# Antidiabetic Potential of Sea Urchin Tripneustes gratilla Nanosuspension Based on In Vitro Enzyme Inhibition, In Vivo Evaluation, and Chemical Profiling Approaches

**Authors:** Ahmed K. B. Aljohani, Aryam S. Alharbi, Asalah B. Alhazmi, Manhal N. Hudhayri, Israa B. Almuwallad, Maya A. Alhazmi, Shuruq M. Almohammadi, Atheer I. Alsaleh, Ahmed Aldhafiri, Heba M. Eltahir, Mekky M. Abouzied, Hamad Alrbyawi, Mohamed S. Mohamed, Mahran Mohamed Abdel-Emam, Fahd M. Abdelkarem

PMC · DOI: 10.3390/cimb48010008 · Current Issues in Molecular Biology · 2025-12-21

## TL;DR

This study explores the antidiabetic potential of a sea urchin extract nanosuspension, showing it can lower blood sugar and protect against diabetes-related damage.

## Contribution

The study introduces a nanosuspension formulation of Tripneustes gratilla extract with demonstrated antidiabetic effects in both in vitro and in vivo models.

## Key findings

- The extract showed strong α-amylase inhibition and moderate α-glucosidase inhibition.
- The nanosuspension improved insulin levels and reduced blood glucose in diabetic rats.
- The extract contains bioactive compounds like terpenes and polyunsaturated fatty acids.

## Abstract

Diabetes mellitus represents one of the main health challenges worldwide, characterized by hyperglycemia and long-term serious microvascular and macrovascular complications. Marine organisms are a promising reservoir of bioactive metabolites for developing effective antidiabetic therapies with fewer side effects. The sea urchin Tripneustes gratilla (T. gratilla) is widely distributed in the Red Sea, with limited reports of its pharmacological activities and chemical characterization. In this study, a nanosuspension formulation of T. gratilla extract (T. gratilla-NS) was developed to enhance the bioavailability of its bioactive constituents. This study investigated the antidiabetic potential of T. gratilla extract through an integrated approach encompassing chemical profiling of the extract, assessment of its alcoholic extract for in vitro inhibitory effects on α-amylase and α-glucosidase, and in vivo evaluation of T. gratilla-NS in an alloxan-induced diabetic rat model. We found that the alcoholic extract showed potent inhibitory action toward α-amylase with IC50 5.31 ± 0.05 µg/mL and moderate inhibitory activity toward α-glucosidase with IC50 21.36 ± 0.06 µg/mL. T. gratilla-NS significantly increased insulin levels, reduced blood glucose levels, and restored pancreatic damage. Furthermore, it enhanced the levels of superoxide dismutase and total antioxidant capacity with a concomitant decrease in malondialdehyde concentration in pancreatic tissue. The observed activities could be attributed to a wide array of diverse compounds, terpenes, mainly sesquiterpenes, diterpenes, steroids, and polyunsaturated fatty acids detected by GC-MS, compounds with a phenolic nucleus equal to 54.26 ± 1.27 mg. GAE/g of extract. This research highlights the dual role of T. gratilla-NS in combating diabetes and subsequently attenuating its associated complications.

## Linked entities

- **Chemicals:** malondialdehyde (PubChem CID 10964)
- **Diseases:** diabetes mellitus (MONDO:0005015)
- **Species:** Tripneustes gratilla (taxon 7673), Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** Diabetes mellitus (MESH:D003920), hyperglycemia (MESH:D006943), pancreatic damage (MESH:D010182)
- **Chemicals:** polyunsaturated fatty acids (MESH:D005231), terpenes (MESH:D013729), steroids (MESH:D013256), alloxan (MESH:D000496), malondialdehyde (MESH:D008315), NS (MESH:D009584), diterpenes (MESH:D004224), glucose (MESH:D005947), T. gratilla (-), sesquiterpenes (MESH:D012717)
- **Species:** Tripneustes gratilla (Hawaiian sea urchin, species) [taxon 7673], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12839668/full.md

## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12839668/full.md

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Source: https://tomesphere.com/paper/PMC12839668