Lavker R, Kaidbey K
Department of Dermatology, University of Pennsylvania Medical Center, Philadelphia 19104, USA.
J Invest Dermatol. 1997 Jan;108(1):17-21. doi: 10.1111/1523-1747.ep12285613.
The wavelength dependence for UVA-induced cumulative damage was investigated in human skin. Epidermal changes (stratum corneum thickening, viable epidermal thickening sunburn cell production), as well as dermal alterations (lysozyme deposition, inflammation), were used as indices of cumulative photoperturbation. UVA wavelengths between 320 nm and 345 nm were more effective than longer wavelengths (360-400 nm) in inducing viable epidermal thickening. Similarly, the shorter wavelengths (320-345 nm) elicited more sunburn cells, although these differences did not reach statistical significance. All UVA bands were equally effective in inducing the dermal markers. At equal fluences, wavelengths > 400 nm produced no measurable cutaneous alterations. These findings suggest that (i) chronic epidermal and dermal damages have different spectral dependence and (ii) the action spectrum for dermal damage in the UVA is broad, extending up to 400 nm, and is different from the acute erythema spectrum in humans.
研究了UVA诱导的累积损伤在人体皮肤中的波长依赖性。将表皮变化(角质层增厚、活表皮增厚、晒伤细胞产生)以及真皮改变(溶菌酶沉积、炎症)用作累积光扰动的指标。在诱导活表皮增厚方面,320 nm至345 nm之间的UVA波长比更长波长(360 - 400 nm)更有效。同样,较短波长(320 - 345 nm)引发的晒伤细胞更多,尽管这些差异未达到统计学意义。所有UVA波段在诱导真皮标志物方面同样有效。在相同通量下,波长> 400 nm未产生可测量的皮肤改变。这些发现表明:(i)慢性表皮和真皮损伤具有不同的光谱依赖性;(ii)UVA中真皮损伤的作用光谱较宽,延伸至400 nm,且与人类急性红斑光谱不同。