Source: https://www.healthline.com/health/endocannabinoid-system
HN Feature™ #36,812,938: we get to take in the bigger picture, as comments are not collapsed algorithmically (IIUC)
<3
There is no aspirin system but salicylates bind to COX, so we may well have had a salicylate receptor if things went slightly differently.
> “ Non-steroidal anti-inflammatory drugs are COX-2 inhibitors that work, in part, by reducing the enzymatic degradation of the endocannabinoid anandamide ”
The human endocannabinoid system has vast and far-reaching implications regarding pain, inflammatory system and metobolic regulation.
> “ Studies at the National Institute on Drug Abuse in Bethesda, Maryland cloned the G-coupled protein receptor (GPCR) in 1990, which is the target for endogenous cannabinoid ligands, and named it, “Cannabinoid Receptor 1 (CB1 or CBR1). This receptor belongs to the Class A rhodopsin-like family of GPCRs [3]. A few years later, the second GPCR: “Cannabinoid Receptor 2” (CB2 or CBR2) was cloned [4]. The CB1 and the CB2 receptors participate in numerous essential biological processes [5]. Some of these are: Neuronal plasticity [6], pain [7], anxiety [8], inflammation [9], neuro-inflammation [10], immune function [11], metabolic regulation [12], and bone growth [13].”
Source: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770351/
To bring it to tech, it'd be like someone claiming that 'database system' was made up by Percona to market MySQL.
If they're knowledgeable on the topic then I'm sure having someone dismiss it as pseudoscience can be frustrating. I get that, but just saying someone's wrong isn't enough to change opinions. It doesn't need to be a research paper with citations, just a link to Wikipedia showing that it exists on a conceptual Level, or even a "I work in pharmaceuticals, it's legit". I'm at fault for not doing my own research as well, but thank you for settling things, looks like a lot of people learned something new
> other effects [...] are also being investigated
So, no.