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A small dose of morphine increases intake of and preference for isotonic saline among rats

M Bertino1, M L Abelson, S H Marglin

  • 1Monell Chemical Senses Center, University of Pennsylvania, Philadelphia 19104.

Insights

Morphine administration increased both the intake and preference for saline solutions in water-deprived rats. These findings indicate a role for endogenous opioids in regulating sodium appetite and overall ingestion behaviors.

Area of Science:

  • Neuroscience
  • Behavioral Pharmacology
  • Physiology

Background:

  • Opioid systems play a crucial role in regulating various physiological processes.
  • Sodium appetite is a critical behavior for maintaining fluid and electrolyte balance.
  • Understanding the neurobiological underpinnings of ingestive behaviors is essential for addressing related disorders.

Purpose of the Study:

  • To investigate the effect of morphine on saline intake and preference in a rat model.
  • To explore the potential involvement of endogenous opioid systems in sodium appetite regulation.

Main Methods:

  • Water-deprived rats were provided with hourly access to water and physiological saline (0.9% NaCl).
  • Rats received injections of morphine (2.0 mg/kg) or a placebo prior to ingestive opportunities.
  • Intake and preference for different concentrations of NaCl (0.9% and 1.5%) were measured.

Main Results:

  • Morphine administration significantly increased the intake of 0.9% NaCl.
  • In 1-hour tests, morphine also enhanced the preference for 0.9% NaCl.
  • Increased intake of 1.5% NaCl was observed following morphine administration.

Conclusions:

  • Endogenous opioids are implicated in the regulation of sodium intake.
  • Opioid systems contribute to the control of ingestive behaviors, including salt appetite.

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