| Literature DB >> 35050108 |
Ana Mariel Torres-Contreras1, Antoni Garcia-Baeza1, Heriberto Rafael Vidal-Limon2, Isaias Balderas-Renteria1, Mónica A Ramírez-Cabrera3, Karla Ramirez-Estrada1.
Abstract
Human skin works as a barrier against the adverse effects of environmental agents, including ultraviolet radiation (UVR). Exposure to UVR is associated with a variety of harmful effects on the skin, and it is one of the most common health concerns. Solar UVR constitutes the major etiological factor in the development of cutaneous malignancy. However, more than 90% of skin cancer cases could be avoided with appropriate preventive measures such as regular sunscreen use. Plants, constantly irradiated by sunlight, are able to synthesize specialized molecules to fight against UVR damage. Phenolic compounds, alkaloids and carotenoids constitute the major plant secondary metabolism compounds with relevant UVR protection activities. Hence, plants are an important source of molecules used to avoid UVR damage, reduce photoaging and prevent skin cancers and related illnesses. Due to its significance, we reviewed the main plant secondary metabolites related to UVR protection and its reported mechanisms. In addition, we summarized the research in Mexican plants related to UV protection. We presented the most studied Mexican plants and the photoprotective molecules found in them. Additionally, we analyzed the studies conducted to elucidate the mechanism of photoprotection of those molecules and their potential use as ingredients in sunscreen formulas.Entities:
Keywords: Mexican plants; UV protection; UVR-damage; antioxidant activity; plant secondary metabolites
Year: 2022 PMID: 35050108 PMCID: PMC8779981 DOI: 10.3390/plants11020220
Source DB: PubMed Journal: Plants (Basel) ISSN: 2223-7747
Ultraviolet radiation classification, characteristics and harmful effects 1.
| Type of UVR | Characteristics | Acute Harmful Skin Effects | Chronic Harmful Skin Effects |
|---|---|---|---|
| Ultraviolet A radiation (UVA) | Is not filtered by the stratospheric ozone layer in the atmosphere | Immediate pigment darkening | Photoaging: skin elasticity reduction and increase wrinkling. |
| Ultraviolet B radiation (UVB) | Filtered by the stratospheric ozone layer in the atmosphere | Edema, | Photoaging |
| Ultraviolet C radiation (UVC) | Completely filtered by the stratospheric ozone layer in the atmosphere | Burn | Skin cancer |
1 Modified from Narayanan et al. [1].
Figure 1Solar ultraviolet radiation (UVR) and the mechanisms of its main biological effects on the skin. UVC (100–280 nm) cannot penetrate the ozone layer; 2–5% of UVB (280–315 nm) crosses the ozone layer and penetrates the epidermis causing DNA damage and an increase in oxidative stress via ROS formation [1,17]. Approximately 95–98% of UVA (315–400 nm) reaches the skin and penetrates deeper into the epidermis and dermis. This causes diverse harmful effects on the skin, mainly through ROS. (1) Skin inflammation via induction of tumor necrosis factor alfa (TNF-α) and activation of pro-inflammatory cytokines as interleukin-1 (IL-1) and interleukin-6 (IL-6). (2) Skin aging by degradation of collagen and elastin through increasing matrix metalloproteinases (MMPs) induced by the nuclear factor-kB (NF-κB) and the activation protein-1 (AP-1). These last two proteins are also transcription factors for pro-inflammatory cytokines. Cytokines can also amplify AP-1 and NF-kB pathways, enhancing the response to UV radiation. (3) Immunosuppression via TNF-α and depletion of Langerhans cells. (4) Oxidative damage and apoptosis (5) Skin cancer by pyrimidine dimers formation [1,18,20]. All these harmful effects can be prevented by phytochemicals with photoprotection activity.
Figure 2Plant secondary metabolites against skin photodamage. Mechanisms of action and skin-related bioactivities. Matrix metalloproteinases (MMPs) activation protein-1 (AP-1); Nuclear factor-kB (NF-κB), ultraviolet radiation (UVR); reactive oxygen species (ROS), reactive nitrogen species (RNS).
Photo protective activities of Mexican plants.
| Plant | Photoprotective Activity | Photoprotective Agent | Biological Model Used | Reference |
|---|---|---|---|---|
|
| Reduction of skin damage, antioxidant activity, UVB absorption. | Methanolic extract | [ | |
|
| Reduction of skin damage, antioxidant activity, UVB absorption. | Methanolic extract | SKH-1 hairless mice, mouse fibroblasts. | [ |
| Reduction of skin damage, antioxidant activity. | Methanolic extract, hydroxycinnamic acids, flavonoids | Clinical trials, in vitro antioxidant tests. | [ | |
| Skin photoprotection, antioxidant activity | Aqueous extract, caffeic acid derivatives. | NHDF human skin fibroblasts. | [ | |
|
| UVB absorption, antioxidant activity, prevention of UVB damage and photoaging. | Flower ethanolic extract, chlorogenic and caffeic acid | Human dermal fibroblast, in vitro antioxidant and SPF tests. | [ |
|
| Inhibition of UVB induced signaling pathways related to skin carcinogenesis, antioxidant activity | Nordihydroguayaric acid (NDGA) | Human keratinocyte cell line HaCaT, in vitro antioxidant tests. | [ |
|
| UVB and UVC absorption, photochemopreventive and antioxidant activity. | Flavonoids, apigenin, pinocembrin and naringenin. | [ | |
|
| Antioxidant activity | Dried extract | in vitro antioxidant and SPF tests | [ |
|
| Antioxidant activity, photoaging reduction, inhibition of metalloproteinases | Ethanolic root extract, | Hairless mouse skin and SPF tests | [ |
|
| Skin antioxidant, antiphotoaging and cytoprotective activity. | Hydroxycinnamic acids, hydrophilic extract. | Human fibroblasts and keratinocytes | [ |
| Oral photoprotective effect: antioxidant, increment of p53+ cells, reduce proliferating cells. | Hydrophilic extract. | Hairless rats, clinical studies | [ | |
|
| Antioxidant, photoprotective, anti-wrinkle, anti-aging | Methanolic extracts | Epithelial keratinocytes and fibroblasts. | [ |
|
| Oral photoprotective and anticancer effect. | Tomato carotenoids enriched extract, lycopene. | Human volunteers, SKH-1 murine model. | [ |
| Skin photoprotection and antioxidant effect | Lycopene | Human dermal fibroblasts. | [ | |
|
| UVA and UVB light protection, antioxidant effect | Methanolic extract, flavonoids, quercetin, rutin. | in vitro antioxidant and SPF tests | [ |
|
| Oral photoprotective effect. | Cocoa beverage flavonols enriched. | Human clinical trials | [ |
|
| Skin photoprotective effect, absorption of UVB radiation | Methanolic extract, polyphenols, resveratrol, methoxystilbene. | Guinea pigs | [ |
| Antioxidant properties, reduced lipid peroxidation and GSH depletion, inhibit UVB-induced skin degeneration | Aqueous extract, eucomic and piscidic acids, opuntiol, flavonols. | Human keratinocytes, HaCaT cells and hairless mice, NIH-3T3 cells | [ |