THC-A : Medical Benefits of THC Without the High

About THC-A:

THC-A occurs when cannabigerol (CBG) is converted to THC-A , before being decarboxylated to THC in the trichome of the Cannabisflower. THC-A is non-psychoactive, acidic precursor of THC  which alleviates: anxiety, depression, anorexia, pain, IBS/Crohn’s, spasticity, seizure (neuromuscular), nausea and much more without the psychoactivity of THC. Studies have even shown tumor suppression of some cancers with THC-A administration. In fact, recent studies have shown that THC-A is far superior to CBD and THC for nausea and the cessation of vomiting. Although, THC and THC-A with CBD are always recommended for any serious cancer cannabinoid therapy, some cancers may be responsive to concentrated THC-A medicines as well.

Scientific studies show..

THC-A does not have any known psychoactive effects on humans in its own right.It has anti inflammatory, neuroprotective, antiemetic (anti-vomiting) and anti-prostate cancer effects. It inhibits COX  enzymes that are involved in inflammation in human colon cell cultures. THC-A has also been shown to decreases oxidative stress, caused by impaired mitochondria which is a major mechanism in neural degeneration in mouse brain cell cultures. At our collective we have tested our products vigorously and have seen a lot of promise for THC-A. In prostate and lymphatic cancer patients, we have seen real progress with THC-A enriched therapies. We believe this is through complicated interactions with, not only cannabinoid receptors (such as CB1, CB2, GPR55, etc.) but the TRP family of calcium channels, due to the targeted effects we see and the types of clinical ailments we are able to alleviate.

 

The Experience

Taking THC-A makes you feel energized, motivated and calm at the same time, while relieving pain, anxiety and increasing appetite. THC-A is a great molecule for nausea as stated and pain, especially chronic pain. You really feel like a new person, thus many people take it int he morning. Personally, I take it in the morning for insomnia, because it helps me sleep much later in the evening and is very subtle and soothing- rather than taking a sleeping pill at night. Instead, I have energy, zest and focus all day long and just as easily calm by the night time and get into slumber. That is the other great thing – focus! THC-A is terrific for people with ADH/D because it help to focus the mind on the tasks at hand. THC-A has been a miracle for so many patients including myself, it’s truly amazing. If you are one of those people who does not like the high of THC , THC-A actually mitigates that anxiety, in case you needed high THC therapy, and were unable to tolerate the “high”, THC-A can alleviate that issue. Side note: I have also received word from some more adventurous souls, that THC-A (at least our Purified Trichome Extract (THC-A) is really good at relaxing people , physically when having a “bad trip” when using psychedelic substances.

Legality in the United States653px-Tetrahydrocannabinolicacid.svg

THC-A is not scheduled by the United Nations’ Convention on Psychotropic Substances. THC-A is not scheduled at the federal level in the United States and is therefore legal to possess, buy, and sell. It is possible that THC-A could legally be considered an analog (of THC) although that is somewhat unlikely since it does not provide a high and THC does. If it were legally considered an analog, sales or possession with intent for human consumption could be prosecuted under the Federal Analogue Act. We actually inquired with FDA officials about the proposed legality of our product and were surprised and relieved that THC-A seems to outright be OK nationally, so long as it doesn’t get anyone “high”.

However the current drug schedule addresses “cannabinoids” as a whole (without specifying exogenous or endogenous, technically that would include the anandamide in our own bodies, and in chocolate, which is strange and illogical). There is currently a application for patent #US20080103193, for a very thoughtful THC-A extraction and enrichment protocol (//www.google.com/patents/US20080103193 I believed applied for by the Aphios conglomerate- which is sponsored by Gillette and other big pharmaceutical and big corporate money, btw). It is unfortunate that this is the awkward vocabulary with which we act in this nation. So the next time you are consuming THC-A you can thank the heavens that nowhere in the United States is it banned.

This really was an interesting investigation of the laws and what they mean and how they ae interpreted by different aspects of government. I guess the thing is if it is edible an not for decarboxylating (i.e., not for smoking) and meant to be consumed as THC-A maybe there is another road block lifted? There are still limits on the amount of THC in the product (must be less than 1% or less by weight), and with the relative instability of THC-A it is important to stabilize the isomer in the product formulation. For now, we remain chained to the issue of feeling “high”, but THC-A offers a moderate solution for many. THC-A may be another stepping stone towards complete freedom for a plant that man, himself has domesticated.

 

The Medical Marijuana Desk Reference is a comprehensive and up-to-date guide on the scientific research of Cannabis species for medical treatment. The Medical Marijuana Desk Reference is a comprehensive and up-to-date guide on the scientific research of Cannabis species for medical treatment. The Medical Marijuana Desk Reference is a comprehensive and up-to-date guide on the scientific research of Cannabis species for medical treatment.

