UV light deterioration
Introduction
Photoaging[1] or dermatoheliosis[2] is a term used for the characteristic changes in the skin induced by chronic exposure to UVA and UVB rays.[3] Tretinoin is the best studied retinoid in the treatment of photoaging.[4].
The deterioration of biological functions and the ability to manage metabolic stress is one of the main consequences of the aging process. Aging is a complex and progressive process that leads to functional and aesthetic changes in the skin. This process can result from both intrinsic (i.e., genetically determined) and extrinsic (i.e., environmental factors) processes. Photoaging is attributed to continuous and prolonged exposure to ultraviolet (UV) radiation of approximately 300 to 400 nm, whether natural or synthetic, on intrinsically aged skin.
Effects of ultraviolet light
Molecular and genetic changes
UVB rays are a primary mutagen that can only penetrate through the epidermal (outermost) layer of the skin, causing DNA mutations. These mutations arise due to chemical changes, the formation of cyclobutane pyrimidine dimers and photoproducts formed between adjacent pyrimidine bases. These mutations may be clinically related to specific signs of photoaging, such as wrinkles, increased elastin, and collagen damage.[5][6].
The epidermal layer does not contain blood vessels or nerve endings, but melanocytes and basal cells are embedded in this layer. When exposed to UVB rays, melanocytes will produce melanin, a pigment that gives skin its color tone. However, UVB rays will cause the formation of freckles and dark spots, which are symptoms of photoaging. With constant exposure to UVB rays, signs of photoaging may appear and precancerous lesions or skin cancer may develop.
UVA rays can penetrate deeper into the skin compared to UVB rays. Therefore, in addition to the epidermal layer, the dermal layer will also be damaged. The dermis is the second main layer of the skin and comprises collagen, elastin, and extrafibrillar matrix that provides structural support to the skin. However, with constant exposure to UVA rays, the size of the dermis layer will reduce, causing the epidermis to begin to peel away from the body. Due to the presence of blood vessels in the dermis, UVA rays can cause dilated or broken blood vessels, which are most commonly visible on the nose and cheeks. UVA rays can also damage DNA indirectly through the generation of reactive oxygen species (ROS), including superoxide anion, peroxide, and singlet oxygen. These ROS damage cellular DNA, as well as lipids and proteins.