# Assessment of Nitric Oxide Release In Vitro via Low-Level Daylight-Equivalent Blue or Red Light Irradiation

**Authors:** Gareth Hazell, Marina Khazova, Paul O’Mahoney

PMC · DOI: 10.3390/antiox15020232 · Antioxidants · 2026-02-10

## TL;DR

This study finds that low-level blue or red light exposure does not significantly increase nitric oxide release in skin cells.

## Contribution

The study clarifies that environmentally relevant low-level visible light does not induce nitric oxide release in skin cells.

## Key findings

- Broad-spectrum blue or red light does not significantly increase NO release in skin cells.
- High-powered LEDs or lasers are typically required for significant NO induction.
- Low-level daylight-equivalent exposure does not measurably affect NO release.

## Abstract

Conflicting evidence exists on whether blue or red light modulates nitric oxide (NO) release within skin cells. Using environmentally relevant doses, irradiances and spectral distribution akin to low-level sunlight, we provide evidence that broad-spectrum blue or red (including infrared) light fails to significantly increase NO release in skin cell monolayers compared to unexposed controls for each individual timepoint assessed. We discuss observed discrepancies between our work and recent photobiomodulation (PBM)-based studies presenting measurable upregulation, noting that significant NO induction typically requires high-powered light-emitting diodes (LEDs) or lasers used in clinical settings within a specific narrow spectral band. Thus, while our findings show no significant effect, they provide an important counterpoint for public health discussions on visible light exposure at terrestrial levels, particularly low-level exposures, between 15 and 30 min midday UK visible light exposure.

## Full-text entities

- **Genes:** NOS2 (nitric oxide synthase 2) [NCBI Gene 4843] {aka HEP-NOS, INOS, NOS, NOS2A}, CP (ceruloplasmin) [NCBI Gene 1356] {aka AB073614, CP-2}
- **Diseases:** squamous cell carcinoma (MESH:D002294), tumour (MESH:D009369), inflammatory (MESH:D007249), injury to (MESH:D014947), malignant melanoma (MESH:D008545), basal cell carcinoma (MESH:D002280), cytotoxic (MESH:D064420), hypertension (MESH:D006973)
- **Chemicals:** NO (MESH:D009569), DAF-FM diacetate (MESH:C503301), S-nitrosothiols (MESH:D026403), Cu (MESH:D003300), water (MESH:D014867), CuCl2 (MESH:C029892), carbon monoxide (MESH:D002248), nitrate (MESH:D009566), cGMP (MESH:D006152), magnesium (MESH:D008274), calcium (MESH:D002118), tryptophan (MESH:D014364), ATP (MESH:D000255), peroxynitrite (MESH:D030421), thiols (MESH:D013438), nitrite (MESH:D009573), RNS (MESH:D026361), superoxide (MESH:D013481), Barolet (-), propidium iodide (MESH:D011419), H2O2 (MESH:D006861), phenol red (MESH:D010637)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938285/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938285/full.md

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Source: https://tomesphere.com/paper/PMC12938285