Cannabidiol

DB09061

small molecule approved investigational

Deskripsi

Cannabidiol, or CBD, is one of at least 85 active cannabinoids identified within the Cannabis plant. It is a major phytocannabinoid, accounting for up to 40% of the Cannabis plant's extract, that binds to a wide variety of physiological targets of the endocannabinoid system within the body. Although the exact medical implications are currently being investigated, CBD has shown promise as a therapeutic and pharmaceutical drug target. In particular, CBD has shown promise as an analgesic, anticonvulsant, muscle relaxant, anxiolytic, antipsychotic and has shown neuroprotective, anti-inflammatory, and antioxidant activity, among other currently investigated uses A32477, A32469. CBD's exact place within medical practice is still currently hotly debated, however as the body of evidence grows and legislation changes to reflect its wide-spread use, public and medical opinion have changed significantly with regards to its usefulness in a number of medical conditions ranging from anxiety to epilepsy.

From a pharmacological perspective, Cannabis' (and CBD's) diverse receptor profile explains its potential application for such a wide variety of medical conditions. Cannabis contains more than 400 different chemical compounds, of which 61 are considered cannabinoids, a class of compounds that act upon endogenous cannabinoid receptors of the body A32584. Cannabinoid receptors are utilized endogenously by the body through the endocannabinoid system, which includes a group of lipid proteins, enzymes, and receptors that are involved in many physiological processes. Through its modulation of neurotransmitter release, the endocannabinoid system regulates cognition, pain sensation, appetite, memory, sleep, immune function, and mood among many other bodily systems. These effects are largely mediated through two members of the G-protein coupled receptor family, cannabinoid receptors 1 and 2 (CB1 and CB2)A32585,A32824. CB1 receptors are found in both the central and peripheral nervous systems, with the majority of receptors localized to the hippocampus and amygdala of the brain. Physiological effects of using cannabis make sense in the context of its receptor activity as the hippocampus and amygdala are primarily involved with regulation of memory, fear, and emotion. In contrast, CB2 receptors are mainly found peripherally in immune cells, lymphoid tissue, and peripheral nerve terminals A32676.

Tetrahydrocannabinol (THC) and cannabidiol (CBD) are two types of cannabinoids found naturally in the resin of the marijuana plant, both of which interact with the cannabinoid receptors that are found throughout the body. Although THC and CBD have been the most studied cannabinoids, there are many others identified to date including cannabinol (CBN), cannabigerol (CBG), DB14050 (CBDV), and DB11755 (THCV) that can be found within the medical cannabis A32830. While both CBD and THC are used for medicinal purposes, they have different receptor activity, function, and physiological effects. If not provided in their activated form (such as through synthetic forms of THC like DB00470 or DB00486), THC and CBD are obtained through conversion from their precursors, tetrahydrocannabinolic acid-A (THCA-A) and cannabidiolic acid (CBDA), through decarboxylation reactions. This can be achieved through heating, smoking, vaporization, or baking of dried unfertilized female cannabis flowers.

The primary psychoactive component of Cannabis, delta 9-tetrahydrocannabinol (?9-THC), demonstrates its effects through weak partial agonist activity at Cannabinoid-1 (CB1R) and Cannabinoid-2 (CB2R) receptors. This activity results in the well-known effects of smoking cannabis such as increased appetite, reduced pain, and changes in emotional and cognitive processes. In contrast to THC's weak agonist activity, CBD has been shown to act as a negative allosteric modulator of the cannabinoid CB1 receptor, the most abundant G-Protein Coupled Receptor (GPCR) in the body A32469. Allosteric regulation is achieved through the modulation of receptor activity on a functionally distinct site from the agonist or antagonist binding site which is clinically significant as direct agonists (such as THC) are limited by their psychomimetic effects such as changes to mood, memory, and anxietyA32469.

In addition to the well-known activity on CB1 and CB2 receptors, there is further evidence that CBD also activates 5-HT1A/2A/3A serotonergic and TRPV1–2 vanilloid receptors, antagonizes alpha-1 adrenergic and µ-opioid receptors, inhibits synaptosomal uptake of noradrenaline, dopamine, serotonin and gamma-aminobutyric acid (GABA), and cellular uptake of anandamide, acts on mitochondria Ca2+ stores, blocks low-voltage-activated (T-type) Ca2+ channels, stimulates activity of the inhibitory glycine-receptor, and inhibits activity of fatty amide hydrolase (FAAH) A31555, A31574.

