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新型美贝维林衍生物的解痉活性和抗炎作用

Spasmolytic Activity and Anti-Inflammatory Effect of Novel Mebeverine Derivatives.

作者信息

Stoyanova Mihaela, Milusheva Miglena, Gledacheva Vera, Stefanova Iliyana, Todorova Mina, Kircheva Nikoleta, Angelova Silvia, Pencheva Mina, Stojnova Kirila, Tsoneva Slava, Nikolova Stoyanka

机构信息

Department of Organic Chemistry, Faculty of Chemistry, University of Plovdiv, 4000 Plovdiv, Bulgaria.

Department of Bioorganic Chemistry, Faculty of Pharmacy, Medical University of Plovdiv, 4002 Plovdiv, Bulgaria.

出版信息

Biomedicines. 2024 Oct 12;12(10):2321. doi: 10.3390/biomedicines12102321.

DOI:10.3390/biomedicines12102321
PMID:39457637
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11505310/
Abstract

: Irritable bowel syndrome (IBS) has a major negative influence on quality of life, causing cramps, stomach pain, bloating, constipation, etc. Antispasmodics have varying degrees of efficacy. Mebeverine, for example, works by controlling bowel movements and relaxing the muscles of the intestines but has side effects. Therefore, more efficient medication is required. : In the current study, we investigated the synthesis of novel mebeverine analogs and determined ex vivo their spasmolytic and in vitro and ex vivo anti-inflammatory properties. The ability to influence both contractility and inflammation provides a dual-action approach, offering a comprehensive solution for the prevention and treatment of both conditions. : The results showed that all the compounds have better spasmolytic activity than mebeverine and good anti-inflammatory potential. Among the tested compounds, , , and have been pointed out as the most active in all the studies conducted. To understand their mechanism of activity, molecular docking simulation was investigated. The docking analysis explained the biological activities with their calculated Gibbs energies and possibilities for binding both centers of albumin. Moreover, the calculations showed that molecules can bind also the two muscarinic receptors and interleukin-β, hence these structures would exert a positive therapeutic effect owed to interaction with these specific receptors/cytokine. : Three of the tested compounds have emerged as the most active and effective in all the studies conducted. Future in vivo and preclinical experiments will contribute to the establishment of these novel mebeverine derivatives as potential drug candidates against inflammatory diseases in the gastrointestinal tract.

摘要

肠易激综合征(IBS)对生活质量有重大负面影响,会导致痉挛、胃痛、腹胀、便秘等。抗痉挛药有不同程度的疗效。例如,美贝维林通过控制肠道运动和放松肠道肌肉起作用,但有副作用。因此,需要更有效的药物。

在本研究中,我们研究了新型美贝维林类似物的合成,并在体外测定了它们的解痉作用以及在体外和体内的抗炎特性。影响收缩性和炎症的能力提供了一种双重作用方法,为这两种病症的预防和治疗提供了全面的解决方案。

结果表明,所有化合物的解痉活性均优于美贝维林,且具有良好的抗炎潜力。在所测试的化合物中,[具体化合物名称未给出]在所有进行的研究中被指出是最具活性的。为了解它们的活性机制,我们进行了分子对接模拟研究。对接分析通过计算吉布斯自由能以及与白蛋白两个结合中心结合的可能性来解释其生物活性。此外,计算结果表明这些分子还可以与两个毒蕈碱受体和白细胞介素-β结合,因此这些结构通过与这些特定受体/细胞因子相互作用将发挥积极的治疗作用。

在所测试的化合物中,有三种在所有进行的研究中表现出最具活性和有效性。未来的体内和临床前实验将有助于确立这些新型美贝维林衍生物作为治疗胃肠道炎症性疾病的潜在候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/ec7eeccd34ff/biomedicines-12-02321-g007a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/52ad0873dc91/biomedicines-12-02321-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/7f3631734faa/biomedicines-12-02321-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/0b2b75b05700/biomedicines-12-02321-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/eab95f9d7707/biomedicines-12-02321-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/cd4133085d8e/biomedicines-12-02321-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/1bbdee53cfca/biomedicines-12-02321-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/819d4952724d/biomedicines-12-02321-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/ec7eeccd34ff/biomedicines-12-02321-g007a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/52ad0873dc91/biomedicines-12-02321-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/7f3631734faa/biomedicines-12-02321-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/0b2b75b05700/biomedicines-12-02321-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/eab95f9d7707/biomedicines-12-02321-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/cd4133085d8e/biomedicines-12-02321-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/1bbdee53cfca/biomedicines-12-02321-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/819d4952724d/biomedicines-12-02321-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2017/11505310/ec7eeccd34ff/biomedicines-12-02321-g007a.jpg

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