# Investigating the protective and therapeutic potential of new generation antioxidant combinations in the brain: an experimental aging model

**Authors:** Büşra Dönmez, Elif Naz Gürsoy, Kanuni Barbaros Balabanli, Şule Coşkun Cevher

PMC · DOI: 10.1007/s10522-026-10399-z · Biogerontology · 2026-02-05

## TL;DR

This study shows that combining squalene and saponin can reduce brain aging-related oxidative stress in rats.

## Contribution

The first demonstration of combined squalene and saponin's protective effects against brain aging in an experimental model.

## Key findings

- Combined SQ and SP reduced oxidative stress markers like MDA, NOx, and PC in brain tissue.
- The treatment increased antioxidant defenses such as GSH and AA levels.
- Aging-related molecules like FOXO3A, NRF2, and SIRT1 were upregulated with the combination.

## Abstract

The increasing elderly population has brought healthy aging into focus. Aging is a multifactorial process characterized by the progressive decline of cellular and tissue functions, largely due to cumulative oxidative stress. Antioxidant-based strategies have therefore gained prominence as potential interventions. This study investigated the protective and therapeutic effects of Squalene (SQ) and Saponin (SP), individually and in combination, on aging-related biomarkers in brain tissue using a D-Galactose (D-Gal)-induced rat model. Forty-eight male Sprague–Dawley rats (200–250 g) were randomly divided into eight groups (n = 6). Aging was induced in four groups via intraperitoneal administration of D-Gal (300 mg/kg/day) for six weeks. One group received no antioxidants, while others were treated orally with SQ (2.66 mL/kg/day), SP (100 mg/kg/day), or their combination. Non-aging groups received the same antioxidant treatments without D-Gal. At the end of the intervention, brain tissues were collected for biochemical analysis. Spectrophotometric assessments included Malondialdehyde (MDA), Glutathione (GSH), Nitric oxide derivatives (NOx), Ascorbic acid (AA), and Protein carbonyls (PC). Forkhead Box O3A (FOXO3A), Nuclear factor erythroid 2-related factor 2 (NRF2), Sirtuin 1 (SIRT1), Paraoxonase 1 (PON1), and Klotho were quantified by ELISA. Combined SQ and SP treatment significantly decreased oxidative stress markers (MDA, NOx, PC) and increased antioxidant defenses (GSH, AA) as well as aging-related molecules (FOXO3A, NRF2, SIRT1, PON1, Klotho) (p < 0.05). Serum Alanine Aminotransferase (ALT) and Aspartate Aminotransferase (AST) levels were also reduced. These findings demonstrate, for the first time, that combined SQ and SP administration can mitigate aging-related oxidative stress and molecular alterations in brain tissue.

## Linked entities

- **Genes:** FOXO3 (forkhead box O3) [NCBI Gene 2309], GABPA (GA binding protein transcription factor subunit alpha) [NCBI Gene 2551], SIRT1 (sirtuin 1) [NCBI Gene 23411], PON1 (paraoxonase 1) [NCBI Gene 5444], CG9701 (uncharacterized protein) [NCBI Gene 39872]
- **Chemicals:** Squalene (PubChem CID 638072), Saponin (PubChem CID 198016), D-Galactose (PubChem CID 206), Malondialdehyde (PubChem CID 10964), Glutathione (PubChem CID 124886), Ascorbic acid (PubChem CID 9888239), Alanine Aminotransferase (PubChem CID 251717)

## Full-text entities

- **Genes:** Got2 (glutamic-oxaloacetic transaminase 2) [NCBI Gene 25721] {aka ASPATA, mAAT}, Pon1 (paraoxonase 1) [NCBI Gene 84024], Podxl (podocalyxin-like) [NCBI Gene 192181] {aka PC, PCLP-1, podocalyxin}, Nfe2l2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 83619], Nos2 (nitric oxide synthase 2) [NCBI Gene 24599] {aka Nos2a, iNos}, Hmox1 (heme oxygenase 1) [NCBI Gene 24451] {aka HEOXG, Heox, Hmox, Ho-1, Ho1, hsp32}, Sirt1 (sirtuin 1) [NCBI Gene 309757] {aka Sir2}, Pon3 (paraoxonase 3) [NCBI Gene 312086], Foxo3 (forkhead box O3) [NCBI Gene 294515] {aka Fkhrl1, Foxo3a}, Kl (Klotho) [NCBI Gene 83504]
- **Diseases:** brain dysfunction (MESH:D001927), inflammation (MESH:D007249), cognitive decline (MESH:D003072), ischemia (MESH:D007511), hepatocellular injury (MESH:D056486), neuronal (MESH:D009410), mitochondrial damage (MESH:D028361), neuroinflammatory (MESH:D000090862), liver dysfunction (MESH:D017093), neurodegeneration (MESH:D019636)
- **Chemicals:** xylazine (MESH:D014991), ethyl acetate (MESH:C007650), 2,4-dinitrophenylhydrazine (MESH:C004787), flavonoids (MESH:D005419), KCl (MESH:D011189), NaCl (MESH:D012965), MDA (MESH:D008315), SP (MESH:D012503), butylated hydroxytoluene (MESH:D002084), H2SO4 (MESH:C033158), ethylenediaminetetraacetic acid (MESH:D004492), Ethanol (MESH:D000431), Alpha-lipoic acid (MESH:D008063), polyunsaturated fatty acids (MESH:D005231), lipid hydroperoxide (MESH:D008054), phosphate (MESH:D010710), ROS (MESH:D017382), meta- phosphoric acid (MESH:C043639), nitrite (MESH:D009573), acid (MESH:D000143), terpenoid (MESH:D013729), oxygen (MESH:D010100), perchloric acid (MESH:C576518), polyphenols (MESH:D059808), nitrate (MESH:D009566), Nitric oxide (MESH:D009569), PC (-), Thiobarbituric acid (MESH:C029684), guanidine HCl (MESH:D019791), SQ (MESH:D013185), RNS (MESH:D026361), AA (MESH:D001205), sodium citrate (MESH:D000077559), D-Gal (MESH:D005690), nitrogen (MESH:D009584), lipid (MESH:D008055), TCA (MESH:D014238), GSH (MESH:D005978), advanced glycation end products (MESH:D017127), Sodium phosphate (MESH:C018279), HCl (MESH:D006851)
- **Species:** Panax japonicus (chikusetsu-ninjin, species) [taxon 44685], Rattus norvegicus (brown rat, species) [taxon 10116], Meleagris gallopavo (common turkey, species) [taxon 9103]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12876541/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12876541/full.md

## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12876541/full.md

---
Source: https://tomesphere.com/paper/PMC12876541