# Cutaneous microvascular function is reduced in winter compared with summer in healthy young adults

**Authors:** James F. Bangle, William E. Jennings, Alyssa J. Guadagni, Georgia R. Albino, Andrew J. Grundstein, S. Tony Wolf

PMC · DOI: 10.14814/phy2.70784 · Physiological Reports · 2026-02-19

## TL;DR

This study found that healthy young adults have reduced blood vessel function in their skin during winter compared to summer, partly due to colder temperatures.

## Contribution

The study identifies seasonal variation in NO-mediated cutaneous vasodilation and links it to temperature changes.

## Key findings

- Cutaneous vasodilation during local heating was significantly lower in winter compared to summer.
- Nitric oxide's contribution to vasodilation decreased in winter.
- Outdoor temperature was positively associated with NO-dependent vasodilation.

## Abstract

Seasonal differences in temperature and ultraviolet radiation (UVR) exposure may alter NO‐mediated vasodilation in the cutaneous microvasculature. We assessed seasonal variation in cutaneous microvascular function in 10 healthy (23 ± 2; 6 men, 4 women) adults in the summer/early‐fall and winter/early‐spring. Microvascular (intradermal microdialysis and local skin heating [42°C]) endothelial function was assessed at two visits separated by ~6 months. Mean daytime (sunrise to sunset) outdoor temperature and 2‐h peak UV Index were recorded for the 30 days prior to each experimental visit. Serum vitamin D concentrations [25(OH)D] were measured for each visit. Multivariate regression analysis evaluated the factors (temperature, UV Index, and [25(OH)D]) that best explained variance in microvascular endothelial function. The local heating response (74.37 ± 12.21 %CVCmax vs. 55.89 ± 15.50 %CVCmax, p = 0.009) and the NO contribution to that response (61.73% ± 9.67% vs. 38.13% ± 13.26%, p = 0.004) were lower in winter/early‐spring compared to summer/early‐fall. The best‐fit regression model suggested that 30‐day average outdoor temperature and 2‐h peak UV Index were positively and negatively associated with NO‐dependent cutaneous vasodilation, respectively. Healthy adults exhibit lower NO‐mediated cutaneous vasodilation in the winter/early‐spring compared with summer/early‐fall, which is partially explained by seasonal differences in outdoor temperature.

## Full-text entities

- **Genes:** Edn1 (endothelin 1) [NCBI Gene 24323] {aka Et1}, NOS3 (nitric oxide synthase 3) [NCBI Gene 4846] {aka EC-NOS, ECNOS, MYMY8, NOSIII, cNOS, eNOS}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, Nos3 (nitric oxide synthase 3) [NCBI Gene 24600] {aka eNos}
- **Diseases:** pigmentation disorders (MESH:D010859), FMD (MESH:D002311), cardiovascular disease (MESH:D002318), Endothelial dysfunction (MESH:D014652), impaired vascular function (MESH:D020141), hypertension (MESH:D006973), skin allergies (MESH:D012871), inflammation (MESH:D007249), cardiometabolic diseases (MESH:D024821), endothelial (MESH:D005642), hyperemia (MESH:D006940), vitamin D deficient (MESH:D014808), obese (MESH:D009765), kidney disease (MESH:D007674)
- **Chemicals:** L-NAME (MESH:D019331), prostaglandins (MESH:D011453), 5-MTHF (MESH:C005984), caffeine (MESH:D002110), 25(OH)D (-), Vitamin D (MESH:D014807), NO (MESH:D009614), NO (MESH:D009569), Calcium (MESH:D002118), reactive oxygen species (MESH:D017382), folate (MESH:D005492), calcitriol (MESH:D002117), sodium nitroprusside (MESH:D009599), melanin (MESH:D008543)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Cell lines:** N5501 — Homo sapiens (Human), Finite cell line (CVCL_UZ57)

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12917853/full.md

## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12917853/full.md

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Source: https://tomesphere.com/paper/PMC12917853