Nuclear Medicine and Biology
Volume 33, Issue 3 , Pages 325-332, April 2006

Effects of anpirtoline on regional serotonin synthesis in the rat brain: an autoradiographic study

  • Arata Watanabe

      Affiliations

    • Permanent address: Department of Neurosurgery, University of Yamanashi, 1110 Shimokato Tamaho-cho, Nakakoma-gun, Yamanashi 409-3898, Japan.
  • ,
  • Akio Nakai

      Affiliations

    • Permanent address: Department of Pediatrics, Faculty of Medical Sciences, University of Fukui, Fukui, Japan.
  • ,
  • Yoshihiro Tohyama

      Affiliations

    • Permanent address: Department of Neurosurgery, Hokkaido University Graduate School of Medicine, North 15, West 7, Kita-ku, Sapporo, Hokkaido 060-8638, Japan.
  • ,
  • Khnah Q. Nguyen
  • ,
  • Mirko Diksic

      Affiliations

    • Corresponding Author InformationCorresponding author. Tel.: +1 514 398 8526; fax: +1 514 398 8195.

Cone Neurological Research Laboratory, Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada H3A 2B4

Received 22 June 2005; received in revised form 9 August 2005; accepted 9 August 2005. published online 13 March 2006.

Abstract 

Anpirtoline has been described as an agonist at 5-HT1B receptors with a relatively high potency. It also acts as an agonist at 5-HT1A receptors, but has a lower potency than at the 5-HT1B sites. There is very little known about the mechanism by which anpirtoline influences regional 5-HT synthesis. The aim of the present study was to investigate the effects of acutely and chronically administered anpirtoline on 5-HT synthesis in the rat brain using the autoradiographic α-[14C]methyl-l-tryptophan method. In the acute study, anpirtoline (2.0 mg/kg) was administered intraperitoneally 30 min before the tracer injection. The control rats were injected with the same volume of saline. In the chronic study, anpirtoline (2 mg/kg per day) was injected subcutaneously in saline once a day for 10 days. There were no significant differences between the plasma-free and total tryptophan concentrations between the anpirtoline treatment and the respective control groups. In the acute experiment, 5-HT synthesis rates in all of the brain areas investigated were significantly decreased by anpirtoline when compared to the saline-treated group. In the chronic anpirtoline experiment, 5-HT synthesis rates of almost all of the projection areas, as well as the raphe nuclei, were normalized or had a tendency to be normalized. These results suggest that it is likely that the terminal 5-HT1B receptors are involved in the regulation of 5-HT synthesis in the projection areas and that 5-HT synthesis, in the raphe, is likely influenced by anpirtoline's 5-HT1A and/or 5-HT1B agonistic properties.

Keywords: Alpha-methyl-l-tryptophan, Autoradiography, Serotonin synthesis rate, Anpirtoline, 5-HT1B agonist

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PII: S0969-8051(05)00203-9

doi:10.1016/j.nucmedbio.2005.08.002

Nuclear Medicine and Biology
Volume 33, Issue 3 , Pages 325-332, April 2006