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Choleretic effect of vasoactive intestinal peptide
Summary
Vasoactive intestinal peptide (VIP) significantly increased bile and sodium output in fasting dogs. Feeding before VIP administration prevented these effects, highlighting VIP
Area of Science:
- Gastroenterology
- Endocrinology
- Physiology
Background:
- Vasoactive intestinal peptide (VIP) is a peptide hormone with diverse physiological roles.
- VIP is known to influence gastrointestinal and biliary functions.
- Understanding VIP's effect on bile secretion is crucial for gastrointestinal research.
Purpose of the Study:
- To investigate the effects of intravenous vasoactive intestinal peptide (VIP) on bile output and composition in anesthetized dogs.
- To determine if feeding status influences VIP's impact on biliary secretion.
Main Methods:
- Anesthetized dogs with common bile duct fistulas were infused intravenously with VIP at dosages of 0.05 and 0.5 mug/kg/min.
- Bile output, sodium, and amylase concentrations were measured in fasting and fed states.
- Control measurements were taken before VIP administration.
Main Results:
- VIP administration significantly increased bile output by approximately 200% in fasting dogs.
- Biliary sodium concentration remained constant, while amylase concentration decreased.
- In fed dogs, VIP had no significant effect on bile output.
- Higher VIP dosage (0.5 mug/kg/min) resulted in a doubled or trebled duration of effect compared to the lower dose.
Conclusions:
- Vasoactive intestinal peptide (VIP) stimulates bile secretion in fasting animals.
- The effect of VIP on bile output is dependent on the animal's feeding status.
- VIP may play a role in regulating bile flow, particularly under fasting conditions.