ArticleJournal of musculoskeletal & neuronal interactions2025
Stigmasterol, a Major Component of
Article in Journal of musculoskeletal & neuronal interactions, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed.
- Stigmasterol upregulates Akt/mTOR/p70S6K signaling through SYVN1 to alleviate osteoporosis in ovariectomized rats.European journal of nutrition · 2026Article
- Research Progress on the Therapeutic Mechanisms of Stigmasterol for Multiple Diseases.Molecules (Basel, Switzerland) · 2025Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectivesThis study investigated the therapeutic effects of stigmasterol (STG), derived from
methodsTwenty-four Male Sprague-Dawley rats (6 weeks old) were used to establish a T2DM model and were divided into four groups: normal diet (ND), high-fat diet (HFD), low-dose STG (STG-L, 100 mg/kg), and high-dose STG (STG-H, 200 mg/kg). The rats received daily gavage treatments for four weeks. Therapeutic effects were assessed by examining femoral bone structure, serum bone formation markers (P1NP, osteocalcin, and osteoprotegerin), bone resorption indices (CTX-1 and RANKL), and osteogenic protein expression (Runx2, osteopontin, and COL1A1).
resultsSTG significantly reduced fasting blood glucose levels and improved insulin resistance in T2DM rats. It enhanced trabecular bone microstructure, with the STG-H group demonstrating superior effects. Compared to the HFD group, STG increased bone mineral density, bone volume fraction (BV/TV), and trabecular thickness, while reducing bone surface-to-volume ratio (BS/BV) and trabecular separation. STG also elevated serum levels of P1NP, osteocalcin, and osteoprotegerin, while reducing CTX-1 and RANKL. Western blot analysis revealed increased expression of Runx2, osteopontin, and COL1A1 in femoral tissues.
conclusionsSTG appears to alleviate osteoporosis in diabetes by improving bone microstructure, promoting bone formation, and reducing bone resorption, indicating its potential as a therapeutic option for managing osteoporosis.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.