光致变色离子通道阻滞剂对角膜冷神经末梢脉冲活动的光化学调节。

IF 7.7 2区 医学 Q1 PHARMACOLOGY & PHARMACY
David Ares-Suárez, Almudena Iñigo-Portugués, Enrique Velasco, Susana Quirce, Fernando Aleixandre-Carrera, Ariadna Díaz-Tahoces, M Carmen Acosta, Wan-Chen Lin, Richard H Kramer, Carlos Belmonte, Juana Gallar, Victor Meseguer
{"title":"光致变色离子通道阻滞剂对角膜冷神经末梢脉冲活动的光化学调节。","authors":"David Ares-Suárez, Almudena Iñigo-Portugués, Enrique Velasco, Susana Quirce, Fernando Aleixandre-Carrera, Ariadna Díaz-Tahoces, M Carmen Acosta, Wan-Chen Lin, Richard H Kramer, Carlos Belmonte, Juana Gallar, Victor Meseguer","doi":"10.1111/bph.70189","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and purpose: </strong>The functional organization of corneal cold nerve endings, critical structures in maintaining the ocular surface, remains poorly understood. Here, the photoisomerizable small-molecule diethylamine-azobenzene-quaternary ammonium (DENAQ) was used to photomodulate activity of cold-sensing nerve terminals in control and chronic tear-deficient corneas. Furthermore, DENAQ was used for in vivo photochemical regulation of the thermally induced blink reflex.</p><p><strong>Experimental approach: </strong>Extracellular nerve terminal impulse activity was recorded on cold terminals in excised corneas of naïve and tear-deficient guinea pigs pre-incubated with DENAQ. Pulses of light at a wavelength of 460 nm were delivered to the perfused corneas. The thermally induced blink reflex was assessed using orbicularis oculi electromyography in anaesthetised rats after topical administration of DENAQ to the eye under blue light and darkness conditions.</p><p><strong>Key results: </strong>Exposure to blue light robustly reduced spontaneous activity of both naïve and tear-deficient cold nerve terminals pre-incubated with DENAQ, while cold-evoked responses remained unaffected. Pre-incubation of excised corneas with DENAQ, along with pharmacological P2X receptor antagonists, prevented the DENAQ-mediated photoreduction of the cold nerve terminal spontaneous activity. In addition, blue light increased cold-evoked reflex blink in eyes pre-treated with DENAQ.</p><p><strong>Conclusion and implications: </strong>DENAQ enters guinea pig cold sensory nerve endings primarily through P2X channels in excised corneas. Subsequently, DENAQ decreases the spontaneous nerve terminal impulse activity upon light irradiation by modulating voltage-gated potassium (K<sub>V</sub>) channel activity. Furthermore, the cold-evoked blink reflex is modulated by light in DENAQ-treated eyes. Chemical photoswitches like DENAQ might be potential new treatments for ocular discomfort and pain in dry eye disease.</p>","PeriodicalId":9262,"journal":{"name":"British Journal of Pharmacology","volume":" ","pages":""},"PeriodicalIF":7.7000,"publicationDate":"2025-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Optochemical modulation of corneal cold nerve terminal impulse activity with a photochromic ion channel blocker.\",\"authors\":\"David Ares-Suárez, Almudena Iñigo-Portugués, Enrique Velasco, Susana Quirce, Fernando Aleixandre-Carrera, Ariadna Díaz-Tahoces, M Carmen Acosta, Wan-Chen Lin, Richard H Kramer, Carlos Belmonte, Juana Gallar, Victor Meseguer\",\"doi\":\"10.1111/bph.70189\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background and purpose: </strong>The functional organization of corneal cold nerve endings, critical structures in maintaining the ocular surface, remains poorly understood. Here, the photoisomerizable small-molecule diethylamine-azobenzene-quaternary ammonium (DENAQ) was used to photomodulate activity of cold-sensing nerve terminals in control and chronic tear-deficient corneas. Furthermore, DENAQ was used for in vivo photochemical regulation of the thermally induced blink reflex.</p><p><strong>Experimental approach: </strong>Extracellular nerve terminal impulse activity was recorded on cold terminals in excised corneas of naïve and tear-deficient guinea pigs pre-incubated with DENAQ. Pulses of light at a wavelength of 460 nm were delivered to the perfused corneas. The thermally induced blink reflex was assessed using orbicularis oculi electromyography in anaesthetised rats after topical administration of DENAQ to the eye under blue light and darkness conditions.</p><p><strong>Key results: </strong>Exposure to blue light robustly reduced spontaneous activity of both naïve and tear-deficient cold nerve terminals pre-incubated with DENAQ, while cold-evoked responses remained unaffected. Pre-incubation of excised corneas with DENAQ, along with pharmacological P2X receptor antagonists, prevented the DENAQ-mediated photoreduction of the cold nerve terminal spontaneous activity. In addition, blue light increased cold-evoked reflex blink in eyes pre-treated with DENAQ.</p><p><strong>Conclusion and implications: </strong>DENAQ enters guinea pig cold sensory nerve endings primarily through P2X channels in excised corneas. Subsequently, DENAQ decreases the spontaneous nerve terminal impulse activity upon light irradiation by modulating voltage-gated potassium (K<sub>V</sub>) channel activity. Furthermore, the cold-evoked blink reflex is modulated by light in DENAQ-treated eyes. Chemical photoswitches like DENAQ might be potential new treatments for ocular discomfort and pain in dry eye disease.</p>\",\"PeriodicalId\":9262,\"journal\":{\"name\":\"British Journal of Pharmacology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":7.7000,\"publicationDate\":\"2025-09-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"British Journal of Pharmacology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1111/bph.70189\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"British Journal of Pharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/bph.70189","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

