# Therapeutic relevance of an EU-GMP certified Cannabis sativa L. strain in a dual in vivo model of cognitive impairment and chronic neuropathic pain

**Authors:** Ivona Costachescu, Raluca-Maria Gogu, Gabriela-Dumitrita Stanciu, Carmen Solcan, Loredana Horodincu, Andrei Szilagyi, Vlad-Constantin Craciun, Daniela-Carmen Ababei, Bogdan-Ionel Tamba

PMC · DOI: 10.3389/fphar.2026.1761426 · Frontiers in Pharmacology · 2026-02-20

## TL;DR

A certified cannabis strain shows strong pain relief and neuroprotection in a rat model of Alzheimer's and chronic pain, suggesting potential as a treatment for these conditions.

## Contribution

Demonstrates the therapeutic potential of a GMP-certified Cannabis sativa strain in a dual model of cognitive impairment and chronic neuropathic pain.

## Key findings

- Cannabixir® Medium Flos provided robust analgesia and reduced neuroinflammation in rats.
- The cannabis strain preserved hippocampal and peripheral nerve integrity when combined with existing drugs.
- Combination therapy showed superior effects compared to tramadol alone in pain and neuroprotection.

## Abstract

Alzheimer’s disease (AD) is a progressive neurodegenerative disorder characterized by cognitive decline and frequently co-occurs with chronic pain. Worldwide, over 55 million people are affected by AD, with nearly half experiencing persistent pain. Chronic pain has been linked to accelerated memory deterioration and an increased risk of dementia, but the interplay between these conditions remains poorly understood. Existing therapies for AD and chronic pain are limited in efficacy, highlighting the need for interventions targeting multiple pathological pathways. The endocannabinoid system, which is altered in both AD and chronic pain, represents a potential therapeutic target, though its role in AD patients with comorbid pain remains unexplored.

The study evaluated the effects of an EU-GMP certified Cannabis sativa L. strain (5 mg/kg, Cannabixir® Medium Flos) on neurobiological alterations in a rat model designed to explore mechanistic interactions between scopolamine-induced transient cognitive impairment and chronic neuropathic pain induced by unilateral sciatic nerve ligation. Treatment outcomes were assessed through nociceptive tests, clinical monitoring and tissue analyses to examine cognitive and pain-related effects.

Cannabixir® Medium Flos induced robust, time-dependent analgesia in thermal nociceptive tests, with the combination of the Cannabis sativa L. strain, donepezil and tramadol producing significantly longer response latencies than tramadol alone. Mechanical sensitivity was minimally affected across treatments. Immunohistochemical analyses revealed that Cannabixir® Medium Flos, either alone or in combination with donepezil or tramadol, produced the most pronounced neuroprotective effects, reducing astrocytic (GFAP) and microglial (Iba1) activation, lowering Caspase-3 and IL-6 expression, and preserving both hippocampal neuronal integrity as well as peripheral nerve structure.

These findings indicate that Cannabixir® Medium Flos, particularly when combined with donepezil and tramadol, provides superior analgesic and neuroprotective effects compared to tramadol alone. Its multi-target action - alleviating thermal nociception, reducing neuroinflammation, limiting apoptosis and preserving neuronal and peripheral nerve integrity—supports its potential as an adjunct therapy in managing dementia with comorbid chronic neuropathic pain. Future studies should explore the molecular mechanisms underlying these effects and assess long-term safety and efficacy across diverse models of neurodegeneration and chronic pain.

