# Comparative Anti-Obesity Potential of Cannabigerol-Dominant Cannabis sativa L. Inflorescence Extracts via Differential Regulation of Lipid Metabolism in 3T3-L1 Cells

**Authors:** Ji-Ye Han, Osoung Kwon, Yun Jung Lee, Minji Choi, Bori Lee, Dae-Ki Kim, Soohyang Noh, Mansoo Cho, Young-Mi Lee

PMC · DOI: 10.3390/ijms27041747 · International Journal of Molecular Sciences · 2026-02-11

## TL;DR

This study shows that cannabis extracts rich in cannabigerol can reduce obesity by altering fat cell development and metabolism.

## Contribution

The novel finding is that cannabigerol-dominant cannabis extracts can regulate lipid metabolism to combat obesity.

## Key findings

- Cannabigerol-dominant cannabis extracts inhibit 3T3-L1 cell differentiation in a dose-dependent manner.
- CE downregulates adipogenic and lipogenic markers like PPARγ, C/EBPα, SREBP-1c, and FAS.
- CE upregulates lipolysis and browning markers such as HSL, ATGL, UCP1, and PGC-1α.

## Abstract

Obesity is a chronic metabolic disorder characterized by excessive accumulation of body fat and is a major risk factor for various diseases, including type 2 diabetes, hypertension, and cardiovascular diseases. This study investigated the anti-obesity effects of cannabigerol-dominant C. sativa inflorescence extracts (CEs) obtained using various ethanol concentrations. The extracts were analyzed by UPLC to determine their major components. Additionally, anti-obesity mechanisms of the extracts were further determined through RT-qPCR and Western blot analysis to evaluate gene and protein expression levels. A total of seven cannabinoids, including cannabigerol as a major constituent, were identified within CE. Differentiation of 3T3-L1 cells was dose-dependently inhibited by CE at all ethanol concentrations. Furthermore, the gene and protein expression levels of key adipogenic and lipogenic markers, such as PPARγ, C/EBPα, SREBP-1c, and FAS, were significantly downregulated by CE treatment. In contrast, the expression of factors involved in lipolysis and white adipose tissue browning, such as HSL, ATGL, UCP1, and PGC-1α, was markedly increased by CE treatment. These effects were enhanced in an ethanol concentration-dependent manner. In conclusion, these results demonstrate that cannabigerol-dominant C. sativa effectively mitigates obesity by suppressing adipogenesis and lipogenesis while concurrently stimulating lipolysis and white adipose tissue browning.

## Linked entities

- **Genes:** PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468], CEBPA (CCAAT enhancer binding protein alpha) [NCBI Gene 1050], Srebf1 (sterol regulatory element binding transcription factor 1) [NCBI Gene 78968], FAS (Fas cell surface death receptor) [NCBI Gene 355], LIPE (lipase E, hormone sensitive type) [NCBI Gene 3991], PNPLA2 (patatin like domain 2, triacylglycerol lipase) [NCBI Gene 57104], UCP1 (uncoupling protein 1) [NCBI Gene 7350], PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891]
- **Chemicals:** cannabigerol (PubChem CID 5315659)
- **Diseases:** obesity (MONDO:0011122), type 2 diabetes (MONDO:0005148)

## Full-text entities

- **Genes:** Ppargc1a (peroxisome proliferative activated receptor, gamma, coactivator 1 alpha) [NCBI Gene 19017] {aka A830037N07Rik, Gm11133, PGC-1, PPARGC-1-alpha, Pgc-1alpha, Pgc1}, Actb (actin, beta) [NCBI Gene 11461] {aka Actx, E430023M04Rik, beta-actin}, Pparg (peroxisome proliferator activated receptor gamma) [NCBI Gene 19016] {aka Nr1c3, PPAR-gamma, PPAR-gamma2, PPARgamma, PPARgamma2}, Lipe (lipase E, hormone sensitive type) [NCBI Gene 16890] {aka 4933403G17Rik, HSL, REH}, Srebf1 (sterol regulatory element binding transcription factor 1) [NCBI Gene 20787] {aka ADD1, SREBP1, bHLHd1}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 14433] {aka Gapd}, Pnpla2 (patatin-like phospholipase domain containing 2) [NCBI Gene 66853] {aka 0610039C21Rik, 1110001C14Rik, Atgl, TTS-2.2}, Cebpa (CCAAT/enhancer binding protein alpha) [NCBI Gene 12606] {aka C/ebpalpha, CBF-A, Cebp}, Ucp1 (uncoupling protein 1 (mitochondrial, proton carrier)) [NCBI Gene 22227] {aka Slc25a7, Ucp}
- **Diseases:** Obesity (MESH:D009765), metabolic (MESH:D008659), injury to (MESH:D014947), inflammatory (MESH:D007249), cancer (MESH:D009369), depression (MESH:D003866), type 2 diabetes (MESH:D003924), bacterial (MESH:D001424), hyperplasia (MESH:D006965), multiple sclerosis (MESH:D009103), hypertension (MESH:D006973), epilepsy (MESH:D004827), insulin resistance (MESH:D007333), cytotoxic (MESH:D064420), hypertrophy (MESH:D006984), cardiovascular disease (MESH:D002318)
- **Chemicals:** terpenoids (MESH:D013729), CBN (MESH:D002187), ORO (MESH:C011049), Delta8-THC (MESH:C035731), water (MESH:D014867), ethanol (MESH:D000431), isopropanol (MESH:D019840), SDS (MESH:D012967), CBNA (MESH:C045780), CBG (MESH:C037036), formazan (MESH:D005562), polytetrafluoroethylene (MESH:D011138), formic acid (MESH:C030544), methanol (MESH:D000432), streptomycin (MESH:D013307), acetonitrile (MESH:C032159), Delta9-THC (MESH:D013759), Lipid (MESH:D008055), CO2 (MESH:D002245), CBGA (MESH:C100679), CBDA (MESH:C006884), Cannabinoid (MESH:D002186), formalin (MESH:D005557), CBD (MESH:D002185), DMSO (MESH:D004121), PVDF (MESH:C024865), penicillin (MESH:D010406), HEPES (MESH:D006531), CBC (MESH:C010695), CE (-), CBDV (MESH:C580853), CBDVA (MESH:C000632924), MTT (MESH:C070243), IBMX (MESH:D015056), dexamethasone (MESH:D003907), CBL (MESH:C022213)
- **Species:** Cannabis sativa subsp. sativa (hemp, subspecies) [taxon 1678924], Cannabis sativa (species) [taxon 3483], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** 3T3-L1 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0123)

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941217/full.md

## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12941217/full.md

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Source: https://tomesphere.com/paper/PMC12941217