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382纳米辐射诱导的即时色素沉着对紫外线B诱导的红斑缺乏光保护作用。

Lack of photoprotection against UVB-induced erythema by immediate pigmentation induced by 382 nm radiation.

作者信息

Black G, Matzinger E, Gange R W

出版信息

J Invest Dermatol. 1985 Nov;85(5):448-9. doi: 10.1111/1523-1747.ep12277170.

Abstract

Immediate pigment darkening (IPD) was induced on the backs of 11 human volunteers of skin types III and IV by exposing the skin to UVA radiation (382 nm). The minimum erythema dose (MED) of UVB radiation was also determined by exposing sites to graduated doses of 304 nm radiation. The order of exposure of distinct anatomic areas was as follow: UVB followed by IPD induction; IPD induction followed by UVB; IPD induction followed 3 h later by UVB; and UVB only. Erythema responses induced by UVB were graded by inspection 24 h later and the MEDs in the 4 areas were compared. The induction of IPD before UVB exposure caused no significant change in the MED compared to sites receiving UVB only, or receiving UVA radiation after UVB, confirming that the IPD reaction does not protect against UVB-induced erythema. There was also no evidence of photorecovery, i.e., an increase in the MED of UVB resulting from exposure to longer wavelength, UV or visible radiation following UVB exposure.

摘要

通过将皮肤暴露于UVA辐射(382纳米),在11名III型和IV型皮肤的人类志愿者背部诱发即时色素沉着(IPD)。通过将部位暴露于304纳米辐射的递增剂量来确定UVB辐射的最小红斑剂量(MED)。不同解剖区域的暴露顺序如下:先UVB后诱发IPD;先诱发IPD后UVB;诱发IPD 3小时后再UVB;仅UVB。24小时后通过检查对UVB诱发的红斑反应进行分级,并比较4个区域的MED。与仅接受UVB或UVB后接受UVA辐射的部位相比,在UVB暴露前诱发IPD不会使MED发生显著变化,这证实IPD反应不能预防UVB诱发的红斑。也没有光修复的证据,即UVB暴露后因暴露于更长波长的紫外线或可见光辐射而导致UVB的MED增加。

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