Publications by authors named "A Yamatodani"

We previously reported that hypothalamic tumor necrosis factor-alpha (TNF-α) mRNA expression via histamine H receptors contributes to the development of cisplatin-induced anorexia; however, its precise mechanisms remain unclear. It has been reported that chemotherapeutic agents induce the suppression of orexin neuron activity, and the administration of orexin inhibits chemotherapeutic agent-induced gastric discomfort. Other studies demonstrated that the central administration of TNF-α impairs the orexinergic system, and that orexin excites the histaminergic system.

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We previously reported that sevoflurane-induced pica, kaolin ingestion behavior, in rats has the potential to reflect postoperative nausea and vomiting (PONV) in humans. It is well-known that corticosteroids, which inhibit both prostaglandin and leukotriene syntheses due to phospholipase A inhibition, are effective for reducing PONV; however, the precise mechanisms remain unclear. We investigated the involvement of the prostaglandin or leukotriene pathway in the development of sevoflurane-induced pica.

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Since the peripheral serotoninergic pathway is involved in the development of radiation-induced nausea and vomiting, referred to as radiation sickness, serotonin 5-HT receptor antagonists are used as a preventive measure, although patients still suffer from these symptoms. Glutamate is known as the excitatory neurotransmitter and is involved in various autonomic symptoms. We investigated the effect of radiation on glutamate release in rats, as measured by in vivo brain microdialysis, and the effects of glutamate receptor antagonists on radiation-induced pica, which can be used as a behavioral assessment of radiation sickness in rats.

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Cancer chemotherapy often induces gastrointestinal symptoms such as anorexia, nausea, and vomiting. Antiemetic agents are effective in inhibiting nausea and vomiting, but patients still experience anorexia. We previously reported that chemotherapeutic agent-induced anorexia is associated with an increase of inflammatory cytokines.

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Introduction: Pica behavior, kaolin ingestion, in rats and mice can be used as an assessment of nausea and vomiting; however, we observed that the incidence of pica behavior in ICR strain mice varied markedly. We investigated the susceptibility of four strains of mice (ICR, BALB/c, C57BL/6, and DBA/2) to the development of pica behavior.

Methods: Mice received cisplatin (7.

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Synopsis of recent research by authors named "A Yamatodani"

  • - A Yamatodani's recent research focuses on the neurobiological mechanisms underlying chemotherapy-induced anorexia and related gastrointestinal symptoms, particularly examining the roles of orexinergic, histaminergic, and glutamatergic pathways.
  • - Key findings include the identification of the orexin system's impairment in cisplatin-induced anorexia and the involvement of leukotriene pathways in sevoflurane-induced pica, a behavioral model reflecting nausea in humans.
  • - Additionally, the studies highlight notable strain differences in the expression of pica behavior among mice, contributing to the understanding of individual susceptibility to treatment-related gastrointestinal side effects.