atara
Bluelighter
Dissociative is a strange category of drugs since we've chosen to lump together two otherwise disparate families of drugs: the NMDA receptor antagonists, and the kappa-opioid receptor agonists.
Until the advent of methoxetamine, it was relatively easy to ignore this, because there was really only one dissociative anyone cared to take: ketamine. Everyone had been scared away from the PCP site antagonists because of a strange mythology surrounding PCP, which seems to have been invented by a paramilitary organization known as "LAPD" in order to justify the murder of Rodney King, and picked up by similar organizations to justify other human rights abuses against colored people in America. Even practicing scientists had been drawn into this view of the category, and so salvia, with its ability to instantly steal the world from the mind, seemed to fit nicely. Other kappa-agonists followed suit.
But today people have grown to expect a certain constellation of effects from dissociatives: anaesthesia, anxiolysis, appetite-suppression, and so forth. More importantly, the mind-set of a dissociative user is often a don't-give-a-fuck feeling with regard to material reality, and this mind-set appears at lower doses than the hallucinations. In many of these categories is salvia quite distinct from the NMDA receptor antagonists, and if we include chewed salvia as opposed to only smoked salvia, the differences become even more pronounced.
Unfortunately I've never had the chance to try salvia, and as I've sort of left that part of my life behind me (thanks to grad school), there is a chance that I won't try it for a very long time. But trip reports of salvia really don't sound like any dissociative experience I've ever had. This line stuck out:
If anything, dissociatives seem to make things less meaningful. The sudden-onset-immersion pattern also isn't seen with dissociatives, but does appear with other kappa agonists, notably pentazocine.
I think that perhaps the kappa-agonists deserve their own categorization and particular analysis, as lumping them in with the PCP site antagonists isn't really clarifying anything. My humble suggestions would be oneirogens (dream-inducers), or makyoleptics (from Zen makyo, "illusion" + Greek -lepsis, "fit/spasm").
Until the advent of methoxetamine, it was relatively easy to ignore this, because there was really only one dissociative anyone cared to take: ketamine. Everyone had been scared away from the PCP site antagonists because of a strange mythology surrounding PCP, which seems to have been invented by a paramilitary organization known as "LAPD" in order to justify the murder of Rodney King, and picked up by similar organizations to justify other human rights abuses against colored people in America. Even practicing scientists had been drawn into this view of the category, and so salvia, with its ability to instantly steal the world from the mind, seemed to fit nicely. Other kappa-agonists followed suit.
But today people have grown to expect a certain constellation of effects from dissociatives: anaesthesia, anxiolysis, appetite-suppression, and so forth. More importantly, the mind-set of a dissociative user is often a don't-give-a-fuck feeling with regard to material reality, and this mind-set appears at lower doses than the hallucinations. In many of these categories is salvia quite distinct from the NMDA receptor antagonists, and if we include chewed salvia as opposed to only smoked salvia, the differences become even more pronounced.
Unfortunately I've never had the chance to try salvia, and as I've sort of left that part of my life behind me (thanks to grad school), there is a chance that I won't try it for a very long time. But trip reports of salvia really don't sound like any dissociative experience I've ever had. This line stuck out:
If anything, dissociatives seem to make things less meaningful. The sudden-onset-immersion pattern also isn't seen with dissociatives, but does appear with other kappa agonists, notably pentazocine.
I think that perhaps the kappa-agonists deserve their own categorization and particular analysis, as lumping them in with the PCP site antagonists isn't really clarifying anything. My humble suggestions would be oneirogens (dream-inducers), or makyoleptics (from Zen makyo, "illusion" + Greek -lepsis, "fit/spasm").