 

Resources and References

    • Baker PB, Taylor BJ, Gough TA. (Jun 1981), “The tetrahydrocannabinol and tetrahydrocannabinolic
    • acid content of cannabis products”, Journal of Pharmacy and Pharmacology 33 (6): 369–72, doi:10.1111/j.2042-7158.1981.tb13806.x, PMID 6115009
    • Sirikantaramas S, Morimoto S, Shoyama Y, Ishikawa Y, Wada Y, Shoyama Y, Taura F. (2004-09-17), “The gene controlling marijuana psychoactivity: molecular cloning and heterologous expression of Delta1-tetrahydrocannabinolic acid synthase from Cannabis sativa L.”, Journal of Biological Chemistry 279 (38): 39767–74, doi:10.1074/jbc.M403693200, PMID 15190053
    • Moore C, Rana S, Coulter C. (2007-06-01), “Simultaneous identification of 2-carboxy-tetrahydrocannabinol, tetrahydrocannabinol, cannabinol and cannabidiol in oral fluid”, J Chromatogr B Analyt Technol Biomed Life Sci. 852 (1-2): 459–64, doi:10.1016/j.jchromb.2007.02.016, PMID 17321807
    • Taura F. (Jun 2009), “Studies on tetrahydrocannabinolic acid synthase that produces the acidic precursor of tetrahydrocannabinol, the pharmacologically active cannabinoid in marijuana”, Drug Discoveries and Therapeutics 3 (3): 83–7, PMID 22495534
    • Dussy FE, Hamberg C, Luginbühl M, Schwerzmann T, Briellmann TA. (2005-04-20), “Isolation of Delta9-THCA-A from hemp and analytical aspects concerning the determination of Delta9-THC in cannabis products”, Forensic Science International 149 (1): 3–10, doi:10.1016/j.forsciint.2004.05.015, PMID 15734104
    • Starks, Michael (1990). Marijuana Chemistry: Genetics, Processing, Potency. Ronin Publishing. ISBN 978-0-9141-7139-3.
    • Ruhaak LR, Felth J, Karlsson PC, Rafter JJ, Verpoorte R, Bohlin L. (2011), “Evaluation of the cyclooxygenase inhibiting effects of six major cannabinoids isolated from Cannabis sativa”,
    • Biological and Pharmaceutical Bulletin 34 (5): 774–8, doi:10.1248/bpb.34.774, PMID 21532172
    • Moldzio R, Pacher T, Krewenka C, Kranner B, Novak J, Duvigneau JC, Rausch WD. (2012-05-07), “Effects of cannabinoids Δ(9)-tetrahydrocannabinol, Δ(9)-tetrahydrocannabinolic acid and cannabidiol in MPP(+) affected murine mesencephalic cultures”, Phytomedicine 19 (8-9): 819–24, doi:10.1016/j.phymed.2012.04.002, PMID 22571976
    •  De Petrocellis L, Ligresti A., Moriello A.S., Iappelli M., Verde R., Stott C.G., Cristino L., Orlando P., and Di Marzo V. (2013-01-01), “Non-THC cannabinoids inhibit prostate carcinoma growth in vitro and in vivo: pro-apoptotic effects and underlying mechanisms”, British Journal of Pharmacology 168 (1): 79–102, doi:10.1111/j.1476-5381.2012.02027.x, PMC 3570006
    • Jung J, Meyer MR, Maurer HH, Neusüss C, Weinmann W, Auwärter V. (Oct 2009), “Studies on the metabolism of the Delta-9-tetrahydrocannabinol precursor delta-9-tetrahydrocannabinolic acid A (Delta9-THCA-A) in rat using LC-MS/MS, LC-QTOF MS and GC-MS techniques”, Journal of Mass Spectrometry 44 (10): 1423–33, doi:10.1002/jms.1624, PMID 19728318
    • Hazekamp A, Bastola K, Rashidi H, Bender J, Verpoorte R. (2007-07-15), “Cannabis tea revisited: a systematic evaluation of the cannabinoid composition of cannabis tea”, Journal of Ethnopharmacology 113 (1): 85–90, doi:10.1016/j.jep.2007.05.019, PMID 17604926
    • Radünz L, Westphal F, Maser E, Rochholz G. (2012-02-10), “THCVA-A – a new additional marker for illegal cannabis consumption”, Forensic Science International 215 (1-3): 171–4, doi:10.1016/j.forsciint.2011.03.001, PMID 21454026
    •  §1308.11 Schedule I.

by Kurt Duchac on May 5, 2015 in Medical Marijuana

Article originally published at ThePotLab.com

Source : //cannaiq.com/thc-a-medical-benefits-of-thc-without-the-high/

 

Auteur: netprauxprin

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