Gastroenterology
Volume 123, Issue 4 , Pages 1120-1128, October 2002

The role of the gastric afferent vagal nerve in ghrelin-induced feeding and growth hormone secretion in rats☆☆

  • Yukari Date

      Affiliations

    • Department of Internal Medicine, Miyazaki Medical College, Miyazaki
    • National Cardiovascular Center Research Institute, Osaka
  • ,
  • Noboru Murakami

      Affiliations

    • Department of Veterinary Physiology, Faculty of Agriculture, Miyazaki University, Miyazaki
  • ,
  • Koji Toshinai

      Affiliations

    • Department of Internal Medicine, Miyazaki Medical College, Miyazaki
  • ,
  • Shigeru Matsukura

      Affiliations

    • Department of Internal Medicine, Miyazaki Medical College, Miyazaki
  • ,
  • Akira Niijima

      Affiliations

    • Department of Physiology, Niigata University School of Medicine, Niigata, Japan
  • ,
  • Hisayuki Matsuo

      Affiliations

    • National Cardiovascular Center Research Institute, Osaka
  • ,
  • Kenji Kangawa

      Affiliations

    • National Cardiovascular Center Research Institute, Osaka
  • ,
  • Masamitsu Nakazato

      Affiliations

    • Department of Internal Medicine, Miyazaki Medical College, Miyazaki

Received 6 May 2002; accepted 13 June 2002.

Abstract 

Background & Aims: Visceral sensory information is transmitted to the brain through the afferent vagus nerve. Ghrelin, a peptide primarily produced in the stomach, stimulates both feeding and growth hormone (GH) secretion. How stomach-derived ghrelin exerts these central actions is still unknown. Here we determined the role of the gastric afferent vagal nerve in ghrelin's functions. Methods: Food intake and GH secretion were examined after an administration of ghrelin intravenously (IV) to rats with vagotomy or perivagal application of capsaicin, a specific afferent neurotoxin. We investigated Fos expression in neuropeptide Y (NPY)-producing and growth hormone–releasing hormone (GHRH)-producing neurons by immunohistochemistry after administration IV of ghrelin to these rats. The presence of the ghrelin receptor in vagal afferent neurons was assessed by using reverse-transcription polymerase chain reaction and in situ hybridization histochemistry. A binding study on the vagus nerve by 125I-ghrelin was performed to determine the transport of the ghrelin receptor from vagus afferent neurons to the periphery. We recorded the electric discharge of gastric vagal afferent induced by ghrelin and compared it with that by cholecystokinin (CCK), an anorectic gut peptide. Results: Blockade of the gastric vagal afferent abolished ghrelin-induced feeding, GH secretion, and activation of NPY-producing and GHRH-producing neurons. Ghrelin receptors were synthesized in vagal afferent neurons and transported to the afferent terminals. Ghrelin suppressed firing of the vagal afferent, whereas CCK stimulated it. Conclusions: This study indicated that the gastric vagal afferent is the major pathway conveying ghrelin's signals for starvation and GH secretion to the brain.

GASTROENTEROLOGY 2002;123:1120-1128

Abbreviations:  GH , growth hormone, GHRH , growth hormone-releasing hormone, ICV , intracerebroventricular, RT-PCR , reverse-transcription polymerase chain reaction

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 30.00 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

 Address requests for reprints to: Masamitsu Nakazato, M.D., Ph.D., Third Department of Internal Medicine, Miyazaki Medical College, Kiyotake, Miyazaki, 889-1692, Japan. e-mail: nakazato@post.miyazaki-med.ac.jp; fax: (81) 985-85-7902.

☆☆ Supported in part by grants in aid from the Ministry of Education, Culture, Sports, Science, and Technology, Japan, and the Ministry of Health, Labor, and Welfare, Japan (to M.N.).

PII: S0016-5085(02)00217-2

doi:10.1053/gast.2002.35954

Gastroenterology
Volume 123, Issue 4 , Pages 1120-1128, October 2002