## Linked entities

- **Proteins:** GFAP (glial fibrillary acidic protein), AIF1 (allograft inflammatory factor 1), Casp3 (caspase 3), IL6 (interleukin 6)
- **Chemicals:** donepezil (PubChem CID 3152), tramadol (PubChem CID 19472)
- **Diseases:** Alzheimer’s disease (MONDO:0004975)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Gfap (glial fibrillary acidic protein) [NCBI Gene 24387], Aif1 (allograft inflammatory factor 1) [NCBI Gene 29427] {aka BART-1, Bart1, iba1, mrf-1}, Iba1 (induction of brown adipocytes 1) [NCBI Gene 114737], Casp3 (caspase 3) [NCBI Gene 12367] {aka A830040C14Rik, AC-3, CASP-3, CC3, CPP-32, CPP32}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, Bche (butyrylcholinesterase) [NCBI Gene 65036], Pdlim3 (PDZ and LIM domain 3) [NCBI Gene 114108] {aka Actn2lp, Alp}, Gfap (glial fibrillary acidic protein) [NCBI Gene 14580], COX1 [NCBI Gene 27215481], Alb (albumin) [NCBI Gene 24186] {aka Alb1, Albza}, Cd163 (CD163 molecule) [NCBI Gene 312701] {aka ED2}, Rbfox3 (RNA binding fox-1 homolog 3) [NCBI Gene 287847] {aka Hrnbp3, Neun, RGD1560070}, Got2 (glutamic-oxaloacetic transaminase 2) [NCBI Gene 25721] {aka ASPATA, mAAT}, Hp (haptoglobin) [NCBI Gene 24464] {aka Ba1-647}, CNR1 (cannabinoid receptor 1) [NCBI Gene 1268] {aka CANN6, CB-R, CB1, CB1A, CB1K5, CB1R}, COX-2 [NCBI Gene 27215472], Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, Casp3 (caspase 3) [NCBI Gene 25402] {aka CPP32-beta, Lice, Yama}, Cnr2 (cannabinoid receptor 2) [NCBI Gene 57302] {aka CB-2, CB2, CB2C, CNR2C, rCB2}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Cd163 (CD163 antigen) [NCBI Gene 93671] {aka CD163v2, CD163v3}
- **Diseases:** inflammation (MESH:D007249), headache (MESH:D006261), neurodegeneration (MESH:D019636), epileptics (MESH:D004827), astrogliosis (MESH:D005911), demyelination (MESH:D003711), peripheral nerve injury (MESH:D059348), Pain (MESH:D010146), brain injury (MESH:D001930), nerve damage (MESH:D000080902), neurotoxic (MESH:D020258), oedema (MESH:C536897), neuropsychiatric symptoms (MESH:D001523), agitation (MESH:D011595), AD (MESH:D000544), mononeuropathy (MESH:D020422), hippocampal atrophy (MESH:D001284), neuroinflammation (MESH:D000090862), axonal degeneration (MESH:D009410), renal dysfunction (MESH:D007674), Chronic pain (MESH:D059350), neuropathic (MESH:D009437), impair learning and memory (MESH:D007859), hypersensitivity (MESH:D004342), dementia (MESH:D003704), synaptic dysfunction (MESH:C536122), necrosis (MESH:D009336), opioid dependence (MESH:D009293), cholinergic deficits (MESH:C535672), acute and chronic pain (MESH:D059787), overdose (MESH:D062787), neuropathy (MESH:D009422), cognitive decline (MESH:D003072), memory deficits (MESH:D008569), analgesia (MESH:D000699)
- **Chemicals:** paraffin (MESH:D010232), hydrogen peroxide (MESH:D006861), CanDG (-), bile acids (MESH:D001647), H&amp;E (MESH:D006371), NaCl (MESH:D012965), Aricept (MESH:D000077265), haematoxylin (MESH:D006416), oxygen (MESH:D010100), Scopolamine (MESH:D012601), xylene (MESH:D014992), Delta9-tetrahydrocannabinol (MESH:D013759), UREA (MESH:D014508), water (MESH:D014867), citrate (MESH:D019343), sodium carboxymethylcellulose (MESH:D002266), Isoflurane (MESH:D007530), endocannabinoid (MESH:D063388), PBS (MESH:D007854), eosin (MESH:D004801), 3,3'-diaminobenzidine (MESH:D015100), Tramadol (MESH:D014147), CBD (MESH:D002185), CHOL (MESH:D002784), ethanol (MESH:D000431), CRE (MESH:D003404), Formalin (MESH:D005557), GLU (MESH:D005947), Cannabinoid (MESH:D002186)
- **Species:** Danio rerio (leopard danio, species) [taxon 7955], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Cannabis sativa (species) [taxon 3483]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12963308/full.md

## References

83 references — full list in the complete paper: https://tomesphere.com/paper/PMC12963308/full.md

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Source: https://tomesphere.com/paper/PMC12963308