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本文引用的文献

1
Association between hair-induced oronasal inflammation and ulcerative dermatitis in C57BL/6 mice.C57BL/6小鼠毛发诱导的口鼻部炎症与溃疡性皮肤炎之间的关联。
Comp Med. 2011 Feb;61(1):13-9.
2
Systemic therapy of atopic dermatitis in children and adults.儿童和成人特应性皮炎的全身治疗
Curr Probl Dermatol. 2011;41:156-164. doi: 10.1159/000323309. Epub 2011 May 12.
3
Maropitant citrate for treatment of ulcerative dermatitis in mice with a C57BL/6 background.柠檬酸马罗匹坦用于治疗具有C57BL/6背景的小鼠的溃疡性皮炎。
J Am Assoc Lab Anim Sci. 2011 Mar;50(2):221-6.
4
Nutritional up-regulation of serotonin paradoxically induces compulsive behavior.营养上调血清素会反常地诱导强迫行为。
Nutr Neurosci. 2010 Dec;13(6):256-64. doi: 10.1179/147683010X12611460764688.
5
Primary follicular dystrophy with scarring dermatitis in C57BL/6 mouse substrains resembles central centrifugal cicatricial alopecia in humans.C57BL/6 小鼠亚系的原发性滤泡性萎缩伴瘢痕性皮炎类似于人类的中心性离心性瘢痕性脱发。
Vet Pathol. 2011 Mar;48(2):513-24. doi: 10.1177/0300985810379431. Epub 2010 Sep 22.
6
An evidence-based review of the efficacy of topical antihistamines in the relief of pruritus.局部用抗组胺药缓解瘙痒疗效的循证综述
J Drugs Dermatol. 2010 Aug;9(8):992-7.
7
Etiopathogenesis of mandibulofacial and maxillofacial abscesses in mice.小鼠下颌面部和颌面脓肿的病因发病机制
Comp Med. 2010 Jun;60(3):200-4.
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Treatment of canine atopic dermatitis: 2010 clinical practice guidelines from the International Task Force on Canine Atopic Dermatitis.犬异位性皮炎的治疗:国际犬异位性皮炎特别工作组2010年临床实践指南
Vet Dermatol. 2010 Jun;21(3):233-48. doi: 10.1111/j.1365-3164.2010.00889.x. Epub 2010 Apr 23.
9
Vitamin E in human health and disease.维生素E与人类健康和疾病
Crit Rev Clin Lab Sci. 2008;45(5):417-50. doi: 10.1080/10408360802118625.
10
Oxidative stress in normal and impaired wound repair.正常及受损伤口修复中的氧化应激
Pharmacol Res. 2008 Aug;58(2):165-71. doi: 10.1016/j.phrs.2008.06.004. Epub 2008 Jun 19.

C57BL/6小鼠的溃疡性皮肤炎表现出与正常伤口愈合一致的氧化应激反应。

Ulcerative dermatitis in C57BL/6 mice exhibits an oxidative stress response consistent with normal wound healing.

作者信息

Williams Lisa K, Csaki Lauren S, Cantor Rita M, Reue Karen, Lawson Greg W

机构信息

Division of Laboratory Animal Medicine, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California, USA.

出版信息

Comp Med. 2012 Jun;62(3):166-71.

PMID:22776048
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3364703/
Abstract

Ulcerative dermatitis (UD) is a common syndrome of unknown etiology that results in profound morbidity in C57BL/6 mice and lines on a C57BL/6 background. The lesions are due to severe pruritus-induced self-trauma, progressing from superficial excoriations to deep ulcerations. UD may be behavioral in origin, with ulcerative lesions resulting from self-mutilating behavior in response to unresolved inflammation or compulsion. Alternatively, abnormal oxidative damage may be a mechanism underlying UD. To evaluate whether UD behaves similarly to normal wounds, consistent with a secondary self-inflicted lesion, or is a distinct disorder with abnormal wound response, we evaluated expression levels of genes representing various arms of the oxidative stress response pathway UD-affected and unwounded C57BL/6J mice. No evidence indicated that UD wounds have a defect in the oxidative stress response. Our findings are consistent with an understanding of C57BL/6 UD lesions as typical rather than atypical wounds.

摘要

溃疡性皮炎(UD)是一种病因不明的常见综合征,会导致C57BL/6小鼠及C57BL/6背景品系出现严重发病情况。这些损伤是由严重瘙痒引起的自我创伤所致,从浅表擦伤发展为深部溃疡。UD可能起源于行为因素,溃疡性损伤是因对未解决的炎症或强迫行为的自残行为而产生。另外,异常氧化损伤可能是UD的潜在机制。为了评估UD的表现是与正常伤口相似(符合继发性自我造成的损伤),还是一种具有异常伤口反应的独特病症,我们评估了代表氧化应激反应途径各个分支的基因在受UD影响的和未受伤的C57BL/6J小鼠中的表达水平。没有证据表明UD伤口在氧化应激反应方面存在缺陷。我们的研究结果与将C57BL/6 UD损伤理解为典型而非非典型伤口的观点一致。