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美洲大蠊提取物促进大鼠溃疡性结肠炎肠黏膜修复。

Periplaneta americana extract promotes intestinal mucosa repair of ulcerative colitis in rat.

作者信息

Xue Nan-Nan, He Miao, Li Yue, Wu Jun-Zhu, Du Wen-Wen, Wu Xiu-Mei, Yang Zi-Zhong, Zhang Cheng-Gui, Li Qi-Yan, Xiao Huai

机构信息

Master, Yunnan Provincial, Key Laboratory of Entomological Biopharmaceutical R&D, Dali University, Yunnan, China. Acquisition of data, manuscript preparation.

PhD, National-Local Joint Engineering Research Center of Entomoceutics, Dali University, Yunnan, China. Critical revision, final approval.

出版信息

Acta Cir Bras. 2020 Nov 23;35(10):e202001002. doi: 10.1590/s0102-865020200100000002. eCollection 2020.

Abstract

PURPOSE

To investigate the mechanism of Periplaneta americana extract promoting intestinal mucosal repair of OXZ-induced colitis in rat.

METHODS

All experiments used an equal number of male and female SD rats (n=48). We injected OXZ into the colon to induce UC rat model. To determine the optimal concentration of P. Americana's extract (PA-40), it was classified into low (L), medium (M), and high (H) doses. After OXZ treatment, each drug was administered by enema for 7 consecutive days. Rats were divided into the following 6 groups: (1) Saline treatment group (NC), (2) OXZ treatment UC model group (MC), (3) OXZ + budesonide group (BUN), (4) OXZ + PA-40 L group, (5) OXZ + PA-40 M group, (6) OXZ + PA-40 H group. Disease activity index (DAI) scores, colon length, histopathological score, serum cytokine level (IL-4, IL-10, iNOS, tNOS), and amount of MPO, EGF, IL-13 in colonic mucosa were measured.

RESULTS

PA treatment had a significant healing effect on the OXZ-colitis model and significantly reduced the lesioned area, especially in the PA-40H groups. PA treatment did not alter the expression of IL-10 and MPO level, but increased EGF (epidermal growth factor) and decrease IL-13 in the colonic tissue. PA inhibited the rise of NOSs (nitric oxide synthase) and decreased the serum IL-4 level.

CONCLUSIONS

The data suggest that Periplaneta americana extract may be a potential compound for the treatment of colonic lesions. The mechanism may be related to inhibiting the secretion of IL-13 and promoting the formation of EGF.

摘要

目的

探讨美洲大蠊提取物促进大鼠奥沙拉嗪诱导的结肠炎肠黏膜修复的机制。

方法

所有实验均使用等量的雄性和雌性SD大鼠(n = 48)。我们将奥沙拉嗪注入结肠以诱导UC大鼠模型。为确定美洲大蠊提取物(PA - 40)的最佳浓度,将其分为低(L)、中(M)、高(H)剂量组。奥沙拉嗪处理后,每种药物连续7天灌肠给药。大鼠分为以下6组:(1)生理盐水处理组(NC),(2)奥沙拉嗪处理的UC模型组(MC),(3)奥沙拉嗪 + 布地奈德组(BUN),(4)奥沙拉嗪 + PA - 40低剂量组,(5)奥沙拉嗪 + PA - 40中剂量组,(6)奥沙拉嗪 + PA - 40高剂量组。测量疾病活动指数(DAI)评分、结肠长度、组织病理学评分、血清细胞因子水平(IL - 4、IL - 10、诱导型一氧化氮合酶、总一氧化氮合酶)以及结肠黏膜中髓过氧化物酶(MPO)、表皮生长因子(EGF)、IL - 13的含量。

结果

PA处理对奥沙拉嗪诱导的结肠炎模型有显著的愈合作用,显著减少病变面积,尤其是在PA - 40高剂量组。PA处理未改变IL - 10的表达和MPO水平,但增加了结肠组织中EGF(表皮生长因子)的含量并降低了IL - 13的含量。PA抑制一氧化氮合酶(NOSs)的升高并降低血清IL - 4水平。

结论

数据表明美洲大蠊提取物可能是治疗结肠病变的潜在化合物。其机制可能与抑制IL - 13的分泌和促进EGF的形成有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af39/7709898/f7c60caca3aa/1678-2674-acb-35-10-e202001002-gf01.jpg

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