Rezolution is comming!!
- 11-29-2010, 12:20 PM
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11-29-2010, 12:46 PM
11-29-2010, 12:47 PM
11-29-2010, 12:48 PM
11-29-2010, 12:49 PM
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11-29-2010, 12:54 PM
11-29-2010, 01:34 PM
You know I will be watching LG
TEAM GET DIESEL
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11-29-2010, 01:41 PM
Very cool, I have high hopes after how well Lipo Burn works. This would fit right into my recomp and I am more than willing to log this .
Edit - Did I just see that this is tablets? What ever happened to a topical 7-keto?
11-29-2010, 01:43 PM
11-29-2010, 01:49 PM
To clarify, Rez is the transdermal 'rub on' that's being discussed out in the supp section, yes, no...maybe so? I printed the pic off and proceeded to rub it on my 'squishy parts'...I sure hope the final product works better than this...although on second thought, I used a black/white lazer printer...perhaps color ink jet would have been the way to go....brb, testing my hypothesis....
11-29-2010, 01:49 PM
11-29-2010, 02:06 PM
11-29-2010, 02:19 PM
11-29-2010, 02:31 PM
11-29-2010, 02:49 PM
11-29-2010, 03:21 PM
11-29-2010, 03:22 PM
Hmmm... stackable with SpeedV2 or no? I may be running that and helping the cause is always a good plan if you ask me.
11-29-2010, 03:27 PM
11-29-2010, 03:29 PM
It's a happy pill that burns fat and gets you amped unlike anything you've ever experienced!
What Rezolution does?
Combines the most potent stimulants (specialized synephrine, geranamine, caffeine) with dopamine precursors (N-Actyl Tyrosine and L-Dopa) plus two herbs that block both Dopamine and Norepinephrine re-uptake (meaning makes dopamine active longer). Add in 5-HTP for increased serotonin and you get a natural high and a stimulant effect that lasts for hours. Sweet spot is 3 capsules (for experienced users)
The two ingredients that make dopamine active longer are:
Dopamine transporter inhibitory and antiparkinsonian effect of common flowering quince extract.
Zhao G, Jiang ZH, Zheng XW, Zang SY, Guo LH.
Common flowering quince (FQ) is the fruit of Chaenomeles speciosa (Sweet) Nakai. FQ-containing ****tails have been applied to the treatment of neuralgia, migraine, and depression in traditional Chinese medicine. The present study assessed whether FQ is effective in dopamine transporter (DAT) regulation and antiparkinsonism by utilizing in vitro and in vivo assays, respectively. FQ at concentrations of 1-1000 microg/ml concentration-dependently inhibited dopamine uptake by Chinese hamster ovary (CHO) cells stably expressing DAT (D8 cells) and by synaptosomes. FQ had a slight inhibitory action on norepinephrine uptake by CHO cells expressing the norepinephrine transporter and no inhibitory effect on gamma-aminobutyric acid (GABA) uptake by CHO cells expressing GABA transporter-1 or serotonin uptake by the serotonin transporter. A viability assay showed that FQ mitigated 1-methyl-4-phenylpyridinium-induced toxicity in D8 cells. Furthermore, in behavioral studies, FQ alleviated rotational behavior in 6-hydroxydopamine-treated rats and improved deficits in endurance performance in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-treated mice. Furthermore, immunohistochemistry revealed that FQ markedly reduced the loss of tyrosine hydroxylase-positive neurons in the substantia nigra in MPTP-treated mice. In summary, FQ is a selective, potent DAT inhibitor and has antiparkinsonian-like effects that are mediated possibly by DAT suppression. FQ has the potential to be further developed for Parkinson's disease treatment.
Inhibitive effects of Fructus Psoraleae extract on dopamine transporter and noradrenaline transporter.
Zhao G, Li S, Qin GW, Fei J, Guo LH.
A petroleum ether extract (FP) from Fructus Psoraleae, seeds of Psoralea corylifolia L. (Leguminosae), was found to strongly inhibit dopamine (DA) uptake by dopamine transporter (DAT) heterogeneously expressed cells (D8 cells) and noradrenaline (NE) uptake by noradrenaline transporter (NET) heterogeneously expressed cells, which, however, had no effect on gamma-aminobutyric acid transporter heterogeneously expressed cells and serotonin transporter heterogeneously expressed cells at the concentration up to 100 microg/ml. These inhibitory effects were also confirmed by experiments on SK-N-SH cell line and synaptosomes from rats' brains. In addition, FP showed a significantly mitigating effect on 1-methyl-4-pyridinium induced injury of D8 cells. Meanwhile, FP dose-dependently reduced the binding of tritium-labeled cocaine analog (-)-2beta-carbomethoxy-3beta-(4-fluorophenyl) tropane to DAT of D8 cells, which suggests that FP may inhibit DAT activity in the same way as cocaine does. Behavioral study showed FP had a long-lasting stimulant effects on the activity of intact mice and reserpinized mice. So FP is proposed as a kind of DAT and NET inhibitor and may be involved in the process of regulating the DA and NE system, and FP or its unknown bioactive compounds may be developed into new medicines for disorders such as Parkinson's disease, depression, Attention Deficit Hyperactivity Disorder (ADHD) or cocaine addiction.
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