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氯菊酯和溴氰菊酯30分钟的暴露会改变皮肤中的离子转运途径。

A 30-Min Exposure on Permethrin and Deltamethrin Modifies Ion Transport Pathways in the Skin.

作者信息

Szewczyk-Golec Karolina, Mądra-Gackowska Katarzyna, Szeleszczuk Łukasz, Szczegielniak Jan, Hołyńska-Iwan Iga

机构信息

Department of Medical Biology and Biochemistry, Faculty of Medicine, Ludwik Rydygier Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Torun, 85-067 Bydgoszcz, Poland.

Department of Geriatrics, Faculty of Health Sciences, Ludwik Rydygier Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Torun, 85-067 Bydgoszcz, Poland.

出版信息

Biomolecules. 2024 Nov 22;14(12):1491. doi: 10.3390/biom14121491.

Abstract

Pyrethroids are pesticides used in agriculture, the textile industry, wood processing, and human and animal medicine. Pyrethroids inhibit voltage-sensitive sodium channels (VSSCs) in insects and mammals. It results in the premature opening and/or delayed closing of the channels, causing a prolonged influx of Na ions into the cell. Insects absorb pyrethroids throughout the entire body surface, while poisoning in humans most often occurs by inhalation and through the skin. In this study, 52 fragments of human skin taken from the eyelid fold were examined. A modified Ussing chamber was used to measure the active ion transport in epithelial tissue and quantify the tissue viability and integrity. Both permethrin and deltamethrin solutions induced changes in the transport of ions, mainly sodium, but by different mechanisms. Permethrin affected the transepithelial transport of sodium ions in a long-term mechanism, while deltamethrin affected the ability to respond to stimuli in an immediate mechanism. Contact with deltamethrin may cause a delay/slowness of sensation, inflammation, hypersensitivity, and/or allergy. The action of permethrin takes place in the intercellular spaces and is associated with the possibility of faster decomposition/metabolism, while deltamethrin interacts with receptors, channels, and the cell membrane, which translates into slower decomposition and longer action in the tissue.

摘要

拟除虫菊酯是用于农业、纺织业、木材加工以及人类和动物医学的杀虫剂。拟除虫菊酯抑制昆虫和哺乳动物体内的电压敏感性钠通道(VSSCs)。这会导致通道过早开放和/或延迟关闭,引起钠离子持续流入细胞。昆虫通过整个体表吸收拟除虫菊酯,而人类中毒最常通过吸入和经皮肤接触发生。在本研究中,对取自眼睑褶皱的52块人类皮肤碎片进行了检查。使用改良的Ussing室来测量上皮组织中的主动离子转运,并量化组织活力和完整性。氯菊酯和溴氰菊酯溶液均会引起离子转运变化,主要是钠离子,但作用机制不同。氯菊酯通过长期机制影响钠离子的跨上皮转运,而溴氰菊酯通过即时机制影响对刺激的反应能力。接触溴氰菊酯可能会导致感觉延迟/迟缓、炎症、超敏反应和/或过敏。氯菊酯的作用发生在细胞间隙,与更快分解/代谢的可能性有关,而溴氰菊酯与受体、通道和细胞膜相互作用,这导致其在组织中分解较慢且作用时间较长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2015/11672964/82d2c04bcb61/biomolecules-14-01491-g001.jpg

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