Xu Lu, Zhao Qin, Xie Yiqiong, Bai Ge, Liu Hongwen, Chen Qi, Duan Hongjue, Wang Lishan, Xu Hang, Sun Yuxiang, Ling Gao, Ge Weihong, Zhu Yun
Department of Pharmacy, Nanjing Drum Tower Hospital Clinical College of Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, Jiangsu Province 210008, China.
Department of Gastroenterology, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing, Jiangsu Province 210008, China.
Colloids Surf B Biointerfaces. 2024 Apr;236:113799. doi: 10.1016/j.colsurfb.2024.113799. Epub 2024 Feb 14.
Inflammatory bowel disease (IBD) remains a global health concern with a complex and incompletely understood pathogenesis. In the course of IBD development, damage to intestinal epithelial cells and a reduction in the expression of tight junction (TJ) proteins compromise the integrity of the intestinal barrier, exacerbating inflammation. Notably, the renin-angiotensin system and angiotensin II receptor type 1 (AT1R) play a crucial role in regulating the pathological progression including vascular permeability, and immune microenvironment. Thus, Telmisartan (Tel), an AT1R inhibitor, loading thermosensitive hydrogel was constructed to investigate the potential of alleviating inflammatory bowel disease through rectal administration. The constructed hydrogel exhibits an advantageous property of rapid transformation from a solution to a gel state at 37°C, facilitating prolonged drug retention within the gut while mitigating irritation associated with rectal administration. Results indicate that Tel also exhibits a beneficial effect in ameliorating colon shortening, colon wall thickening, cup cell lacking, crypt disappearance, and inflammatory cell infiltration into the mucosa in colitis mice. Moreover, it significantly upregulates the expression of TJ proteins in colonic tissues thereby repairing the intestinal barrier damage and alleviating the ulcerative colitis (UC) disease process. In conclusion, Tel-loaded hydrogel demonstrates substantial promise as a potential treatment modality for IBD.
炎症性肠病(IBD)仍然是一个全球关注的健康问题,其发病机制复杂且尚未完全明确。在IBD发展过程中,肠道上皮细胞受损以及紧密连接(TJ)蛋白表达减少会损害肠道屏障的完整性,加剧炎症。值得注意的是,肾素-血管紧张素系统和1型血管紧张素II受体(AT1R)在调节包括血管通透性和免疫微环境在内的病理进展中起关键作用。因此,构建了负载AT1R抑制剂替米沙坦(Tel)的热敏水凝胶,以研究通过直肠给药缓解炎症性肠病的潜力。所构建的水凝胶具有在37°C时从溶液快速转变为凝胶状态的有利特性,有助于药物在肠道内长时间保留,同时减轻与直肠给药相关的刺激。结果表明,替米沙坦在改善结肠炎小鼠的结肠缩短、结肠壁增厚、杯状细胞缺失、隐窝消失以及黏膜炎症细胞浸润方面也具有有益作用。此外,它能显著上调结肠组织中TJ蛋白的表达,从而修复肠道屏障损伤并减轻溃疡性结肠炎(UC)的病程。总之,负载替米沙坦的水凝胶作为IBD的一种潜在治疗方式显示出巨大的前景。