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皮肤神经肽:心理压力与慢性炎症性皮肤病之间缺失的环节?

Cutaneous neuropeptides: the missing link between psychological stress and chronic inflammatory skin disease?

作者信息

Keller Jesse Joel

机构信息

Department of Dermatology, Oregon Health & Science University, 3303 S Bond Ave CH16D, Portland, OR, 97239, USA.

出版信息

Arch Dermatol Res. 2023 Sep;315(7):1875-1881. doi: 10.1007/s00403-023-02542-4. Epub 2023 Jan 26.

Abstract

A "brain-skin" connection has been long been observed between chronic stress and chronic inflammatory skin disease including urticaria, psoriasis, atopic dermatitis, and prurigo nodularis. The relationship appears to be bidirectional. Chronic psychological stress has been shown to sustain hyperactivity of the sympathetic branch of the autonomic nervous system. Chronic stress is proinflammatory and in the context of several dermatologic disorders may be associated with an increase in dermal nerve fiber density, mast cells, nerve growth factor and calcitonin-gene-related peptide (CGRP). Furthermore, CGRP elicits a T2-polarized T-cell response that is a hallmark of chronic pruritic conditions such as atopic dermatitis and prurigo nodularis. This T2 response contributes directly to acute pruritus as well as the sensitization of cutaneous sensory neurons that are critical for chronic pruritus. Prurigo nodularis is a debilitating skin disorder featuring prominent nerve structural, neuropeptide, and T2 cytokine aberrations that is a model deserving of future study.

摘要

长期以来,人们一直观察到慢性应激与包括荨麻疹、银屑病、特应性皮炎和结节性痒疹在内的慢性炎症性皮肤病之间存在“脑-皮肤”联系。这种关系似乎是双向的。慢性心理应激已被证明会维持自主神经系统交感神经分支的过度活跃。慢性应激具有促炎作用,在几种皮肤病的情况下,可能与真皮神经纤维密度、肥大细胞、神经生长因子和降钙素基因相关肽(CGRP)的增加有关。此外,CGRP会引发T2极化的T细胞反应,这是特应性皮炎和结节性痒疹等慢性瘙痒性疾病的一个标志。这种T2反应直接导致急性瘙痒以及对慢性瘙痒至关重要的皮肤感觉神经元的致敏。结节性痒疹是一种使人衰弱的皮肤疾病,其特征是神经结构、神经肽和T2细胞因子明显异常,是一个值得未来研究的模型。

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