CBD is currently available in Canada within a 1:1 formulation with tetrahydrocannbinol (THC) (as the formulation known as "nabiximols") as the brand name product Sativex. It is approved for use as adjunctive treatment for symptomatic relief of spasticity in adult patients with multiple sclerosis (MS). Sativex was also given a conditional Notice of Compliance (NOC/c) for use as adjunctive treatment for the symptomatic relief of neuropathic pain in adult patients with multiple sclerosis and as adjunctive analgesic treatment for moderate to severe pain in adult patients with advanced cancer L886.

In April 2018, a Food and Drug Administration advisory panel unanimously recommended approval of Epidiolex (cannabidiol oral solution) for the treatment of two rare forms of epilepsy - Lennox-Gastaut syndrome and Dravet syndrome, which are among the two most difficult types of epilepsy to treat L2721, L2719. Epidiolex was granted Orphan Drug designation as well as Fast Track Approval from the FDA for further study in these hard to treat conditions. Notably, phase 3 clinical trials of Epidiolex have demonstrated clinically significant improvement in Lennox-Gastaut syndrome and Dravet syndrome L2720. On June 25th, 2018, Epidiolex was approved by the FDA to be the first CBD-based product available on the US market.

Struktur Molekul 2D

Berat 314.469
Wujud solid

Peta Jejaring Molekuler
Legenda: ObatTargetGenEnzim(Panah → menunjukkan arah efek / relasi)TransporterCarrier

Profil Farmakokinetik

Waktu Paruh (Half-Life) The CBD component of sublingual Sativex was found to have a half life (t1/2) of 1.44hr, while buccal Sativex was found to have a half life (t1/2) of 1.81hr.
Volume Distribusi Cannabinoids are distributed throughout the body; they are highly lipid soluble and accumulate in fatty tissue. The release of cannabinoids from fatty tissue is responsible for the prolonged terminal elimination half-life.
Klirens (Clearance) -

Absorpsi

Following a single buccal administration, maximum plasma concentrations of both CBD and THC typically occur within two to four hours. When administered buccally, blood levels of THC and other cannabinoids are lower compared with inhalation of smoked cannabis. The resultant concentrations in the blood are lower than those obtained by inhaling the same dose because absorption is slower, redistribution into fatty tissues is rapid and additionally some of the THC undergoes hepatic first pass metabolism to 11-OH-THC, a psycho-active metabolite. The CBD component of sublingual Sativex was found to have a Tmax of 1.63hr and a Cmax of 2.50ng/mL, while buccal Sativex was found to have a Tmax of 2.80hr and a Cmax of 3.02ng/mL.

Metabolisme

THC and CBD are metabolized in the liver by a number of cytochrome P450 isoenzymes, including CYP2C9, CYP2C19, CYP2D6 and CYP3A4. They may be stored for as long as four weeks in the fatty tissues from which they are slowly released at sub-therapeutic levels back into the blood stream and metabolized via the renal and biliary systems. The main primary metabolite of CBD is 7-hydroxy-cannabidiol.

Rute Eliminasi

Elimination from plasma is bi-exponential with an initial half-life of one to two hours. The terminal elimination half-lives are of the order of 24 to 36 hours or longer. Sativex is excreted in the urine and faeces.

Interaksi Makanan

4 Data
  • 1. Avoid excessive or chronic alcohol consumption. Ingesting alcohol may increase the risk of sedation.
  • 2. Avoid grapefruit products. Grapefruit inhibits the CYP3A metabolism of cannabidiol, which may increase its serum concentration. Cannabidiol dose reduction may be necessary if used together.
  • 3. Avoid St. John's Wort. This herb induces the CYP3A metabolism of cannabidiol and may reduce its serum concentration. The dose of cannabidiol may need to be increased if used together.
  • 4. Take with food. Taking cannabidiol with food (particularly high-fat food) increases its bioavailability. The absorption of cannabidiol is more consistent when meal macronutrients remain the same.

