Suppr超能文献

丁香酚对逼尿肌的作用:治疗膀胱过度活动症的潜力。

Effect of Eugenol on Detrusor Muscle: Potential for Overactive Bladder Treatment.

作者信息

Araújo Marília Cavalcante, Pereira-Gonçalves Átila, Cardeal Dos Santos André Nogueira, Freire José Ednésio da Cruz, Peireira-de-Morais Luís, Henrique-Félix Francisco Sydney, Sousa-Júlio Nicoly Câmara Castro, Leal-Cardoso José Henrique, Coelho-de-Souza Andrelina Noronha

机构信息

Experimental Physiology Laboratory, Superior Institute of Biomedical Sciences, State University of Ceará, Fortaleza, Brazil.

Faculty of Education and Integrated Science, State University of Ceará, Crateús, Brazil.

出版信息

Int Neurourol J. 2024 Dec;28(4):253-263. doi: 10.5213/inj.2448326.163. Epub 2024 Dec 31.

Abstract

PURPOSE

This investigation was conducted to elucidate the effects of eugenol on bladder contractility through experimental and in silico approaches.

METHODS

To assess the impact of eugenol on muscular contractility, longitudinal strips of bladder tissue, measuring 2 mm by 6 mm, were mounted in perfusion chambers connected to an isometric force transducer. Furthermore, molecular docking studies were conducted to explore the potential of eugenol to target the M3 muscarinic acetylcholine receptor (M3R) and voltage-operated calcium channels (VOCCs) in muscle cells, utilizing in silico techniques.

RESULTS

Eugenol exhibited a concentration-dependent inhibitory effect on both the phasic and tonic components of the contraction induced by 60mM K+ and carbachol, completely suppressing this contraction at a concentration of 3mM. Additionally, eugenol inhibited the concentration-contraction curve elicited by Ba2+.

CONCLUSION

The in vitro and in silico results suggest that the mechanism of eugenol likely involves blockade of VOCCs and/or M3R, implicating eugenol as a promising molecule for the treatment of overactive bladder.

摘要

目的

本研究旨在通过实验和计算机模拟方法阐明丁香酚对膀胱收缩力的影响。

方法

为评估丁香酚对肌肉收缩力的影响,将2毫米×6毫米的膀胱组织纵向条带安装在与等长力传感器相连的灌注室中。此外,利用计算机模拟技术进行分子对接研究,以探索丁香酚作用于肌肉细胞中M3毒蕈碱型乙酰胆碱受体(M3R)和电压门控钙通道(VOCCs)的可能性。

结果

丁香酚对60mM K +和卡巴胆碱诱导的收缩的相位和张力成分均表现出浓度依赖性抑制作用,在3mM浓度时完全抑制该收缩。此外,丁香酚抑制了Ba2 +引起的浓度-收缩曲线。

结论

体外和计算机模拟结果表明,丁香酚的作用机制可能涉及对VOCCs和/或M3R的阻断,这表明丁香酚是治疗膀胱过度活动症的一个有前景的分子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42f5/11710953/fdc6d0b71d06/inj-2448326-163f1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验