摘要

背景与目的:角膜冷神经末梢是维持眼表的关键结构,其功能组织尚不清楚。本研究利用光异构化小分子二乙胺偶氮苯季铵(DENAQ)对正常和慢性缺泪角膜冷感神经末梢的活性进行光调节。此外,DENAQ被用于热诱导眨眼反射的体内光化学调节。实验方法:用DENAQ预孵育的naïve和泪液缺失豚鼠,在切除角膜的冷端记录细胞外神经末梢冲动活动。在460纳米波长的光脉冲被传送到灌注角膜。在蓝光和黑暗条件下,局部给药后,用眼轮匝肌电图评估麻醉大鼠的热诱导眨眼反射。关键结果:蓝光暴露显著降低了用DENAQ预先孵育的naïve和缺泪冷神经末梢的自发活动,而冷诱发反应未受影响。与药理学P2X受体拮抗剂一起,用DENAQ预先孵育切除的角膜,阻止了DENAQ介导的冷神经末端自发活性的光还原。此外,蓝光增加了经DENAQ预处理的眼睛的冷诱发反射眨眼。结论和意义:DENAQ主要通过切除角膜的P2X通道进入豚鼠冷感觉神经末梢。随后,DENAQ通过调节电压门控钾(KV)通道活性来降低光照射下自发神经末梢脉冲活动。此外,在denaq处理过的眼睛中,冷诱发的眨眼反射受到光的调节。像DENAQ这样的化学光开关可能是治疗干眼症引起的眼部不适和疼痛的潜在新疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optochemical modulation of corneal cold nerve terminal impulse activity with a photochromic ion channel blocker.

Background and purpose: The functional organization of corneal cold nerve endings, critical structures in maintaining the ocular surface, remains poorly understood. Here, the photoisomerizable small-molecule diethylamine-azobenzene-quaternary ammonium (DENAQ) was used to photomodulate activity of cold-sensing nerve terminals in control and chronic tear-deficient corneas. Furthermore, DENAQ was used for in vivo photochemical regulation of the thermally induced blink reflex.

Experimental approach: Extracellular nerve terminal impulse activity was recorded on cold terminals in excised corneas of naïve and tear-deficient guinea pigs pre-incubated with DENAQ. Pulses of light at a wavelength of 460 nm were delivered to the perfused corneas. The thermally induced blink reflex was assessed using orbicularis oculi electromyography in anaesthetised rats after topical administration of DENAQ to the eye under blue light and darkness conditions.

Key results: Exposure to blue light robustly reduced spontaneous activity of both naïve and tear-deficient cold nerve terminals pre-incubated with DENAQ, while cold-evoked responses remained unaffected. Pre-incubation of excised corneas with DENAQ, along with pharmacological P2X receptor antagonists, prevented the DENAQ-mediated photoreduction of the cold nerve terminal spontaneous activity. In addition, blue light increased cold-evoked reflex blink in eyes pre-treated with DENAQ.

Conclusion and implications: DENAQ enters guinea pig cold sensory nerve endings primarily through P2X channels in excised corneas. Subsequently, DENAQ decreases the spontaneous nerve terminal impulse activity upon light irradiation by modulating voltage-gated potassium (KV) channel activity. Furthermore, the cold-evoked blink reflex is modulated by light in DENAQ-treated eyes. Chemical photoswitches like DENAQ might be potential new treatments for ocular discomfort and pain in dry eye disease.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
15.40
自引率
12.30%
发文量
270
审稿时长
2.0 months
期刊介绍: The British Journal of Pharmacology (BJP) is a biomedical science journal offering comprehensive international coverage of experimental and translational pharmacology. It publishes original research, authoritative reviews, mini reviews, systematic reviews, meta-analyses, databases, letters to the Editor, and commentaries. Review articles, databases, systematic reviews, and meta-analyses are typically commissioned, but unsolicited contributions are also considered, either as standalone papers or part of themed issues. In addition to basic science research, BJP features translational pharmacology research, including proof-of-concept and early mechanistic studies in humans. While it generally does not publish first-in-man phase I studies or phase IIb, III, or IV studies, exceptions may be made under certain circumstances, particularly if results are combined with preclinical studies.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信