Interaksi Obat

1804 Data
Cilostazol The serum concentration of Cilostazol can be increased when it is combined with Cannabidiol.
Ramipril Cannabidiol may decrease the antihypertensive activities of Ramipril.
Remikiren Cannabidiol may decrease the antihypertensive activities of Remikiren.
Guanadrel Cannabidiol may decrease the antihypertensive activities of Guanadrel.
Olmesartan Cannabidiol may decrease the antihypertensive activities of Olmesartan.
Chlorthalidone Cannabidiol may decrease the antihypertensive activities of Chlorthalidone.
Nitroprusside Cannabidiol may decrease the antihypertensive activities of Nitroprusside.
Minoxidil Cannabidiol may decrease the antihypertensive activities of Minoxidil.
Bendroflumethiazide Cannabidiol may decrease the antihypertensive activities of Bendroflumethiazide.
Fosinopril Cannabidiol may decrease the antihypertensive activities of Fosinopril.
Trandolapril Cannabidiol may decrease the antihypertensive activities of Trandolapril.
Metolazone Cannabidiol may decrease the antihypertensive activities of Metolazone.
Benazepril Cannabidiol may decrease the antihypertensive activities of Benazepril.
Cyclothiazide Cannabidiol may decrease the antihypertensive activities of Cyclothiazide.
Candoxatril Cannabidiol may decrease the antihypertensive activities of Candoxatril.
Mecamylamine Cannabidiol may decrease the antihypertensive activities of Mecamylamine.
Moexipril Cannabidiol may decrease the antihypertensive activities of Moexipril.
Lisinopril Cannabidiol may decrease the antihypertensive activities of Lisinopril.
Nitroglycerin Cannabidiol may decrease the antihypertensive activities of Nitroglycerin.
Hydroflumethiazide Cannabidiol may decrease the antihypertensive activities of Hydroflumethiazide.
Cryptenamine Cannabidiol may decrease the antihypertensive activities of Cryptenamine.
Perindopril Cannabidiol may decrease the antihypertensive activities of Perindopril.
Fenoldopam Cannabidiol may decrease the antihypertensive activities of Fenoldopam.
Eprosartan Cannabidiol may decrease the antihypertensive activities of Eprosartan.
Chlorothiazide Cannabidiol may decrease the antihypertensive activities of Chlorothiazide.
Quinapril Cannabidiol may decrease the antihypertensive activities of Quinapril.
Telmisartan The metabolism of Cannabidiol can be decreased when combined with Telmisartan.
Methyldopa Cannabidiol may decrease the antihypertensive activities of Methyldopa.
Hydrochlorothiazide Cannabidiol may decrease the antihypertensive activities of Hydrochlorothiazide.
Trichlormethiazide Cannabidiol may decrease the antihypertensive activities of Trichlormethiazide.
Deserpidine Cannabidiol may decrease the antihypertensive activities of Deserpidine.
Pentolinium Cannabidiol may decrease the antihypertensive activities of Pentolinium.
Trimethaphan Cannabidiol may decrease the antihypertensive activities of Trimethaphan.
Diazoxide Cannabidiol may decrease the antihypertensive activities of Diazoxide.
Bretylium Cannabidiol may decrease the antihypertensive activities of Bretylium.
Terazosin Cannabidiol may decrease the antihypertensive activities of Terazosin.
Captopril Cannabidiol may decrease the antihypertensive activities of Captopril.
Epoprostenol Cannabidiol may decrease the antihypertensive activities of Epoprostenol.
Polythiazide Cannabidiol may decrease the antihypertensive activities of Polythiazide.
Cilazapril Cannabidiol may decrease the antihypertensive activities of Cilazapril.
Saprisartan Cannabidiol may decrease the antihypertensive activities of Saprisartan.
Spirapril Cannabidiol may decrease the antihypertensive activities of Spirapril.
Dexpropranolol Cannabidiol may decrease the antihypertensive activities of Dexpropranolol.
Diethylnorspermine Cannabidiol may decrease the antihypertensive activities of Diethylnorspermine.
Temocapril Cannabidiol may decrease the antihypertensive activities of Temocapril.
Trimazosin Cannabidiol may decrease the antihypertensive activities of Trimazosin.
Nicorandil Cannabidiol may decrease the antihypertensive activities of Nicorandil.
Rauwolfia serpentina root Cannabidiol may decrease the antihypertensive activities of Rauwolfia serpentina root.
Enalaprilat Cannabidiol may decrease the antihypertensive activities of Enalaprilat.
