Pomegranate peel extract nanoparticles enhance insulin production and antioxidant activity of diabetic rats

Hanan Yousri Ibrahim Al Sayed1, Mostafa I Abdelglil2, Hanan Ramadan H Mohamed1

  • 1Zoology Department, Faculty of Science, Cairo University, Giza 12613, Egypt.

Tissue & Cell
|March 3, 2026
PubMed

Insights

Pomegranate peel extract nanoparticles (PPE-NPs) show promise in treating Type 1 Diabetes Mellitus (T1DM) in rats. This study found PPE-NPs improved key health markers and organ function in diabetic rats.

Area of Science:

  • Biomedical Science
  • Pharmacology
  • Nanotechnology

Background:

  • Type 1 Diabetes Mellitus (T1DM) is a prevalent chronic disease in children and adolescents.
  • Pomegranate peel extract (PPE) possesses various therapeutic properties, including anti-inflammatory effects.
  • Chitosan nanoparticles offer a method to stabilize and deliver PPE.

Purpose of the Study:

  • To prepare and characterize Pomegranate Peel Extract-Chitosan Nanoparticles (PPE-NPs).
  • To evaluate the therapeutic potential of PPE-NPs in a rat model of Type 1 Diabetes Mellitus.

Main Methods:

  • PPE-NPs were synthesized using ionotropic gelation and characterized by spectroscopy and microscopy.
  • Type 1 Diabetes Mellitus was induced in rats using streptozotocin.
  • Diabetic rats were treated with chitosan nanoparticles or PPE-NPs, and various physiological and histological parameters were assessed.

Main Results:

  • PPE-NP administration significantly increased serum insulin, albumin, HDL-cholesterol, and antioxidant levels.
  • Treatment with PPE-NPs reduced glucose, triglycerides, LDL-cholesterol, and markers of oxidative stress and DNA damage.
  • Gene expression of adiponectin and leptin was significantly upregulated by PPE-NPs, with improved pancreatic, liver, and kidney histology.

Conclusions:

  • Pomegranate peel extract nanoparticles (PPE-NPs) demonstrate significant therapeutic effects in a rat model of Type 1 Diabetes Mellitus.
  • PPE-NPs enhance pancreatic, hepatic, and renal functions and structures in diabetic rats.
  • Potential antidiabetic mechanisms include improved beta-cell histology, increased insulin, and antioxidant activity.
Abstract