Five groups of rats were included: (1) free-fed controls (2) pair-fed controls (3) prednisolone (delcortol, 4 mg × kg−1 × day−1) (4) prednisolone and GH (1 mg × kg−1 × day−1) (5) prednisolone and Ipamorelin (0.5 mg × kg−1 × day−1). After seven days the hepatic capacity of urea-N synthesis (CUNS) was determined in parallel with measurements of liver mRNA levels of urea cycle enzymes, whole-body N-balance, and N-contents of various organs.
Compared to pair-fed controls, prednisolone increased CUNS (p < 0.01) as well as the expression of urea cycle genes (p < 0.01), and decreased N-balance (p < 0.01) as well as organ N-contents (p < 0.05). Compared to prednisolone treated animals, co-administration of GH reduced CUNS by 33 % (p < 0.01), normalized urea cycle gene expression, improved N-balance 2.5-fold, and normalized or improved organ N-contents. In prednisolone treated rats Ipamorelin reduced CUNS by 20 % (p < 0.05), decreased the expression of urea cycle enzymes, neutralised N-balance, and normalized or improved organ N-contents.
Accelerated nitrogen wasting in the liver and other organs caused by prednisolone treatment was counteracted by treatment with either GH or its secretagogue Ipamorelin, though at the doses given less efficiently by the latter. This functional study of animals confirms that the GH secretagogue exerts GH related metabolic effects and may be useful in the treatment of steroid-induced catabolism.