# Targeting Circadian Rhythm for the Regulation of Skin Collagen Metabolism

**Authors:** Cheng Wang, Tianlin Song, Yurong Zhang, Nihong Li, Ling Xie, Min Xie, Xingwu Jiang, Guanglei Lü, Yun Meng, Chaochao Wang, Lijun Yue, Wei Yang, Yang Li, Yelin Wu, Liang Chen

PMC · DOI: 10.1111/jocd.70638 · 2026-01-13

## TL;DR

This study shows that collagen metabolism in skin follows a daily rhythm and that timed application of two compounds improves skin quality.

## Contribution

The study introduces a time-coordinated application of baicalin and PT-1 to synergistically enhance collagen metabolism.

## Key findings

- Collagen assembly genes peak during the day, while synthesis and degradation genes peak at night in fibroblasts.
- Time-coordinated application of baicalin and PT-1 increased collagen fiber density in mice and improved skin quality in humans.
- Clinical trial results showed significant improvements in skin luminance, firmness, and nasolabial fold depth.

## Abstract

Collagen is essential for maintaining skin structure and function, and the circadian rhythm is known to regulate a wide range of physiological processes.

To investigate whether collagen metabolism in human skin fibroblasts exhibits circadian regulation, and to evaluate whether the time‐coordinated application of baicalin at daytime and palmitoyl tripeptide‐1 (PT‐1) at nighttime synergistically promotes collagen fiber formation and improves overall skin quality.

A circadian‐synchronized human skin fibroblast model was established. The expression of collagen metabolism‐related genes was analyzed using qPCR and immunofluorescence. Subsequently, an 8‐week topical application study was conducted in mice using a regimen of daytime baicalin and nighttime PT‐1. Finally, a clinical trial involving 30 female participants was conducted, employing the same time‐coordinated application scheme.

Fibroblasts exhibited opposing day‐night rhythms: genes for collagen assembly (e.g., LOX) peaked during the day, while those involved in synthesis/secretion (e.g., Sec61a2, Mia3, Pde4d, Vps33b) and degradation (e.g., CTSK, MMP1) peaked at night. Time phase‐dependent interventions showed baicalin enhanced daytime assembly, while PT‐1 boosted nighttime synthesis. In mice, a timed day‐night combination therapy increased collagen fiber density. Clinical trial (n = 30) confirmed the efficacy, showing significant improvements in skin luminance (+16.29%), nasolabial fold depth (−36.35%), and firmness (R2: +24.35%).

Collagen metabolism is regulated by circadian rhythms. Chronomodulated baicalin and PT‐1 application synergistically optimize collagen metabolism and improve skin quality.

