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10-29-2005, 05:20 AM #1Senior Member
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DNP - Need help finding a study... (Female Reproductive affects)
OKay, I have heard that women should NOT use this because it may damage their eggs.
Is this just a thought? Or does anyone here know of a study regarding this.
I have searched Pubmed/Medline, Google, and read the Profile on it here.
Yes, I have seen other people post threads or contribute to threads stating this potential problem for women, however, I haven't seen a thread with supportive information.
If ANYONE has ANY bookmarked access to a worthwhile thread on this drug as it relates to the female reproductive system, please please please, post it here. It'd be usefull to the community, and my friends.
Regards.
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10-29-2005, 08:49 AM #2Originally Posted by TrumanHW
alo
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10-29-2005, 10:23 AM #3
From what I read here on the forum (posted by a lady) it does kill eggs! So if the female wants to have kids still its best for her to wait. Same with male, it kills your boyz and makes you cum yellow, but men produce semen everday women are born with a certain number of eggs and thats it.
Alo you're in the medical field, you can easily explain this better.
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10-29-2005, 11:09 AM #4Senior Member
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Yeah, I've read the same thing more than once... but I'm trying to find out how we "know" this.
Bump for facts....
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10-29-2005, 11:13 AM #5Associate Member
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i'm curious as to why a mitochondrial uncoupler like dnp would affect a sex cell differently than a somatic cell. same cell structures AFAIK. and if there is something specific to sex cells, shouldn't DNP affect sperm cells also?
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10-29-2005, 11:40 AM #6
hmmm....
Last edited by alo5603; 10-29-2005 at 11:44 AM. Reason: typo
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10-29-2005, 11:43 AM #7Originally Posted by macgyver_48
alo
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10-29-2005, 11:44 AM #8Senior Member
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Alo! Well worded. Lets find a study.
I guess just as important as potentially killing some eggs ... is anything that may produce a higher risk of birth defect. Lets dig... this subject needs an answer...
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10-29-2005, 11:45 AM #9Originally Posted by TrumanHW
alo
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10-29-2005, 11:48 AM #10Associate Member
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so DNP works by allowing H+ to flow through the cell membrane, bypassing ATP synthase protein, and therefore preventing ATP from being generated by the cell.
working on the assumption that DNP is processed out of the body, and doesn't permanently alter the cell membrane, where is the effect on the sex cells coming from?
and if it does permanently alter the cell membrane of the female's sex cells, what is different about the body cells that they aren't permanently altered?
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10-29-2005, 11:50 AM #11Associate Member
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sorry should've clarified i was talking about mitochondrial cell
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10-29-2005, 11:55 AM #12Originally Posted by macgyver_48
alo
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10-29-2005, 12:00 PM #13Associate Member
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i was under the impression that DNP affected ALL mitochondria in the body in the same fashion
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10-29-2005, 12:02 PM #14Originally Posted by macgyver_48
alo
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10-29-2005, 12:04 PM #15Associate Member
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interesting... could you briefly describe where differences occur in mitochondria (i.e. location and function)
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10-29-2005, 12:13 PM #16Associate Member
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found this on wikipedia:
mtDNA is typically passed on only from the mother during sexual reproduction (mitochondrial genetics), meaning that the mitochondria are clones. This means that there is little change in the mtDNA from generation to generation, unlike nuclear DNA which changes by 50% each generation. Since the mutation rate is easily measured, mtDNA is a powerful tool for tracking matrilineage, and has been used in this role for tracking many species back thousands of generations.
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10-29-2005, 12:19 PM #17
thats a good read, but think about this, mitochondria found in muscle tissue is part of that particular cell, and muscle itself is a regenerating tissue, therefore it is meant to take stress, regardless if its drugs or bb, etc. Reproductive tissue, and its mitochondria are a diff type. Reproductive cells are not meant to regenerate under that particular stress, yes it does have regenerative properties, like all tissue in the body, but not under that particular stress. Therefore, its obvious you couldnt compare the two types of tissue when administering an agent like DNP . Im starting to wonder if there exists a study on this, it would be extremely dangerous to do, if it was done, it would probably have to have been done years back before we had all the inhumane laws we have now.
alo
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10-29-2005, 12:20 PM #18Originally Posted by macgyver_48
alo
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10-29-2005, 12:24 PM #19Associate Member
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yah, i was hoping to find something from the 40's regarding birth defects, but apparently there was no internet back then, lol. there was a doctor that prescribed it for weight loss in the 80's tho, i wonder if anybody bothered to do follow-ups on his patients.
do you recall whether mitochondrial replicate themselves or if they are created piece by piece by the nucleus and golgi apparatus? i want to say they are self replicating since they have their own DNA.
if this is the case, i wonder if the primary oocytes experience mitochondrial regeneration while they just sit around and wait to get knocked up.
