In vitro anti-diabetic activities of phytochemicals isolated from Cornus officinalis fruits

Four previously undescribed compounds, including two dihydroisocoumarin glycosides (1 and 2), a truxillic acid derivative (4), and a cadinane-type sesquiterpene (5), were isolated from the fruits of Cornus officinalis Sieb. et Zucc., along with seven known ones (3, 6-11). Their chemical structures were determined by extensive spectroscopic methods and computational analyses. All isolated compounds were evaluated for the effects on glucose consumption in insulin-resistant (IR) HepG2 cells. The compounds exhibited no significant cytotoxicity at 10.0 μM in the CCK-8 assay. Compounds 2, 3, and 8 significantly increased glucose consumption (P < 0.05) at 5.0 and 10.0 μM. The 2-NBDG labeling indicated that compounds 2 and 8 significantly increased glucose uptake at 10 μM. Moreover, compounds 2 and 8 also significantly increased insulin receptor (INSR) expression, indicating their potential to upregulate the INSR in the cytomembrane and enhance glucose uptake.

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Publication Details

Journal
Fitoterapia
Published
2025-11-11
DOI
https://doi.org/10.1016/j.fitote.2025.106984
Primary Topic
Natural Antidiabetic Agents Studies
Type
article
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article

In vitro anti-diabetic activities of phytochemicals isolated from Cornus officinalis fruits

Xiaoke Zheng, Meng Yang, Shuangshuang Xie, Shi‐Qi Zhou et al.
Fitoterapia
Natural Antidiabetic Agents Studies
article

In vitro anti-diabetic activities of phytochemicals isolated from Cornus officinalis fruits

Xiaoke Zheng, Meng Yang, Shuangshuang Xie, Shi‐Qi Zhou, Yan‐Jun Sun, Zhi‐You Hao, Meng Li, Xiaolan Wang, Chaoyuan Xiao, Yan-Gang Cao, Junyang Zhang, Wei-Sheng Feng
article en

Abstract

Four previously undescribed compounds, including two dihydroisocoumarin glycosides (1 and 2), a truxillic acid derivative (4), and a cadinane-type sesquiterpene (5), were isolated from the fruits of Cornus officinalis Sieb. et Zucc., along with seven known ones (3, 6-11). Their chemical structures were determined by extensive spectroscopic methods and computational analyses. All isolated compounds were evaluated for the effects on glucose consumption in insulin-resistant (IR) HepG2 cells. The compounds exhibited no significant cytotoxicity at 10.0 μM in the CCK-8 assay. Compounds 2, 3, and 8 significantly increased glucose consumption (P < 0.05) at 5.0 and 10.0 μM. The 2-NBDG labeling indicated that compounds 2 and 8 significantly increased glucose uptake at 10 μM. Moreover, compounds 2 and 8 also significantly increased insulin receptor (INSR) expression, indicating their potential to upregulate the INSR in the cytomembrane and enhance glucose uptake.

FitoterapiaVol. 188
Henan University of Traditional Chinese Medicine (CN), First Affiliated Hospital of Henan University (CN)
Openalex Percentile: Top 54%
Natural Antidiabetic Agents Studies
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