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Sax HC, Talamini MA, Hasselgren PO, et al. Increased synthesis of secreted hepatic proteins during abdominal sepsis. J Surg Res. 1988;44(2):109-16doi: 10.1016/0022-4804(88)90038-8.
Sax, H. C., Talamini, M. A., Hasselgren, P. O., Rosenblum, L., Ogle, C. K., & Fischer, J. E. (1988). Increased synthesis of secreted hepatic proteins during abdominal sepsis. The Journal of surgical research, 44(2), 109-16. https://doi.org/10.1016/0022-4804(88)90038-8
Sax, H C, et al. "Increased synthesis of secreted hepatic proteins during abdominal sepsis." The Journal of surgical research vol. 44,2 (1988): 109-16. doi: https://doi.org/10.1016/0022-4804(88)90038-8
Sax HC, Talamini MA, Hasselgren PO, Rosenblum L, Ogle CK, Fischer JE. Increased synthesis of secreted hepatic proteins during abdominal sepsis. J Surg Res. 1988 Feb;44(2):109-16. doi: 10.1016/0022-4804(88)90038-8. PMID: 3339873.
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Elsevier Science

J Surg Res. 1988 Feb;44(2):109-16. doi: 10.1016/0022-4804(88)90038-8.

Increased synthesis of secreted hepatic proteins during abdominal sepsis.

The Journal of surgical research

H C Sax, M A Talamini, P O Hasselgren, L Rosenblum, C K Ogle, J E Fischer

Affiliations

  1. Department of Surgery, University of Cincinnati Medical Center, OH 45267.

PMID: 3339873 DOI: 10.1016/0022-4804(88)90038-8

Abstract

To study the effect of intraabdominal sepsis on hepatic protein synthesis, male Sprague-Dawley rats underwent celiotomy with either cecal ligation and puncture (CLP) or sham operation. Eight and sixteen hours later total hepatic protein synthesis was measured by flooding dose technique. Specific synthetic rates of structural or secreted hepatic proteins were further studied 16 hr after CLP in an isolated perfused liver model. Total hepatic protein synthesis was significantly elevated at 16 hr (59 +/- 6%/day vs 37 +/- 6%/day, P less than 0.05), but not 8 hr post-CLP. Structural hepatic protein synthesis was unchanged after CLP; however, the synthetic rates of the acute-phase secretory proteins alpha 1-acid glycoprotein, transferrin and complement component C3 were significantly increased 16 hr after CLP. However, the albumin synthetic rate was not increased during sepsis. We conclude that sepsis causes augmentation of hepatic protein synthesis primarily to increase acute-phase proteins for host defense.

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