# Rice bran extract attenuates cognitive impairment by enhancing pancreatic β-cell insulin secretion in STZ-induced diabetic rats targeting the PPARγ/PDX1 pathway

**Authors:** Madonna Magdy Youssef, Mohammed Farrag El-Yamany, Reham Mahmoud Abdel-Kader, Ola Ahmed Heikal

PMC · DOI: 10.1007/s11011-025-01639-1 · 2025-06-19

## TL;DR

Rice bran extract improves cognitive function in diabetic rats by boosting insulin production through a specific cellular pathway.

## Contribution

The study reveals that rice bran extract enhances insulin secretion and cognitive function in diabetic rats via the PPARγ/PDX1 pathway.

## Key findings

- Rice bran extract increased insulin levels and improved pancreatic function in diabetic rats.
- RBE boosted gene expression of PPARγ, SERCA, and PrKC, but not PDX1.
- RBE restored cognitive abilities in diabetic rats as shown by behavioral tests.

## Abstract

Type I diabetes (T1D), also known as juvenile diabetes, is an autoimmune disease that causes gradual destruction of pancreatic cells and leads to intellectual disability, neuropathy, cognitive impairment, and impaired learning ability in children. Despite standard treatment with synthetic human insulin, T1D patients can maintain up to 40% of their insulin-producing islets. PPARγ receptor activation research that aims to restore β-cell biology could help reverse the loss of pancreatic mass that comes with getting older and improve β-cell function. Egyptian RB ethanol extract (RBE), previously reported with PPARγ agonist activity, showed an increase in insulin secretion both in vivo and in INS-1 cells. The exact antidiabetic RBE mechanism is still unclear. The present study aims to investigate the molecular RBE mechanism in glucose-stimulating insulin secretion and restoration of β cell function. A diabetic rat streptozotocin (STZ) model was used; five groups were designed. The STZ-diabetic rats were treated with RBE daily for 21 days compared to an insulin-treated group. Biochemical parameters and quantitative RT-PCR of β-cell genes related to the PPAR/PDX1 signaling pathway were performed, and the influence on cognitive ability was confirmed by behavioral testing (Y-maze and NOR) and histological examination. The RBE-treated group reversed blood glucose, Glut2, Ca2 +, and insulin levels in diabetic rats, with pancreatic insulin levels significantly increasing compared to the insulin group. With the exception of PDX1, RBE boosted PPARγ, SERCA, and PrKC gene expression. RBE also restored cognitive functions. This study suggests that RBE may enhance memory and cognition by increasing peripheral insulin secretion through PPARγ regulator activity.

Schematic pathway for insulin secretion via PPAR-γ dependent pathway in type 1 diabetes

The online version contains supplementary material available at 10.1007/s11011-025-01639-1.

Glucose transport in β-cells plays a significant role for insulin secretion.

Egyptian Rice bran extract treatment enhanced insulin secretion.

Egyptian Rice bran extract boosted PPARℽ, SERCA, and PrKC gene expression.

Egyptian Rice bran extract restored pancreatic structure more effectively.

RBE may enhance memory and cognition by increasing peripheral insulin secretion.

The online version contains supplementary material available at 10.1007/s11011-025-01639-1.

## Linked entities

- **Genes:** PDX1 (pancreatic and duodenal homeobox 1) [NCBI Gene 3651], PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468], SERCA (Sarco/endoplasmic reticulum Ca(2+)-ATPase) [NCBI Gene 49297], prkC (protein serine/threonine kinase) [NCBI Gene 936132], SLC2A2 (solute carrier family 2 member 2) [NCBI Gene 6514]
- **Diseases:** Type I diabetes (MONDO:0005147), T1D (MONDO:0005147)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Pdx1 (pancreatic and duodenal homeobox 1) [NCBI Gene 29535] {aka Idx1, Ipf1, Stf1}, Pparg (peroxisome proliferator-activated receptor gamma) [NCBI Gene 25664] {aka PPARgamma2}, Ppara (peroxisome proliferator activated receptor alpha) [NCBI Gene 25747] {aka PPAR}, Prkcg (protein kinase C, gamma) [NCBI Gene 24681] {aka PKC, PKCI, Prkc, Prkcc, RATPKCI}, Slc2a2 (solute carrier family 2 member 2) [NCBI Gene 25351] {aka GTT2, Glut2}
- **Diseases:** loss of pancreatic mass (MESH:D010195), impaired learning ability (MESH:D007859), neuropathy (MESH:D009422), diabetic (MESH:D003920), cognitive impairment (MESH:D003072), T1D (MESH:D003922), intellectual disability (MESH:D008607), autoimmune disease (MESH:D001327)
- **Chemicals:** STZ (MESH:D013311), Rice bran extract (MESH:D000073879), blood glucose (MESH:D001786), Ca2 + (-), glucose (MESH:D005947)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** INS-1 — Rattus norvegicus (Rat), Rat insulinoma, Cancer cell line (CVCL_0352)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12178994/full.md

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Source: https://tomesphere.com/paper/PMC12178994