# Impact of Sappan Wood Extract as Iron Chelator Adjuvant on Iron Concentration and Macrophage Polarization in Rat Spleen

**Authors:** Mohammad Ghozali, Ratu Safitri, Erick Khristian, Amethyst Puspita Ainni, Yasmi Purnamasari Kuntana, Muhamad Hasan Bashari, Jeri Nobia Purnama

PMC · DOI: 10.30476/ijms.2024.103099.3629 · Iranian Journal of Medical Sciences · 2025-07-01

## TL;DR

This study explores how Sappan wood extract, when used with an iron chelator, can reduce iron buildup and improve immune cell balance in rats with iron overload.

## Contribution

The study introduces Sappan wood extract as a novel adjuvant for iron chelation therapy, showing its efficacy in modulating macrophage polarization.

## Key findings

- Sappan wood extract at 50 mg/Kg BW reduced spleen iron levels and increased anti-inflammatory M2 macrophages.
- At 100 mg/Kg BW, the extract decreased pro-inflammatory M1 macrophage intensity significantly.
- Sappan wood extract showed therapeutic potential comparable to Deferiprone in iron overload conditions.

## Abstract

Iron accumulation in the spleen of thalassemia patients disrupts macrophage polarization, impairs immune function, and increases mortality. Sappan wood (Biancaea sappan L.) extract exhibits iron-chelating and immunomodulatory properties, making it a potential adjuvant with Deferiprone (DFP). This study aimed to assess the effects of Sappan wood extract (SWE) as a DFP adjuvant in rat models of iron overload.

This experimental study was conducted from January to March 2024 at Padjadjaran University, Indonesia. Thirty-five rats were divided into seven groups: normal, iron overload (IO) induced by iron dextran (ID) at a cumulative dose of 60 mg/Kg body weight (BW), positive control receiving DFP, and four groups receiving DFP+SWE at different doses of 50, 100, 150, and 200 mg/Kg BW. Iron levels and macrophage polarization (pro-inflammatory M1 and anti-inflammatory M2) in the spleen were assessed.

SWE at 50 mg/Kg BW significantly reduced spleen iron levels to 60.77 ppm/mg and increased M2 intensity (P<0.001 compared to the IO group). At 100 mg/Kg BW, SWE effectively decreased M1 macrophage intensity (P=0.001 compared to the IO group).

SWE at 50 mg/Kg BW was comparable to DFP in reducing the spleen iron levels and M1 macrophage intensity, while 100 mg/Kg BW enhanced M2 macrophage polarization. These findings highlighted SWE’s potential as a therapeutic adjuvant in IO conditions.

## Linked entities

- **Chemicals:** iron (PubChem CID 23925), Deferiprone (PubChem CID 2972), iron dextran (PubChem CID 105075)
- **Diseases:** thalassemia (MONDO:0000984), iron overload (MONDO:0800385)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Diseases:** thalassemia (MESH:D013789), inflammatory (MESH:D007249), IO (MESH:D019190)
- **Chemicals:** DFP (MESH:D000077543), ID (MESH:D007505), Iron (MESH:D007501), SWE (-)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12334789/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12334789/full.md

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Source: https://tomesphere.com/paper/PMC12334789