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大麻二酚减轻肠道细胞的炎症损伤,拓展基于生物材料的治疗方法。

Cannabidiol attenuates inflammatory impairment of intestinal cells expanding biomaterial-based therapeutic approaches.

作者信息

Boehm Elisa, Droessler Linda, Amasheh Salah

机构信息

Institute of Veterinary Physiology, School of Veterinary Medicine, Freie Universität Berlin, Oertzenweg 19b, 14163, Berlin, Germany.

出版信息

Mater Today Bio. 2023 Sep 20;23:100808. doi: 10.1016/j.mtbio.2023.100808. eCollection 2023 Dec.

Abstract

Cannabis-based biomaterials have the potential to deliver anti-inflammatory therapeutics specifically to desired cells, tissues, and organs, enhancing drug delivery and the effectiveness of anti-inflammatory treatment while minimizing toxicity. As a major component of Cannabis, Cannabidiol (CBD) has gained major attention in recent years because of its potential therapeutic properties, e.g., for restoring a disturbed barrier resulting from inflammatory conditions. The aim of this study was to test the hypothesis that CBD has beneficial effects under normal and inflammatory conditions in the established non-transformed intestinal epithelial cell model IPEC-J2. CBD induced a significant increase in transepithelial electrical resistance (TER) values and a decrease in the paracellular permeability of [³H]-D-Mannitol, indicating a strengthening effect on the barrier. Under inflammatory conditions induced by tumor necrosis factor alpha (TNFα), CBD stabilized the TER and mitigated the increase in paracellular permeability. Additionally, CBD prevented the barrier-disrupting effects of TNFα on the distribution and localization of sealing TJ proteins. CBD also affected the expression of TNF receptors. These findings demonstrate the potential of CBD as a component of Cannabis-based biomaterials used in the development of novel therapeutic approaches against inflammatory pathogenesis.

摘要

基于大麻的生物材料有潜力将抗炎治疗剂特异性地递送至所需的细胞、组织和器官,提高药物递送效率和抗炎治疗效果,同时将毒性降至最低。作为大麻的主要成分,大麻二酚(CBD)近年来因其潜在的治疗特性而备受关注,例如,用于修复炎症状态下受损的屏障。本研究的目的是验证以下假设:在已建立的非转化肠上皮细胞模型IPEC-J2中,CBD在正常和炎症条件下均具有有益作用。CBD导致跨上皮电阻(TER)值显著增加,[³H]-D-甘露醇的细胞旁通透性降低,表明对屏障有增强作用。在肿瘤坏死因子α(TNFα)诱导的炎症条件下,CBD稳定了TER并减轻了细胞旁通透性的增加。此外,CBD阻止了TNFα对紧密连接(TJ)蛋白分布和定位的屏障破坏作用。CBD还影响了TNF受体的表达。这些发现证明了CBD作为基于大麻的生物材料的一种成分在开发针对炎症发病机制的新型治疗方法中的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a5f/10539670/e93f2ebdcfe6/ga1.jpg

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