Antioxidant and Photoprotective Capacity of Secondary Metabolites Isolated from Pseudocyphellaria berberina

Exposure to sunlight, whose main component is UV radiation (UVR), leads to various skin damage such as sunburns, premature aging, or more severe issues such as increased symptoms of autoimmune disease and skin cancer. Therefore, there is a growing interest in developing improved photoprotective agents that can protect skin from sunlight incidence and antioxidants that counteract the oxidative stress caused by it. Lichens are a source of such agents since they adapt to extreme environments including those with high UVR by biosynthesizing metabolites with those properties. In this study, brialmontin 2 (<b>1</b>), physciosporin (<b>2</b>), and pseudocyphellarin A (<b>3</b>) were isolated for the first time from the lichen <i>Pseudocyphellaria berberina</i> (G. Forst.) D. J. Galloway & P. James, along with calycin (<b>4</b>) and 22-hydroxystictan-3-one (<b>5</b>). Their structural characterization was carried out by spectroscopy (<sup>1</sup>H and <sup>13</sup>C NMR). Sun protection factor (SPF) along with critical wavelength (λ<sub>crit</sub>), a UVA/UVB ratio (UVA/UVB-r) of <b>one</b> to <b>five,</b> and acetone extract (<b>AE</b>) were evaluated spectrophotometrically as a measure of their UVB and UVA photoprotective capacities, respectively. Additionally, their antioxidant activity was measured by scavenging DPPH free radicals (RSA). Compounds <b>2</b>, <b>4,</b> and <b>AE</b> showed "medium" UVB photoprotective capacities (with SPFs between 15 and 30). Additionally, <b>4</b> and <b>AE</b> presented "maximum" UVA photoprotective capacities (λ<sub>crit</sub> > 370 nm and UVA/UVB-r > 0.8), whereas this activity was "good" for <b>2</b> and <b>3</b> (λ<sub>crit</sub> 350 to 370 nm and UVA/UVB-r 0.4 to 0.6), and "moderate" for <b>1</b> (λ<sub>crit</sub> 335 to 350 nm and UVA/UVB-r 0.2 to 0.4). All compounds and <b>AE</b> showed antioxidant activity, standing out were <b>AE</b> and <b>4</b> with activity comparable to the controls (ca. 95 and 81 RSA %, respectively, at 1000 ppm). <b>AE</b> and <b>4</b> are dual agents with photoprotective (UVB-UVA) and antioxidant capacities that could help prevent skin damage associated with sunlight. In silico assays suggest that <b>4</b> spontaneously diffuses into the stratum corneum with limited absorption through the skin. Additionally, <b>4</b> lacks potential toxicity to Normal Human Epidermal Keratinocytes (showing viability ca. 70% at 100 ppm); therefore, it is a candidate for the development of sunscreen formulations.

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Publication Details

Journal
Molecules
Published
2025-09-22
DOI
https://doi.org/10.3390/molecules30183833
Primary Topic
Lichen and fungal ecology
Type
article
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article

Antioxidant and Photoprotective Capacity of Secondary Metabolites Isolated from Pseudocyphellaria berberina

Cecilia Rubio, Norma A. Valencia-Islas, Natalia Quiñones, Carolina Campos et al.
Molecules
Lichen and fungal ecology
article

Antioxidant and Photoprotective Capacity of Secondary Metabolites Isolated from Pseudocyphellaria berberina

Cecilia Rubio, Norma A. Valencia-Islas, Natalia Quiñones, Carolina Campos, José Rojas, Javiera Ramírez
article en

Abstract

Exposure to sunlight, whose main component is UV radiation (UVR), leads to various skin damage such as sunburns, premature aging, or more severe issues such as increased symptoms of autoimmune disease and skin cancer. Therefore, there is a growing interest in developing improved photoprotective agents that can protect skin from sunlight incidence and antioxidants that counteract the oxidative stress caused by it. Lichens are a source of such agents since they adapt to extreme environments including those with high UVR by biosynthesizing metabolites with those properties. In this study, brialmontin 2 (<b>1</b>), physciosporin (<b>2</b>), and pseudocyphellarin A (<b>3</b>) were isolated for the first time from the lichen <i>Pseudocyphellaria berberina</i> (G. Forst.) D. J. Galloway & P. James, along with calycin (<b>4</b>) and 22-hydroxystictan-3-one (<b>5</b>). Their structural characterization was carried out by spectroscopy (<sup>1</sup>H and <sup>13</sup>C NMR). Sun protection factor (SPF) along with critical wavelength (λ<sub>crit</sub>), a UVA/UVB ratio (UVA/UVB-r) of <b>one</b> to <b>five,</b> and acetone extract (<b>AE</b>) were evaluated spectrophotometrically as a measure of their UVB and UVA photoprotective capacities, respectively. Additionally, their antioxidant activity was measured by scavenging DPPH free radicals (RSA). Compounds <b>2</b>, <b>4,</b> and <b>AE</b> showed "medium" UVB photoprotective capacities (with SPFs between 15 and 30). Additionally, <b>4</b> and <b>AE</b> presented "maximum" UVA photoprotective capacities (λ<sub>crit</sub> > 370 nm and UVA/UVB-r > 0.8), whereas this activity was "good" for <b>2</b> and <b>3</b> (λ<sub>crit</sub> 350 to 370 nm and UVA/UVB-r 0.4 to 0.6), and "moderate" for <b>1</b> (λ<sub>crit</sub> 335 to 350 nm and UVA/UVB-r 0.2 to 0.4). All compounds and <b>AE</b> showed antioxidant activity, standing out were <b>AE</b> and <b>4</b> with activity comparable to the controls (ca. 95 and 81 RSA %, respectively, at 1000 ppm). <b>AE</b> and <b>4</b> are dual agents with photoprotective (UVB-UVA) and antioxidant capacities that could help prevent skin damage associated with sunlight. In silico assays suggest that <b>4</b> spontaneously diffuses into the stratum corneum with limited absorption through the skin. Additionally, <b>4</b> lacks potential toxicity to Normal Human Epidermal Keratinocytes (showing viability ca. 70% at 100 ppm); therefore, it is a candidate for the development of sunscreen formulations.

MoleculesVol. 30(18)
Universidad Nacional de Colombia (CO), University of Valparaíso (CL)
Openalex Percentile: Top 80%
Lichen and fungal ecology
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