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瞬时受体电位通道 A1(TRPA1)和瞬时受体电位通道 M8(TRPM8)作为皮肤微血管冷感受器的相关性。

Relevance of TRPA1 and TRPM8 channels as vascular sensors of cold in the cutaneous microvasculature.

机构信息

Section of Vascular Biology and Inflammation, School of Cardiovascular Medicine and Research, BHF Cardiovascular Centre of Research Excellence, King's College London, Room 3.74, FWB, 150 Stamford Street, London, SE1 9NH, UK.

出版信息

Pflugers Arch. 2018 May;470(5):779-786. doi: 10.1007/s00424-017-2085-9. Epub 2017 Nov 21.

Abstract

Cold exposure is directly related to skin conditions, such as frostbite. This is due to the cold exposure inducing a vasoconstriction to reduce cutaneous blood flow and protect against heat loss. However, a long-term constriction will cause ischaemia and potentially irreversible damage. We have developed techniques to elucidate the mechanisms of the vascular cold response. We focused on two ligand-gated transient receptor potential (TRP) channels, namely, the established "cold sensors" TRP ankyrin 1 (TRPA1) and TRP melastin (TRPM8). We used the anaesthetised mouse and measured cutaneous blood flow by laser speckle imaging. Two cold treatments were used. A generalised cold treatment was achieved through whole paw water immersion (10 °C for 5 min) and a localised cold treatment that will be potentially easier to translate to human studies was carried out on the mouse paw with a copper cold probe (0.85-cm diameter). The results show that TRPA1 and TRPM8 can each act as a vascular cold sensor to mediate the vasoconstrictor component of whole paw cooling as expected from our previous research. However, the local cooling-induced responses were only blocked when the TRPA1 and TRPM8 antagonists were given simultaneously. This suggests that this localised cold probe response requires both functional TRPA1 and TRPM8.

摘要

冷暴露与皮肤状况直接相关,如冻伤。这是因为冷暴露会引起血管收缩,减少皮肤血流量,防止热量流失。然而,长期的收缩会导致缺血和潜在的不可逆转的损伤。我们已经开发出了阐明血管冷反应机制的技术。我们专注于两种配体门控瞬时受体电位 (TRP) 通道,即已确立的“冷传感器”TRP 锚蛋白 1 (TRPA1) 和 TRP 黑色素瘤 (TRPM8)。我们使用麻醉小鼠并通过激光散斑成像测量皮肤血流量。使用了两种冷处理。通过整个爪子水浸(10°C 持续 5 分钟)实现全身性冷处理,而使用铜冷探头(直径 0.85 厘米)在小鼠爪子上进行局部冷处理,这可能更容易转化为人体研究。结果表明,TRPA1 和 TRPM8 都可以作为血管冷传感器,介导整个爪子冷却的血管收缩成分,这与我们之前的研究预期一致。然而,只有当同时给予 TRPA1 和 TRPM8 拮抗剂时,局部冷却引起的反应才会被阻断。这表明这种局部冷探头反应需要功能性 TRPA1 和 TRPM8。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d88f/5942358/54cdc36e3769/424_2017_2085_Fig1_HTML.jpg

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