大麻缓解醋酸诱导的大鼠溃疡性结肠炎:靶向CB1/SIRT/MAPK信号通路

IF 2.9 4区 医学 Q3 IMMUNOLOGY Immunopharmacology and Immunotoxicology Pub Date : 2024-12-25 DOI:10.1080/08923973.2024.2445733
Rania Elgohary, Enayat A Omara, Abeer Salama
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引用次数: 0

摘要

背景:溃疡性结肠炎(UC)是一种常见的炎症性肠病(IBD),可引起直肠和结肠最内层的持久炎症。目的:探讨大麻对大鼠醋酸性结肠炎的改善作用。材料与方法:1组:正常对照组直肠内给予0.9%生理盐水溶液;2组:醋酸(AA)组患者直肠内给予醋酸2 mL,浓度为4% (v/v),加入0.9% NaCl溶液)1次;第3组和第4组:溃疡性结肠炎诱导大鼠,先直肠内注射乙酸,再注射紫花苜蓿(20和40 mg/kg,每天,连续8天)。结果:苜蓿预处理后结肠结构异常明显改善。此外,它显著降低MDA水平,防止GSH含量的消耗。此外,芥蓝对NF-κB、MAPK、ERK、PI3K、AKT、HIF-1α和TLR4等促炎细胞因子均有抑制作用。此外,它显著上调结肠组织中SIRT和CB1的水平。结论:本研究通过抑制TLR-4 MAPK/ERK、PI3K和NFκB信号通路,为芥蓝对aa诱导的UC大鼠CB1受体激活提供了新的影响。
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Cannabis sativa alleviates experimentally acetic acid- induced ulcerative colitis in rats: targeting CB1/SIRT/MAPK signaling pathways.

Background: Ulcerative colitis (UC) is a frequent inflammatory bowel disease (IBD) that causes long-lasting inflammation in the innermost lining of the rectum and colon.

Objective: The aim of this study was to evaluate the therapeutic effect of Cannabis sativa (C. sativa) on the amelioration of acetic acid-induced colitis in rats.

Materials and methods: Group 1: normal control group was intrarectally administered saline solution (0.9%); group 2: acetic acid (AA) group was given AA intra-rectally (2 mL of 4% (v/v) in 0.9% NaCl) once.; group 3&4: This group represented the ulcerative colitis-induced rats that were injected with acetic acid intra-rectally, then s.c. injection with C. sativa (20 and 40 mg/kg daily for 8 days).

Results: Colonic architectural abnormality significantly improved after pretreatment with C. sativa. Additionally, it significantly reduced the MDA level and prevented the depletion of GSH content. Moreover, C. sativa administration showed suppressive activities on pro-inflammatory cytokines, including NF-κB, MAPK, ERK, PI3K, AKT, HIF-1α, and TLR4. Moreover, it significantly upregulated the level of SIRT and CB1 in the colon tissue.

Conclusion: This study provided a novel impact for CB1 receptor activation produced by C. sativa against AA-induced UC in rats through inhibiting the TLR-4 MAPK/ERK, PI3K, and NFκB signaling pathways.

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来源期刊
CiteScore
5.40
自引率
0.00%
发文量
133
审稿时长
4-8 weeks
期刊介绍: The journal Immunopharmacology and Immunotoxicology is devoted to pre-clinical and clinical drug discovery and development targeting the immune system. Research related to the immunoregulatory effects of various compounds, including small-molecule drugs and biologics, on immunocompetent cells and immune responses, as well as the immunotoxicity exerted by xenobiotics and drugs. Only research that describe the mechanisms of specific compounds (not extracts) is of interest to the journal. The journal will prioritise preclinical and clinical studies on immunotherapy of disorders such as chronic inflammation, allergy, autoimmunity, cancer etc. The effects of small-drugs, vaccines and biologics against central immunological targets as well as cell-based therapy, including dendritic cell therapy, T cell adoptive transfer and stem cell therapy, are topics of particular interest. Publications pointing towards potential new drug targets within the immune system or novel technology for immunopharmacological drug development are also welcome. With an immunoscience focus on drug development, immunotherapy and toxicology, the journal will cover areas such as infection, allergy, inflammation, tumor immunology, degenerative disorders, immunodeficiencies, neurology, atherosclerosis and more. Immunopharmacology and Immunotoxicology will accept original manuscripts, brief communications, commentaries, mini-reviews, reviews, clinical trials and clinical cases, on the condition that the results reported are based on original, clinical, or basic research that has not been published elsewhere in any journal in any language (except in abstract form relating to paper communicated to scientific meetings and symposiums).
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