## Linked entities

- **Genes:** LOX (lysyl oxidase) [NCBI Gene 4015], SEC61A2 (SEC61 translocon subunit alpha 2) [NCBI Gene 55176], MIA3 (MIA SH3 domain ER export factor 3) [NCBI Gene 375056], PDE4D (phosphodiesterase 4D) [NCBI Gene 5144], VPS33B (VPS33B late endosome and lysosome associated) [NCBI Gene 26276], CTSK (cathepsin K) [NCBI Gene 1513], MMP1 (matrix metallopeptidase 1) [NCBI Gene 4312]
- **Chemicals:** baicalin (PubChem CID 64982), palmitoyl tripeptide-1 (PubChem CID 10231864)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Sec61a2 (SEC61 translocon subunit alpha 2) [NCBI Gene 57743], CRY1 (cryptochrome circadian regulator 1) [NCBI Gene 1407] {aka DSPD, PHLL1}, Mmp13 (matrix metallopeptidase 13) [NCBI Gene 17386] {aka Clg, MMP-13, Mmp1}, COL1A2 (collagen type I alpha 2 chain) [NCBI Gene 1278] {aka EDSARTH2, EDSCV, OI4}, Lox (lysyl oxidase) [NCBI Gene 16948] {aka TSC-160, rrg}, MMP1 (matrix metallopeptidase 1) [NCBI Gene 4312] {aka CLG}, Vps33b (vacuolar protein sorting 33B) [NCBI Gene 233405], PDIA2 (protein disulfide isomerase family A member 2) [NCBI Gene 64714] {aka PDA2, PDI, PDIP, PDIR}, CTSK (cathepsin K) [NCBI Gene 1513] {aka CTS02, CTSO, CTSO1, CTSO2, PKND, PYCD}, SIRT1 (sirtuin 1) [NCBI Gene 23411] {aka SIR2, SIR2L1, SIR2alpha}, MIA3 (MIA SH3 domain ER export factor 3) [NCBI Gene 375056] {aka D320, ODCD2, TANGO, TANGO1, UNQ6077}, ZNF77 (zinc finger protein 77) [NCBI Gene 58492] {aka pT1}, NPAS2 (neuronal PAS domain protein 2) [NCBI Gene 4862] {aka MOP4, PASD4, bHLHe9}, SEC61A2 (SEC61 translocon subunit alpha 2) [NCBI Gene 55176], BMAL1 (basic helix-loop-helix ARNT like 1) [NCBI Gene 406] {aka ARNTL, ARNTL1, BMAL1c, JAP3, MOP3, PASD3}, LOX (lysyl oxidase) [NCBI Gene 4015] {aka AAT10}, VPS33B (VPS33B late endosome and lysosome associated) [NCBI Gene 26276] {aka KDIDAR, PFIC12}, Mia3 (MIA SH3 domain ER export factor 3) [NCBI Gene 338366] {aka 9130229H14Rik, A930039G15Rik, B230399H06Rik, Gm1525, TANGO1, Tango}, Ctsk (cathepsin K) [NCBI Gene 13038] {aka MMS10-Q, Ms10q, catK}, PDE4D (phosphodiesterase 4D) [NCBI Gene 5144] {aka ACRDYS2, DPDE3, HSPDE4D, PDE43, PDE4DN2, STRK1}, Pde4d (phosphodiesterase 4D, cAMP specific) [NCBI Gene 238871] {aka 9630011N22Rik, Dpde3}, ATXN2L (ataxin 2 like) [NCBI Gene 11273] {aka A2D, A2LG, A2LP, A2RP}
- **Diseases:** pulmonary fibrosis (MESH:D011658), erythema (MESH:D004890), cytotoxicity (MESH:D064420), pigmentation (MESH:D010859), edema (MESH:D004487), inflammation (MESH:D007249), systemic diseases (MESH:D034721), wrinkles (MESH:D019773), skin laxity (MESH:D007593), HSF (MESH:D012871), allergies (MESH:D004342)
- **Chemicals:** glucose (MESH:D005947), AGEs (MESH:D017127), Niacinamide (MESH:D009536), Trizol (MESH:C411644), xylene (MESH:D014992), Vitamin C (MESH:D001205), Peptide (MESH:D010455), dexamethasone (MESH:D003907), Baicalin (MESH:C038044), DMEM (-), eosin (MESH:D004801), H&amp;E (MESH:D006371), penicillin (MESH:D010406), paraformaldehyde (MESH:C003043), Retinol (MESH:D014801), Triton X-100 (MESH:D017830), streptomycin (MESH:D013307), ethanol (MESH:D000431), CCK-8 (MESH:D012844), isoflurane (MESH:D007530), titanium (MESH:D014025), water (MESH:D014867), NAD+ (MESH:D009243), flavonoid (MESH:D005419), paraffin (MESH:D010232), CO2 (MESH:D002245), hematoxylin (MESH:D006416)
- **Species:** Scutellaria baicalensis (Baikal skullcap, species) [taxon 65409], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** C +- 2 C, C-22 C
- **Cell lines:** HSF — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0594)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12797011/full.md

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Source: https://tomesphere.com/paper/PMC12797011