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Increased aversion to bitter-tasting fluids in the Brattleboro rat
Physiology & Behavior
|January 1, 1987
Summary
Brattleboro rats with diabetes insipidus (BDI) exhibit high water intake due to hormone deficiency, but show reduced motivation to drink when faced with aversive tastes. Their motivation to drink is lower than control rats, despite a higher taste threshold for quinine.
Area of Science:
- Physiology
- Animal Behavior
- Endocrinology
Background:
- Brattleboro rats with diabetes insipidus (BDI) exhibit polydipsia, often attributed to vasopressin deficiency.
- Increased fluid consumption in BDI rats may not solely reflect an increased drive to drink.
- Investigating the motivation to drink in BDI rats is crucial for understanding their physiological responses.
Purpose of the Study:
- To assess the drinking motivation of BDI rats compared to Long Evans (LE) rats.
- To determine if BDI rats have a decreased motivation to drink when faced with aversive stimuli.
- To differentiate between physiological thirst and behavioral drive to drink in BDI rats.
Main Methods:
- Administering quinine solutions of varying concentrations as the sole fluid source to BDI and LE rats.
- Measuring 24-hour fluid balance in rats exposed to quinine.
- Conducting two-bottle preference tests with quinine solutions.
- Using sucrose octa-acetate as an alternative aversive taste stimulus.
Main Results:
- BDI rats significantly reduced fluid intake more than LE rats at high quinine concentrations (100 mg/l), indicating reduced drinking motivation.
- BDI rats demonstrated a higher taste threshold for quinine compared to LE rats.
- BDI rats drastically reduced fluid intake when sucrose octa-acetate was the sole fluid source, while LE rats increased consumption.
Conclusions:
- The high water intake in BDI rats is not solely driven by an increased motivation to drink.
- BDI rats exhibit a decreased motivation to drink when presented with aversive taste stimuli.
- Taste aversion plays a significant role in regulating fluid intake in BDI rats, independent of their underlying polydipsia.