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通过 GSK3β 激活的动态分析组氨酸介导的乙酰胆碱诱导出汗的衰减。

Dynamic analysis of histamine-mediated attenuation of acetylcholine-induced sweating via GSK3β activation.

机构信息

Department of Dermatology, Course of Integrated Medicine, Graduate School of Medicine, Osaka University, Osaka, Japan.

Department of Dermatology, Course of Integrated Medicine, Graduate School of Medicine, Osaka University, Osaka, Japan.

出版信息

J Invest Dermatol. 2014 Feb;134(2):326-334. doi: 10.1038/jid.2013.323. Epub 2013 Jul 30.

Abstract

Sweating has been associated with the exacerbation of atopic dermatitis (AD) in diverse ways. Acetylcholine (ACh)-mediated sweating is known to be attenuated in AD, but its cause remains obscure. To address this issue, the impact of histamine on ACh-induced sweating was evaluated. Sweating was measured by counting the number of active sweat pores by the starch-iodine reaction and dynamic optical coherence tomography; sweat was visualized using two-photon excitation fluorescence microscopy in mice and the quantitative sudomotor axon reflex test in humans. Both histamine receptor antagonists and H1 receptor (H1R)-knockout (KO) mice were used to determine methodological specificity. Histamine demonstrably inhibited ACh-induced sweating in both mice and humans via H1R-mediated signaling. In sweat glands, ACh inactivated glycogen synthase kinase 3β (GSK3β), a kinase involved in endocytosis and secretion, whereas simultaneous stimulation with histamine activated GSK3β. Results of two-photon excitation fluorescence microscopy confirmed the dynamic motion of sweat and sweat glands after ACh treatment, showing that simultaneous stimulation with histamine altered their dynamic properties. These results indicate that histamine inhibits sweat gland secretions by blocking ACh-induced inactivation of GSK3β. Histamine-mediated hypohidrosis might be involved in the mechanism of abnormal skin dryness in patients with AD.

摘要

出汗与特应性皮炎(AD)的恶化有多种关联。已知 AD 中乙酰胆碱(ACh)介导的出汗会减弱,但原因尚不清楚。为了解决这个问题,评估了组胺对 ACh 诱导出汗的影响。通过淀粉-碘反应和动态光学相干断层扫描来计数活跃的汗孔来测量出汗;在小鼠中使用双光子激发荧光显微镜和在人类中使用定量出汗轴突反射试验来可视化汗水。使用两种组胺受体拮抗剂和 H1 受体(H1R)敲除(KO)小鼠来确定方法学特异性。组胺通过 H1R 介导的信号转导,明显抑制了小鼠和人类的 ACh 诱导的出汗。在汗腺中,ACh 使参与内吞作用和分泌的糖原合酶激酶 3β(GSK3β)失活,而同时用组胺刺激则激活了 GSK3β。双光子激发荧光显微镜的结果证实了 ACh 处理后汗和汗腺的动态运动,表明组胺的同时刺激改变了它们的动态特性。这些结果表明,组胺通过阻断 ACh 诱导的 GSK3β失活来抑制汗腺分泌。组胺介导的少汗可能参与了 AD 患者皮肤干燥异常的机制。

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