Lesion of the area postrema/nucleus of the solitary tract (AP/NTS) attenuates the anorectic effects of amylin and calcitonin gene-related peptide (CGRP) in rats

Peptides. 1998;19(2):309-17. doi: 10.1016/s0196-9781(97)00292-1.


The area postrema/nucleus of the solitary tract (AP/NTS) region plays an important role in the control of food intake since it receives peripheral satiety signals via splanchnic and vagal afferents. Due to the lack of the blood brain barrier in this region, blood borne signals can directly be monitored in the AP/NTS. Furthermore, receptors for anorectic peptides such as amylin or calcitonin gene-related peptide (CGRP) have been found in the AP/NTS. It was therefore the aim of the present study to investigate the role of the AP/NTS region in mediating the anorectic effects of these peptides. Thermal ablation of the AP/NTS resulted in a significant reduction of the anorectic effects of IP injected amylin (5 microg/kg) and CGRP (5 microg/kg) in food deprived rats. The anorectic actions of CCK and BBS were also reduced by the AP/NTS lesion which agrees with previous studies. We conclude that the AP/NTS region is an important brain site for mediating the anorectic effects of amylin and CGRP. It remains to be clarified whether this effect is due to amylin and CGRP action on receptors within the AP/NTS region or peripheral receptors on afferent nerves projecting to the AP/NTS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Afferent Pathways / drug effects
  • Afferent Pathways / physiology
  • Amyloid / pharmacology*
  • Amyloid / physiology
  • Animals
  • Anorexia / chemically induced*
  • Anorexia / physiopathology*
  • Body Weight / drug effects
  • Calcitonin Gene-Related Peptide / pharmacology*
  • Calcitonin Gene-Related Peptide / physiology
  • Eating / drug effects*
  • Eating / physiology*
  • Food Deprivation
  • Islet Amyloid Polypeptide
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Satiation / drug effects
  • Satiation / physiology
  • Solitary Nucleus / drug effects*
  • Solitary Nucleus / injuries
  • Solitary Nucleus / physiology*


  • Amyloid
  • Islet Amyloid Polypeptide
  • Calcitonin Gene-Related Peptide