What is the central question of this study? The aim was to propose an animal model for investigating the effects of immunosuppressive monotherapy on gastrointestinal motility using a non-invasive biomagnetic technique. What is main finding and its importance? In our experimental study, immunosuppressive drugs currently in use accelerated gastric emptying whilst increasing the frequency and amplitude of gastric contractions after treatment, except for Mycophenolate and azathioprine. Alternating current biosusceptometry is a useful tool to evaluate side-effects of drugs on the gastrointestinal tract, which will help in understanding the symptoms and improving clinical management of patients. The aim was to propose an animal model for investigating the effects of immunosuppressive monotherapy on gastrointestinal motility using a non-invasive biomagnetic technique. Male Wistar rats were randomly distributed into the following treatment groups: ciclosporin, tacrolimus, prednisone, sirolimus, mycophenolate mofetil, everolimus, azathioprine and control. Each animal was treated for 14 days by gavage with dosages ranging from 1 to 20 mg kg day considering the area-to-volume ratio and hepatic metabolism. Gastrointestinal transit and gastric contractility measurements were evaluated by alternating current biosusceptometry before and after treatment. Gastric emptying was faster in animals treated with tacrolimus, prednisone, sirolimus and everolimus compared with control animals (126.7 ± 12.7 min). There was a significant increase in the frequency of contractions after ciclosporin, tacrolimus, azathioprine and sirolimus treatment compared with control animals (4.6 ± 0.3 cycles min ). Increases in the amplitude of contraction were observed after treatment with tacrolimus, sirolimus and everolimus compared with control rats (34.9 ± 6.0 dB). The results showed that our animal model was suitable for demonstrating that most immunosuppressive drugs currently in use impaired at least one gastrointestinal motility parameter. As a non-invasive technique, alternating current biosusceptometry is a potentially useful tool for evaluation of side-effects of drugs in gastrointestinal tract, helping us to understand the symptoms to improve clinical management of patients.
Our aim was to verify the effects of prednisone related to gastrointestinal motility, intestinal histology, and mucosal mast cells in rats. Two-month-old male Wistar rats were randomly assigned to control group (vehicle) animals receiving saline 0.9% (n = 7) or treated orally with 0.625 mg/kg/day of prednisone (n = 7) or 2.5 mg/kg/day of prednisone (n = 7) during 15 days. Mast cells and other histologic analyses were performed in order to correlate to gastric emptying, cecum arrival, and small intestine transit evaluated by Alternating Current Biosusceptometry. Results showed that prednisone in adult rats increased the frequency of gastric contractions, hastened gastric emptying, slowed small intestinal transit, and reduced mucosal mast cells. Histologically, the treatment with both doses of prednisone decreased villus height, whereas longitudinal and circular muscles and crypt depth were not affected. These findings indicate an impairment of intestinal absorption which may be linked to several GI dysfunctions and symptoms. The relationship between gastrointestinal motor disorders and cellular immunity needs to be clarified in experimental studies since prednisone is one of the most prescribed glucocorticoids worldwide.
Background:
Triple immunosuppressive therapy is associated with several gastrointestinal disorders. The aim of
this study was to investigate the effects induced by the triple immunosuppressive therapy on the gastrointestinal
tract of rats.
Methods:
Male Wistar rats were randomly assigned into three experimental groups: Control:
filtered water; TAC+MPS+PRED: treated with Tacrolimus plus Mycophenolate Sodium plus Prednisone; and
CSA+AZA+PRED: treated with Cyclosporine plus Azathioprine plus Prednisone. The treatment was done for 14
days by gavage. Gastric emptying and contractility were evaluated by the Alternating Current Biosusceptometry
(ACB) and Electrogastrography (EGG). Histological, biochemical and hematological analysis were also
performed.
Results:
Gastric emptying time was slower in the CSA + AZA + PRED group in comparison with
control (p < 0.01) and TAC + MPS + PRED groups (p < 0.001). Animals treated with TAC + MPS + PRED
showed accelerated gastric emptying (p<0.05) compared to control. The amplitude of gastric contractions in both
immunosuppressed groups was higher than observed in the control. The frequency of gastric contractions for the CSA+AZA+PRED group was also increased (p<0.01). Results obtained by EGG were similar to those recorded
with the ACB. The thickness of circular layer from stomach muscle decreased in both immunosuppressed
groups, while longitudinal layer was reduced only in the CSA+AZA+PRED group.
Conclusion:
Triple
immunosuppressive therapy alters gastric motility and compromise the muscular layers and the association
between CSA, AZA, and PRED provokes the major alterations in structure and gastric function. Specific
gastrointestinal side effects resulting from different immunosuppressive therapies still need to be elucidated in
order to provide more effective and personalized therapy for patients.
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