Unchanged capacity of urea synthesis during acute phase response in rats
Version of Record online: 19 AUG 2010
© 2010 The Authors. European Journal of Clinical Investigation © 2010 Stichting European Society for Clinical Investigation Journal Foundation
European Journal of Clinical Investigation
Volume 41, Issue 1, pages 16–22, January 2011
How to Cite
Thomsen, K. L., Aagaard, N. K., Nielsen, S. S., Grønbæk, H., Jessen, N., Frystyk, J. and Vilstrup, H. (2011), Unchanged capacity of urea synthesis during acute phase response in rats. European Journal of Clinical Investigation, 41: 16–22. doi: 10.1111/j.1365-2362.2010.02369.x
- Issue online: 8 DEC 2010
- Version of Record online: 19 AUG 2010
- Received 26 March 2010; accepted 22 July 2010
- hepatic amino nitrogen conversion;
- messenger ribonucleic acid;
Eur J Clin Invest 2010; 41 (1): 16–22
Background The acute phase response presents a catabolic event related to increased waste of amino-N via hepatic urea synthesis despite an increased need for amino-N incorporation into acute phase proteins. In our previous studies, tumour necrosis factor-α (TNF-α) acutely up-regulated the in vivo capacity of urea–nitrogen synthesis (CUNS) in rats before the hepatic acute phase response was established. To extend these observations, this study aimed to clarify the regulation of N elimination via urea during the later stages of the acute phase response.
Methods Twenty-four hours after i.v. injection of 25 μg kg−1 TNF-α or placebo, we determined the in vivo CUNS, hepatocyte urea cycle enzyme protein levels and mRNA levels of the urea cycle enzyme genes in pair-fed rats. In addition, serum acute phase proteins and their liver mRNA levels were measured.
Results After TNF-α, CUNS and hepatocyte urea cycle enzyme protein expressions were unchanged while urea cycle enzyme mRNA levels decreased. Liver mRNA levels of α2MG, haptoglobin and α1AGP rose and their serum levels increased equally.
Conclusion Despite a fully established 24-h acute phase response, there was no change in the in vivo capacity for disposal of amino-N by urea synthesis or in the urea cycle enzyme proteins, although the expression of the urea cycle enzyme genes was decreased. Thus, in vivo urea synthesis was not orchestrated together with acute phase protein synthesis so as to limit N waste despite genetic regulation to this effect. This may contribute towards catabolism of inflammation.