heatlessbbq
Bluelighter
I like that 3 month rule when it comes to MDMA breaks.
Ok @Negi hasn’t come back to refute anything yet. I’d just like to add one more thing that only makes my argument stronger.
While yes there is rough “species to species” dosage transition charts, they are rough at best. As is the case with MDMA, where dosages actually correlate pretty well rat to human.
In this study..
Effects of Dose and Route of Administration on Pharmacokinetics of (±)-3,4-Methylenedioxymethamphetamine in the Rat
Michael H. Baumann, Dorota Zolkowska, [...], and Marilyn A. Huestis
They talk about the MDMA cMax values for 2mg/kg in rats was similar to 1.5mg/kg in humans.
So with this in mind, we can now assume that many of these research studies are actually safer than you once assumed.. Wouldn’t you agree Negi?
-GC
Administration of 10 mg/kg MDMA in our study produced a robust 5-HT syndrome but no long-term 5-HT depletion, suggesting that this dose is not neurotoxic under the conditions used here.
Administration of 2 mg/kg MDMA by intraperitoneal and subcutaneous routes produced an MDMA Cmax of ∼200 ng/ml, a concentration close to the MDMA Cmax in humans who receive 1.3 to 1.7 mg/kg by the oral route under controlled conditions
MDMA t1/2 was ∼45 min for rats given 2 mg/kg, and this interval is much shorter than the t1/2 of 7 to 9 h observed in humans
Given the rapid MDMA clearance in rats, repeated intraperitoneal or subcutaneous injections of low-dose MDMA in this species might be an acceptable model for single oral doses in humans.
However, what is most apparent is that a dose of 2 mg/kg in humans produces a peak plasma concentration that is only achieved by giving approximately 7 mg/kg to rats.
given that a 100 mg MDMA dose (1.4 mg/kg) provokes a 0.6°C oral temperature rise in humans (Farré et al.2007) and a similar increase in rectal temperature is seen following an approximate fourfold higher dose (5 mg/kg IP) to rats (Colado et al.1995).
I tend to look at the information as a whole from many research article sources
Lol ya I tend to write novels...
In summary it’s not wise to redose more than once in a single night with MDMA (beyond a small booster not long after the first) both in terms of neurotoxicity and overall pleasurable effects.
Which is something people already know..
But then I also deconstruct the whole “3 month rule” and show why it’s more of rule based around averages per year. And in fact it may even be safer to consume closer together so long as you keep your antioxidant system “topped off.”
Based on research along with my own use.. If your use is kept to 4-8 times a year max, and you keep up on your antioxidants, there’s no worries.
-GC
Take anti oxidant vitamin supplements daily or eat alot of fruit and vegetables like tomatoes which are rich in anti oxidants. Keeps you looking younger and protects your body from free radical damageHow can one keep their antioxidants “topped off”??
PS - Newbie here
How can one keep their antioxidants “topped off”??
PS - Newbie here
I’ll finish with my own personal data. I’ve been rolling for 15yrs, and have found that there doesn’t seem to be any downsides to rolling b2b SO LONG AS I TAKE THE PROPER ANTIOXIDANTS!!!
[...]
Most can’t follow all the rules required to safely roll b2b.. Most can’t keep it to one reasonable dose the first night. Eating healthy the days before and after. Taking antioxidant supplements.
Sure, take them if you want. But when people in the thread are saying stuff like:
They are ascribing much more to the supplements than "eh, it's $2 and it will probably help".