Kalsiyum fruktoboratın SIRT1 enzim aktivitesi üzerindeki konsantrasyona bağlı inhibitör etkisi: Borik asit ile karşılaştırmalı bir analiz
JOURNAL OF BASIC AND CLINICAL HEALTH SCIENCES, cilt.10, ss.397-402, 2026 (ESCI, TRDizin)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 10
- Basım Tarihi: 2026
- Doi Numarası: 10.30621/jbachs.1949511
- Dergi Adı: JOURNAL OF BASIC AND CLINICAL HEALTH SCIENCES
- Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), TR DİZİN (ULAKBİM)
- Sayfa Sayıları: ss.397-402
- Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
- Dokuz Eylül Üniversitesi Adresli: Evet
Özet
ABSTRACT
Purpose: SIRT1 functions in regulatory mechanisms including cellular aging, apoptosis, glucose and lipid
metabolism, oxidative stress and inflammation. Studies show that SIRT1 inhibitors may affect various
types of cancer and metabolic disorders, making SIRT1 an important therapeutic target. Boric acid is an
inorganic boron compound with antimicrobial, antifungal and potential anticancer effects. Calcium
fructoborate, another boron compound found in vegetables and fruits, has anti-inflammatory, antioxidant
and anti-tumor effects. This study aimed to investigate the inhibitory potential of calcium fructoborate on
SIRT1 activity and to evaluate its possible use as a chemical tool for future studies targeting SIRT1
regulation.
Material and Methods: In this study, the effect of calcium fructoborate on SIRT1 activity was investigated
by a fluorescence-based method using human recombinant SIRT1.
Results: Calcium fructoborate inhibited SIRT1 activity in a concentration-dependent manner. Calcium
fructoborate significantly inhibited SIRT1 activity by 42% at a concentration of 20 mM (p < 0.001). Boric
acid did not produce a statistically significant or consistent concentration-dependent change in SIRT1
activity within the tested concentration range.
Conclusion: These preliminary cell-free findings suggest that calcium fructoborate inhibits SIRT1 activity,
indicating its potential as a chemical tool for studying the biological functions of SIRT1. However, the
biological relevance of this effect and its potential therapeutic implications require confirmation through
further studies in cellular and in vivo models.