i think im going to be trying this product out in the next couple days
what im going to do is run it with inhibit-E and i think i will start out doing 12 on 12 off and then depending on how i feel from that i will either do another 12 on 12 off or i will go for longer than 12 days
regardless i will be doing inhibit E for 8 weeks
what do you guys think?
anyone have feedback on their results using DAA?
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Thread: pure DAA
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08-17-2010, 03:06 PM #1
pure DAA
i rep back
Lefticle my b1tch
Tonic Log
http://forum.bodybuilding.com/showthread.php?t=132307753
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08-17-2010, 03:10 PM #2
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08-17-2010, 03:15 PM #3
do you think its best to use it for 6 weeks at 3 grams a day?
and do you think that using inhibit E during cycle is best or lets say i do it for 6 weeks do you think it would be wise to start the inhibit e week 2 of the DAA so it extends 4 weeks after the use of the DAA to supress any possible estrogeni rep back
Lefticle my b1tch
Tonic Log
http://forum.bodybuilding.com/showthread.php?t=132307753
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08-17-2010, 03:22 PM #4
I believe 6 weeks is the minimum cycle lenght for any test-booster if you want to see some actual improvement in strenght and body composition. I also believe 3 grams is the minimum dosage to get a decent test increase.
Last, you need estrogens alongside testosterone to increase anabolism. Focus on the T/E ratio,not total E. I wouldn't use any AI.Olympus Labs/Lyfestyle Research & Development (R&D) Director
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08-17-2010, 03:22 PM #5
I'd use the DAA much much longer. People get off of test boosters too quick. IF you can find one that does actually boost your testosterone you are going to need to stay on it for quite a while to really get the benefits form it.
For simplicity sake lets say your test goes from 550 to 750 free test going from 1.8% to 2.4%...you need LOTS OF TIME at that 750/2.4 amount to really get the benefits.
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08-17-2010, 03:28 PM #6
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08-17-2010, 03:34 PM #7
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08-17-2010, 03:34 PM #8
i actually have been taking it for about 6 weeks but also taking 1-2iu's hgh and hghup and fodalgia. will be posting reviews and blood work soon.
of course it throws off my review directly on daa because I am taking other things. I don't "feel" a difference since starting daa but curious to see what the bloodwork says.
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08-17-2010, 03:36 PM #9
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08-17-2010, 03:39 PM #10
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08-17-2010, 03:40 PM #11
THEHUGE is this enough for L-dopa?
http://www.bodybuilding.com/store/now/dopamuc.html
250mg a day, that would be 4 caps correct?
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08-17-2010, 03:40 PM #12
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08-17-2010, 03:43 PM #13
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08-17-2010, 03:48 PM #14
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08-17-2010, 03:50 PM #15
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08-17-2010, 03:55 PM #16
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08-17-2010, 04:00 PM #17
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08-17-2010, 04:07 PM #18
Isn't agmatine a NMDA antagonist? Ingesting a couple grams a day of DAA is not exactly like injecting a massive amount of NMDA directly into your brain. Once again, DAA has been widely used for years here in EU and no neurotoxicity reported(and none should be expected). 90 days is the standard administration lenght(a full spermiogenic cycle).
BTW,mucuna pruriens has neuroprotective properties.Olympus Labs/Lyfestyle Research & Development (R&D) Director
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08-17-2010, 04:08 PM #19
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08-18-2010, 04:21 AM #20
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08-18-2010, 05:31 AM #21
- Join Date: Apr 2009
- Location: Perth, WA, Australia
- Age: 36
- Posts: 131
- Rep Power: 206
Thanks for the information the Huge.. i am a week into my DAA cycle and was dreading stopping after 2 weeks.. will def be on it for 4-6 weeks now..
already noticed slight increase in aggression.. takes almost nothing to set me off and bit better endurance in gym. no libido increase at all yet.. but i work so damn hard at work then gym then squash and baseball etc.. can too much physical activity kill libido?
also HUGE.. l-dopa a must with this stack.. how much difference would it be if i get some and add it in?
thanks heaps mate
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08-18-2010, 05:34 AM #22
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08-18-2010, 08:09 AM #23
Good info Huge- I have some DAA coming, I'm interested to see if it works as well as ProMax- my final review = pretty blown away by it, definitely the best test booster I've ever used and it lasted for about 2 weeks after I stopped taking pills. I was shedding pretty heavily, I'll be using spiro in the future to hopefully combat that issue. Disclaimer for anyone else reading- I am super prone to hair loss and any kind of test increase will make me drop hair.
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08-18-2010, 11:06 AM #24
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08-18-2010, 12:51 PM #25
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09-14-2010, 01:47 PM #26
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09-14-2010, 02:02 PM #27
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09-14-2010, 02:16 PM #28
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09-14-2010, 02:31 PM #29
It is not mistaken reasoning. It's evidence based reasoning. We kinda know what happens up to 12 days, not what happens after that. Some people probably did bloods while being longer on DAA and I think it is very unlikely that the results would diminish rapidly after 12 days, but we don't have clinical proof for it. Based on that, people have to choose for themselves if they're gonna do 12 day cycles or longer. But neither choice is either wrong or right.
I'm still worried about possible endotoxicity. Also, I'm curious to see the long term effects of DAA on various hormones. Has anyone done bloodwork on 4+ weeks that includes LH?
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09-14-2010, 09:04 PM #30
Seems like the THEHUGE is right on this one, however I do not know if there is more complexity to NMDA and it's manipulation since this is above my education level.
Neurosci Res. 2005 Aug;52(4):387-92.
Effect of agmatine on heteromeric N-methyl-D-aspartate receptor channels.
Askalany AR, Yamakura T, Petrenko AB, Kohno T, Sakimura K, Baba H.
Division of Anesthesiology, Niigata University Graduate School of Medical and Dental Sciences, Niigata 951-8510, Japan.
Abstract
Endogenous polyamines like spermine are known to have four distinct effects on recombinant N-methyl-d-aspartate (NMDA) receptor channels: voltage-dependent inhibition, glycine-dependent stimulation, glycine-independent stimulation and decreased affinity to the agonist (l-glutamate). These effects are highly dependent on the constituting epsilon subunits (epsilon1-epsilon4) of the recombinant NMDA receptor channels. Agmatine reportedly inhibits native NMDA receptor channels in cultured hippocampal neurons. In the present investigation, the effects of agmatine on the epsilon/zeta heteromeric NMDA receptor channels expressed in Xenopus laevis oocytes were examined using the two-electrode voltage clamp method. Agmatine inhibited the four epsilon/zeta (epsilon1/zeta1, epsilon2/zeta1, epsilon3/zeta1 and epsilon4/zeta1) channels with similar sensitivity (an IC50 value of about 300microM at -70mV). This effect was dependent on the membrane potential and was more pronounced at hyperpolarized membrane potentials (voltage-dependent inhibition). Agmatine did not exhibit other stimulatory (glycine-dependent and -independent effects) or inhibitory (decreased affinity to l-glutamate) effects. These properties are similar to the pharmacological profile of well-characterized NMDA receptor channel blockers like phencyclidine and ********. Thus, regarding the effects on the NMDA receptor channels, agmatine is not like other endogenous polyamines rather it acts as a channel blocker.
PMID: 15982768 [PubMed - indexed for MEDLINE]
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