# Protective Effect of Resolvin D1, D2, and Their Methyl Esters on Oxidative Stress and Hyaluronidase—Induced Hyaluronic Acid Degradation

**Authors:** Zahra Kariminezhad, Mahdi Rahimi, Julio Fernandes, Hassan Fahmi, Mohamed Benderdour

PMC · DOI: 10.3390/antiox15020163 · Antioxidants · 2026-01-25

## TL;DR

This study shows that Resolvin D1 and D2 derivatives can protect hyaluronic acid in osteoarthritis treatments by reducing oxidative stress and enzyme breakdown.

## Contribution

The study introduces Resolvin D1 and D2 methyl esters as novel dual-function agents to enhance hyaluronic acid stability in osteoarthritis treatments.

## Key findings

- Resolvin D1 methyl ester shows strong antioxidant activity in hydrogen atom transfer-based assays.
- Resolvin derivatives effectively inhibit ROS-induced and enzyme-induced hyaluronic acid degradation.
- These compounds could improve the therapeutic persistence of hyaluronic acid injections in osteoarthritic joints.

## Abstract

Hyaluronic acid (HA) injections are commonly employed in the management of osteoarthritis (OA), yet their therapeutic benefits are often limited by oxidative degradation and enzymatic breakdown within the joint. This study investigates whether Resolvin D1, Resolvin D2, and their methyl ester derivatives can enhance the efficacy of HA injections by acting as dual-function agents with both antioxidant and enzyme inhibitory properties. A comprehensive series of in vitro assays—including ORAC, FRAP, DPPH, ABTS, HRS, and SOD—were performed to evaluate antioxidant capacity, using Trolox, Ascorbic acid, β-Carotene, and Quercetin as reference standards. The potential to inhibit HA degradation was assessed through ROS-induced HA fragmentation and hyaluronidase inhibition assay, with epigallocatechin gallate (EGCG) serving as a positive control. The results indicate that Resolvin derivatives, particularly the methyl ester form of Resolvin D1, display mechanism-dependent antioxidant activity, showing pronounced effects in hydrogen atom transfer-based assays (e.g., ORAC and HRS), as well as in ABTS•+ and superoxide-related systems, along with protection against ROS and enzyme-induced HA degradation. These findings suggest that incorporating Resolvin derivatives may represent a promising strategy to improve HA-based viscosupplementation by enhancing stability and therapeutic persistence in osteoarthritic joints.

## Linked entities

- **Chemicals:** Resolvin D1 (PubChem CID 44251266), Resolvin D2 (PubChem CID 11383310), Trolox (PubChem CID 40634), Ascorbic acid (PubChem CID 9888239), β-Carotene (PubChem CID 573), Quercetin (PubChem CID 5280343), epigallocatechin gallate (PubChem CID 1287)
- **Diseases:** osteoarthritis (MONDO:0005178)

## Full-text entities

- **Genes:** SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, ALOX15 (arachidonate 15-lipoxygenase) [NCBI Gene 246] {aka 12-LOX, 15-LOX, 15-LOX-1, LOG15}, CEMIP (cell migration inducing hyaluronidase 1) [NCBI Gene 57214] {aka CCSP1, CEMIP1, HYBID, KIAA1199, TMEM2L}, ALOX5 (arachidonate 5-lipoxygenase) [NCBI Gene 240] {aka 5-LO, 5-LOX, 5LPG, LOG5}, SRSF5 (serine and arginine rich splicing factor 5) [NCBI Gene 6430] {aka HRS, SFRS5, SRP40}
- **Diseases:** stiffness (MESH:C566112), joint (MESH:D007592), toxicity (MESH:D064420), joint pain (MESH:D018771), membrane (MESH:D015433), joint degeneration (MESH:D009410), pain (MESH:D010146), inflammation (MESH:D007249), injury to (MESH:D014947), cartilage breakdown (MESH:D002357), OA (MESH:D010003)
- **Chemicals:** glycosaminoglycan (MESH:D006025), polyunsaturated fatty acids (MESH:D005231), D-glucuronic acid (MESH:D020723), formamide (MESH:C031066), dn (MESH:C022306), H2O2 (MESH:D006861), 7S,16R,17S-trihydroxy-4Z,8E,10Z,12E,14E,19Z-docosahexaenoic acid (MESH:C545423), Superoxide anions (MESH:D013481), 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (-), dextran (MESH:D003911), N-acetyl-D-glucosamine (MESH:D000117), R (MESH:D001120), K2S2O8 (MESH:C009007), FL (MESH:D019793), beta-Carotene (MESH:D019207), ABTS (MESH:C002502), lipid (MESH:D008055), DHA (MESH:D004281), Agarose (MESH:D012685), alpha-tocopherol (MESH:D024502), OH- (MESH:C031356), 2,2'-azobis(2-methylpropionamidine) dihydrochloride (MESH:C046728), TPTZ (MESH:C002849), polyphenols (MESH:D059808), flavonoid (MESH:D005419), ROS (MESH:D017382), peroxyl radical (MESH:C049375), xanthophylls (MESH:D024341), PBS (MESH:D007854), acetate (MESH:D000085), hydrogen (MESH:D006859), zeaxanthin (MESH:D065146), formazan (MESH:D005562), Oxygen (MESH:D010100), (-)-Epigallocatechin gallate (MESH:C045651), NaCl (MESH:D012965), Trolox (MESH:C010643), 4-(dimethylamino) benzaldehyde (MESH:C510241), singlet oxygen (MESH:D026082), methanol (MESH:D000432), 2,2-Diphenyl-1-picrylhydrazyl (MESH:C004931), ester (MESH:D004952), 2-(4-Iodophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H-tetrazolium (MESH:C110656), C (MESH:D002244), Resolvin D1 (MESH:C518399), N2 (MESH:D009584), Quercetin (MESH:D011794), bromophenol blue (MESH:D001978), PEG (MESH:D011092), uric acid (MESH:D014527), EDTA (MESH:D004492), DCFH-DA (MESH:C029569), disaccharide (MESH:D004187), D2 (MESH:C091377), EPA (MESH:D015118), H2O (MESH:D014867), lycopene (MESH:D000077276), tetrazolium salt (MESH:D013778), CuCl2 (MESH:C029892), free radical (MESH:D005609)
- **Species:** Hepatovirus A (no rank) [taxon 12092], Homo sapiens (human, species) [taxon 9606], Bos taurus (bovine, species) [taxon 9913]
- **Cell lines:** HA — Homo sapiens (Human), Neuroblastoma, Cancer cell line (CVCL_D044)

## Full text

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## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12937457/full.md

## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937457/full.md

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Source: https://tomesphere.com/paper/PMC12937457