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组胺受体拮抗剂对尿刊酸顺式异构体诱导的免疫抑制的影响。

The effect of histamine receptor antagonists on immunosuppression induced by the cis-isomer of urocanic acid.

作者信息

Norval M, Gilmour J W, Simpson T J

机构信息

Department of Medical Microbiology, University of Edinburgh Medical School, Scotland, UK.

出版信息

Photodermatol Photoimmunol Photomed. 1990 Dec;7(6):243-8.

PMID:1983293
Abstract

Urocanic acid (UCA) is found in the stratum corneum predominantly as the trans-isomer; on ultraviolet B (UVB) irradiation, isomerization to the cis-isomer occurs. Cis-UCA has been shown to mimic the consequences of UVB irradiation in generating transient suppression of contact and delayed hypersensitivity (DH) responses. In an attempt to elucidate the mechanisms of action of UCA, the effects of 2 histamine receptor antagonists, cimetidine and terfenadine, were examined. One day after skin painting murine ears with cis-UCA, the number of ATPase- cells was reduced from 1068 to 408 mm-2. However, if cimetidine or terfenadine was applied at the same time as cis-UCA, the number of ATPase- cells was reduced only slightly from the control value, to 1028 and 892 respectively. Cis-UCA given subcutaneously or epidermally 5 h before infection of mice with herpes simplex virus suppressed the DH response on subsequent challenge with the virus. If cimetidine or terfenadine was added at the same time as cis-UCA, little suppression of the DH response to the virus occurred. Thus 2 effects of cis-UCA, on the number of ATPase+ epidermal cells and on DH response, were reduced or abrogated by histamine receptor antagonists, which may indicate that cis-UCA acts through histamine-like receptors in the skin.

摘要

尿刊酸(UCA)主要以反式异构体的形式存在于角质层中;在紫外线B(UVB)照射下,会发生异构化形成顺式异构体。已表明顺式UCA在产生接触性迟发性超敏反应(DH)的短暂抑制方面模拟了UVB照射的后果。为了阐明UCA的作用机制,研究了两种组胺受体拮抗剂西咪替丁和特非那定的作用。在用顺式UCA涂抹小鼠耳部皮肤一天后,ATP酶阳性细胞的数量从1068减少到408个/mm²。然而,如果在涂抹顺式UCA的同时应用西咪替丁或特非那定,ATP酶阳性细胞的数量仅比对照值略有减少,分别降至1028和892个。在用单纯疱疹病毒感染小鼠前5小时皮下或表皮给予顺式UCA,可抑制随后用该病毒攻击时的DH反应。如果在给予顺式UCA的同时加入西咪替丁或特非那定,则对该病毒的DH反应几乎没有抑制作用。因此,组胺受体拮抗剂可减少或消除顺式UCA对ATP酶阳性表皮细胞数量和DH反应的两种作用,这可能表明顺式UCA通过皮肤中的组胺样受体发挥作用。

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