# P-Hydroxybenzaldehyde from Gastrodia elata Blume Reduces Hydroxyurea-Induced Cellular Senescent Phenotypes in Human SH-SY5Y Cells via Enhancing Autophagy

**Authors:** Shuhui Qu, Daijiao Tang, Lingxuan Fan, Yuan Dai, Hai-Jing Zhong, Wei Cai, Cheong-Meng Chong

PMC · DOI: 10.3390/ph19020207 · Pharmaceuticals · 2026-01-25

## TL;DR

P-Hydroxybenzaldehyde from Gastrodia elata reduces signs of cellular aging in human cells by boosting autophagy.

## Contribution

This study identifies P-HBA as a novel compound from Gastrodia elata that mitigates cellular senescence via autophagy enhancement.

## Key findings

- TME and P-HBA reduce hydroxyurea-induced DNA damage and SA-β-Gal activity in SH-SY5Y cells.
- P-HBA's anti-senescent effect is diminished by the autophagy inhibitor chloroquine.
- P-HBA enhances autophagy to counteract cellular senescence.

## Abstract

Background/Objectives: The rhizome of Gastrodia elata Blume (Tianma) is a functional food with medicinal value in China, used to improve the health of the central nervous system and reported to exhibit anti-cellular senescent activity. P-hydroxybenzaldehyde (P-HBA) is a key aromatic compound isolated from Tianma; however, its potential to mitigate cellular senescence remains unclear. Methods: We employed ultra-performance liquid chromatography-mass spectrometry to identify the chemical characterization of Tianma extract. Cell viability assay, senescence-associated-β-galactosidase (SA-β-Gal) assay, and immunofluorescence staining and autophagy analysis were used to evaluate the anti-senescent activity of P-HBA and other Tianma components. Results: Our findings demonstrate that Tianma methanol extract (TME) and P-HBA significantly reduce cellular senescent inducer hydroxyurea (HU)-induced DNA damage, SA-β-Gal activity increase, and autophagic dysfunction in human SH-SY5Y cells. Notably, an autophagy inhibitor, chloroquine, can reduce anti-cellular senescent activity of P-HBA. Conclusions: These results suggest that P-HBA exhibits the effect of reducing cellular senescent phenotypes, and its effect is achieved by enhancing autophagy.

## Linked entities

- **Chemicals:** P-hydroxybenzaldehyde (PubChem CID 126), hydroxyurea (PubChem CID 3657), chloroquine (PubChem CID 2719)
- **Species:** Gastrodia elata (taxon 91201), Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, CDKN2A (cyclin dependent kinase inhibitor 2A) [NCBI Gene 1029] {aka ARF, CAI2, CDK4I, CDKN2, CMM2, INK4}, MAP1LC3A (microtubule associated protein 1 light chain 3 alpha) [NCBI Gene 84557] {aka ATG8E, LC3, LC3A, MAP1ALC3, MAP1BLC3}, LMNA (lamin A/C) [NCBI Gene 4000] {aka CDCD1, CDDC, CMD1A, CMT2B1, EMD2, FPL}, H2AX (H2A.X variant histone) [NCBI Gene 3014] {aka H2A.X, H2A/X, H2AFX}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, GLB1 (galactosidase beta 1) [NCBI Gene 2720] {aka EBP, ELNR1, MPS4B}, LMNB1 (lamin B1) [NCBI Gene 4001] {aka ADLD, LMN, LMN2, LMNB, MCPH26}, MAP1LC3B (microtubule associated protein 1 light chain 3 beta) [NCBI Gene 81631] {aka ATG8F, LC3B, MAP1A/1BLC3, MAP1LC3B-a}, H3P16 (H3 histone pseudogene 16) [NCBI Gene 644914] {aka H3.6, H3F3AP6, p21}, SIRT3 (sirtuin 3) [NCBI Gene 23410] {aka SIR2L3}
- **Diseases:** AD (MESH:D000544), cerebral ischemia (MESH:D002545), inflammatory (MESH:D007249), headache (MESH:D006261), neurodegeneration (MESH:D019636), injury to (MESH:D014947), mitochondrial dysfunction (MESH:D028361), Parkinson's disease (MESH:D010300), neuroblastoma (MESH:D009447), paralysis (MESH:D010243), infection (MESH:D007239), cytotoxicity (MESH:D064420), dizziness (MESH:D004244), spasms (MESH:D013035), epilepsy (MESH:D004827), impaired brain homeostasis (MESH:D001927), brain injury (MESH:D001930), hypertension (MESH:D006973), amnesia (MESH:D000647), migraine (MESH:D008881), cognitive or motor deficits (MESH:D003072)
- **Chemicals:** F12 (MESH:C007782), Triton  X-100 (MESH:D017830), acetonitrile (MESH:C032159), streptomycin (MESH:D013307), methanol (MESH:D000432), P-HBA (MESH:C011483), formic acid (MESH:C030544), D-gal (MESH:D005690), CCK-8 (MESH:D012844), BeSO4 (MESH:C020711), Vanillin (MESH:C100058), SA-beta-Gal (-), Gastrodin (MESH:C045345), SA (MESH:D000077145), penicillin (MESH:D010406), PBS (MESH:D007854), HU (MESH:D006918), DMSO (MESH:D004121), DAPI (MESH:C007293), CQ (MESH:D002738), Parishin C (MESH:C554064), PCA (MESH:C009091), CO2 (MESH:D002245), PFA (MESH:C003043)
- **Species:** Gastrodia elata (species) [taxon 91201], Homo sapiens (human, species) [taxon 9606], Nematoda (nematode, phylum) [taxon 6231]
- **Mutations:** JAK2V617F
- **Cell lines:** CRL- — Sigmodon hispidus (Hispid cotton rat), Spontaneously immortalized cell line (CVCL_YD58), SH-SY5Y — Homo sapiens (Human), Neuroblastoma, Cancer cell line (CVCL_0019), P-HBA — Atilax paludinosus (Marsh mongoose), Finite cell line (CVCL_6365)

## Full text

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## Figures

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## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943341/full.md

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Source: https://tomesphere.com/paper/PMC12943341