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用于溃疡性皮肤病的抗氧化疗法:一种潜在的皮肤搔抓障碍模型。

Antioxidant Therapies for Ulcerative Dermatitis: A Potential Model for Skin Picking Disorder.

作者信息

George Nneka M, Whitaker Julia, Vieira Giovana, Geronimo Jerome T, Bellinger Dwight A, Fletcher Craig A, Garner Joseph P

机构信息

Department of Pathology and Laboratory Medicine, Division of Laboratory Animal Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.

Department of Animal Sciences, Purdue University, West Lafayette, Indiana, United States of America.

出版信息

PLoS One. 2015 Jul 13;10(7):e0132092. doi: 10.1371/journal.pone.0132092. eCollection 2015.

Abstract

Skin Picking Disorder affects 4% of the general population, with serious quality of life impacts, and potentially life threatening complications. Standard psychoactive medications do not help most patients. Similarly, Mouse Ulcerative Dermatitis (skin lesions caused by excessive abnormal grooming behavior) is very common in widely used inbred strains of mice, and represents a serious animal welfare issue and cause of mortality. Treatment options for Ulcerative Dermatitis are largely palliative and ineffective. We have proposed mouse Ulcerative Dermatitis as a model for human Skin Picking Disorder based on similar epidemiology, behavior, and its comorbidity and mechanistic overlap with hair pulling (trichotillomania). We predicted that mouse Ulcerative Dermatitis would be treated by N-Acetylcysteine, as this compound is highly effective in treating both Skin Picking Disorder and Trichotillomania. Furthermore, we hypothesized that N-Acetylcysteine's mode of action is as a precursor to the production of the endogenous antioxidant glutathione in the brain, and therefore intranasal glutathione would also treat Ulcerative Dermatitis. Accordingly, we show in a heterogenous prospective trial, the significant reduction in Ulcerative Dermatitis lesion severity in mice receiving either N-acetylcysteine (oral administration) or glutathione (intranasal). The majority of mice treated with N-acetylcysteine improved slowly throughout the course of the study. Roughly half of the mice treated with glutathione showed complete resolution of lesion within 2-4 weeks, while the remainder did not respond. These findings are the first to show that the use of N-acetylcysteine and Glutathione can be curative for mouse Ulcerative Dermatitis. These findings lend additional support for mouse Ulcerative Dermatitis as a model of Skin Picking Disorder and also support oxidative stress and glutathione synthesis as the mechanism of action for these compounds. As N-Acetylcysteine is poorly tolerated by many patients, intranasal glutathione warrants further study as potential therapy in Skin Picking, trichotillomania and other body-focused repetitive behavior disorders.

摘要

皮肤搔抓障碍影响着4%的普通人群,对生活质量有严重影响,并且可能引发危及生命的并发症。标准的精神活性药物对大多数患者并无帮助。同样,小鼠溃疡性皮肤病(由过度异常梳理行为导致的皮肤损伤)在广泛使用的近交系小鼠中非常常见,这是一个严重的动物福利问题,也是导致小鼠死亡的原因。溃疡性皮肤病的治疗方法大多只是缓解症状,效果不佳。基于相似的流行病学、行为表现,以及它与拔毛癖(拔毛症)的共病情况和机制重叠,我们提出将小鼠溃疡性皮肤病作为人类皮肤搔抓障碍的模型。我们预测N-乙酰半胱氨酸可以治疗小鼠溃疡性皮肤病,因为这种化合物在治疗皮肤搔抓障碍和拔毛癖方面都非常有效。此外,我们假设N-乙酰半胱氨酸的作用方式是作为大脑中内源性抗氧化剂谷胱甘肽产生的前体,因此鼻内给予谷胱甘肽也可以治疗溃疡性皮肤病。相应地,我们在一项异质性前瞻性试验中表明,接受N-乙酰半胱氨酸(口服)或谷胱甘肽(鼻内给药)的小鼠,其溃疡性皮肤病损伤严重程度显著降低。在整个研究过程中,大多数接受N-乙酰半胱氨酸治疗的小鼠改善缓慢。大约一半接受谷胱甘肽治疗的小鼠在2至4周内损伤完全消退,而其余小鼠则没有反应。这些发现首次表明,使用N-乙酰半胱氨酸和谷胱甘肽可以治愈小鼠溃疡性皮肤病。这些发现进一步支持了将小鼠溃疡性皮肤病作为皮肤搔抓障碍的模型,也支持氧化应激和谷胱甘肽合成作为这些化合物的作用机制。由于许多患者对N-乙酰半胱氨酸耐受性较差,鼻内给予谷胱甘肽作为皮肤搔抓、拔毛癖和其他身体聚焦重复行为障碍的潜在治疗方法值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/defc/4500395/e7716475448b/pone.0132092.g001.jpg

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