# Cannabidiol in Neurology: Current Insights and Translational Perspectives

**Authors:** Magdalena Białoń, Marta Kędziora, Katarzyna Starowicz

PMC · DOI: 10.3390/ph19020330 · 2026-02-17

## TL;DR

Cannabidiol (CBD) shows promise for treating neurological disorders without psychoactive effects, but more research is needed to understand its full potential and risks.

## Contribution

This review provides a comprehensive assessment of CBD's therapeutic potential and safety in neurological conditions based on preclinical and clinical studies.

## Key findings

- CBD has therapeutic potential for epilepsy, chronic pain, and neurodegenerative diseases.
- CBD is generally safe but may cause mild side effects and drug interactions.
- Epidiolex and Sativex are currently approved CBD-based medications for specific neurological conditions.

## Abstract

Cannabidiol (CBD) is one of the most studied compounds of Cannabis sativa and has attracted significant interest due to its therapeutic and beneficial properties, which have been confirmed in numerous preclinical and clinical studies over the last few years. A great advantage of CBD over the other widely known Cannabis sativa ingredient, Δ-9-tetrahydrocannabinol (THC), is that CBD does not exert intoxicating and psychoactive effects, making it an attractive candidate for therapeutic applications in neurological disorders. CBD has been shown to exert antioxidant, analgesic, anti-inflammatory, and neuroprotective effects, with therapeutic potential for various neurological conditions. To date, the only drug that consists solely of highly purified CBD is Epidiolex, which is used in the management of severe forms of epilepsy such as Dravet syndrome and Lennox–Gastaut syndrome. Another legal medication containing CBD (albeit with the addition of THC) is Sativex, used to alleviate spasticity in multiple sclerosis. Besides epilepsy, preclinical data suggest that CBD alone may be potentially beneficial in treating chronic pain, multiple sclerosis, Alzheimer’s and Parkinson’s diseases, or stroke. The safety profile of CBD is generally considered favorable, as the most commonly reported adverse effects are mild (e.g., somnolence, diarrhea). However, much attention should be paid as CBD-driven drug–drug interactions have been reported. This review article aims to assess the outcomes of preclinical and clinical research on CBD’s effects in various neurological conditions while also addressing potential risks and concerns related to its use.

## Linked entities

- **Chemicals:** Cannabidiol (PubChem CID 644019), CBD (PubChem CID 644019), THC (PubChem CID 16078)
- **Diseases:** epilepsy (MONDO:0005027), Dravet syndrome (MONDO:0100135), Lennox–Gastaut syndrome (MONDO:0016532), multiple sclerosis (MONDO:0005301), Alzheimer’s disease (MONDO:0004975), Parkinson’s disease (MONDO:0005180), stroke (MONDO:0005098)

