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2003 Fiscal Year Final Research Report Summary

Molecular pharmacological study on the roles of the central noradreneric neurosis in the higher central actions of morphine

Research Project

Project/Area Number 14370743
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Biological pharmacy
Research InstitutionKYOTO UNIVERSITY

Principal Investigator

SATOH Masamichi  Kyoto.University, Grad. Sch. of Pharmaceu. Sci., Professor, 薬学研究科, 教授 (80025709)

Co-Investigator(Kenkyū-buntansha) NAKAGAWA Takayuki  Kyoto University, Grad. Sch. of Pharmaceu. Sci., Instructor, 薬学研究科, 助手 (30303845)
MINAMI Masabumi  Kyoto University, Grad. Sch. of Pharmaceu. Sci., Assistant Professor, 薬学研究科, 助教授 (20243040)
Project Period (FY) 2002 – 2003
Keywordsμ-Opioid receptor / Morphine / Noradrenergic neuron / Transgenic mouse / Knockout mouse / Dopamine-β-hydroxylase / Analgesic effect / Locus coeruleus
Research Abstract

μ-Opioid receptor, a receptor far morphine, is intensely expressed in the noradrenergic neurons located in the locus coeruleus.. These neurons project into various brain regions including the cerebral cortex, hippocampus and amygdala, and are implicated in memory, emotion and stress responses. However, the molecular bases for the regulation of memory, emotion and stress responses through the opioid system remain to be elucidated. In this study, we generated the genetically modified mouse line in which μ-opioid receptors are expressed only in the not adrenergic neurons by means of the crossbreeding between the μ-opioid receptor KO mouse and the transgenic mouse in which the expression of human μ-opioid receptor gene is regulated by DBH (dopamine β-hydroxyrase) promoter. Using this newly generated mouse line, we showed that the μ-opioid receptors expressed in the noradrenergic neurons are involved in the regulation of stress responses, such as the escape behavior and corticosteroid hormone release induced by the stress. In addition, using the μ-opioid receptor KO mice, we demonstrated that most of the analgesic effect of buprenorphine, one of the analgesics clinically used in Japan, is mediated by μ-opioid receptors. These findings are considered to be useful for the understanding of the roles of μ-opioid receptors in the stress responses and for the improvement of clinical use of buprenorphine.

  • Research Products

    (12 results)

All Other

All Publications (12 results)

  • [Publications] Watanabe, T. et al.: "Involvement of noradrenergic system within the central nucleus of the amygdala in naloxone-precipitated morphine withdrawal-induced conditioned place aversion in rats"Psychopharmacology. 170. 80-88 (2003)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Tanimoto, S. et al.: "Differential contributions of the basolateral and central nuclei of the amygdala in the negative affective component of chemical somatic and visceral pains in rats."European Journal of Neuroscience. 18. 2343-2350 (2003)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Nakagawa, T. et al.: "Differential patterns of c-fos mRNA expression in the amygdaloid nuclei induced by chemical somatic and visceral noxious stimuli in rats."Neuroscience Letters. 344. 197-200 (2003)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ozawa, T. et al.: "Effect of gene transfer of GLT-1, a glutamate transporter, into the locus coeruleus by recombinant adenoviruses on morphine physical dependence in rats."European Journal of Neuroscience. 19. 221-226 (2004)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Fukui, M. et al.: "Involvement of locus coeruleus noradrenergic neurons in supraspinal antinociception by α,β-methylene-ATP in rats."Journal of Pharmacological Sciences. 94. 153-160 (2004)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Ide, S.et al.: "Buprenorphine antinociception is abolished, but naloxone-sensitive reward is retained, in μ-opioid receptor knockout mice"Neuropsychopharmacology. (in press). (2004)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Watanabe, T.et al.: "Involvement of noradrenergic system within he central nucleus of the amygdala in nalox-one-precipitated morphine withdrawal-induced conditioned place aversion in rats"Psychopharmacology. 170. 80-88 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Tanimoto, S.et al.: "Differential contributions of the basolateral and central nuclei of the amygdala in the negative affective component of chemical somatic and visceral pains in rats."European Journal of Neuroscience. 18. 2343-2350 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Nakagawa, T.et al.: "Differential patterns of c-fos mRNA expression in the amygdaloid nuclei induced by chemical somatic and visceral noxious stimuli in rats."Neuroscience Letters. 344. 197-200 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ozawa, T.et al.: "Effect of gene transfer of GLT-1, a glutamate transporter, into the locus coeruleus by recombinant adenoviruses on morphine physical dependence in rats."European Journal of Neuroscience. 19. 221-226 (2004)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Fukui, M.et al.: "Involvement of locus coeruleus noradrenergic neurons in supraspinal antinociception by α, β-methylene-ATP in rats."Journal of Pharmacological sciences. 94. 153-160 (2004)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Ide, S.et al.: "Buprenorphine antinociception is abolished, but naloxone-sensitive reward is retained, in μ-opioid receptor knockout mice"Neuropsychopharmacology. (in press).

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 2005-04-19  

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