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10-29-2005, 12:33 PM #20Originally Posted by macgyver_48
They do in fact replicate, had to dig up some of my old hw lol, and the cells in muscular tissue due at a much faster pace i might add. That would explain the regenerative process, maybe they dont build itself back up at all, they just replicate themselves. But then again, if it is replicating, wouldnt it replicate the damage DNP could do to it? I wonder.....
alo
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10-29-2005, 12:35 PM #21Associate Member
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my understanding is that damage to the DNA would produce lasting mutations or defects, and that damage to surrounding organelles and structures, while passed on through cellular division, would eventually be "worked out" over time.
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10-29-2005, 12:40 PM #22Originally Posted by macgyver_48
alo
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10-29-2005, 12:45 PM #23Associate Member
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looks like its time to go to a third world country for some secret research...
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10-29-2005, 12:48 PM #24Originally Posted by macgyver_48
alo
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10-29-2005, 02:57 PM #25Senior Member
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Well this was some good pontificating - but ... just because have good answers doesn't mean we can assume the likely outcome. We simple need to find a study ... need to.
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10-29-2005, 03:22 PM #26Associate Member
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here's some practical application for DNP . almost nobody needs to use it. especially not your average woman looking to "drop a few pounds." so in the real world, all of this is moot, she just needs to put down the ho-ho's and exercise.
prolactin would supposedly release that stubborn female pattern fat on the hips and thighs, but then you run into other problems (unless you don't mind a little extra cream in your coffee)
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10-29-2005, 09:33 PM #27Senior Member
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http://patft.uspto.gov/netacgi/nph-Parser?
Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=/netahtml/srchnum.htm&r=1&f=G&l=50&s1=4
,673,691.WKU.&OS=PN/4,673,691&RS=PN/4,673,691
And here's the toxocology report on it, saying nothing about reproductive
effects:
DINITROPHENOL
CASRN: 25550-58-7
For other data, click on the Table of Contents
Human Health Effects:
Human Toxicity Excerpts:
Signs and symptoms of acute poisoning in human beings include nausea,
restlessness, flushed skin, sweating, rapid respiration, tachycardia,
fever, cyanosis, and finally, collapse and coma. The illness runs a rapid
course; death or recovery occurs within 24 to 48 hours. If production of
heat exceeds the capacity for its dissipation, fatal hyperthermia may
result.
[Hardman, J.G., L.E. Limbird, P.B. Molinoff, R.W. Ruddon, A.G. Goodman
(eds.). Goodman and Gilman's The Pharmacological Basis of Therapeutics. 9th
ed. New York, NY: McGraw-Hill, 1996., p. 1691]**PEER REVIEWED**
Poisoning results first in ... a feeling of warmth with weakness and
fatigue. ... Death, if it occurs, is sudden and rigor mortis ensues almost
immediately.
[International Labour Office. Encyclopedia of Occupational Health and
Safety. Vols. I&II. Geneva, Switzerland: International Labour Office,
1983., p. 636]**PEER REVIEWED**
In a poisoned person, the result is an almost immediate incr in oxygen
consumption, body temp, breathing rate, and heart rate. Because circulation
and resp do not accelerate in proportion to the metabolic demand, anoxia
and acidosis develop. ... It is a milder corrosive to skin and mucous
membranes than phenol, but concentrated soln have produced corrosion of the
oropharyngeal, esophageal, and gastric mucous membranes. It exerts direct
actions on the cerebrum and lower brain centers consisting of stimulation
followed by depression. It may produce a necrotizing tubular injury of the
kidneys. If the acute phase of poisoning is survived, the patient usually
tolerates successfully the later complications, which may include renal
insufficiency and a toxic hepatitis. The fulminating type of poisoning is
characterized by sudden onset, severe symptoms, and prompt death (within 24
hours). Death is due to resp or circulatory collapse, especially the
former. Many factors undoubtedly contribute to this collapse, notably
hyperpyrexia ... dehydration, muscle rigor (due to heat and/or lactic
acid), and occasionally pulmonary edema. ... In subacute poisoning due to
repeated daily exposures, some individuals complain of lassitude, headache,
and malaise, while others experience a disarming sense of well being,
energy and drive.