Angiotensin 1-7 Cannabidiol may decrease the antihypertensive activities of Angiotensin 1-7.
Imidapril Cannabidiol may decrease the antihypertensive activities of Imidapril.
BQ-123 Cannabidiol may decrease the antihypertensive activities of BQ-123.
Cicletanine Cannabidiol may decrease the antihypertensive activities of Cicletanine.
Zofenopril Cannabidiol may decrease the antihypertensive activities of Zofenopril.
Guanoxan Cannabidiol may decrease the antihypertensive activities of Guanoxan.
Delapril Cannabidiol may decrease the antihypertensive activities of Delapril.
Vincamine Cannabidiol may decrease the antihypertensive activities of Vincamine.
Linsidomine Cannabidiol may decrease the antihypertensive activities of Linsidomine.
Guanoxabenz Cannabidiol may decrease the antihypertensive activities of Guanoxabenz.
Tolonidine Cannabidiol may decrease the antihypertensive activities of Tolonidine.
Endralazine Cannabidiol may decrease the antihypertensive activities of Endralazine.
Cadralazine Cannabidiol may decrease the antihypertensive activities of Cadralazine.
Cyclopenthiazide Cannabidiol may decrease the antihypertensive activities of Cyclopenthiazide.
Bietaserpine Cannabidiol may decrease the antihypertensive activities of Bietaserpine.
Guanazodine Cannabidiol may decrease the antihypertensive activities of Guanazodine.
Methoserpidine Cannabidiol may decrease the antihypertensive activities of Methoserpidine.
Guanoclor Cannabidiol may decrease the antihypertensive activities of Guanoclor.
Muzolimine Cannabidiol may decrease the antihypertensive activities of Muzolimine.
Xipamide Cannabidiol may decrease the antihypertensive activities of Xipamide.
Tocopherylquinone Cannabidiol may decrease the antihypertensive activities of Tocopherylquinone.
Benazeprilat Cannabidiol may decrease the antihypertensive activities of Benazeprilat.
Fosinoprilat Cannabidiol may decrease the antihypertensive activities of Fosinoprilat.
Ramiprilat Cannabidiol may decrease the antihypertensive activities of Ramiprilat.
Perindoprilat Cannabidiol may decrease the antihypertensive activities of Perindoprilat.
Quinaprilat Cannabidiol may decrease the antihypertensive activities of Quinaprilat.
Furosemide Cannabidiol may decrease the antihypertensive activities of Furosemide.
Enalapril Cannabidiol may decrease the antihypertensive activities of Enalapril.
Nimodipine Cannabidiol may decrease the antihypertensive activities of Nimodipine.
Bisoprolol Cannabidiol may decrease the antihypertensive activities of Bisoprolol.
Indapamide Cannabidiol may decrease the antihypertensive activities of Indapamide.
Irbesartan The metabolism of Irbesartan can be decreased when combined with Cannabidiol.
Guanethidine Cannabidiol may decrease the antihypertensive activities of Guanethidine.
Hydralazine Cannabidiol may decrease the antihypertensive activities of Hydralazine.
Pinacidil Cannabidiol may decrease the antihypertensive activities of Pinacidil.
Macitentan Cannabidiol may decrease the antihypertensive activities of Macitentan.
Aliskiren Cannabidiol may decrease the antihypertensive activities of Aliskiren.
Efonidipine Cannabidiol may decrease the antihypertensive activities of Efonidipine.
Lacidipine Cannabidiol may decrease the antihypertensive activities of Lacidipine.
Niguldipine Cannabidiol may decrease the antihypertensive activities of Niguldipine.
Selexipag The metabolism of Selexipag can be decreased when combined with Cannabidiol.
Naftopidil Cannabidiol may decrease the antihypertensive activities of Naftopidil.
Dexniguldipine Cannabidiol may decrease the antihypertensive activities of Dexniguldipine.
Amlodipine The metabolism of Cannabidiol can be decreased when combined with Amlodipine.
Buthiazide Cannabidiol may decrease the antihypertensive activities of Buthiazide.
Esmolol The metabolism of Esmolol can be decreased when combined with Cannabidiol.
Betaxolol The metabolism of Betaxolol can be decreased when combined with Cannabidiol.
Metoprolol The metabolism of Metoprolol can be decreased when combined with Cannabidiol.
Atenolol The metabolism of Atenolol can be decreased when combined with Cannabidiol.
Timolol The metabolism of Timolol can be decreased when combined with Cannabidiol.
Guanabenz The metabolism of Guanabenz can be decreased when combined with Cannabidiol.

