Pretreatment with a CRF antagonist amplifies feeding inhibition induced by fourth ventricular cocaine- and amphetamine-regulated transcript peptide.

Background: Pre-treatment with the corticotropin-releasing factor antagonist α-helical CRF9-41 prevents inhibition of gastric emptying by cocaine-and amphetamine-regulated transcript peptide at a dorsal hindbrain level, but its inhibition of sucrose intake is not affected. This is suggestive of sepa...

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Publicado en:BMC Neuroscience Vol. 20; no. 1
Autores principales: Smedh, Ulrika, Scott, Karen A., Moran, Timothy H.
Formato: research Journal Article
Publicado: BioMed Central 3/18/2019
Acceso en línea:Ver este registro en EBSCOhost
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      jtl: BMC Neuroscience
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      dt: 3/18/2019
      vid: 20
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      pub: BioMed Central
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        NLM30885137
        135400396
        10.1186/s12868-019-0494-8
        NLM30885137
        135400396
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        atl: Pretreatment with a CRF antagonist amplifies feeding inhibition induced by fourth ventricular cocaine- and amphetamine-regulated transcript peptide.
      aug:
        au:
          Smedh, Ulrika
          Scott, Karen A.
          Moran, Timothy H.
        affil: The Surgical Metabolic Research Laboratory, Department of Surgery, Institute of Clinical Sciences, Sahlgrenska Academy University of Gothenburg, and Sahlgrenska University Hospital, 413 45, Gothenburg, Sweden
      sug:
        subj:
          Nerve Tissue Proteins Pharmacodynamics
          Brain Stem Drug Effects
          Peptides Pharmacodynamics
          Corticotropin-Releasing Hormone Antagonists and Inhibitors
          Eating Drug Effects
          Central Nervous System Agents Pharmacodynamics
          Peptides Metabolism
          Eating Physiology
          Animal Studies
          Corticotropin-Releasing Hormone Metabolism
          Rats
          Brain Stem Metabolism
          Male
          Injections, Intraventricular
          Nerve Tissue Proteins Metabolism
          Corticotropin-Releasing Hormone Pharmacodynamics
          Cerebral Ventricles
          Validation Studies
          Comparative Studies
          Evaluation Research
          Multicenter Studies
          Male
      ab: Background: Pre-treatment with the corticotropin-releasing factor antagonist α-helical CRF9-41 prevents inhibition of gastric emptying by cocaine-and amphetamine-regulated transcript peptide at a dorsal hindbrain level, but its inhibition of sucrose intake is not affected. This is suggestive of separable underlying mechanisms of action in the caudal brainstem for cocaine-and amphetamine-regulated transcript peptide with regard to food intake and gastrointestinal functions. Here we further examine cocaine-and amphetamine-regulated transcript peptide-corticotropin-releasing factor receptor interactions in caudal brainstem controls of solid food intake. Injections of combinations of vehicle, cocaine-and amphetamine-regulated transcript peptide (0.5 μg or 1 μg) or α-helical CRF9-41 were given into the fourth cerebral ventricle of rats. Nocturnal solid food intake was recorded over 22 h.Results: Pre-treatment with α-helical CRF9-41 into the fourth ventricle significantly increased the responsivity to cocaine-and amphetamine-regulated transcript peptide on hypophagia. In a separate control experiment, α-helical CRF9-41 pre-treatment blocked CRF-induced food intake inhibition indicative of its antagonistic effectiveness.Conclusions: We conclude that an endogenous Corticotropin-releasing factor agonist may modulate suppression of food intake caused by cocaine-and amphetamine-regulated transcript peptide at a dorsal hindbrain level in the absence of stress. A potential caudal brainstem mechanism whereby cocaine-and amphetamine-regulated transcript peptide effects on food intake is attenuated via corticotropin-releasing factor receptor activity causing tonic inhibition, is suggested.
      pubtype: Academic Journal
      doctype:
        research
        Journal Article
      ougenre: Article
    language: English
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