp. MI-2
Borrelia sp. MI-5
Borrelia sp. MI-6
Borrelia sp. MI-8
Borrelia sp. MI-9
Borrelia sp. MOD-1
Borrelia sp. MOD-5
Borrelia sp. MOK-3a
Borrelia sp. MOS-1b
Borrelia sp. NE49
Borrelia sp. NE581
Borrelia sp. PHaP
Borrelia sp. PSigII
Borrelia sp. SCGT-10
Borrelia sp. SCGT-8a
Borrelia sp. SCI-2
Borrelia sp. SCW-30h
Borrelia sp. SI-1
Borrelia sp. SI-10
Borrelia sp. SM-1
Borrelia sp. W97F51
Borrelia sp. Z41293
Borrelia sp. Z41493
Borrelia spielmanii
Borrelia tanukii
Borrelia turdi
Borrelia valaisiana
Candidatus Borrelia texasensis
this one still has no name [bonk]

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Do unto others as you would have them do unto you.
Remember Iam not a Doctor Just someone struggling like you with Tick Borne Diseases.

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Aligondo Bruce
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borrelia actually have small genomes for a bacteria. they have a small amount of total DNA. the problem is that it is distributed on a record number of plasmids.{~20,+ the chromosome}
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Marnie
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They have more than the syphilis spirochete as I understand...

So they are even MORE complex...

Mg is capable of "stimulating DNA REPAIR"...mdschoice website which I have linked numerous times.

DNA repair?! WOW!!!

P.S. Enzymes are proteins and Mg (and other nutrients are needed to MAKE all proteins). Mg also controls many, many enzymes. The liver stores a lot of Mg...

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Lymied
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So is the P450 pathway a collection of enzymes in the liver that process stuff? OR is it an entire metabolic system?

I find Tree's hypothesis here quite interesting...could the P450 enzymes from other mammals be collected in the tick and thus produce a spirochete with a varied DNA? OR is the DNA already established and unchanging in the spirochete.

I have done a little research with the P450 pathway because I had a Stevens-Johnson Syndrome type reaction to Sulpha drugs. It is a hereditary condition and I found out after having it that it is what my half brother had ten years ago.

They have established that Stevens-Johnsons patients cannot process medications and other toxins as well as others because of a screwed up P450 pathway. See http://www.nationalreviewofmedicine.com/issue/2004_04_30/clinical09_09.html

So I find all of this interesting while I still have such a minimal understanding of it.

I have been mulling over it in my head after my sulfa reaction - wondering if this could be part of the piece that contributes to why some people's bodies can handle lyme and fight it and others can't...

Just fun to question and think about for me...

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bpeck
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Lymied:
The P450 enzyme system is PART of the entire metabolic system. It's not the entire system-

Yes- there are genetic differences in some people's p450 enzymes pathways, thats why is so dangerous to call all adverse reactions when taking an abx a herx. It could well be your bodies in ability to metabolize the drug the way other people do.

Barb

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mlkeen
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Mg= DNA repair. Yet another reason I love Mg! Thanks Marnie.
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Marnie
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"Cytochrome P450 is a family of the body's more powerful detox ENZYMES . Over 60 key forms are known, with hundreds of genetic variations possible,

producing a wide variety of susceptibility to specific toxins.

As the saying goes, "One man's meat is another man's poison".

Keep in mind...enzymes are PROTEINS.

P450 enzymes are not ONLY in the liver.

"Long term inhibition of heme synthesis due to P450 insufficiency may cause anemia. "

These enzymes can be damaged by ...ethanol...thanks to nasty Bb.

"Mechanisms by which: 1) consumption of alcoholic beverages increases liver damage from acetaminophen and 2)
arsenic decreases cytochromes P450 in the liver and the relation of such decreases to development of cancer and liver
damage."


What ELSE does ethanol do...

Acute and chronic ethanol administration results in a decrease in cellular Mg2+ content and an alteration of Mg2+ TRANSPORT in liver cells.

PMID: 16257349

This activity is also associated with the generation of free radicals with resulting lipid peroxidation and membrane damage as well as depletion of mitochondrial reduced glutathione (GSH) and its ultimate precursor, namely methionine activated to S-adenosylmethionine (SAMe).

Its repletion restores liver functions.

Administration of polyenylphosphatidylcholine (PPC), a mixture of unsaturated phosphatidylcholines (PC) extracted from soybeans,

*restores the structure of the membranes and the function of the corresponding enzymes.

Ethanol impairs the conversion of beta-carotene to vitamin A and depletes hepatic vitamin A and, when it is given together with vitamin A or beta-carotene, hepatotoxicity is potentiated. Our present therapeutic approach is to reduce excess alcohol consumption by the Brief Intervention technique found to be very successful.

We correct hepatic SAMe depletion and supplementation with PPC has some favorable effects on parameters of liver damage which continue to be evaluated.

PMID: 16363067

The mechanism by which ethanol induces beta-endorphin (beta-EP) NEURONS DEATH during the developmental period was determined using fetal rat hypothalamic neurons in primary cultures. The addition of ethanol to hypothalamic cell cultures stimulated apoptotic cell death of primarily beta-EP neurons by increasing caspase-3 activity.
PMID: 16326933

Black Tea Extract (BTE), a phytocompound has been attributed with a plethora of health-promoting actions. We have previously demonstrated that BTE inhibits chronic hepatitis in a rat model induced with high-fat and ethanol (EtOH). This study reports that BTE prevents altered pancreatic acinar cell functions, oxidative stress, inflammatory changes and DNA damage in the EtOH+cholecystokinin (CCK)-induced model of pancreatitis.

These findings suggest that BTE prevents pancreatitis caused by chronic EtOH+CCK toxicity presumably by enhancing *antioxidant*, anti-inflammatory and antiapoptotic activity in rats.

PMID: 16289561

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treepatrol
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My brain hurts:)

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