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黄连素对急性坏死性胰腺炎及相关肺损伤的影响。

Effects of Berberine on Acute Necrotizing Pancreatitis and Associated Lung Injury.

作者信息

Choi Sun-Bok, Bae Gi-Sang, Jo Il-Joo, Song Ho-Joon, Park Sung-Joo

机构信息

From the *Hanbang Body-fluid Research Center, and †Department of Herbology, School of Oriental Medicine, Wonkwang University, Iksan, Jeonbuk, South Korea.

出版信息

Pancreas. 2017 Sep;46(8):1046-1055. doi: 10.1097/MPA.0000000000000877.

Abstract

OBJECTIVES

We set out to examine whether berberine (BBR) might affect the severity of pancreatitis and pancreatitis-associated lung injury in choline-deficient ethionine-supplemented (CDE) diet-induced severe acute pancreatitis.

METHODS

Severe acute pancreatitis was induced by feeding a CDE diet for 3 days. Berberine was administered intraperitoneally during CDE diet. Mice were killed on days 1, 2, and 3 after the onset of CDE diet. The severity of pancreatitis was assessed by evaluating changes to the pancreas and lung and survival rate. Blood, pancreas, and lung were harvested for further examination. Furthermore, the regulating mechanisms of BBR were evaluated on the pancreas.

RESULTS

Administration of BBR significantly inhibited histological damage to the pancreas and lung and decreased serum level of amylase and lipase, myeloperoxidase activity, cytokine production, and the mortality rate. Furthermore, administration of BBR inhibited activation of nuclear factor kappa B, c-Jun N-terminal kinases, and p38 in the pancreas during CDE diet.

CONCLUSIONS

These findings suggest that BBR attenuates the severity of pancreatitis by inhibiting activation of nuclear factor kappa B, c-Jun N-terminal kinase, and p38 and that BBR could be used as a beneficial agent to regulate AP.

摘要

目的

我们旨在研究小檗碱(BBR)是否可能影响胆碱缺乏乙硫氨酸补充(CDE)饮食诱导的重症急性胰腺炎中胰腺炎的严重程度以及胰腺炎相关的肺损伤。

方法

通过喂食CDE饮食3天诱导重症急性胰腺炎。在CDE饮食期间腹腔注射小檗碱。在CDE饮食开始后的第1、2和3天处死小鼠。通过评估胰腺和肺的变化以及存活率来评估胰腺炎的严重程度。采集血液、胰腺和肺用于进一步检查。此外,在胰腺上评估BBR的调节机制。

结果

给予BBR可显著抑制胰腺和肺的组织学损伤,并降低血清淀粉酶和脂肪酶水平、髓过氧化物酶活性、细胞因子产生以及死亡率。此外,给予BBR可抑制CDE饮食期间胰腺中核因子κB、c-Jun氨基末端激酶和p38的激活。

结论

这些发现表明,BBR通过抑制核因子κB、c-Jun氨基末端激酶和p38的激活来减轻胰腺炎的严重程度,并且BBR可作为调节急性胰腺炎的有益药物。

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