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Hispidulin attenuates the social withdrawal in isolated disrupted-in-schizophrenia-1 mutant and chronic phencyclidine-treated mice.
Mouri, Akihiro; Lee, Hsin-Jung; Mamiya, Takayoshi; Aoyama, Yuki; Matsumoto, Yurie; Kubota, Hisayoshi; Huang, Wei-Jan; Chiou, Lih-Chu; Nabeshima, Toshitaka.
Afiliação
  • Mouri A; Advanced Diagnostic System Research Laboratory, Fujita Health University, Graduate School of Health Sciences, Toyoake, Japan.
  • Lee HJ; Department of Regulatory Science for Evaluation and Development of Pharmaceuticals and Devices, Fujita Health University, Graduate School of Health Sciences, Toyoake, Japan.
  • Mamiya T; Japanese Drug Organization of Appropriate Use and Research, Nagoya, Japan.
  • Aoyama Y; Department of Pharmacology, College of Medicine, National Taiwan University, Taipei, Taiwan.
  • Matsumoto Y; Department of Chemical Pharmacology, Faculty of Pharmacy, Meijo University, Nagoya, Japan.
  • Kubota H; Department of Chemical Pharmacology, Faculty of Pharmacy, Meijo University, Nagoya, Japan.
  • Huang WJ; Department of Chemical Pharmacology, Faculty of Pharmacy, Meijo University, Nagoya, Japan.
  • Chiou LC; Department of Regulatory Science for Evaluation and Development of Pharmaceuticals and Devices, Fujita Health University, Graduate School of Health Sciences, Toyoake, Japan.
  • Nabeshima T; Graduate Institute of Pharmacognosy, Taipei Medical University, Taipei, Taiwan.
Br J Pharmacol ; 177(14): 3210-3224, 2020 07.
Article em En | MEDLINE | ID: mdl-32133633
ABSTRACT
BACKGROUND AND

PURPOSE:

Hispidulin is a flavonoid isolated from Clerodendrum inerme that was found to inhibit intractable motor tics. Previously, we found that hispidulin attenuates hyperlocomotion and the disrupted prepulse inhibition induced by methamphetamine and N-methyl-d-aspartate (NMDA) receptor antagonists, two phenotypes of schizophrenia resembling positive symptoms. Hispidulin can inhibit COMT, a dopamine-metabolizing enzyme in the prefrontal cortex (PFC) that is important for social interaction. Here, we investigated whether hispidulin would affect social withdrawal, one of the negative symptoms of schizophrenia. EXPERIMENTAL

APPROACH:

We examined whether acute administration of hispidulin would attenuate social withdrawal in two mice models, juvenile isolated disrupted-in-schizophrenia-1 mutant (mutDISC1) mice and chronic phencyclidine (PCP)-treated naïve mice. KEY

RESULTS:

In chronic PCP-treated mice, hispidulin (10 mg·kg-1 , i.p.) attenuated social withdrawal similar to that observed with dopamine D1 receptor antagonist (SCH-23390, 0.02 mg·kg-1 , i.p.) and was mimicked by the selective COMT inhibitor, OR-486 (10 mg·kg-1 , i.p.). Hispidulin increased extracellular dopamine levels in the PFC of chronic PCP-treated mice. In isolated mutDISC1 mice, hispidulin also reversed social withdrawal. In both models, intra-PFC microinjection of a D1 agonist (SKF-81297 10 nmol/mouse/bilateral) reversed the impairment of Ser897 phosphorylation at the GluN1 subunit of NMDA receptors, suggesting the association between GluN1 Ser897 -phosphorylation and D1 activation in the PFC exits in both models. CONCLUSIONS AND IMPLICATIONS Hispidulin attenuated social withdrawal by activating D1 receptors indirectly through elevated dopamine levels in the PFC by COMT inhibition. This nature of hispidulin suggests that it a potential novel therapeutic candidate for the treatment of negative symptoms in schizophrenia.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esquizofrenia / Flavonas Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esquizofrenia / Flavonas Idioma: En Ano de publicação: 2020 Tipo de documento: Article