[Gosselin, R.E., R.P. Smith, H.C. Hodge. Clinical Toxicology of Commercial
Products. 5th ed. Baltimore: Williams and Wilkins, 1984., p. III-157]**PEER
REVIEWED**
Miscellaneous hazards in the use of dinitrophenol include neutropenia,
agranulocytosis, and cataract formation.
[Gosselin, R.E., R.P. Smith, H.C. Hodge. Clinical Toxicology of Commercial
Products. 5th ed. Baltimore: Williams and Wilkins, 1984., p. III-157]**PEER
REVIEWED**
The hose on a weed sprayer ruptured, spraying dinitrophenol into the eye of
a worker. Chemical conjunctivitis developed and it was treated with Blinex,
Neosporin opthalmic ointment, and an eye patch. His vision was impaired for
one month.
[Peoples SA et al; Occupational Health Problems Resulting from Exposure to
Dinitrophenol and its Substituted Formulas in California in 1975 and 1976,
ACF 59-433 p.4 (1977)]**PEER REVIEWED**
A tractor driver was opening a can of dinitrophenol when it sprayed into
his face and eyes. ... /The patient's/ face peeled from contact
with /dinitrophenol/.
[Peoples SA et al; Occupational Health Problems Resulting from Exposure to
Dinitrophenol and its Substituted Formulas in California in 1975 and 1976.
ACF 59-433 p.6 (1977)]**PEER REVIEWED**
Highly toxic. Dust inhalation may be fatal.
[Sax, N.I. and R.J. Lewis, Sr. (eds.). Hawley's Condensed Chemical
Dictionary. 11th ed. New York: Van Nostrand Reinhold Co., 1987., p. 421]
**PEER REVIEWED**
Allergic reactions to explosives and war gases were reviewed with regard to
identification of the primary allergens and the clinical monitoring of
affected subjects. Sensitization was reported for powders, explosives,
fuses and war gases. ...
[Foussereau J et al; Occupational Contact Dermatitis, Clinical and Chemical
Aspects 171-6 (1982)]**PEER REVIEWED**
Human Toxicity Values:
The fatal dose in adults is about 1 to 3 g by mouth, and 3 g has proved
fatal even in divided doses over a period of 5 days.
[Gosselin, R.E., R.P. Smith, H.C. Hodge. Clinical Toxicology of Commercial
Products. 5th ed. Baltimore: Williams and Wilkins, 1984., p. III-157]**PEER
REVIEWED**
*****Truman-Note the typically reccomended does of up to 600mgs/day ******
******************is apparently 60% of the fatal dose?**********************
The acute fatal dose of dinitrophenol /SRP: Unspecified mixture of isomers/
is approximately 1 g.
[Dreisbach, R.H. Handbook of Poisoning. 11th ed. Los Altos, CA: Lange
Medical Publications. 1983., p. 127]**PEER REVIEWED**
Skin, Eye and Respiratory Irritations:
Dust and vapor of dinitrophenol have been reported to be irritating to
mucous membrane in industrial exposure ... .
[Grant, W.M. Toxicology of the Eye. 3rd ed. Springfield, IL: Charles C.
Thomas Publisher, 1986., p. 359]**PEER REVIEWED**
Drug Warnings:
Salicylates, which contain a phenolic group, must be avoided during
treatment for exposure to dinitrophenols.
[Hardman, J.G., L.E. Limbird, P.B. Molinoff, R.W. Ruddon, A.G. Goodman
(eds.). Goodman and Gilman's The Pharmacological Basis of Therapeutics. 9th
ed. New York, NY: McGraw-Hill, 1996., p. 1691]**PEER REVIEWED**
Medical Surveillance:
Men regularly exposed to dinitrophenol should have their urine regularly
tested for dinitrophenol or aminonitrophenol ... .
