Skip to main content
Log in

Efficacy of urinary trypsin inhibitor in the treatment of rats with severe sepsis and its effects on coagulation and immunity

  • Original Article
  • Published:
Molecular & Cellular Toxicology Aims and scope Submit manuscript

Abstract

Background

Sepsis is a condition of severe septicemia and septic shock caused by infection, accompanied by multiple organ dysfunction often leading to patients’ admission to the intensive care unit (ICU) and death.

Objective

This study aims to investigate the efficacy of urinary trypsin inhibitor in the treatment of rats with severe sepsis, and to analyze its effects on coagulation and immunity. Sixty Sprague Dawley rats were randomly divided into a model control group (MCG), an ulinastatin group (UG), and a normal control group (n = 20 each). Rats in the model CG and UG were modeled for severe sepsis through cecal ligation and puncture, and the 72 h survival of the rats in the three groups was recorded. The expression of IL-18 and TNF-α before urinary trypsin inhibitor administration and 72 h after administration was detected by an ELISA. Activated partial thromboplastin time (APTT), prothrombin time (PT), thrombin time (TT), and fibrinogen (FIB) were determined using a fully automatic coagulation analyzer. CD4 + , CD8 + , and CD4 + /CD8 + levels were quantitated by flow cytometry.

Results

After administration, compared with those in the MCG, rats in the UG showed higher survival rates (P < 0.05), lower IL-18 and TNF-α expression (P < 0.05), lower APTT, PT, and TT (P < 0.05), higher FIB (P < 0.05), higher CD4 + and CD4 +/CD8 + levels (P < 0.05), and significantly lower CD8 + levels (P < 0.05).

Conclusion

Urinary trypsin inhibitor can increase the survival rate of rats with severe sepsis, reduce their inflammatory responses, and ameliorate coagulation disorders and immune dysfunction.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7

Similar content being viewed by others

References

Download references

Acknowledgements

None.

Funding

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Author information

Authors and Affiliations

Authors

Contributions

In this work, BT and ZL conceived the study and designed the experiments. JY, SW and HZ contributed to the data collection, performed the data analysis and interpreted the results. BT wrote the manuscript; ZL contributed to the critical revision of article. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Zhiheng Li.

Ethics declarations

Conflict of interests

Author Biao Tang, Jiemin Yao, Shengtian Wu, Haibin Zhu, Zhiheng Li declares that have no conflict of interest.

Ethical approval

All applicable international, national and/or institutional guidelines for the care and use of animals were followed. This study was approved by the Animal Ethics Committee of The Second Nanning People’s Hospital.

Informed consent

This article does not contain any studies with human participants performed by any of the authors.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Tang, B., Yao, J., Wu, S. et al. Efficacy of urinary trypsin inhibitor in the treatment of rats with severe sepsis and its effects on coagulation and immunity. Mol. Cell. Toxicol. 19, 753–765 (2023). https://doi.org/10.1007/s13273-022-00303-4

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13273-022-00303-4

Keywords

Navigation