Mc. Moore et al., Disposition of a mixed meal by conscious dogs after seven days of treatment with cyclosporine A and prednisone, J PARENT EN, 24(4), 2000, pp. 244-250
Background: Combination immunosuppressive therapy, that often includes pred
nisone and cyclosporine A (CyA), is commonly used in the treatment of organ
transplant patients. We hypothesized that CyA and prednisone treatment wou
ld alter the roles of the liver and peripheral tissues in the disposal of c
arbohydrates from a meal, Methods: Using the arteriovenous difference techn
ique, we examined the disposition of an intragastrically delivered mixed me
al in eight 24-hour fasted conscious dogs that had received CyA 15 mg.kg(-1
) daily and prednisone 5 mg twice daily for 7 consecutive days before study
(CyA-prednisone group). The results were compared with those from a group
of 13 dogs (control group) receiving the same meal but no drugs. Results: N
either arterial blood glucose concentrations nor arterial plasma insulin or
glucagon concentrations differed significantly between the groups at any t
ime. Cumulative net gut glucose output was equivalent to 43 +/- 9 vs 57% +/
- 7% of the glucose in the meal in CyA-prednisone vs control (p =.12). The
CyA-prednisone group exhibited greater (p <.05) mean net hepatic glucose up
takes (15.4 +/- 4.6 vs 4.3 +/- 2.2 mu mol.kg(-1).min(-1)) and net hepatic f
ractional extractions of glucose (7.8 +/- 1.6 and 1.5% +/- 1.0%) than the c
ontrol group. Arterial blood lactate concentrations and net hepatic lactate
output were greater in the CyA-prednisone group than the control group (p
<.05). Hepatic glycogen content at the end of the study was 2.5-fold greate
r in the CyA-prednisone group than in the control group (p <.05). The nonhe
patic tissues disposed of approximately 91% of the absorbed glucose in the
control group but only approximately 26% in the CyA-prednisone group (p <.0
5). Conclusions: CyA-prednisone treatment caused a marked shift in the carb
ohydrate disposal from a meal, enhancing the hepatic glucose uptake and dec
reasing peripheral glucose disposal.