Chen Jianqing, Yang Hongliang, Sheng Zunlai
College of Veterinary Medicine, Northeast Agricultural University, Harbin, China.
College of Animal Science and Technology, Northeast Agricultural University, Harbin, China.
Front Pharmacol. 2020 Jan 31;10:1681. doi: 10.3389/fphar.2019.01681. eCollection 2019.
Acute diarrhea is still a common and serious disease. The causes of acute diarrhea are very complicated. Therefore, we need to find a medicine to control diarrhea symptoms, save time for diagnosis of pathogens, and prevent drug abuse. Ellagic acid (EA), a natural polyphenol drug, has anti-diarrhea effects. However, the action mechanisms of EA for non-specific diarrhea have not been characterized.
To study the mechanisms of EA, mice were divided into four groups. Group C were intraperitoneally injected with 0.1 ml physiological saline and orally given 0.2 ml physiological saline, and then after experiment began 0.5 h, orally administered 0.3 ml physiological saline. Group D were intraperitoneally injected with 0.1 ml physiological saline and orally given 0.2 ml castor oil, and then after experiment began 0.5 h, orally administered 0.3 ml physiological saline. Group E were intraperitoneally injected with 0.1 ml physiological saline and orally given 0.2 ml castor oil, and then after experiment began 0.5 h, orally administered 0.3 ml EA (10 mg/ml). Group V were intraperitoneally injected with 0.1ml GW9662 (1m g/ml) and orally given 0.2 ml castor oil, and then after experiment began 0.5 h, orally administered 0.3 ml EA (10 mg/ml). Transcriptome were performed on ileum tissues of mice in group D and E. Histological examination and qRT-PCR were performed on ileum tissues of mice in group C, D, E, and V.
We found that a total of 273 differentially expressed genes (DEGs) were obtained, including 160 up-regulated DEGs and 113 down-regulated DEGs. The DEGs were enriched in 458 Gene Ontology (GO) terms and 15 Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways, respectively. The peroxisome proliferator activated receptor (PPAR) signaling pathway was the most significantly enriched in KEGG pathways. We used the PPAR-specific antagonist GW9662 to validate the anti-diarrhea and anti-inflammatory effect of EA in group V compared with group E. Conclusively, EA protected ileums against castor oil-induced inflammation and diarrhea by activating the PPAR signaling pathway and a method was used to study the mechanism of EA.
急性腹泻仍是一种常见且严重的疾病。急性腹泻的病因非常复杂。因此,我们需要找到一种药物来控制腹泻症状,为病原体诊断节省时间,并防止药物滥用。鞣花酸(EA)是一种天然多酚类药物,具有止泻作用。然而,EA对非特异性腹泻的作用机制尚未明确。
为研究EA的作用机制,将小鼠分为四组。C组腹腔注射0.1 ml生理盐水,口服0.2 ml生理盐水,然后在实验开始0.5小时后,口服0.3 ml生理盐水。D组腹腔注射0.1 ml生理盐水,口服0.2 ml蓖麻油,然后在实验开始0.5小时后,口服0.3 ml生理盐水。E组腹腔注射0.1 ml生理盐水,口服0.2 ml蓖麻油,然后在实验开始0.5小时后,口服0.3 ml EA(10 mg/ml)。V组腹腔注射0.1ml GW9662(1mg/ml),口服0.2 ml蓖麻油,然后在实验开始0.5小时后,口服0.3 ml EA(10 mg/ml)。对D组和E组小鼠的回肠组织进行转录组分析。对C组、D组、E组和V组小鼠的回肠组织进行组织学检查和qRT-PCR。
我们发现共获得273个差异表达基因(DEG),其中上调DEG有160个,下调DEG有113个。这些DEG分别富集于458个基因本体(GO)术语和15条京都基因与基因组百科全书(KEGG)通路。过氧化物酶体增殖物激活受体(PPAR)信号通路在KEGG通路中富集最为显著。我们使用PPAR特异性拮抗剂GW9662验证了与E组相比V组中EA的止泻和抗炎作用。最终得出,EA通过激活PPAR信号通路保护回肠免受蓖麻油诱导的炎症和腹泻影响,并且采用了一种方法来研究EA的作用机制。