weren't you looking for each sepertei have 7 vials of teen. i was going to run anyway. I was planning on 200 mg test c anyway. Is this good.
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weren't you looking for each sepertei have 7 vials of teen. i was going to run anyway. I was planning on 200 mg test c anyway. Is this good.
i have 7 vials of teen. i was going to run anyway. I was planning on 200 mg test c anyway. Is this good.
@ChestRockwell
I might have some complete blood profile panels still on file from when I ran tren only cycles. I'll check and see on Monday when I go back to my office. From memory, I know that my HDL and LDL were extremely affected, among other things.
I was running fina tren at the time. 100mg eod.
I checked and I don't have bloodwork in my files that go back that far. Wish I could've contributed.
some ramblings are logged on here during that period...probably "TEK TALKS" thread maybe. No bloods but I was pinning like 100-140mg fina ED for about 6 weeks and Brutus told me my brain was going to melt....@TANGO.ECHO.KILO ran tren only for a while, I believe he went through hell after a few weeks in. Not sure if he ran bloods?
Tren was the only thing that made my nuts shrink up to raisins.
You can transfer 10 amps at a time to a sealed sterile vial and then use whatever dose you want. Slin pins make accurate dosing easy if you're doing less than 1 ml per injection.
yea this is true.
Of course the reproducibility of such testing is dependent upon
KNOWING the product itself
is qualitatively and quantitatively consistent with what's on the label
Jim
the rubber on the syringes doesnt get mest up and wear into the oil?You can also just fill multiple syringes and have them ready. When I want to pin 0.6 ml and have amps. I just open 3 amps and put 0.6 in 5 syringes and put the cap back over the needles. The math works out. I put them in a ziplock to stay clean. Diabetics often fill a bunch of syringes at once since they pin 3 times a day.
the rubber on the syringes doesnt get mest up and wear into the oil?
I understand that you can't tell us much about it until after the article is ready and published.I would tend to speculate, in a trenbolone-only blast, this would very likely have to do with the significantly suppressed estradiol levels caused by the lack of aromatization present.
Animal models suggest one of the causes of testicular atrophy is related to damaged fluid reabsorption capabilities, which leads to fluid accumulation and testicular back-pressure. Estrogen is thought to be a major part of this fluid reabsorption process.
Hess RA. Estrogen in the adult male reproductive tract: a review. Reprod Biol Endocrinol. 2003 Jul 9;1:52. Review.
tren doesn't aromatize? and if it does it's converted to an estrogenic-shaped molecule that doesn't activate estrogen receptors?
2 Lack of estrogen makes Tren only cycles unbearable?
Just curious if it's Trenbolone itself activating Estrogen receptors, or if it's an Tren-estrogenic derivative from aromatization?Great questions @master.on
This is correct, as most animal trials support this hypothesis by demonstrating reduced estradiol levels as compared to control and/or testosterone treatment groups. Interestingly enough, trenbolone may actually have the ability to activate the estrogen receptor but this has not been continuously demonstrated.
This is certainly a possibility. The research teams working hard to promote it as a potential HRT tout the lack of aromatization and 5alpha reduction as being positive things, especially in regards to prostate cancer risk. However, by suppressing aromatase and 5 alpha reduction, there are a lot of potential long-term risks associated with this which would have to be uncovered during long-term human trials.
Just curious if it's Trenbolone itself activating Estrogen receptors, or if it's an Tren-estrogenic derivative from aromatization?
This looks similar to literature suggesting Boldenone DOES aromatize, but nobody seems to get nasty estrogenic sides from it.
So maybe them both (EQ and Tren) aromatize to very weak derivatives?
YepI haven't seen any evidence to suggest this, no. There was a group who speculated that trenbolone, via androstendione, (derived from dehydroepiandrosterone) can be aromatized to estrone and, subsequently, converted to E2 by actions of 17β-hydroxysteroid dehydrogenase in tissues, such as fat, expressing the required enzymes.
My personal stance currently is that this isn't a possibility because I've found no evidence that trenbolone can metabolize to androstendione.
As far as we know, trenbolone's primary metabolites are 17β-hydroxy- and 17-oxo-metabolites of trenbolone in rodents or 17α-hydroxy-metabolites of trenbolone in ruminants such as livestock. In humans, ingested trenbolone is primarily excreted intact as trenbolone, as the 17α epimer (epitrenbolone; 17α-TBOH) or as trendione (TBO).
Probably this is going to be the main scope of your article, so I understand you can't tell us much now
Why long, high dose, solo (no other steroids, no hcg) cycles of other steroids that don't seem to aromatize (like Primo, Mast) that sharply lower natural Test/Estradiol/LH/FSH don't feel as nasty as Tren does?
It would be interesting to see if HCG at high enough doses (1000 IU/week) which increases Test and E2 makes Tren-only sides (more) bearable.I don't mind sharing, as I can always elaborate further in the document.
I think this suggests that suppressing estrogen isn't the only mechanism at play here as it relates to trenbolone's ability to reduce quality of life. Now, as with most things in the hormone world, this will be quite individual in nature. For example, trenbolone tends to wreck me after a relatively short time during preps.
However, I've routinely thrived using it during growth phases on multiple occasions. Here is a hypothesis I've been really thinking more about lately. Could the effects being reported by trenbolone user's be secondary? Meaning that trenbolone tends to wreak havoc with sleep cycles and perhaps even circadian processes in general (I'm speculating out of my ass here mind you).
Could our quality of life suffer due to the lack of sleep over time, combined with sustained periods of energy intake deficit? In this way, those would be the primary drivers with trenbolone being the catalyst...
It would be interesting to see if HCG at high enough doses (1000 IU/week) which increases Test and E2 makes Tren-only sides (more) bearable.
