Jinhong Tablet Reduces Damage of Intestinal Mucosal Barrier in Rats with Acute Biliary Infection via Bcl-2/Bax mRNA and Protein Regulation

OBJECTIVE: To explore the effects and mechanism of Jinhong Tablet on intestinal mucosal barrier function and SIRS in rats with acute biliary infection.

METHODS: 36 SD male rats were divided into three groups: sham operation (control), acute biliary infection (ABI) model, and Jinhong Tablet (Jinhong) group. Jinhong group were force-fed with Jinhong Tablet, while the other two groups received oral saline. At days 3 and 5, morphological changes of intestinal mucosa were assessed. Serum diamine oxidase (DAO), D-lactate, and endotoxin levels were measured. And the genes bcl-2 and bax in intestinal tissues were tested by real-time PCR and Western blotting.

RESULTS: Intestinal damage was significantly less severe in Jinhong group compared with ABI group, as indicated by Chiu's scoring, TUNEL analysis, and serum DAO, D-lactic acid, and endotoxin levels. Additionally, the expression of bax mRNA and protein was decreased and the ratio of bcl-2/bax mRNA and protein was increased compared with ABI group.

CONCLUSION: Jinhong Tablet had a positive intervention on acute biliary infection through improving inflammation and intestinal mucosal barrier, inhibiting excessive apoptosis of intestinal epithelial cells via bax and bcl-2 gene, and protein regulation.

Medienart:

E-Artikel

Erscheinungsjahr:

2017

Erschienen:

2017

Enthalten in:

Zur Gesamtaufnahme - volume:2017

Enthalten in:

Evidence-based complementary and alternative medicine : eCAM - 2017(2017) vom: 03., Seite 4985926

Sprache:

Englisch

Beteiligte Personen:

Liang, Xiaoqiang [VerfasserIn]
Ni, Xiao [VerfasserIn]
Wang, YongQi [VerfasserIn]
Xie, Jinkun [VerfasserIn]
Zhang, Xuelin [VerfasserIn]
Gu, Honggang [VerfasserIn]
Zhang, Jingzhe [VerfasserIn]

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Volltext

Themen:

Journal Article

Anmerkungen:

Date Revised 11.03.2022

published: Print-Electronic

Citation Status PubMed-not-MEDLINE

doi:

10.1155/2017/4985926

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM278991572