From Herbal Tea to Science: Phytochemical and Biological Investigation of <i>Ajuga chamaepitys</i> subsp. chia (Lamiaceae) With Molecular Docking Analysis

The hypothesis that insulin resistance and impaired insulin-like growth factor signaling contribute to Alzheimer's disease (AD) has led to the designation of AD as "type 3 diabetes." Ajuga chamaepitys subsp. chia is traditionally used in T & uuml;rkiye as an analgesic, tonic, and for the external treatment of hemorrhoids and wound healing. This study evaluates antioxidant, antidiabetic, and anticholinesterase activities of methanolic, aqueous extracts, and essential oils from the flowering aerial parts of A. chamaepitys subsp. chia, along with their phytochemical profiles (GC-MS/MS), morphological-anatomical characteristics, and molecular docking analysis. The essential oil yield was 0.002%, comprising 45 compounds (92.5%), with beta-pinene (19.8%), alpha-pinene (12.8%), and germacrene D (10.0%) as major constituents, dominated by monoterpene (39.8%) and sesquiterpene hydrocarbons (23.5%). The methanolic extract exhibited moderate bioactivity, achieving 28.36% alpha-amylase inhibition at 5000 mu g/mL and 21.85% acetylcholinesterase inhibition at 100 mu g/mL, while also demonstrating notable antioxidant activity with 23.013% ABTS center dot+ and 8.114% DPPH center dot scavenging. It showed the highest total phenolic (14.261 mu g GAE/mg) and tannin content (34.444 mu g TAE/mg) among the tested extracts. Morphologically, the plant features hairy stems and tripartite leaves with a cuticle, trichomes, and diacytic stomata, while anatomically, it presents collenchyma, starch-filled parenchyma, and a distinct cambium in the stem. Molecular docking studies revealed that germacrene D exhibited strong binding affinities to acetylcholinesterase, butyrylcholinesterase, alpha-amylase, and alpha-glucosidase, suggesting multitarget inhibition potential. These findings support the traditional use of A. chamaepitys subsp. chia and highlight its promise as a natural source for therapeutic agents targeting oxidative stress, diabetes, and neurodegenerative diseases.

Dergi

FOOD SCIENCE & NUTRITION

Yıl

2025

Cilt

13

Sayı

8

ISSN

2048-7177

DOI

10.1002/fsn3.70749

WoS UID

WOS:001559319600041