GLP1激动剂杜拉鲁肽对醋酸诱导的大鼠溃疡性结肠炎的保护作用:GLP-1、TFF-3和TGF-β/PI3K/NF-κB信号通路的参与。

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Raghda N El Mahdy, Manar A Nader, Manar G Helal, Sally E Abu-Risha, Marwa E Abdelmageed
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引用次数: 0

摘要

结肠的慢性炎症称为溃疡性结肠炎(UC),其特点是粘膜表面受到刺激,并从直肠延伸到近端结肠部分。这项研究的目的是确定杜拉鲁肽(Dula)是否能保护大鼠避免因接触醋酸(AA)而患上结肠炎。大鼠被随机分为七组(每组八只):正常对照组、杜拉对照组、AA组(直肠注射2毫升3% v/v AA)、磺胺沙拉嗪(SLZ)组(第11天至第21天口服SLZ(100毫克/千克),第22天直肠注射AA)和杜拉组(每周一次皮下注射50、100或150微克/千克杜拉,连续三周,第22天注射AA,诱发溃疡性结肠炎,第23天采集结肠组织和血液样本)。通过产生结肠组织学偏差,如炎症过程、鹅口疮细胞死亡、腺体增生和粘膜溃疡,杜拉减轻了 AA 诱导的结肠炎。此外,这些变化还降低了血液乳酸脱氢酶(LDH)、C 反应蛋白(CRP)、结肠重量和结肠重量/长度比。此外,杜拉还降低了氧化应激生物标志物丙二醛(MDA),增加了抗氧化酶(总抗氧化能力(TAC)、还原型谷胱甘肽(GSH)和超氧化物歧化酶(SOD)的浓度)。杜拉还能明显减少结肠细胞结构中转化生长因子-1(TGF-β1)、磷脂酰肌醇-3-激酶(PI3K)、蛋白激酶 B(AKT)信号通路以及炎症细胞因子:核因子卡巴 B(NF-κB)、白细胞介素-6(IL-6)和干扰素-γ(IFN-γ)的表达。此外,杜拉还能提高对肠粘膜再生和伤口愈合至关重要的胰高血糖素样肽-1(GLP-1)和三叶因子-3(TFF-3)的水平。通过调节 TGF-β1 以及 PI3K/AKT 和 NF-κB 等其他炎症通路、调节氧化剂/抗氧化剂平衡以及改善肠道屏障的完整性,杜拉能预防 AA 引起的大鼠结肠炎。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protective effect of Dulaglutide, a GLP1 agonist, on acetic acid-induced ulcerative colitis in rats: involvement of GLP-1, TFF-3, and TGF-β/PI3K/NF-κB signaling pathway.

A chronic inflammatory condition of the colon called ulcerative colitis (UC) is characterized by mucosal surface irritation that extends from the rectum to the near proximal colon portions. The rationale of this work was to conclude if dulaglutide (Dula) could protect rats from developing colitis caused by exposure to acetic acid (AA). Rats were randomly divided into seven groups (each with eight rats): Normal control, Dula control, AA (received 2 milliliters of 3% v/v AA through the rectum), Sulfasalazine (SLZ); given SLZ (100 mg/kg) orally from day 11 to day 21 then AA intrarectally on day 22 and Dula groups ( pretreated with 50, 100 or 150 μg/kg subcutaneous injection of Dula - once weekly for three weeks and AA on day 22 to induce ulcerative colitis, colon tissues and blood samples were taken on day 23. By generating colonic histological deviations such as inflammatory processes, goblet cell death, glandular hyperplasia, and mucosa ulcers, Dula dropped AA-induced colitis. Additionally, these modifications diminished blood lactate dehydrogenase (LDH), C-reactive protein (CRP), colon weight, and the weight/length ratio of the colon. In addition, Dula decreased the oxidative stress biomarker malondialdehyde (MDA) and increased the antioxidant enzymes (total antioxidant capacity (TAC), reduced glutathione (GSH), and superoxide dismutase (SOD) concentrations). Dula also significantly reduced the expression of transforming growth factor-1 (TGF-β1), phosphatidylinositol-3-kinase (PI3K), protein kinase B (AKT) signaling pathway, and the inflammatory cytokines: nuclear factor kappa B (NF-κB), interleukin-6 (IL-6), and interferon-γ (IFN-γ) in colonic cellular structures. In addition, Dula enforced the levels of glucagon-like peptide-1 (GLP-1) and trefoil factor-3 (TFF-3) that were crucial to intestinal mucosa regeneration and healing of wounds. By modulating TGF-β1 in conjunction with other inflammatory pathways like PI3K/AKT and NF-κB, regulating the oxidant/antioxidant balance, and improving the integrity of the intestinal barrier, Dula prevented AA-induced colitis in rats.

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来源期刊
CiteScore
6.20
自引率
5.60%
发文量
142
审稿时长
4-8 weeks
期刊介绍: Naunyn-Schmiedeberg''s Archives of Pharmacology was founded in 1873 by B. Naunyn, O. Schmiedeberg and E. Klebs as Archiv für experimentelle Pathologie und Pharmakologie, is the offical journal of the German Society of Experimental and Clinical Pharmacology and Toxicology (Deutsche Gesellschaft für experimentelle und klinische Pharmakologie und Toxikologie, DGPT) and the Sphingolipid Club. The journal publishes invited reviews, original articles, short communications and meeting reports and appears monthly. Naunyn-Schmiedeberg''s Archives of Pharmacology welcomes manuscripts for consideration of publication that report new and significant information on drug action and toxicity of chemical compounds. Thus, its scope covers all fields of experimental and clinical pharmacology as well as toxicology and includes studies in the fields of neuropharmacology and cardiovascular pharmacology as well as those describing drug actions at the cellular, biochemical and molecular levels. Moreover, submission of clinical trials with healthy volunteers or patients is encouraged. Short communications provide a means for rapid publication of significant findings of current interest that represent a conceptual advance in the field.
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