tuppingtoncity
Bluelighter
https://doi.org/10.1093/braincomms/fcag093
This paper is pretty interesting. Although purely hypothetical, I'm glad to see someone at least proposing a mechanism for what is in my opinion one of the most fascinating neuropharmacological mysteries to me in the realm of psychedelics.
The first hypothesis suggested by the paper tries to explain DiPT's tonal distortion mechanism as a result of tonotopic disruption. The second hypothesis suggests that there may be some sort of potassium channel disruption causing DiPT to alter the stiffness of cochlear membranes.
I don't know enough about the auditory system to know if these hypotheses are tenable, but the latter seems straightforward to test experimentally. Not entirely sure about the first, maybe some fMRI magic?
This paper is pretty interesting. Although purely hypothetical, I'm glad to see someone at least proposing a mechanism for what is in my opinion one of the most fascinating neuropharmacological mysteries to me in the realm of psychedelics.
The first hypothesis suggested by the paper tries to explain DiPT's tonal distortion mechanism as a result of tonotopic disruption. The second hypothesis suggests that there may be some sort of potassium channel disruption causing DiPT to alter the stiffness of cochlear membranes.
I don't know enough about the auditory system to know if these hypotheses are tenable, but the latter seems straightforward to test experimentally. Not entirely sure about the first, maybe some fMRI magic?

