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March 30, 2026ACS Omega0 citationsOpen Access

Regulatory Effects of Pumpkin Seed Extract on Glucose Metabolism and Insulin Signaling in Diabetic Models

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YLYu‐Cheng LinPHPang-Kuei HsuMPMin‐Hsiung Pan

Key Points

  • This study aims to explore the antidiabetic effects of pumpkin seed extract on glucose metabolism and insulin signaling in diabetic models.
  • Used defatted pumpkin seed extract prepared by supercritical fluid extraction.
  • Administered PSE to streptozotocin-induced diabetic rats.
  • Conducted oral glucose tolerance tests to assess insulin sensitivity.
  • Performed RNA sequencing of insulin-resistant C2C12 myotubes to analyze gene expression.
  • Conducted western blot analysis to evaluate insulin receptor and Akt phosphorylation.
  • PSE supplementation significantly reduced fasting blood glucose, HbA1c, and fasting insulin levels.
  • Improved insulin sensitivity observed in a dose-dependent manner during glucose tolerance tests.
  • Increased expression of genes related to PI3K/Akt signaling and mitochondrial function found in C2C12 myotubes.
  • Enhanced phosphorylation of the insulin receptor and Akt was noted, suggesting activation of insulin signaling in skeletal muscle.

Abstract

Diabetes mellitus is a chronic metabolic disorder characterized by impaired insulin signaling and glucose homeostasis. In this study, a defatted pumpkin seed extract (PSE), prepared via supercritical fluid extraction, was investigated for its potential antidiabetic effects. In streptozotocin-induced diabetic rats, PSE supplementation significantly reduced fasting blood glucose, HbA1c (glycated hemoglobin), and fasting insulin levels and homeostasis model assessment of insulin resistance. Oral glucose tolerance tests revealed enhanced insulin sensitivity in a dose-dependent manner. RNA sequencing of insulin-resistant C2C12 myotubes revealed differentially expressed genes related to PI3K/Akt signaling and mitochondrial function. Western blot analysis further demonstrated increased phosphorylation of the insulin receptor and Akt, suggesting the PSE-mediated activation of insulin signaling in skeletal muscle. These preclinical findings warrant further clinical and safety evaluation of PSE and PSE-02 as nutraceutical candidates.

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Cite This Study

Lin et al. (2026) studied this question.

synapsesocial.com/papers/69ca12d4883daed6ee095213https://doi.org/10.1021/acsomega.5c13268
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