# Exploration of Potential Antidepressant Active Ingredients of Albiziae Flos via HS–GC–MS, Chemometrics, and Network Pharmacology

**Authors:** Dan Yang, Dan He, Yiwu Wang, Yuan Shen, Jialing Yu, Ruijia Yang, Lin Yang

PMC · DOI: 10.1155/jamc/2885034 · Journal of Analytical Methods in Chemistry · 2026-03-01

## TL;DR

This study explores the antidepressant properties of Albiziae Flos using advanced analytical and pharmacological methods to identify active compounds and their mechanisms.

## Contribution

The study introduces a novel integrated approach combining HS–GC–MS, chemometrics, and network pharmacology to evaluate AF's volatile components and antidepressant mechanisms.

## Key findings

- Identified 34 volatile compounds in Albiziae Flos with high consistency across 16 batches.
- Network pharmacology revealed 15 active components and 131 potential targets linked to antidepressant effects.
- Molecular docking showed strong binding affinity between linalool oxide and core targets via hydrogen and hydrophobic interactions.

## Abstract

Albiziae Flos (AF) is a traditional Chinese medicine with an extensive historical background. This study presented an integrated approach combining headspace–gas chromatography–mass spectrometry (HS–GC–MS), chemometrics, and network pharmacology to comprehensively evaluate the volatile components of AF and explore their potential antidepressant mechanisms. A total of 34 volatile compounds were identified through HS–GC–MS analysis. Fingerprint assessment revealed high consistency among 16 batches (similarity: 0.790–0.998), while chemometric analysis successfully discriminated samples from different geographical origins. Network pharmacology screening identified 15 active components and 131 potential targets, revealing multicomponent, multitarget characteristics of AF’s antidepressant effects. Molecular docking simulations demonstrated strong binding affinity between linalool oxide configurations and 12 core targets, primarily through hydrogen bonding and hydrophobic interactions. This work lies in its comprehensive investigation of AF’s volatile components using an integrated analytical–pharmacological approach, providing both a methodological framework for quality assessment and mechanistic insights for antidepressant drug development. Our findings established scientific foundations for quality control of AF and revealed its potential antidepressant mechanisms through multiple pathways.

## Linked entities

- **Chemicals:** linalool oxide (PubChem CID 22310)
- **Diseases:** depression (MONDO:0002050)

