• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

The hypothalamo-pituitary axis responses to lipopolysaccharide-induced endotoxemia in mice lacking inducible nitric oxide synthase

Research Project

Project/Area Number 16591630
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Urology
Research InstitutionUniversity of Occupational and Environmental Health

Principal Investigator

AKASAKA Soichiro  University of Occupational and Environmental Health, Japan, School of Medicine, Instructor, 医学部, 助手 (30320360)

Co-Investigator(Kenkyū-buntansha) NOMURA Masayoshi  University of Occupational and Environmental Health, Japan, School of Medicine, Instructor, 医学部, 助手 (80369066)
SASAGURI Takakazu  University of Occupational and Environmental Health, Japan, University Hospital, Associate Professor, 大学病院, 助教授 (70341493)
Project Period (FY) 2004 – 2005
Project Status Completed (Fiscal Year 2005)
Budget Amount *help
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2005: ¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 2004: ¥1,800,000 (Direct Cost: ¥1,800,000)
KeywordsExperimental cystitis / Estrogen / Testosterone / cyclophosphamide / Bladder / Inflammation / 内臓痛 / アポトーシス / 間質性膀胱炎 / 視床下部-下垂体系 / サイクロフォスファミド膀胱炎 / 下部尿路症状 / 尿意切迫感
Research Abstract

Nitric oxide (NO) generated by inducible NO synthase (iNOS) may be implicated in the biological responses of the central nervous system to immune stimuli. To elucidate the role of iNOS in the hypothalamo-pituitary axis in responses to endotoxemia, using iNOS knockout (KO) mice, we examined the levels of c-fos, a neural activational marker, and corticotropin-releasing hormone (CRH) gene transcription in the paraventricular nucleus (PVN) and central amygdala (CeAMY) during lipopolysaccharide (LPS)-induced endotoxemia. In addition, the serum adrenocorticotropic hormone (ACTH) levels were also examined during endotoxemia. Following the intraperitoneal administration of LPS (1 mg/kg), the levels of the c-fos gene expression significantly increased in the PVN and the CeAMY regardless of the genotype. However, the disruption of the iNOS gene resulted in a significant decrease in the c-fos gene induction in the PVN in comparison to that observed in control mice. LPS administration caused a significant increase in CRH mRNA levels in the PVN and CeAMY regardless of genotype. However, the LPS-induced upregulation of CRH mRNA was significantly attenuated in the PVN of iNOS KO mice in comparison to that in the control mice. In contrast, no such genotype differences in the neural activity or CRH gene transcription were observed in the CeAMY. The serum ACTH responses to LPS were also significantly blunted in the iNOS KO mice in comparison to the control mice. These results suggest that iNOS-derived NO may therefore play a stimulatory role in the activity of the hypothalamo-pituitary axis during endotoxemia.

Report

(3 results)
  • 2005 Annual Research Report   Final Research Report Summary
  • 2004 Annual Research Report
  • Research Products

    (8 results)

All 2005 Other

All Journal Article (8 results)

  • [Journal Article] Involvement of estrogen in the pathogenesis of cyclophosphamide-induced cystitis in rats.2005

    • Author(s)
      Terado M
    • Journal Title

      Endocrine 26(1)

      Pages: 55-63

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2005 Annual Research Report 2005 Final Research Report Summary
  • [Journal Article] Effects of nitric oxide synthase isoform delection on oxytocin and vasopressin messenger RNA in mouse hypothalamus.2005

    • Author(s)
      Nomura M
    • Journal Title

      Neuroreport 16(4)

      Pages: 413-417

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2005 Final Research Report Summary
  • [Journal Article] Involvement of estrogen in the pathogenesis of cyclophosphamide-induced cystitis in rats.2005

    • Author(s)
      Terado M, Nomura M, Mineta K, Nishii H, Fujimoto N, et al.
    • Journal Title

      Endocrine 26-1

      Pages: 55-63

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2005 Final Research Report Summary
  • [Journal Article] Effects of nitric oxide synthase isoform deletion on oxytocin and vasopressin messenger RNA in mouse hypothalamus2005

    • Author(s)
      Nomura M
    • Journal Title

      Neuroreport 16(4)

      Pages: 413-417

    • Related Report
      2005 Annual Research Report
  • [Journal Article] Roles of inducible nitric oxide synthase in the hypothalamus-pituitary axis in response to lipopolysaccharide-induced endotoxemia in mice.

    • Author(s)
      Akasaka S
    • Journal Title

      Molecular Brain Research (ln press)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2005 Final Research Report Summary
  • [Journal Article] Roles of inducible nitric oxide synthase in the hypothalamus-pituitary axis in response to lipopolysaccharide-induced endotoxemia in mice.

    • Author(s)
      Akasaka S, Nomura M, Nishii H, Fujimoto N, et al.
    • Journal Title

      Molecular Brain Research (in press)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2005 Final Research Report Summary
  • [Journal Article] Effects of nitric oxide synthase isoform delection on oxytocin and vasopressin messenger RNA in mouse hypothalamus

    • Author(s)
      Nomura M, Tsutsui M, Shimokawa H, Fujimoto N, Ueta Y, et al.
    • Journal Title

      Neuroreport 16-4

      Pages: 413-417

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2005 Final Research Report Summary
  • [Journal Article] Roles of inducible nitric oxide synthase in the hypothalamus-pituitary axis in response to lipopolysaccharide-induced endotoxemia in mice

    • Author(s)
      Akasaka S
    • Journal Title

      Molecular Brain Research (In press)

    • Related Report
      2005 Annual Research Report

URL: 

Published: 2004-04-01   Modified: 2016-04-21  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi