Evidence map›Paper›PMID 38929866›Full record

ArticleJournal of personalized medicine2024

Effects of NF-κB Inhibitor on Sepsis Depend on the Severity and Phase of the Animal Sepsis Model.

Ye Jin Park, Jinkun Bae, Jae-Kwang Yoo, So-Hee Ahn, Seon Young Park, Yun-Seok Kim, Min Ji Lee, Seon Young Moon, Tae Nyoung Chung, Chulhee Choi and 1 more

Abstract read
In one paragraph

Article in Journal of personalized medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Ye Jin ParkDepartment of Emergency Medicine, CHA University School of Medicine, Seongnam 13497, Republic of Korea.
Jinkun BaeDepartment of Emergency Medicine, CHA University School of Medicine, Seongnam 13497, Republic of Korea.ORCID 0000-0001-9605-7965
Jae-Kwang YooILIAS Biologics Inc., Daejeon 34014, Republic of Korea.
So-Hee AhnILIAS Biologics Inc., Daejeon 34014, Republic of Korea.
Seon Young ParkILIAS Biologics Inc., Daejeon 34014, Republic of Korea.
Yun-Seok KimDepartment of Emergency Medicine, CHA University School of Medicine, Seongnam 13497, Republic of Korea.
Min Ji LeeDepartment of Emergency Medicine, CHA University School of Medicine, Seongnam 13497, Republic of Korea.
Seon Young MoonDepartment of Emergency Medicine, CHA University School of Medicine, Seongnam 13497, Republic of Korea.
Tae Nyoung ChungDepartment of Emergency Medicine, CHA University School of Medicine, Seongnam 13497, Republic of Korea.ORCID 0000-0003-3537-4136
Chulhee ChoiILIAS Biologics Inc., Daejeon 34014, Republic of Korea.ORCID 0000-0001-5542-9136
Kyuseok KimDepartment of Emergency Medicine, CHA University School of Medicine, Seongnam 13497, Republic of Korea.ORCID 0000-0002-7991-9428

Funding

NRF 2020R1A2C3004508
6 · The paper itself

Abstract

Hyperinflammation occurs in sepsis, especially in the early phase, and it could have both positive and negative effects on sepsis. Previously, we showed that a new concept of NF-κB inhibitor, exosome-based super-repressor IκBα (Exo-srIκB) delivery, has a beneficial effect on sepsis. Here, we further investigate the therapeutic effects of Exo-srIκB at different severities and phases of sepsis using an animal polymicrobial intra-abdominal infection model. We used a rat model of fecal slurry polymicrobial sepsis. First, we determined the survival effects of Exo-srIκB on sepsis according to the severity. We used two different severities of the animal sepsis model. The severe model had a mortality rate of over 50%. The mild/moderate model had a less than 30% mortality rate. Second, we administered the Exo-srIκB at various time points (1 h, 6 h, and 24 h after fecal slurry administration) to determine the therapeutic effect of Exo-srIκB at different phases of sepsis. Lastly, we determined the effects of the Exo-srIκB on cytokine production, arterial blood gas, electrolyte, and lactate. The survival gain was statistically significant in the severe sepsis model when Exo-srIκB was administered 6 h after sepsis. Interleukin 6 and interleukin-10 were significantly decreased in the kidney when administered with Exo-srIκB. The laboratory data showed that lactate, glucose, and potassium levels were significantly lowered in the NF-κB inhibitor group. In conclusion, Exo-srIκB exhibited a beneficial therapeutic effect when administered 6 h post fecal slurry administration in a severe sepsis model.

Indexed as

hyperinflammationNF-κB inhibitorrats

Identifiers

PMID38929866
PMCPMC11204870

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.