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Eucommia ulmoides Bark Extract Attenuates Oxidative Damage and H2O2-Induced Hair Follicle Suppression in Cellular and
Xiaojin Liu1,2, Shuyue Chen1,2, Yanyan Zhang1,2
1Anhui Provincial Key Laboratory of Molecular Enzymology and Mechanism of Major Metabolic Diseases, College of Life Sciences, Anhui Normal University, Wuhu 241000, China.
Abstract:
Oxidative stress contributes to hair follicle aging, melanocyte dysfunction, and androgen-related hair disorders, yet chemically characterized botanical interventions with multi-target activities remain incompletely defined. This study evaluated the antioxidant, follicle-supporting, and antiandrogenic potential of Eucommia ulmoides bark extract (EUE) using integrated in vitro and in vivo approaches and characterized EUE by HPLC-DAD using geniposidic acid and chlorogenic acid as representative marker compounds. Chlorogenic acid and geniposidic acid were present at 3.21 ± 0.01 and 1.88 ± 0.15 mg/g extract, respectively. In replicate-well assays using H2O2-challenged B16 melanoma cells, EUE increased superoxide dismutase activity and reduced malondialdehyde accumulation. Technical-triplicate RT-qPCR measurements and a single Western blot experiment showed descriptive changes in Nrf2 and HO-1 markers; these observations are exploratory and require independent biological replication. In HDPCs, replicate-well viability assays and technical-triplicate RT-qPCR measurements indicated concentration-associated viability changes and descriptive changes in VEGF, Wnt5a, and β-catenin transcripts. EUE also inhibited 5α-reductase activity in a cell-free assay, although the non-monotonic response and the much higher mass concentrations used relative to finasteride preclude potency equivalence. In male C57BL/6 mice, topical EUE attenuated H2O2-induced suppression of hair follicle elongation and improved follicular morphology. Overall, EUE is a chemically characterized botanical extract with preliminary biological activities relevant to oxidative stress- and androgen-associated hair disorders; independent replication, active-compound identification, marker-specific permeation, and protein-level validation of the measured markers remain necessary.
