StayCurrentMD · Intestinal tract and parenteral multi-organ sequential pathological injury caused by necrotizing enterocolitis
Article1 min read·Published Nov 2020Older

Intestinal tract and parenteral multi-organ sequential pathological injury caused by necrotizing enterocolitis

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Article · Nov 2020 · 1 min read

In brief

In brief

Experimental rat model demonstrates that necrotizing enterocolitis triggers sequential inflammatory injury across multiple organ systems including intestine, lung, liver, and kidney, with varying timelines of damage and repair. Peak injury occurs within 24 hours, with organ repair processes predominating by day 4 and complete resolution by day 7, accompanied by distinct patterns of apoptosis and cellular proliferation markers across affected tissues.

Written by the GCMD Library team from the article.

Background: To explore the relationship between the pathological changes of the colon, terminal ileum, lung, liver and kidney, and the changes of Bax, PCNA and PAF in a rat model of NEC.

Methods: One hundred and forty neonatal SD rats were randomly divided into NEC group and control group (70 in each group). NEC group was given hypoxia, cold stimulation and artificial feeding twice a day for 3 consecutive days. The control group was only fed normally. After modeling, From the 1st day to the 7th day, 10 rats were sampled in each group for pathological examination of colon, terminal ileum, lung, liver and kidney tissue. The levels of Bax, PCNA and PAF were investigated by immunohistochemistry.

Results: Compared with the normal group, in the NEC group, on the 1st day, the colon, terminal ileum, lung, liver and kidney showed inflammatory damage. On the 5th day, the inflammatory injury was reduced. The inflammation disappeared on the 7th day. There were differences in the time of apoptosis in the intestine. In the intestine, the proliferation of PCNA was weak at first and then strong. Bax in liver and kidney showed marked apoptosis and apoptosis time increased in the lung. The expression of PCNA increased in lung, liver and kidney, and the expression of PAF increased in lung and liver.

Conclusions: NEC can lead to secondary injury of different degrees in colon, terminal ileum, lung, liver and kidney, and the degree and time of injury and repair were different. In general, organ repair played a leading role on the 4th day after modeling.

DOI: 10.1186/s12887-020-02304-5

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