Pharmacognosy intro
Dong Quai's primary active compounds include phthalides (Z-ligustilide at 40-60% of the volatile fraction, Z-butylidenephthalide, senkyunolide A) which are antispasmodic and vasodilatory; ferulic acid as the primary phenolic acid providing antioxidant, anti-inflammatory, and anti-platelet aggregation activity; polysaccharides (Angelica sinensis polysaccharides/ASP) with immunomodulatory and hematopoietic stimulation properties; and coumarins (osthole, bergapten) which carry phototoxicity risk. The mechanism of action features a dual uterine modulation: Z-ligustilide and ferulic acid produce paradoxical effects, stimulating the atonic uterus while relaxing the hypertonic uterus. This is NOT simple "uterine tonic" but regulatory. ASP polysaccharides stimulate bone marrow proliferation and increase erythropoietin, providing a mechanistic basis for the traditional "blood builder" reputation. Ferulic acid inhibits NF-κB activation and reduces TNF-α, IL-1β, and IL-6 production. Phthalides relax vascular smooth muscle via calcium channel modulation. Dong Quai is NOT estrogenic in isolation, whole-root extract does not show significant estrogen receptor binding in most assays.