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依托咪酯抑制小鼠急性组胺和氯喹诱导的搔抓行为。

Ethosuximide inhibits acute histamine- and chloroquine-induced scratching behavior in mice.

机构信息

Department of Physiology and Pharmacology, Hotchkiss Brain Institute, Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.

出版信息

Mol Brain. 2021 Mar 2;14(1):46. doi: 10.1186/s13041-021-00762-1.

Abstract

We have recently reported that the Cav3.2 T-type calcium channel which is well known for its key role in pain signalling, also mediates a critical function in the transmission of itch/pruritus. Here, we evaluated the effect of the clinically used anti-seizure medication ethosuximide, a well known inhibitor of T-type calcium channels, on male and female mice subjected to histaminergic- and non-histaminergic itch. When delivered intraperitoneally ethosuximide significantly reduced scratching behavior of mice of both sexes in response to subcutaneous injection of either histamine or chloroquine. When co-delivered subcutaneously together with either pruritogenic agent ethosuximide was also effective in inhibiting scratching responses in both male and female animals. Overall, our results are consistent with an important role of Cav3.2 T-type calcium channels in modulating histamine-dependent and histamine-independent itch transmission in the primary sensory pathway. Our findings also suggest that ethosuximide could be explored further as a possible therapeutic for the treatment of itch.

摘要

我们最近报道称,Cav3.2 T 型钙通道以其在疼痛信号转导中的关键作用而闻名,它还介导了瘙痒/瘙痒感传递中的关键功能。在这里,我们评估了临床使用的抗癫痫药物乙琥胺对接受组氨酸能和非组氨酸能瘙痒的雄性和雌性小鼠的影响。当腹腔内给药时,乙琥胺显著减少了两种性别的小鼠对皮下注射组胺或氯喹的搔抓行为。当与任何一种致痒剂一起皮下共同给予时,乙琥胺也能有效抑制雄性和雌性动物的搔抓反应。总体而言,我们的结果一致表明,Cav3.2 T 型钙通道在调节原发性感觉通路中组氨酸依赖性和非组氨酸依赖性瘙痒传递中起重要作用。我们的发现还表明,乙琥胺可能作为一种治疗瘙痒的潜在治疗方法进一步探索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6099/7927410/6e254457ec03/13041_2021_762_Fig1_HTML.jpg

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