Non-NMDA receptors in the lateral parabrachial nucleus modulate sodium appetite

Brain Res. 2009 Dec 8:1301:44-51. doi: 10.1016/j.brainres.2009.08.094. Epub 2009 Sep 9.

Abstract

Glutamatergic mechanisms have been implicated in the control of fluid ingestion. In the present study, we investigated whether non-N-methyl-d-aspartate (NMDA) glutamatergic receptors in the lateral parabrachial nucleus (LPBN) are involved in the control of water and sodium intake. Male Sprague-Dawley rats had cannulas implanted bilaterally into the LPBN. They were acutely depleted of water and sodium by injections of the diuretic furosemide (Furo; 10 mg/kg, bw) and given a low dose of the angiotensin-converting enzyme inhibitor, captopril (Cap; 5 mg/kg, bw). Bilateral LPBN injections of the non-NMDA receptor antagonist DNQX (2 and 5 nmol/0.2 microl) increased the ingestion of 0.3 M NaCl and water of Furo/Cap treated rats. The increased ingestion produced by DNQX was abolished by pretreating the LPBN with alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid (AMPA), a non-NMDA receptor agonist. AMPA injected alone into the LPBN reduced water and 0.3 M NaCl intake. Injections of DNQX (5 nmol/0.2 microl) into the LPBN also produced ingestion of 0.3 M NaCl after sc injections of the beta-adrenoceptor agonist, isoproterenol, a hypotensive drug that typically produces only water intake. Food intake, arterial blood pressure and heart rate were not altered by DNQX LPBN injections. We conclude that agonists acting on non-NMDA receptors in the LPBN exert an inhibitory influence on sodium intake during acute fluid depletion with hypotension and after isoproterenol treatment. A possible interaction of serotonin with glutamate within the LPBN is discussed.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Antihypertensive Agents / pharmacology
  • Appetite / drug effects
  • Appetite / physiology*
  • Captopril / pharmacology
  • Catheters, Indwelling
  • Diuretics / pharmacology
  • Drinking / drug effects*
  • Drinking / physiology
  • Eating / drug effects*
  • Eating / physiology
  • Excitatory Amino Acid Agonists / pharmacology
  • Excitatory Amino Acid Antagonists / pharmacology
  • Furosemide / pharmacology
  • Hypotension / chemically induced
  • Male
  • Pons / drug effects
  • Pons / metabolism*
  • Quinoxalines / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, AMPA / metabolism*
  • Sodium, Dietary*
  • Time Factors
  • Water Deprivation
  • alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid / pharmacology

Substances

  • Antihypertensive Agents
  • Diuretics
  • Excitatory Amino Acid Agonists
  • Excitatory Amino Acid Antagonists
  • Quinoxalines
  • Receptors, AMPA
  • Sodium, Dietary
  • FG 9041
  • alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid
  • Furosemide
  • Captopril