Integrative Metabolomics and Systems Pharmacology Reveal PPARγ-Centered Antidiabetic Mechanisms of Caulerpa racemosa and Its Bioactive Compounds
Type 2 diabetes mellitus (T2DM) is a complex metabolic disorder requiring safe, multitarget therapeutic strategies. Marine macroalgae represent an underexplored source of bioactives with pleiotropic metabolic effects. This study investigated the antidiabetic potential of an ultrasound-assisted ethanolic extract of <i>Caulerpa racemosa</i> (UAECr) and its key phytosterol, campesterol, through an integrative framework combining metabolomics, network pharmacology, molecular docking, molecular dynamics simulation, and in vitro validation. Untargeted ultra-high-performance liquid chromatography-high-resolution mass spectrometry (UHPLC-HRMS) metabolomics characterized UAECr constituents, followed by in silico bioactivity prediction, target-network analysis, molecular docking, and 100 ns molecular dynamics simulation of the peroxisome proliferator-activated receptor gamma (PPARγ)-campesterol complex. Functional validation was performed in differentiated 3T3-L1 adipocytes assessing glucose uptake, PPARγ expression, dipeptidyl peptidase 4 (DPP-4) inhibition, and cytotoxicity. Metabolomics identified campesterol as a prominent bioactive. Network pharmacology highlighted PPARγ as a central hub, supported by strong docking affinity of campesterol toward PPARγ (-11.4 kcal/mol) and DPP-4 (-8.3 kcal/mol). Molecular dynamics simulations demonstrated stable PPARγ-campesterol interactions, with preserved protein compactness and low residue fluctuation. In vitro, UAECr and campesterol significantly enhanced glucose uptake (up to 134% vs. control, <i>p</i> < 0.001), upregulated PPARγ expression (4-fold, <i>p</i> < 0.0001), and moderately inhibited DPP-4 activity (<i>p</i> < 0.01) without cytotoxicity. <i>C. racemosa</i>-derived extracts and campesterol exert antidiabetic effects primarily via stable PPARγ-mediated insulin sensitization with complementary DPP-4 modulation, supporting its potential as a marine-derived functional food candidate.
Authors
- Dante Saksono Harbuwono (ORCID: https://orcid.org/0000-0002-6006-2719)
- Nurpudji Astuti Taslim (ORCID: https://orcid.org/0000-0003-1349-5367)
- Fahrul Nurkolis (ORCID: https://orcid.org/0000-0003-2151-0854)
- Happy Kurnia Permatasari (ORCID: https://orcid.org/0000-0002-4777-624X)
- Adha Fauzi Hendrawan (ORCID: https://orcid.org/0009-0004-9222-1173)
- Arifa Mustika
- Reggie Surya
- Evhy Apryani
- Izza Afkarina
- Annette d’Arqom
- Nurmawati Fatimah
- Raymond Rubianto Tjandrawinata
Institutions
- Atma Jaya Catholic University of Indonesia (ID)
- Universitas Gadjah Mada (ID)
- Binus University (ID)
- University of Brawijaya (ID)
- Sunan Kalijaga State Islamic University Yogyakarta (ID)
- Universitas Airlangga (ID)
- Muhammadiyah University of Yogyakarta (ID)
- Rumah Sakit Umum Pusat Nasional Dr. Cipto Mangunkusumo (ID)
- Hasanuddin University (ID)
Publication Details
- Journal
- Marine Drugs
- Published
- 2026-02-17
- DOI
- https://doi.org/10.3390/md24020082
- Primary Topic
- Seaweed-derived Bioactive Compounds
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Lembaga Penelitian dan Pengabdian Kepada Masyarakat