They didn't separate isomers cause they wanted to make it as multimodal as possible and since both isomers are psychoactive they decided that racemic tramadol is the best one for pain - providing both serotonine reuptake inhibition, noradrenaline reuptake inhibition, serotonine release, mu-opioid binding and even its potent opioid metabolite still function as a noradrenaline reuptake inhibitor.No need to apologize, thank you for your candor.
The beginning of your story sounds very familiar. I've always experienced life as unsatisfactory, a problem to be solved. Most of my past behavior can be characterized as resistance to the current reality and hoping for relief in the future.
A while ago, I ate a piece of hash which turned out to be more potent than I had anticipated. I was overwhelmed by fear, yet something in me decided to let go completely. I was ready and willing to die on the spot if necessary. That moment, the fear dissolved completely and I had an amazing trip. Interestingly, I lived the next couple of weeks in some kind of pseudo-enlightened state where everything seemed to just flow naturally.
Sadly, my normal state of consciousness returned after a while. Yet, after 20 years of stagnation I've started turning my life around, trying to use all the tools at my disposal. I'm awfully grateful to tramadol for providing relief and showing me what is possible, yet I recognize that looking the beast in the eye when it rears its ugly head is an equally important duty as the flip side of the coin.
So, I gather that any level of consistent, long-term use of tramadol will escalate towards addiction. I was going to ask whether incorporating month-long breaks would be a way to prevent this, but I guess the crux of the matter is that an external enforcement mechanism is necessary to prevent abuse.
Sounds like you're on to something. I found the following in A call to develop tramadol enantiomer for overcoming the tramadol crisis by reducing addiction:
It is very monoaminergic in both reuptake inbibition, serotonine release and indirect dopamine release due to opioid mechanism and combination of every single one of these mechanisms provides the best analgesic effects for acute, chronic and due to monoaminergic properties for neuropathic pain.
Also, it has quite long half-life which is getting even higher when u take multiple doses theough the day.
Compared to codeine it is whole different beast and for me, very good cyp2d6 metaboliser 100mg of tramadol is actually considerably more potent and longer lasting than 10mg of morphine sulphate ( both tram and morphine oral consumption ) .
