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橙花叔醇缓解结肠炎症:体内和体外模型的实验研究。

Nerolidol Mitigates Colonic Inflammation: An Experimental Study Using both In Vivo and In Vitro Models.

机构信息

Department of Physiology, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain 17666, UAE.

Zayed Bin Sultan Center for Health Sciences, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain 17666, UAE.

出版信息

Nutrients. 2020 Jul 8;12(7):2032. doi: 10.3390/nu12072032.

DOI:10.3390/nu12072032
PMID:32650602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7400891/
Abstract

Nerolidol (NED) is a naturally occurring sesquiterpene alcohol present in various plants with potent anti-inflammatory effects. In the current study, we investigated NED as a putative anti-inflammatory compound in an experimental model of colonic inflammation. C57BL/6J male black mice (C57BL/6J) were administered 3% dextran sodium sulfate (DSS) in drinking water for 7 days to induce colitis. Six groups received either vehicle alone or DSS alone or DSS with oral NED (50, 100, and 150 mg/kg body weight/day by oral gavage) or DSS with sulfasalazine. Disease activity index (DAI), colonic histology, and biochemical parameters were measured. TNF-α-treated HT-29 cells were used as in vitro model of colonic inflammation to study NED (25 µM and 50 µM). NED significantly decreased the DAI and reduced the inflammation-associated changes in colon length as well as macroscopic and microscopic architecture of the colon. Changes in tissue Myeloperoxidase (MPO) concentrations, neutrophil and macrophage mRNA expression (CXCL2 and CCL2), and proinflammatory cytokine content (IL-1β, IL-6, and TNF-α) both at the protein and mRNA level were significantly reduced by NED. The increase in content of the proinflammatory enzymes, COX-2 and iNOS induced by DSS were also significantly inhibited by NED along with tissue nitrate levels. NED promoted Nrf2 nuclear translocation dose dependently. NED significantly increased antioxidant enzymes activity (Superoxide dismutase (SOD) and Catalase (CAT)), Hemeoxygenase-1 (HO-1), and SOD3 mRNA levels. NED treatment in TNF-α-challenged HT-29 cells significantly decreased proinflammatory chemokines (CXCL1, IL-8, CCL2) and COX-2 mRNA levels. NED supplementation attenuates colon inflammation through its potent antioxidant and anti-inflammatory activity both in in vivo and in vitro models of colonic inflammation.

摘要

橙花叔醇(NED)是一种天然存在的倍半萜醇,存在于各种具有强大抗炎作用的植物中。在本研究中,我们研究了 NED 作为一种潜在的抗炎化合物在结肠炎症的实验模型中。C57BL/6J 雄性黑鼠(C57BL/6J)给予饮用水中的 3%葡聚糖硫酸钠(DSS)7 天以诱导结肠炎。六组分别给予载体、DSS 或 DSS 加口服 NED(50、100 和 150 mg/kg 体重/天灌胃)或 DSS 加柳氮磺胺吡啶。测量疾病活动指数(DAI)、结肠组织学和生化参数。使用 TNF-α 处理的 HT-29 细胞作为结肠炎症的体外模型研究 NED(25 µM 和 50 µM)。NED 显著降低 DAI,并减少与炎症相关的结肠长度变化以及结肠的宏观和微观结构变化。NED 显著降低组织髓过氧化物酶(MPO)浓度、中性粒细胞和巨噬细胞 mRNA 表达(CXCL2 和 CCL2)以及促炎细胞因子含量(IL-1β、IL-6 和 TNF-α)的蛋白和 mRNA 水平。DSS 诱导的促炎酶 COX-2 和 iNOS 的含量增加也被 NED 显著抑制,同时组织硝酸盐水平也被抑制。NED 促进 Nrf2 核易位呈剂量依赖性。NED 显著增加抗氧化酶活性(超氧化物歧化酶(SOD)和过氧化氢酶(CAT))、血红素加氧酶-1(HO-1)和 SOD3 mRNA 水平。NED 治疗 TNF-α 刺激的 HT-29 细胞显著降低促炎趋化因子(CXCL1、IL-8、CCL2)和 COX-2 mRNA 水平。NED 补充通过其在体内和体外结肠炎症模型中的强大抗氧化和抗炎活性减轻结肠炎症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c6b/7400891/b2c76c513923/nutrients-12-02032-g007a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c6b/7400891/20c4dbe8c7a8/nutrients-12-02032-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c6b/7400891/5ff289f9b734/nutrients-12-02032-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c6b/7400891/d01162eaca00/nutrients-12-02032-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c6b/7400891/df4624397b1e/nutrients-12-02032-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c6b/7400891/05a92a383ef8/nutrients-12-02032-g006a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c6b/7400891/b2c76c513923/nutrients-12-02032-g007a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c6b/7400891/20c4dbe8c7a8/nutrients-12-02032-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c6b/7400891/9e33f656d078/nutrients-12-02032-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c6b/7400891/5ff289f9b734/nutrients-12-02032-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c6b/7400891/d01162eaca00/nutrients-12-02032-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c6b/7400891/df4624397b1e/nutrients-12-02032-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c6b/7400891/05a92a383ef8/nutrients-12-02032-g006a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c6b/7400891/b2c76c513923/nutrients-12-02032-g007a.jpg

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