World Journal of Gastroenterology · 2002 · 60 citations · 40 references
MedicineEndocrinologyPharmacologyPharmacodynamicsReproductive EndocrinologyReproductive PhysiologyDigestive PhysiologyGastrointestinal FunctionGastrointestinal PhysiologyGastrointestinal TransitOxytocin PhysiologyProgesterone TherapyAltered Gastrointestinal MotilityGastric Emptying TimeGastrointestinal Motility ControlIntestinal Transit TimeMaternal OxytocinProgesterone PharmacodynamicsProgesterone PharmacologySmall Intestinal Transit
AIM: To study the dose-dependent of progesterone (P) effect and the interaction between the oxytocin (OT) and P on gastrointestinal motility. METHODS: In order to monitor the gastric emptying and intestinal transit, the SD male rats were intubated via a catheter with normal saline (3 ml/kg) containing Na(2)(51)CrO(4) (0.5 microCi/ml) and 10% charcoal. OT was dissolved into normal saline and P was dissolved into 75% alcohol. RESULTS: Low does of P (1 mg/kg, i.p.) enhanced the gastric emptying (75+/-3%, P<0.05) and high dose of P (5 mg/kg, i.p.) inhibit it (42+/-11.2%, P<0.01). P (1 mg/kg) increased the intestinal transit (4.2+/-0.3, P<0.05) while the higher dose (10-20 mg/kg) had no effect. OT (0.8 mg/kg, i.p.) inhibited the gastric emptying (23.5+/-9.8%, P<0.01). The inhibitory effects of P(20 mg/kg) (32+/-9.7%, P<0.05) and OT (0.8 mg/kg) on gastric emptying enhanced each other when the two chemicals were administrated simultaneously (17+/-9.4%, P<0.01). CONCLUSION: Low dose of P increased GI motility while high dose of P decreased it. During the later period of pregnancy, elevated plasma level of OT may also participate in the gastrointestinal inhibition.
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Inhibition of oxytocin receptor function by direct binding of progesterone
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