Decreased marble burying behavior in female mice lacking neuromedin-B receptor (NMB-R) implies the involvement of NMB/NMB-R in 5-HT neuron function

Brain Res. 2002 Jun 28;942(1-2):71-8. doi: 10.1016/s0006-8993(02)02696-3.

Abstract

Neuromedin B (NMB) is a mammalian bombesin-like peptide distributed widely in the central nervous system. This peptide exerts its function via the NMB receptor (NMB-R). Female NMB-R-deficient mice were used to study the role that NMB/NMB-R may play in 5-HT neuron function since this relationship was suggested in previous in vitro studies. As 5-HT neurons are thought to modulate marble burying behavior, a role for NMB-R in this behavior was assessed. Relative to wild-type mice, NMB-R-deficient mice showed decreased marble burying behavior. However, depletion of 5-HT by treatment with p-chlorophenylalanine (p-CPA) increased burying behavior in NMB-R-deficient mice suggesting that increased levels of 5-HT in the brain cause a decrease in burying behavior in NMB-R-deficient mice. While HPLC analysis showed that 5-HT content in the whole brain does not differ between NMB-R-deficient and wild-type mice, an immunohistochemical analysis of brain sections showed that 5-HT expression in the dorsal raphe (DR) nucleus is elevated in NMB-R-deficient mice. Furthermore, a quantitative RT-PCR analysis revealed that 5-HT(1A)-receptor gene expression is downregulated in NMB-R-deficient mice at the whole brain level. These behavioral and biological results suggest that NMB/NMB-R may modulate 5-HT neuronal activity by affecting DR function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal / physiology*
  • Down-Regulation / genetics
  • Female
  • Fenclonine / pharmacology
  • Immunohistochemistry
  • Male
  • Mice
  • Mice, Knockout
  • Motor Activity / genetics
  • Neurokinin B / analogs & derivatives*
  • Neurokinin B / metabolism*
  • Neurons / metabolism*
  • RNA, Messenger / metabolism
  • Raphe Nuclei / metabolism*
  • Raphe Nuclei / physiopathology
  • Receptors, Bombesin / deficiency*
  • Receptors, Bombesin / genetics
  • Receptors, Serotonin / genetics
  • Receptors, Serotonin, 5-HT1
  • Serotonin / deficiency*
  • Serotonin Antagonists / pharmacology

Substances

  • RNA, Messenger
  • Receptors, Bombesin
  • Receptors, Serotonin
  • Receptors, Serotonin, 5-HT1
  • Serotonin Antagonists
  • Serotonin
  • Neurokinin B
  • neuromedin B
  • Fenclonine