Target Protein

Cannabinoid receptor 1 CNR1
Cannabinoid receptor 2 CNR2
G-protein coupled receptor 12 GPR12
Glycine receptor subunit alpha-1 GLRA1
Glycine receptor (alpha-1/beta) GLRA1
Glycine receptor subunit alpha-3 GLRA3
N-arachidonyl glycine receptor GPR18
G-protein coupled receptor 55 GPR55
5-hydroxytryptamine receptor 1A HTR1A
5-hydroxytryptamine receptor 2A HTR2A
Neuronal acetylcholine receptor subunit alpha-7 CHRNA7
Delta-type opioid receptor OPRD1
Mu-type opioid receptor OPRM1
Peroxisome proliferator-activated receptor gamma PPARG
Transient receptor potential cation channel subfamily V member 1 TRPV1
Voltage-dependent T-type calcium channel subunit alpha-1G CACNA1G
Voltage-dependent T-type calcium channel subunit alpha-1H CACNA1H
Voltage-dependent T-type calcium channel subunit alpha-1I CACNA1I
Transient receptor potential cation channel subfamily A member 1 TRPA1
Transient receptor potential cation channel subfamily M member 8 TRPM8
Transient receptor potential cation channel subfamily V member 2 TRPV2
Transient receptor potential cation channel subfamily V member 3 TRPV3
Transient receptor potential cation channel subfamily V member 4 TRPV4
Non-selective voltage-gated ion channel VDAC1 VDAC1
5-hydroxytryptamine receptor 3A HTR3A
Adenosine receptor A1 ADORA1
Prostaglandin G/H synthase 1 PTGS1
Prostaglandin G/H synthase 2 PTGS2
Acetyl-CoA acetyltransferase, mitochondrial ACAT1
Steroid 17-alpha-hydroxylase/17,20 lyase CYP17A1
3-hydroxy-3-methylglutaryl-coenzyme A reductase HMGCR
Glutathione reductase, mitochondrial GSR
Glutathione peroxidase 1 GPX1
Indoleamine 2,3-dioxygenase 1 IDO1
NAD(P)H dehydrogenase [quinone] 1 NQO1
Catalase CAT
Superoxide dismutase [Cu-Zn] SOD1
Serotonin N-acetyltransferase AANAT
N-acylethanolamine-hydrolyzing acid amidase NAAA

Referensi & Sumber

Artikel (PubMed)
  • PMID: 26264914
    Ibeas Bih C, Chen T, Nunn AV, Bazelot M, Dallas M, Whalley BJ: Molecular Targets of Cannabidiol in Neurological Disorders. Neurotherapeutics. 2015 Oct;12(4):699-730. doi: 10.1007/s13311-015-0377-3.
  • PMID: 24281562
    Zhornitsky S, Potvin S: Cannabidiol in humans-the quest for therapeutic targets. Pharmaceuticals (Basel). 2012 May 21;5(5):529-52. doi: 10.3390/ph5050529.
  • PMID: 28861484
    Ujvary I, Hanus L: Human Metabolites of Cannabidiol: A Review on Their Formation, Biological Activity, and Relevance in Therapy. Cannabis Cannabinoid Res. 2016 Mar 1;1(1):90-101. doi: 10.1089/can.2015.0012. eCollection 2016.
  • PMID: 28680405
    Ruggiero RN, Rossignoli MT, De Ross JB, Hallak JEC, Leite JP, Bueno-Junior LS: Cannabinoids and Vanilloids in Schizophrenia: Neurophysiological Evidence and Directions for Basic Research. Front Pharmacol. 2017 Jun 21;8:399. doi: 10.3389/fphar.2017.00399. eCollection 2017.
  • PMID: 26218440
    Laprairie RB, Bagher AM, Kelly ME, Denovan-Wright EM: Cannabidiol is a negative allosteric modulator of the cannabinoid CB1 receptor. Br J Pharmacol. 2015 Oct;172(20):4790-805. doi: 10.1111/bph.13250. Epub 2015 Oct 13.
  • PMID: 17828291
    Pertwee RG: The diverse CB1 and CB2 receptor pharmacology of three plant cannabinoids: delta9-tetrahydrocannabinol, cannabidiol and delta9-tetrahydrocannabivarin. Br J Pharmacol. 2008 Jan;153(2):199-215. doi: 10.1038/sj.bjp.0707442. Epub 2007 Sep 10.
  • PMID: 29307505
    MacCallum CA, Russo EB: Practical considerations in medical cannabis administration and dosing. Eur J Intern Med. 2018 Mar;49:12-19. doi: 10.1016/j.ejim.2018.01.004. Epub 2018 Jan 4.
  • PMID: 26015168
    Baron EP: Comprehensive Review of Medicinal Marijuana, Cannabinoids, and Therapeutic Implications in Medicine and Headache: What a Long Strange Trip It's Been .... Headache. 2015 Jun;55(6):885-916. doi: 10.1111/head.12570. Epub 2015 May 25.
Menampilkan 8 dari 17 artikel.

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