## Full-text entities

- **Genes:** Faah (fatty acid amide hydrolase) [NCBI Gene 14073], ABCB1 (ATP binding cassette subfamily B member 1) [NCBI Gene 5243] {aka ABC20, CD243, CLCS, ENPAT, GP170, MDR1}, Cck (cholecystokinin) [NCBI Gene 12424], UGT2B7 (UDP glucuronosyltransferase family 2 member B7) [NCBI Gene 7364] {aka UDPGT 2B7, UDPGT 2B9, UDPGT2B7, UDPGTH2, UDPGTh-2, UGT2B9}, Cntf (ciliary neurotrophic factor) [NCBI Gene 12803], CYP2C9 (cytochrome P450 family 2 subfamily C member 9) [NCBI Gene 1559] {aka CPC9, CYP2C, CYP2C10, CYPIIC9, P450-2C9, P450IIC9}, Ecs (epistatic circling SWR/J) [NCBI Gene 13604], PPP2R2A (protein phosphatase 2 regulatory subunit Balpha) [NCBI Gene 5520] {aka B55, B55A, B55ALPHA, PR52A, PR55A, PR55alpha}, CYP3A4 (cytochrome P450 family 3 subfamily A member 4) [NCBI Gene 1576] {aka CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4}, Fkbp5 (FK506 binding protein 5) [NCBI Gene 14229] {aka D17Ertd592e, Dit1, FKBP-5, FKBP51}, Pvalb (parvalbumin) [NCBI Gene 19293] {aka PV, Parv, Pva}, Il33 (interleukin 33) [NCBI Gene 77125] {aka 9230117N10Rik, Il-33, Il1f11, NF-HEV}, Cnr1 (cannabinoid receptor 1) [NCBI Gene 12801] {aka CB-R, CB1, CB1A, CB1B, CB1R}, Bcl2 (B cell leukemia/lymphoma 2) [NCBI Gene 12043] {aka Bcl-2, C430015F12Rik, D630044D05Rik, D830018M01Rik}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, FAAH (fatty acid amide hydrolase) [NCBI Gene 2166] {aka FAAH-1, FAAH1, PSAB}, Nos2 (nitric oxide synthase 2, inducible) [NCBI Gene 18126] {aka MAC-NOS, NOS-II, Nos-2, Nos2a, i-NOS, iNOS}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Scn2a (sodium channel, voltage-gated, type II, alpha) [NCBI Gene 110876] {aka 6430408L10, A230052E19Rik, Nav1.2, Scn2a1}, PTPA (protein phosphatase 2 phosphatase activator) [NCBI Gene 5524] {aka PARK25, PP2A, PPP2R4, PR53}, Trem2 (triggering receptor expressed on myeloid cells 2) [NCBI Gene 83433] {aka TREM-2, Trem2a, Trem2b, Trem2c}, Cks1b (CDC28 protein kinase 1b) [NCBI Gene 54124] {aka 2410005G18Rik, 2610005D03Rik, Cks1, sid1334}, PGP (phosphoglycolate phosphatase) [NCBI Gene 283871] {aka AUM, G3PP, PGPase}, Snca (synuclein, alpha) [NCBI Gene 20617] {aka NACP, alpha-Syn, alphaSYN}, Trpv2 (transient receptor potential cation channel, subfamily V, member 2) [NCBI Gene 22368] {aka GRC, OTRPC2, VRL-1, Vrl1}, Vcam1 (vascular cell adhesion molecule 1) [NCBI Gene 22329] {aka CD106, Vcam-1}, Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}, Sod2 (superoxide dismutase 2, mitochondrial) [NCBI Gene 20656] {aka MnSOD, Sod-2}, Trpv1 (transient receptor potential cation channel, subfamily V, member 1) [NCBI Gene 193034] {aka OTRPC1, TRPV1alpha, TRPV1beta, VR-1, Vr1}, Tlr4 (toll-like receptor 4) [NCBI Gene 21898] {aka Lps, Ly87, Ran/M1, Rasl2-8}, TRPV1 (transient receptor potential cation channel subfamily V member 1) [NCBI Gene 7442] {aka VR1}, HTR1A (5-hydroxytryptamine receptor 1A) [NCBI Gene 3350] {aka 5-HT-1A, 5-HT1A, 5HT1a, ADRB2RL1, ADRBRL1, G-21}, CYP2C19 (cytochrome P450 family 2 subfamily C member 19) [NCBI Gene 1557] {aka CPCJ, CYP2C, CYPIIC17, CYPIIC19, P450C2C, P450IIC19}, Sod1 (superoxide dismutase 1, soluble) [NCBI Gene 20655] {aka B430204E11Rik, Cu/Zn-SOD, CuZnSOD, Ipo-1, Ipo1, SODC}, Th (tyrosine hydroxylase) [NCBI Gene 21823], Icam1 (intercellular adhesion molecule 1) [NCBI Gene 15894] {aka CD54, Icam-1, Ly-47, MALA-2}, Nfe2l2 (nuclear factor, erythroid derived 2, like 2) [NCBI Gene 18024] {aka Nrf2}, Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, CYP4F3 (cytochrome P450 family 4 subfamily F member 3) [NCBI Gene 4051] {aka CPF3, CYP4F, CYPIVF3, LTB4H}, Iba1 (induction of brown adipocytes 1) [NCBI Gene 114737], Cat (catalase) [NCBI Gene 12359] {aka 2210418N07, Cas-1, Cas1, Cs-1}, Bax (BCL2-associated X protein) [NCBI Gene 12028], Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, Il17a (interleukin 17A) [NCBI Gene 16171] {aka Ctla-8, Ctla8, IL-17, IL-17A, Il17}, Casp3 (caspase 3) [NCBI Gene 12367] {aka A830040C14Rik, AC-3, CASP-3, CC3, CPP-32, CPP32}
