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原发性和继发性雷诺现象中皮肤瞬时受体电位通道的表达及微血管对冷却的反应性

Skin transient receptor potential channels expression and microvascular reactivity to cooling in primary and secondary Raynaud's phenomenon.

作者信息

Guigui A, Hodaj E, Rendu J, Bidart M, Petre G, Pluchart H, Coutton C, Coste B, Cracowski J L, Blaise S, Roustit M

机构信息

Univ. Grenoble Alpes, Inserm, CHU Grenoble Alpes, HP2, Grenoble, France.

Univ. Grenoble Alpes, Inserm, CHU Grenoble Alpes, CIC 1406, Grenoble, France.

出版信息

Physiol Rep. 2025 Sep;13(17):e70557. doi: 10.14814/phy2.70557.

Abstract

Temperature-sensitive Transient Receptor Potential (TRP) channels contribute to modulating skin vascular tone. Their role in Raynaud's Phenomenon (RP) remains unknown. We aimed to investigate TRPs expression in the skin, along with microvascular reactivity to cooling in patients with primary and secondary RP, compared with healthy subjects. Skin blood flow was measured in 10 regions of interest on the dorsum of the hand before, during, and after a 30-min cooling at 8°C. Skin biopsies were performed from a subset of participants at the distal phalanx before and after cooling. RNAs were extracted, sequenced, and TRPs mRNA expression quantified. TRPs mRNA were successfully quantified, but no significant differences in their expression were observed between groups, or in response to cooling. There was a decreased perfusion at the distal phalanx over time, in secondary RP compared with primary RP (adjusted p = 0.03) or healthy subjects (adjusted p = 0.042). Gene expression profiles were more similar between primary RP and healthy subjects than with secondary RP. This study shows an impairment of microvascular reactivity to cold in secondary, but not in primary RP. Transcriptomic data suggest involvement of the NO pathway in secondary RP, while TRP channel expression appears unchanged; however, their function could be impaired, which should be further investigated.

摘要

温度敏感型瞬时受体电位(TRP)通道有助于调节皮肤血管张力。它们在雷诺现象(RP)中的作用尚不清楚。我们旨在研究原发性和继发性RP患者皮肤中TRP的表达,以及与健康受试者相比,皮肤微血管对冷却的反应性。在8°C下进行30分钟冷却之前、期间和之后,测量手背10个感兴趣区域的皮肤血流量。对一部分参与者在冷却前后的远端指骨进行皮肤活检。提取RNA、进行测序并对TRP的mRNA表达进行定量。成功对TRP的mRNA进行了定量,但在各组之间或对冷却的反应中未观察到其表达有显著差异。与原发性RP或健康受试者相比,继发性RP中远端指骨的灌注随时间减少(校正p = 0.03)或(校正p = 0.042)。原发性RP与健康受试者之间的基因表达谱比与继发性RP之间更相似。这项研究表明,继发性RP中存在微血管对寒冷的反应受损,但原发性RP中没有。转录组学数据表明,NO途径参与了继发性RP,而TRP通道表达似乎未改变;然而,它们的功能可能受损,这有待进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26b4/12422803/9c0a541fca77/PHY2-13-e70557-g001.jpg

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