# Artemisia herba alba Outperforms Indomethacin with Multitarget Efficacy and Safety in CFA Arthritic Model

**Authors:** Hicham Wahnou, Martin Ndayambaje, Imane Nait Irahal, Zaynab Ouadghiri, Wafaa Taha, Asmaa Mazti, Riad El Kebbaj, Youness Limami, Mounia Oudghiri

PMC · DOI: 10.3390/antiox15020190 · Antioxidants · 2026-02-02

## TL;DR

Artemisia herba alba extract shows better anti-inflammatory and safety effects than indomethacin in treating arthritis in rats.

## Contribution

Demonstrates the multitarget efficacy and safety of Artemisia herba alba in a preclinical arthritis model.

## Key findings

- Artemisia herba alba reduced joint inflammation and pain hypersensitivity in arthritic rats.
- The extract preserved liver and kidney function without causing oxidative stress.
- It showed antioxidant activity and cartilage protection compared to indomethacin.

## Abstract

Rheumatoid arthritis remains a major clinical challenge requiring safer and more effective alternatives to conventional non-steroidal anti-inflammatory drugs (NSAIDs). This pioneering study evaluated the anti-inflammatory, analgesic, antioxidant, and safety effects of Artemisia herba alba extract in complete Freund’s adjuvant (CFA)-induced arthritis in rats. Animals received oral Artemisia herba alba (250 or 500 mg/kg), indomethacin (3 mg/kg), or saline for 15 days. CFA induced marked joint inflammation, mechanical allodynia, locomotor impairment, and oxidative stress. Treatment with Artemisia herba alba 500 mg/kg significantly reduced paw swelling, improved mobility in the open-field test, and markedly attenuated pain hypersensitivity. In parallel, biochemical analyses showed restoration of total antioxidant capacity, prevention of lipid peroxidation, and normalization of creatinine levels. Unlike indomethacin, which induced hepatotoxicity (elevated ASAT (Aspartate Aminotransferase)/ALAT (Alanine Aminotransferase)) and pronounced oxidative stress, Artemisia herba alba preserved liver and kidney function and did not produce histopathological alterations. Histological findings further indicated reduced inflammatory infiltrate and cartilage protection, particularly at 500 mg/kg. Taken together, these results suggest that Artemisia herba alba displays a multitarget effect with anti-inflammatory, antioxidant and analgesic activity, along with a superior safety profile compared with indomethacin, consistent with reports from other phenolic-rich natural products. However, findings should be interpreted in light of the small sample size and preclinical study design, and further mechanistic and clinical investigations are warranted.

## Linked entities

- **Proteins:** ABCB7 (ATP binding cassette subfamily B member 7), alaT (tRNA-Ala)
- **Chemicals:** indomethacin (PubChem CID 3715), creatinine (PubChem CID 588)
- **Diseases:** rheumatoid arthritis (MONDO:0008383)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Got1 (glutamic-oxaloacetic transaminase 1) [NCBI Gene 24401] {aka AAT1, ASAT, Aspat, Gaspat, cAspAT, cCAT}, Sds (serine dehydratase) [NCBI Gene 25044] {aka RATSDHE1, SDH2, Sdh, Sdhe1, TDH}, Got2 (glutamic-oxaloacetic transaminase 2) [NCBI Gene 25721] {aka ASPATA, mAAT}, Ptgs2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 29527] {aka COX-2, Cox2, PGHS-2, PHS II, Pghs2}, Tac1 (tachykinin, precursor 1) [NCBI Gene 24806] {aka PPTA3, Ppt5fl, RATPPTA3, TAC}, Il1b (interleukin 1 beta) [NCBI Gene 24494] {aka IL-1F2}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, Cat (catalase) [NCBI Gene 24248] {aka CS1, Cas1, Cat01, Catl, Cs-1}, Gpt (glutamic--pyruvic transaminase) [NCBI Gene 81670] {aka ALAT, Gpt1}, Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}
- **Diseases:** Arthritis (MESH:D001168), Rheumatoid arthritis (MESH:D001172), joint deformity (MESH:D016916), stiffness (MESH:C566112), infections (MESH:D007239), oedema (MESH:C536897), gastrointestinal disorders (MESH:D005767), loss of function (MESH:D006315), weight loss (MESH:D015431), toxicity (MESH:D064420), joint damage (MESH:D007592), bone erosion (MESH:D014077), joint pain (MESH:D018771), arthritis impaired kidney function (MESH:D007674), hepatic or renal toxicity (MESH:D056486), liver injury (MESH:D017093), hypersensitivity (MESH:D004342), joint destruction (MESH:D008105), immune dysregulation (OMIM:614878), mechanical (MESH:D041781), synovial hyperplasia (MESH:D006965), Allodynia (MESH:D006930), erythema (MESH:D004890), chronic (MESH:D002908), inflammation (MESH:D007249), injury (MESH:D014947), pain (MESH:D010146), mitochondrial function (MESH:D028361), locomotor impairment (MESH:D001523), anxiety (MESH:D001007), edema (MESH:D004487), weight gain (MESH:D015430), autoimmune (MESH:D001327), Arthritic (MESH:D015535), motor deficits (MESH:D009461), cartilage degradation (MESH:D002357)
- **Chemicals:** H2O2 (MESH:D006861), Artemisia herba alba extract (-), H&amp;E (MESH:D006371), ammonium molybdate (MESH:C022175), hematoxylin (MESH:D006416), sodium phosphate (MESH:C018279), Indomethacin (MESH:D007213), Urea (MESH:D014508), MDA (MESH:D008315), Ketamine (MESH:D007649), Lipid (MESH:D008055), luteolin (MESH:D047311), PBS (MESH:D007854), eosin (MESH:D004801), TBARS (MESH:D017392), flavonoids (MESH:D005419), Creatinine (MESH:D003404), formalin (MESH:D005557), sulfuric acid (MESH:C033158), paraffin (MESH:D010232), DCIP (MESH:D015086), NaCl (MESH:D012965), carrageenan (MESH:D002351), xylene (MESH:D014992), quercetin (MESH:D011794), EDTA (MESH:D004492), 2,2-diphenyl-1-picrylhydrazyl (MESH:C004931), Free radical (MESH:D005609), phenolic acids (MESH:C017616), essential oils (MESH:D009822), ethanol (MESH:D000431), molybdate (MESH:C044659)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Rodentia (rodent, order) [taxon 9989], Homo sapiens (human, species) [taxon 9606], Artemisia herba-alba (white wormwood, species) [taxon 72329]

## Full text

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## Figures

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## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938658/full.md

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Source: https://tomesphere.com/paper/PMC12938658