ABSTRACT
We compared the in vivo efficacy of two selective CRF2 agonists, mouse urocortin II (mUcn II) and human urocortin III (hUcn III), using food intake, anxious behavior, or ACTH release in CD-1 or Balb/c mice as indices of biological stress responses. All three peptides produced anorexia (Minimal Effective Dose (M.E.D.) for CRF and mUcn II = 0.03 nmol; M.E.D. for hUcn III = 0.3 nmol). Only mUcn II and CRF appeared to increase anxious behaviors in the elevated plus maze test (M.E.D. = 0.3 and 0.01 nmol, respectively). CRF increased the release of plasma ACTH (M.E.D. of 0.3 nmol), while mUcn II and hUcn III had no effect on ACTH release. These data suggest that the CRF2 receptor subtype plays a primary role in the activation of behavioral, but not neuroendocrine, stress responses.
Subject(s)
Anxiety/drug therapy , Corticotropin-Releasing Hormone/administration & dosage , Receptors, Corticotropin-Releasing Hormone/agonists , Stress, Physiological/drug therapy , Adrenocorticotropic Hormone/blood , Animals , Anxiety/blood , Eating/drug effects , Female , Humans , Male , Mice , Mice, Inbred BALB C , Pituitary-Adrenal System/drug effects , Stress, Physiological/blood , UrocortinsABSTRACT
The central melanocortin system has been demonstrated to play an important role in regulating different aspects of energy homeostasis. Understanding the specific contributions of MC3 and MC4 receptors, however, requires specific agonists and antagonists for each of the predominant forms of brain melanocortin receptors, MC3-R and MC4-R. We report here the characterization of a small peptide mimetic MC4-R-specific agonist that possesses both high affinity (K(i)=11.3 nM) and potency (EC(50)=1.62 nM) in vitro and is capable of inhibiting feeding behavior in mice when administered intracerebroventricularly (i.c.v.). Depending on the paradigm, acute (1 h following an overnight fast) or long-term (greater than 6 h under normal nocturnal feeding conditions) feeding inhibition was observed following icv injection. No effect on long-term feeding inhibition was observed with this compound in MC4-R knockout mice, and central administration of this compound had no effect on either metabolic rate or insulin release.
Subject(s)
Energy Metabolism/physiology , Homeostasis/physiology , Receptor, Melanocortin, Type 4/agonists , Tetrahydroisoquinolines/pharmacology , Triazoles/pharmacology , Animals , Cell Line , Eating/drug effects , Eating/physiology , Energy Metabolism/drug effects , Homeostasis/drug effects , Humans , Male , Mice , Mice, Knockout , Receptor, Melanocortin, Type 4/deficiency , Receptor, Melanocortin, Type 4/physiology , Tetrahydroisoquinolines/chemical synthesis , Triazoles/chemical synthesisABSTRACT
The aim of the present study was to investigate the effects of activation or blockade of the CRF(2) receptor subtype on cardiovascular function in conscious rats following systemic i.v. administration of the CRF(2) receptor peptide agonist urocortin 2 given alone and the selective CRF(2) receptor peptide antagonist antisauvagine-30 given alone. Urocortin 2 caused a dose-dependent reduction in mean arterial blood pressure and a dose-dependent increase in heart rate. Pretreatment with antisauvagine-30 blocked the hypotensive effect of urocortin 2. Antisauvagine-30 failed to produce any statistically significant effects on mean arterial blood pressure and heart rate at doses that completely blocked the effects of urocortin 2. These data verify the cardiovascular effects of selective CRF(2) receptor activation, but find no evidence for an endogenous CRF(2)-mediated tone.
