# Black Currant Extract Protects against Oxidative Stress in SH-SY5Y Cells and High-Fat Diet-Induced Cognitive Impairment in C57BL/6 Mice

**Authors:** Sungbin Im, Kwan Joong Kim, Gyo-Ha Hwang, Tae Gyu Nam, Jong Suk Lee, Ho Jin Heo, Dae-Ok Kim

PMC · DOI: 10.4014/jmb.2601.01068 · Journal of Microbiology and Biotechnology · 2026-03-11

## TL;DR

Black currant extract protects brain cells from oxidative stress and improves cognitive function in mice fed a high-fat diet.

## Contribution

This study demonstrates the neuroprotective effects of black currant extract through antioxidant activity and cognitive improvement in a mouse model of metabolic syndrome.

## Key findings

- BCE restored SH-SY5Y cell viability to 77% of control levels under oxidative stress.
- BCE treatment improved spatial memory consolidation in high-fat diet-fed mice.
- BCE inhibited acetylcholinesterase and butyrylcholinesterase in a dose-dependent manner.

## Abstract

Black currant (Ribes nigrum L.) is rich in anthocyanins and other phenolic compounds with diverse health benefits. This study investigated the neuroprotective effects of black currant extract (BCE) using integrated in vitro and in vivo approaches. UHPLC-MS/MS analysis identified four major anthocyanins in BCE: delphinidin 3-O-glucoside, delphinidin 3-O-rutinoside, cyanidin 3-O-glucoside, and cyanidin 3-O-rutinoside. In vitro, BCE protected SH-SY5Y neuroblastoma cells against H2O2-induced oxidative stress in a dose-dependent manner, restoring cell viability to 77% of control levels at 50 mg/l. BCE also exhibited dose-dependent inhibition of acetylcholinesterase and butyrylcholinesterase, demonstrating cholinergic-enhancing properties. In vivo, C57BL/6 mice were fed a high-fat diet (HFD) for 4 weeks to induce obesity, followed by 4 weeks of oral BCE administration (50 or 200 mg/kg /day) with continued HFD feeding. Cognitive function was assessed using the Y-maze, passive avoidance, and Morris water maze tests. BCE treatment (50 mg/kg/day) significantly increased the time spent in the target quadrant compared with the HFD-only group (p < 0.05), suggesting that BCE mitigates HFD-induced cognitive impairment by enhancing spatial memory consolidation. BCE also showed trends toward improved performance in Y-maze and passive avoidance tests, though these did not reach statistical significance. These findings demonstrate that BCE exerts multi-target neuroprotective effects through antioxidant activity, cholinesterase inhibition, and amelioration of obesity-associated cognitive deficits, supporting its potential as a functional food ingredient for cognitive health in metabolic syndrome.

## Linked entities

- **Chemicals:** H2O2 (PubChem CID 784)
- **Diseases:** metabolic syndrome (MONDO:0000816), obesity (MONDO:0011122)

## Full-text entities

- **Genes:** ACHE (acetylcholinesterase (Yt blood group)) [NCBI Gene 43] {aka ACEE, ARACHE, N-ACHE, YT}, BCHE (butyrylcholinesterase) [NCBI Gene 590] {aka BCHED, CHE1, CHE2, E1}
- **Diseases:** Cognitive Impairment (MESH:D003072), metabolic syndrome (MESH:D024821), neuroblastoma (MESH:D009447), obesity (MESH:D009765)
- **Chemicals:** H2O2 (MESH:D006861), BCE (-), anthocyanins (MESH:D000872), cyanidin 3-O-glucoside (MESH:C462279), Fat (MESH:D005223), cyanidin 3-O-rutinoside (MESH:C428983)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Ribes nigrum (European black currant, species) [taxon 78511]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12991935/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12991935/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12991935/full.md

---
Source: https://tomesphere.com/paper/PMC12991935