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A Study of Functional Abnormality by Environmental Contaminants.

Research Project

Project/Area Number 01560339
Research Category

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

Allocation TypeSingle-year Grants
Research Field Applied veterinary science
Research InstitutionOsaka Prefecture University

Principal Investigator

NISHIMURA Masakazu  UNIVERSITY OF OSAKA PREFECTURE, DEPARTMENT OF VETERINARY SCIENCE, ASSOCIATE PROFESSOR., 農学部, 助教授 (50011995)

Co-Investigator(Kenkyū-buntansha) KISO Yasuo  UNIVERSITY OF OSAKA PREFECTURE, DEPARTMENT OF VETERINARY SCIENCE, ASSISTANT PROF, 農学部, 助手 (10142374)
Project Period (FY) 1989 – 1990
Project Status Completed (Fiscal Year 1989)
Budget Amount *help
¥1,600,000 (Direct Cost: ¥1,600,000)
Fiscal Year 1989: ¥1,600,000 (Direct Cost: ¥1,600,000)
KeywordsIprodione / Developmental toxicity / Neuronal Development / Functional malformation
Research Abstract

The effects of daily injection of iprodione to pregnant mice on neuronal functions of the new born mice were investigated. Iprodione (IPRD, Wako Pure Chemicals, Osaka) was dissolved in dimethyl sulfoxide (DMSO, Wako Pure Chemicals, Osaka) at a concentration of 100 mg/ml. Daily injection of IPRD (100 mg/kg) to the pregnant mice was started day 0 on gestation (Group 1)or 15th day on gestation (Group 2) and continued through delivery. Control pregnant mice was given vehicle on day o through delivery. New born mice from Group 2 had no behavioral sighns significantly different from the control neonates. However, both sexes of mice born from Group I showed body-weight-gain reduced significantly (P<0.05). These mice at 4 weeks old showed abnormally higher reactivity (P<0.05), Spontaneous activity (P<0.05) and touch response (P<0.05). The resting membrane potentials, frequency (F) of miniature end-plate potentials (m.e.p.ps) and the quantal content (m) of end-plate potentials (e.p.ps) were measured intracellularly at end-plates of diaphragm of male mouse in a high-Mg^<2+> bathing solution containing several concentrations of Ca^<2+>. The resting membrane potentials of end-plates were significantly decreased in 7 or 8 weeks old mice from Group 1. Also, in these mice, F was significantly (P<0.05) higher and m was significantly (P<0.05) larger than the controls, respectively. Slope of the regression line for 1n(m)-1n[Ca] relationship was approx. 3 in these mice, while control was 4. Thus, the treatment with IPRD of the mice for whole pregnant period may have a causal of abnormality of neuronal development.

Report

(2 results)
  • 1989 Annual Research Report   Final Research Report Summary
  • Research Products

    (3 results)

All Other

All Publications (3 results)

  • [Publications] Masakazu Nishimura and Yasuo Kiso: "The effect of chronic treatment with iprodione of pregnant mice on neuronal functions of the new born mice." J.Toxicol.Sci.(1990)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1989 Final Research Report Summary
  • [Publications] Masakazu Nishimura and Yasuo Kiso: "The effect of chronic treatment with iprodione of pregnant mice on neuronal functions of the new born mice." J. Toxicol. Sci. (1990).

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1989 Final Research Report Summary
  • [Publications] Masakazu Nishimura and Yasuo Kiso: "The effect of chronic treatment with iprodione of pregnant mice on neuronal functions of the new born mice." J.Toxicol.Sci.(1990). (1990)

    • Related Report
      1989 Annual Research Report

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Published: 1989-04-01   Modified: 2016-04-21  

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