## Full-text entities

- **Genes:** OR1E1 (olfactory receptor family 1 subfamily E member 1) [NCBI Gene 8387] {aka HGM071, OR13-66, OR17-2, OR17-32, OR1E5, OR1E6}, SLC6A4 (solute carrier family 6 member 4) [NCBI Gene 6532] {aka 5-HTT, 5-HTTLPR, 5HTT, HTT, OCD1, SERT}, CROT (carnitine O-octanoyltransferase) [NCBI Gene 54677] {aka COT}, RAB9BP1 (RAB9B, member RAS oncogene family pseudogene 1) [NCBI Gene 9366] {aka RAB9P1}, FAM13C (family with sequence similarity 13 member C) [NCBI Gene 220965] {aka FAM13C1}, CASP5 (caspase 5) [NCBI Gene 838] {aka ICE(rel)III, ICEREL-III, ICH-3}, GRM5 (glutamate metabotropic receptor 5) [NCBI Gene 2915] {aka GPRC1E, MGLUR5, PPP1R86, mGlu5}, MAOB (monoamine oxidase B) [NCBI Gene 4129], PHACTR4 (phosphatase and actin regulator 4) [NCBI Gene 65979] {aka PPP1R124}, PSPHP1 (phosphoserine phosphatase pseudogene 1) [NCBI Gene 8781] {aka CO9, PSPHL}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, PTGS2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 5743] {aka COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2}, ENPEP (glutamyl aminopeptidase) [NCBI Gene 2028] {aka APA, CD249, gp160}, SLC28A2 (solute carrier family 28 member 2) [NCBI Gene 9153] {aka CNT2, HCNT2, HsT17153, SPNT1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, ARMC6 (armadillo repeat containing 6) [NCBI Gene 93436] {aka R30923_1}, PPARA (peroxisome proliferator activated receptor alpha) [NCBI Gene 5465] {aka NR1C1, PPAR, PPAR-alpha, PPARalpha, hPPAR}, WIPF1 (WAS/WASL interacting protein family member 1) [NCBI Gene 7456] {aka PRPL-2, WAS2, WASPIP, WIP}, NR3C1 (nuclear receptor subfamily 3 group C member 1) [NCBI Gene 2908] {aka GCCR, GCR, GCRST, GR, GRL}, SOX30 (SRY-box transcription factor 30) [NCBI Gene 11063], ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, GPR143 (G protein-coupled receptor 143) [NCBI Gene 4935] {aka NYS6, OA1}, MAOA (monoamine oxidase A) [NCBI Gene 4128] {aka BRNRS, MAO-A}, CLEC4D (C-type lectin domain family 4 member D) [NCBI Gene 338339] {aka CD368, CLEC-6, CLEC6, CLECSF8, Dectin-3, MCL}, XDH (xanthine dehydrogenase) [NCBI Gene 7498] {aka XAN1, XDH/XO, XO, XOR}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, ITGB8 (integrin subunit beta 8) [NCBI Gene 3696], IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, VIP (vasoactive intestinal peptide) [NCBI Gene 7432] {aka PHM27}, DKFZP547J0410 [NCBI Gene 26107]
- **Diseases:** insomnia (MESH:D007319), restlessness (MESH:D011595), mental disorders (MESH:D001523), SD (MESH:D012735), ischemic heart disease (MESH:D017202), MF (MESH:C567116), dry (MESH:D015352), neuroinflammation (MESH:D000090862), cocaine addiction (MESH:D019970), HCA (MESH:D003027), inflammation (MESH:D007249), sleep disorder (MESH:D012893), -MS (MESH:D009103), Chagas disease (MESH:D014355), Depression (MESH:D003866)
- **Chemicals:** alpha-terpineol (MESH:C016775), Heptaldehyde (MESH:C046204), quercetin (MESH:D011794), nitrogen (MESH:D009584), Benzaldehyde (MESH:C032175), 2-Acetylpyrrole (MESH:C051267), isoquercitrin (MESH:C016527), Eicosane (MESH:C050821), (+)-limonene (MESH:D000077222), corticosterone (MESH:D003345), ketones (MESH:D007659), 2-Pyrrolecarbaldehyde (MESH:C051266), esters (MESH:D004952), Nonanoic acid (MESH:C008776), rutin (MESH:D012431), (+)-limonene oxide (MESH:C028940), (Z)-Linalool oxide (-), Acrylic acid (MESH:C036658), helium (MESH:D006371), Hexanoic acid (MESH:C037652), Pyridine (MESH:C023666), linalool (MESH:C018584), dopamine (MESH:D004298), phenylacetaldehyde (MESH:C013192), alkanes (MESH:D000473), hotrienol (MESH:C476493), 2-Methoxy-4-vinyl phenol (MESH:C526552), isorhamnetin (MESH:C047368), hydrogen (MESH:D006859), alcohols (MESH:D000438), isoamyl alcohol (MESH:C029683), flavonoids (MESH:D005419), 1-Hexanol (MESH:C036260), Tridecane (MESH:C094074), glucose (MESH:D005947), 5-hydroxytryptamine (MESH:D012701), ethanol (MESH:D000431), cyanidin-3-O-glucoside (MESH:C462279), aldehydes (MESH:D000447), 2,5-Dimethylfuran (MESH:C037555), 2-Heptanone (MESH:C011917), water (MESH:D014867), (S)-linalool oxide (MESH:C000593345), pelargonaldehyde (MESH:C008664), fluoxetine (MESH:D005473), lipid (MESH:D008055), quercitrin (MESH:C012526), sucrose (MESH:D013395), olefins (MESH:D000475), Cedrenol (MESH:C534303), hexanal (MESH:C010463), volatile oil (MESH:D009822)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Albizia julibrissin (silk tree, species) [taxon 3813]
- **Cell lines:** PC12 — Rattus norvegicus (Rat), Rat adrenal gland pheochromocytoma, Cancer cell line (CVCL_0481)

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## References

54 references — full list in the complete paper: https://tomesphere.com/paper/PMC12950218/full.md

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Source: https://tomesphere.com/paper/PMC12950218