- **Diseases:** tuberous sclerosis (MESH:D014402), erythema (MESH:D004890), DS (MESH:D004831), allodynia (MESH:D006930), MS (MESH:D009103), pulmonary problems (MESH:D019973), memory deficits (MESH:D008569), inflammatory focal lesions (MESH:D005490), chronic disability (MESH:D002908), axonal damage (MESH:D001480), neurological impairment (MESH:D009422), cognitive decline (MESH:D003072), chronic pain (MESH:D059350), breast cancer (MESH:D001943), depression (MESH:D003866), Autoimmune Encephalomyelitis (MESH:D004681), neuropathic pain (MESH:D009437), LID (MESH:D004409), epileptiform activity (MESH:D014277), dry mouth (MESH:D014987), neuronal death (MESH:D009410), hypersensitivity (MESH:D004342), decreased appetite (MESH:D001068), Dementia (MESH:D003704), amyloid (MESH:C000718787), anxious/aggressive behaviors (MESH:D010554), peripheral neuropathy (MESH:D010523), liver toxicity (MESH:D056486), audiogenic seizures (MESH:D020195), psychosis (MESH:D011618), slowness of movement (MESH:D020754), agitation (MESH:D011595), impaired social interaction (MESH:C563663), dizziness (MESH:D004244), developmental toxicity (MESH:D064420), Epilepsy (MESH:D004827), spasm (MESH:D013035), somnolence (MESH:D006970), tremor (MESH:D014202), brain damage (MESH:D001925), SNI (MESH:D000080902), demyelination (MESH:D003711), posttraumatic epilepsy (MESH:D013313), psoriatic arthritis (MESH:D015535), atonic seizures (MESH:D012640), osteoarthritis (MESH:D010003), CCI (MESH:D020208), hypotension (MESH:D007022), ischemia (MESH:D007511), Neurological Disorders (MESH:D009461), Dravet and Lennox-Gastaut syndromes (MESH:D065768), axonal loss (MESH:D012183), balance difficulties (MESH:D051346), Chronic low back pain (MESH:D017116), anxiety disorders (MESH:D001008), degenerative brain disorder (MESH:D020271), autoimmune disease (MESH:D001327), focal epilepsy (MESH:D004828), skin rash (MESH:D005076), diarrhea (MESH:D003967)
- **Chemicals:** taxane (MESH:C080625), dopamine (MESH:D004298), morphine (MESH:D009020), Cannabinoids (MESH:D002186), CBD (MESH:D002185), glucose (MESH:D005947), rotenone (MESH:D012402), fluoxetine (MESH:D005473), endocannabinoid (MESH:D063388), AM630 (MESH:C094023), lipid (MESH:D008055), LPS (MESH:D008070), amitriptyline (MESH:D000639), nitrite (MESH:D009573), mirtazapine (MESH:D000078785), kainate (MESH:D007608), oil (MESH:D009821), valproate (MESH:D014635), L-DOPA (MESH:D007980), 2-AG (MESH:C094503), 7-COOH-CBD (-), cisplatin (MESH:D002945), olanzapine (MESH:D000077152), anandamide (MESH:C078814), glutamate (MESH:D018698), risperidone (MESH:D018967), Sativex (MESH:C587251), NO (MESH:D009569), 6-OHDA (MESH:D016627), streptozotocin (MESH:D013311), Delta-9-tetrahydrocannabinol (MESH:D013759), paclitaxel (MESH:D017239), FeCl3 (MESH:C024555), citalopram (MESH:D015283), capsazepine (MESH:C071423), fat (MESH:D005223), reserpine (MESH:D012110), clobazam (MESH:D000078306), oxygen (MESH:D010100)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Cannabis sativa (species) [taxon 3483], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** BV-2 — Mus musculus (Mouse), Transformed cell line (CVCL_0182), PC12 — Rattus norvegicus (Rat), Rat adrenal gland pheochromocytoma, Cancer cell line (CVCL_0481)

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943572/full.md

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Source: https://tomesphere.com/paper/PMC12943572