Related Experiment Videos
Increased fat consumption induced by morphine administration in rats
Pharmacology, Biochemistry, and Behavior
|June 1, 1982
Summary
Morphine sulfate administration altered rat feeding patterns, increasing fat intake and decreasing carbohydrate intake. Protein consumption remained largely unchanged across different dietary self-selection regimes.
Area of Science:
- Nutritional Neuroscience
- Behavioral Pharmacology
- Animal Nutrition
Background:
- Opioid drugs, such as morphine, are known to affect feeding behavior and appetite regulation.
- Understanding how macronutrient selection is influenced by pharmacological agents is crucial for comprehending food intake control.
- Previous research has indicated that opioids can alter taste preferences and food reward pathways.
Purpose of the Study:
- To investigate the effects of varying doses of morphine sulfate on caloric intake and macronutrient self-selection in male rats.
- To determine if morphine influences the choice between protein, fat, and carbohydrate under different dietary conditions.
Main Methods:
- Male rats were administered different doses of morphine sulfate (0.0, 1.0, 10.0, 20.0 mg/kg).
- Animals had access to either a standard chow or a self-selection diet with high-fat or isocaloric fat options.
- Nutrient intake was measured over a six-hour period post-injection at multiple time points (1, 2, 4, 6 hours).
Main Results:
- Morphine administration led to a significant increase in fat intake across both self-selection dietary regimes.
- Carbohydrate intake was suppressed in a dose-dependent manner following morphine injections.
- Protein intake showed minimal alterations regardless of morphine dose or dietary availability.
Conclusions:
- Morphine sulfate selectively alters macronutrient selection in rats, promoting fat consumption while reducing carbohydrate intake.
- These findings suggest that opioid pathways play a significant role in modulating dietary fat preference and carbohydrate aversion.
- The observed changes in macronutrient choice highlight the complex interplay between opioid signaling and appetite regulation.