[International Labour Office. Encyclopedia of Occupational Health and
Safety. Vols. I&II. Geneva, Switzerland: International Labour Office,
1983., p. 637]**PEER REVIEWED**
In exposed workers, blood concentration of /dinitro-derivatives/ should not
exceed 10 ug/g. A white cell count should be performed if the exposed
person has an unexplained persistent fever. Individuals who have a fall in
white blood cell counts should avoid further exposure. /Dinitro-
derivatives/
[Dreisbach, R.H. Handbook of Poisoning. 11th ed. Los Altos, CA: Lange
Medical Publications. 1983., p. 127]**PEER REVIEWED**
Probable Routes of Human Exposure:
Exposure may occur by the inhalation of the vapor, dusts, or sprays of soln
of dinitrophenol. It penetrates the intact skin but, as it is a brilliant
yellow dye, skin contamination is readily recognized. Systemic poisoning
has occurred during both production and use. If exposure to dinitrophenol
is suspected by the nature of the occupation and by staining of the skin,
particularly of the hands and around the mouth and nose, individuals should
immediately be removed from futher expsoure, made to lie down, and the
course of poisoning carefully watched
[International Labour Office. Encyclopedia of Occupational Health and
Safety. Vols. I&II. Geneva, Switzerland: International Labour Office,
1983., p. 636-7]**PEER REVIEWED**
Those involved in dye manufacture, picric acid manufacture, photographic
chemicals.
[Sittig, M. Handbook of Toxic and Hazardous Chemicals and Carcinogens,
1985. 2nd ed. Park Ridge, NJ: Noyes Data Corporation, 1985., p. 379]**PEER
REVIEWED**
Occupational exposure to dinitrophenols may occur through inhalation and
dermal contact with this compound at workplaces where dinitrophenols are
produced or used. (SRC)
**PEER REVIEWED**
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10-30-2005, 04:14 PM #28Senior Member
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bump ... by the way, that is originally researched by Hooker...
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10-30-2005, 09:55 PM #29Senior Member
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hey alo
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10-30-2005, 10:00 PM #30
I will look around, but I doubt I can find any studies. DNP is not a hormone nor is it even intended for human use so I dont think I can find anything other than anecdotal info.
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10-30-2005, 10:03 PM #31
Needless to say women that are pregnant or may become pregnant should not be even thinking about DNP .
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10-30-2005, 10:31 PM #32Originally Posted by TrumanHW
alo
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10-31-2005, 12:46 AM #33Senior Member
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Alo - cataracs is dose dependant likelihood? Or is it at any dose?
Did you guys read the above study?
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10-31-2005, 12:51 AM #34Originally Posted by alo5603
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10-31-2005, 02:32 AM #35Senior Member
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Texas-Girl... I haven't heard of someone NOT coming back on line ... but I have heard of long delays, and low testosterone levels . Anyway, the nuts are an organ, they atrophy, they hypertrophy ... if they're of size to handle the workload - they produce according to the HTPA stimulation to do so. Think about it - the whole NFL's been on this for 20+ years, conservatively - we'd know more about that issue by now... if it was a legitimate concern.
As far as the reports I posted above, they were from hooker. Check out this BRILLIAN process he used in finding the results!
I've been looking in medline all day for that information.
I happen to know that DNP was discovered as a weight loss agent when factory workers who were working where DNP was used to create certain shades of yellow began losing weight. Were they sterile? I'm looking into class action law suites for sterility filed at that time against paint companies by their workers, and there aren't any that I see.
We're lucky to have had Anthony's active contributions while we did... Above, are the REAL issues with DNP - not those people SPECULATE to have been likely, or could be, or heard of, or were afraid of, but the REAL side affects.
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10-31-2005, 10:49 AM #36
well texas, truman summed it up nice for me so there ya go lol.
Truman, the doses were not dose dependant, they ranged from 50mgs a day up to 600mgs (crazy women lol), so it seems to be more of a random thing, depending i would imagine on how sensitive their eyes were. As for males, it was extremely rare for them to develop cataracts, why i do not know, im lookin in to it now.
alo
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10-31-2005, 09:56 PM #37Originally Posted by TrumanHW
BTW If I need to know something I'll just ask you to do the research for me. You get some good info
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11-01-2005, 12:35 PM #38Senior Member
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No - not that NFL AAS usage is conservative ... but that conservatively speaking ... if there was a problem with restoring testical volume and capacity to perform, there'd be more literature about it. Those monsters have been on HIGH doses of stupid stacks since high school no doubt, and didn't have access to good stack suggestions until they reached pro status, or had money, or the last 3 years of the internet. That's just the way it's been ... and in spite that, there's STILL limited number of long term problems from it.
:-)
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11-01-2005, 09:01 PM #39Originally Posted by TrumanHW
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11-01-2005, 11:05 PM #40Senior Member
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You always have to wonder that. I mean, it will enhance an existing problem... and supposedly, over time, test users become subject to grandeur.
Is this a guy you're dating? What examples do you have of the problems you're experiencing, whats the time line of your dating, and how do you contrast them to his off-cycle disposition?
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