Virgin Coconut Oil Alleviates Dextran Sulphate-Induced Inflammatory Bowel Disease and Modulates Inflammation and Immune Response in Mice.

IF 6.8 4区 医学 Q1 NUTRITION & DIETETICS
Silpa Prabha, Sanjay Tamoli, Achuthan C Raghavamenon, Kanjoormana Aryan Manu
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Abstract

Objective: Virgin coconut oil (VCNO), an unrefined kernel oil from Cocos nucifera L., has considerable medicinal and nutritive value. Experimental evidence suggests its antioxidant, anti-inflammatory, chemoprotective, analgesic, and hypolipidemic effects. Presently, the effect of VCNO on ameliorating dextran sodium sulfate (DSS)-induced inflammatory bowel disease and cyclophosphamide (CTX)-induced immunosuppression in experimental animals was analyzed.

Method: DSS (4%) was administered to BALB/c mice through drinking water for 12 days to induce inflammatory bowel disease, and VCNO (500, 750, and 1000 mg/kg bwt) was supplemented orally for 12 days. For anti-inflammatory studies, lipopolysaccharide (LPS, 250 µg/animal) was injected into the intraperitoneal cavity of Swiss albino mice followed by 7 days' pretreatment of VCNO (500, 750, and 1000 mg/kg bwt). To understand the mechanism of action, serum from all animals was collected after 6 hours of LPS challenge and levels of proinflammatory cytokines were analyzed using enzyme-inked immunosorbent assay. In addition to this, immunosuppression was induced by CTX (50 mg/kg bwt, po) in Swiss albino mice.

Results: Oral administration of VCNO effectively reversed the pathologies associated with inflammatory bowel disease induced by DSS, including loss of body weight, increased disease activity index, shortening of colon length, diarrhea, and rectal bleeding. Histopathological examination showed that VCNO restored the damage in colon tissue induced by DSS. Similar trends were noticed in levels of myeloperoxidase and mRNA expression of proinflammatory cytokines in colon tissue. In addition to this, supplementation of VCNO markedly reduced the hike in the level of serum proinflammatory cytokines in LPS-challenged mice. Further, administration of VCNO effectively increased spleen and thymus indexes and stimulated the production of interferon-γ in serum.

Conclusions: Overall, this study revealed that VCNO alleviates inflammatory bowel disease and inflammation; concurrently, it can revert immunosuppression.

初榨椰子油可减轻右旋糖酐诱导的炎症性肠病,并调节小鼠的炎症和免疫反应。
目的:初榨椰子油(VCNO)是椰子中未精制的仁油,具有较高的药用和营养价值。实验证据表明其具有抗氧化、抗炎、化学保护、镇痛和降血脂作用。目前,分析了VCNO对右旋糖酐硫酸钠(DSS)诱导的实验动物炎症性肠病和环磷酰胺(CTX)诱导的免疫抑制的改善作用。方法:采用饮水法给BALB/c小鼠注射DSS(4%)12只 诱导炎症性肠病的天数,以及VCNO(500、750和1000 毫克/千克体重)口服补充12 天。对于抗炎研究,脂多糖(LPS,250 µg/只动物)注射到瑞士白化小鼠的腹腔内,然后注射7 VCNO预处理天数(500、750和1000 毫克/千克体重)。为了了解作用机制,在6 使用酶联免疫吸附测定法分析LPS激发的小时数和促炎细胞因子的水平。除此之外,CTX(50 毫克/千克体重,po)。结果:口服VCNO可有效逆转DSS诱导的炎症性肠病相关病理,包括体重减轻、疾病活动指数增加、结肠长度缩短、腹泻和直肠出血。组织病理学检查显示VCNO恢复了DSS诱导的结肠组织损伤。结肠组织中髓过氧化物酶水平和促炎细胞因子mRNA表达也出现了类似的趋势。除此之外,补充VCNO显著降低了LPS攻击小鼠血清促炎细胞因子水平的升高。此外,VCNO可有效提高脾脏和胸腺指数,并刺激血清中干扰素-γ的产生。结论:总体而言,本研究表明VCNO可减轻炎症性肠病和炎症;同时,它可以逆转免疫抑制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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