Allylbenzene
Bluelighter
- Joined
- Jul 25, 2025
- Messages
- 1,130
In Britain we have online vendors with CBG isolate and high CBG hemp strains/extracts. From a quick search I see you have vendors selling lab tested 20% CBG strains.
CBG is the plants precursor for THC and CBD. It's pretty unique because it's main effect is to block adrenaline and increase natural opioids. It does this by activating a receptor called "alpha-2 adrenergic". It only slightly activates the cannabinoid-1 receptor iirc.I don't really know what CBG stands for specifically, but when it's present over 2.5% in my product then I'm pretty much gonna grab it regardless of the other numbers. CBG been doin' me RIGHT and it's a damn shame I don't know exactly what it is.
CBG is the plants precursor for THC and CBD. It's pretty unique because it's main effect is to block adrenaline and increase natural opioids. It does this by activating a receptor called "alpha-2 adrenergic". It only slightly activates the cannabinoid-1 receptor iirc.
Ah, look into an "overactive stress response". Theres some dietary factors that can contribute to this (eg phytoestrogens, polyunsaturated fats).It blocks adrenaline?!
That's it. That's how it calms me down.
I'm often barraged with fight-or-flight responses to things that just don't warrant it. I've never been diagnosed but a few doctors have noticed that I seem to have adrenaline dumps in their offices. It normally comes to light when they're trying to get a read on my blood pressure.
horncreekhemp.com
Cat s get high,by just smelling Catnip, a 15 minute Opioid/ Hallucinating high.Sure. Now that you have an idea what effects those terpenes have, it could help to choose suitable strains.
What I wrote about stimulating & relaxing terpenes was literal. Well...many terpenes have both stimulating & relaxing qualities but I was writing about the dominant effect.
Terpinolene strains would be a good fit for your needs. Along with citral it's the only terpene I know that interacts with 5-HT2A which is the receptor associated with psychedelics (LSD, magic mushrooms, DMT etc).
You could try terpene isolates sure, it's a good way to see what they're like. You could also use essential oils ("pre-mixed terpenes") that are described as having the effect you're after. In the sense that people know the effects of a strain, people know the effects of essential oils.
It sounds like you're looking for uplifting, mental calm + focus with subtle body relaxation effects. I'd go for a mix of lemon (uplifting, focus), lavander (calm, body relaxation), sandalwood ("zen"), optional: lemon myrtle (introspective)
Lemon oil for the limonene & smaller % of pinene. Lavander oil for the linalool. Sandalwood oil is a unique one you won't find any dispensary strains for. Lemon myrtle oil is mostly citral.
Diluted in some coconut/olive oil and applied to inner wrists/arms I found works well.
Keeping it simple, the best oil for somatic release is Sandalwood so combined with cannabis = excellent.
Cats, unlike humans have working vomeronasal organs (which respond to pheromones). Ours have lost their neural connections and are vestigial, so humans are unlikely to have as powerful of a response to a smell.Cat s get high,by just smelling Catnip, a 15 minute Opioid/ Hallucinating high.
Conforming it impossible as my cat does understand me better the i did her.
Wonder which Terpene, best guess, in catnip is responsible.
https://en.wikipedia.org/wiki/Nepetalactone , no Terpene a Nepalactone
Lavender oil, does have direct effect on human rest, through the nose.
https://flowerpursuits.com/why-does-lavender-relax-you/#google_vignette
That alpha-pinene paper uses doses of 20-100 mg/kg to see effects in mice. That has almost no relationship to the concentrations which humans are exposed to in cannabis or aromatherapy. Even scaling for metabolism, that still works out to basically drinking a shot of pure terpene to get the effects they got.I did talk about this, all 3 charts are technically right.
Overall linalool is sedating & mentally relaxing via it's actions at GABA + adenosine (which are both inhibitory aka calming) and reducing the effects of glutamate.
The pinenes (theres 2 different versions) have a combination of uplifting/stimulating effects (via D1 + 5-HT1A receptors, increased dopamine, increased acetylcholine, BDNF) and calming effects (via GABA, opioid).
I don't recommend trying this in such high doses but here's an example of what theraputic-grade lemon oil can do.
Lemon oil contains ~60% limonene, ~20% beta-pinene.
So it's all about the dose really. 5 drops of lemon oil might be calm + uplfting but 20+ drops things get more energising and euphoric.![]()
Nature's Herb Forum-Lemon Oil is Definitely Psychedelic!
So far I've done 3 high dose experiments with lemon essential oil, and I've experienced psychedelic effects all 3 times. 1st experiment (30 drops lemowww.tapatalk.com
In a sense, THC will tend to amplify the terpene effects in it's own unique way.
Also if something reduces cortisol (stress) then that will have an uplifting effect and greatly facilitate any healing practices.
Since you're looking to support somatic release and nervous system work, I'd prioritise anti-stress, good mood (uplifting), focus and calm. From experience i'd say Sandalwood does this quite well, but terpene wise - lemon (limonene, pinene), lavander (linalool) + cannabinoids works too. Or both cannabis + Sandalwood for synergy.
Regardless, from an actual practical perspective 1 drop pure alpha-pinene is sufficient. It works well stand-alone but is best combined with others like ocimene, phellandrene, valencene and limonene. Dermal absorption is far more efficient than ingestion but possibly comparable to vaping/smoking.That alpha-pinene paper uses doses of 20-100 mg/kg to see effects in mice. That has almost no relationship to the concentrations which humans are exposed to in cannabis or aromatherapy.
I think relying on those kinds of studies for navigating dosages and deducing potency will always blind the reader to anything practical.That alpha-pinene paper uses doses of 20-100 mg/kg to see effects in mice.