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The contribution of nitroxide on neonatal polymorphonuclear cells (PMNs)

Research Project

Project/Area Number 06807066
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field Pediatrics
Research InstitutionKANSAI MEDICAL UNIVERSITY

Principal Investigator

TANIUCHI Shoichiro  Kansai Medical University, Medicine Assistant Professor, 医学部, 講師 (70171832)

Co-Investigator(Kenkyū-buntansha) TAKAYA Junji  Kansai Medical University, Medicine Instructor, 医学部, 助手 (80247923)
KODERA Urara  Kansai Medical University, Medicine Instructor, 医学部, 助手 (90198614)
KINOSHITA Yo  Kansai Medical University, Medicine Associate Professor, 医学部, 助教授 (10105778)
Project Period (FY) 1994 – 1995
Project Status Completed (Fiscal Year 1995)
Budget Amount *help
¥1,800,000 (Direct Cost: ¥1,800,000)
Fiscal Year 1995: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1994: ¥1,000,000 (Direct Cost: ¥1,000,000)
KeywordsNeonates / Polymorphonuclear leukocytes / Nitric oxide / Superoxide
Research Abstract

To elucidate the susceptibility to bacterial infections in neonates, we evaluated the effects of nitric oxide (NO) on MCLA and LCL in PMNs with 12 cord bloods and 8 adults using L-arginene, a NO precursor and L-NMMA,a NOS inhibitor. There was no significant difference of the LCL intensity on MCLA n two groups in PMA stimulated PMNs. Adding L-arginine to PMNs, no significant reduction of the LCL intensity was observed in both groups. In the presence of L-NMNA,the LCL intensity significantly increased in the both groups (P<0.05).
The LCL intensity of lumino-dependent chemiluminescence (LDC) in cord PMNs stimulated with PMA significantly decreased than that of LDC in adult PMNs (P<0.001). Adding L-arginene, the LCL intensity of LCL significant increased in both groups (adult, neonate ; p<0.05). Similar increases in both groups were found (adult ; 11%, neonate ; 9%). In the presence of L-NMNA,the LCL intensity significantly increased in the both groups (P<0.01). Remarkable increases of the LCL were observed in adult PMNs, compared with cord PMNs.
From our results, a reduction of the LCL intensity of LDC in cord PMNs may be partly related to a decrease of NO production, suggesting that a cause of the susceptibility to bacterial infection could be ascribed to a decreased NO production in neonates.

Report

(3 results)
  • 1995 Annual Research Report   Final Research Report Summary
  • 1994 Annual Research Report
  • Research Products

    (4 results)

All Other

All Publications (4 results)

  • [Publications] 谷内昇一郎、他6名: "臍帯血好中球におけるサブポピュレーションの存在 -F-アクチンでの検討-." 日本産婦人科・新生児血液学会誌. 6. 83-84 (1996)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] 藤原 亨、他3名: "細菌感染症に対する免疫グロブリン療法の有効性-貧食からの検討-" 小児感染免疫. 8. 7-10 (1996)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Fujiwara,T.et al: "Effect of immunoglobulin therapy on phagocytosis by polymorphornuclear leucocytes in wholebllod of neonates." Clin Exp Immunol. 107. (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1995 Final Research Report Summary
  • [Publications] Fujiwara, T., Taniuchi, S., Hattori, K., Kobayashi, T., Kinoshita, Y.and Kobayashi, Y.: "Effect of immunoglobulin therapy on phagocytosis by polymorphornuclear leucocytes in wholeblood of neonates." Clin Exp Immunol. 107. (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1995 Final Research Report Summary

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Published: 1994-04-01   Modified: 2016-04-21  

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