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A NEW NEUROTOXICOLOGICAL TEST SYSTEM USING NERVE CELL LINE

Research Project

Project/Area Number 10670366
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Public health/Health science
Research InstitutionJIKEI UNIVERSITY SCHOOL OF MEDICINE

Principal Investigator

SUZUKI Yuji  JIKEI UNIVERSITY SCHOOL OF MEDICINE,ASSOSIATE PROFFESOR, 医学部, 助教授 (30163017)

Project Period (FY) 1998 – 1999
Project Status Completed (Fiscal Year 1999)
Budget Amount *help
¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1999: ¥600,000 (Direct Cost: ¥600,000)
KeywordsNeurotoxicology / micronuclei / apoptosis / nerve cell / action potential / cisplatin / calcium ion / 膜電位 / カルシウム / スクリーニング / 小核 / キャスパーゼ / タンネル法 / DNA / ハイブリド細胞
Research Abstract

Many new chemicals have produced in this century from industrial circles. We established a in vitro neurotoxicological test system for the purpose of assessing the neurotoxic potential of these chemicals.
(1) Induction of micronuclei and apoptosis
Hybrid cell line N18DRG-D2 of BALB/c mouse dorsal root ganglion neuron and mouse neuroblastoma cell (N18TG-D2) was used in this study. Induction of micronuclei by propidium iodide peaked at 96 hours of cisplatin treatment and frequency of micronuclei induced by cisplatin increased dose dependent manner. However, number of apoptotic micronuclei (double staining with proidium iodide and TUNEL method) did not increase following cisplatin treatment.
(2) Alteration of membrane action potential
Membrane action potential was determined using a fluorophotometer after stained with 3, 3'-dipenty loxacarbocyanine iodide. Fluorescence intensity of N18DRG-D2 was attenuated after exposure to cisplatin.
(3) Alteration of intracellular calcium ion concentration
Membrane action potential was determined using a fluorophotometer after stained with fura-2. Fluorescence intensity of N18DRG-D2 was attenuated after exposure to cisplatin.
These results suggested that a new neurotoxicological test system using N18DRG-2 cell line might be useful for estimating neurotoxic substances.

Report

(3 results)
  • 1999 Annual Research Report   Final Research Report Summary
  • 1998 Annual Research Report
  • Research Products

    (7 results)

All Other

All Publications (7 results)

  • [Publications] Masateru Ikehata: "Mutagenicity and co-mutagenicity of static magnetic fields detected by bacterial mutation assay."Mutation Research. 427・2. 147-156 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Yuichi Miyakoshi: "Micronucleus test using cultured new born rat astrocytes"Industrial Health. 37・2. 95-102 (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] MASATERU IKEHATA: "MUTAGENICITY AND CO-MUTAGENICITY OF STATIC MAGENTIC FIELDS DETECTED BY BACTERIAL MUTATION ASSAY"MUTATION RESEARCH. 427. 147-156 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] YUICHI MIYAKOSHI: "MICRONUCLEUS TEST USING NEW BORN RAT ASTROCYTES"INDUSTRIAL HEALTH. 37. 95-102 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Masateru Ikehata: "Mutagenicity and co-mutagenicity of static magnetic fields detected by bacterial mutation assay"Mutation Research. 427・2. 147-156 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Yuichi Miyakoshi: "Micronucleus test using cultured new born rat astrocytes"Industrial Health. 37・2. 95-102 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Miyakoshi,Y.: "Micronucleus test using cultured new born rat astrocytes" Industrial Health. 37・1. 95-102 (1999)

    • Related Report
      1998 Annual Research Report

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Published: 1999-04-01   Modified: 2016-04-21  

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