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Featured researches published by Kazunori Furukawa.


Chemico-Biological Interactions | 1984

Induction by butylated hydroxytoluene of rat liver γ-glutamyl transpeptidase activity in comparison to expression in carcinogen-induced altered lesions

Kazunori Furukawa; Yoshiichi Maeura; Noriko T. Furukawa

Butylated hydroxytoluene (BHT) at concentrations of 300-6000 ppm in the diet caused a dose-dependent increase in gamma-glutamyl transpeptidase (GGT) activity in normal F344 male rat liver at 18 weeks. However, the activities of glutathione S-transferases (GSTs) of rat liver cytosol were enhanced only at concentrations of 3000 or 6000 ppm BHT. Histochemically, the enhanced GGT activity was localized to hepatocytes surrounding the portal areas. Autoradiographic measurements of DNA synthesis showed that dietary BHT did not increase the level of cell proliferation and the GGT-positive hepatocytes did not exhibit different rates of DNA synthesis from those of GGT-negative cells. Feeding of the liver carcinogen N-2-fluorenylacetamide (FAA) induced foci and nodules of GGT-positive altered cells which exhibited higher rates of DNA synthesis than those of surrounding GGT-negative hepatocytes. Following iron loading, the periportal GGT-positive hepatocytes produced by BHT accumulated cellular iron, whereas the cells in FAA-induced lesions excluded iron. These results suggest that dietary BHT induces GGT activity in periportal hepatocytes without proliferation of the cells and that induction does not represent fetal expression or a preneoplastic alteration.


Cellular Signalling | 1998

Relation between spontaneous contraction and sarcoplasmic reticulum function in cultured neonatal rat cardiac myocytes.

Hisakazu Kimura; Haruo Takemura; Kenshi Imoto; Kazunori Furukawa; Hideyo Ohshika; Yohichi Mochizuki

The relation between spontaneous contraction, Ca2+ oscillations, and sarcoplasmic reticulum (SR) function was studied in cultured neonatal rat cardiac myocytes. Spontaneous contraction and Ca2+ oscillations were irregular at day 2 of culture but became regular at day 6 of culture in neonatal rat cardiac myocytes. The rate of spontaneous contraction and the frequency of Ca2+ oscillations were decreased by verapamil and were abolished in the absence of extracellular Ca2+ at both day 2 and day 6 of culture. Ryanodine and thapsigargin increased the rate of contraction and the frequency of Ca2+ oscillations at day 2 of culture but did not affect contractions and Ca2+ oscillations at day 6 of culture. Ultrastructural observation showed that the structure of SR developed less at day 6 of culture. The present results suggest that spontaneous contraction and Ca2+ oscillations are due mainly to extracellular Ca2+ influx but not to Ca2+ release from SR in neonatal rat cardiac myocytes.


Virchows Archiv B Cell Pathology Including Molecular Pathology | 1988

Morphometric and cytochemical evaluation of clofibrate-induced peroxisomal proliferation in adult rat hepatocytes cultured on floating collagen gels

Kazunori Furukawa; Yohichi Mochizuki; Norimasa Sawada; Mikio Gotoh; Hideyuki Tsukada

SummaryThe present ultrastructural morphometric and cytochemical studies demonstrate clofibrate induced changes in peroxisomes in adult rat hepatocytes maintained for 14 days in primary culture on floating collagen gels. Catalase activity and the number and diameter of peroxisomes were reduced in hepatocytes cultured for between 2/3 and 7 days. However, hepatocytes cultured for 7–14 days had well-developed peroxisomes containing crystalloid nucleoids. The number of anucleoid peroxisomes in hepatocytes treated with 2 mM Na clofibrate increased with culture age, and by day 14 the number was 2.9 times greater than in freshly isolated hepatocytes. Catalase activity, as well as the number of nucleoid-containing peroxisomes were much greater in treated hepatocytes than in untreated controls, but decreased slightly with culture age. The diameter of peroxisomes was not reduced in the treated cells. These results suggest that the treatment with Na clofibrate is effective both for proliferation and maintenance of peroxisomes and for enhancing catalase activity. In treated hepatocytes, matrical plates were formed in peroxisomes from days 5 to 14 and the number of plate-containing peroxisomes increased with culture age.


Cancer Research | 1985

Effects of the Hepatocarcinogen Nafenopin, a Peroxisome Proliferator, on the Activities of Rat Liver Glutathione-requiring Enzymes and Catalase in Comparison to the Action of Phenobarbital

Kazunori Furukawa; Satoshi Numoto; Keizo Furuya; Noriko T. Furukawa


Carcinogenesis | 1984

Effects of the hepatocarcinogenic peroxisome-proliferating hypolipidemic agents Clofibrate and Nafenopin on the rat liver cell membrane enzymes γ-glutamyltranspeptidase and alkaline phosphatase and on the early stages of liver carcinogenesis

Satoshi Numoto; Kazunori Furukawa; Keizo Furuya


Carcinogenesis | 1982

Effects of various concentrations of ethyl-α-p-chlorophenoxyisobutyrate (clofibrate) on diethylnitrosamine-induced hepatic tumorigenesis in the rat

Yohichi Mochizuki; Kazunori Furukawa; Norimasa Sawada


Tumor Research | 1988

Establishment and Characterization of a Human Cell Line Derived from a Squamous Cell Carcinoma of the Tongue

Toshikazu Yokoi; Akira Yamaguchi; Tetsuyo Odajima; Kazunori Furukawa


In Vitro Cellular & Developmental Biology – Plant | 1987

Enrichment and characterization of clonogenic epithelial cells from adult rat liver and initiation of epithelial cell strains

Kazunori Furukawa; Tomiko Shimada; Patricia J. England; Yohichi Mochizuki


Cancer Research | 1983

Induction of Transformation by Six Classes of Chemical Carcinogens in Adult Rat Liver Epithelial Cells

Tomiko Shimada; Kazunori Furukawa; Dawn M. Kreiser; Andrea Cawein


Cell Biology International Reports | 1988

Polygonal networks, «geodomes», of adult rat hepatocytes in primary culture

Yohichi Mochizuki; Kazunori Furukawa; Toshihiro Mitaka; Toshikazu Yokoi; Toshinori Kodama

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Yohichi Mochizuki

Sapporo Medical University

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Hideyo Ohshika

Sapporo Medical University

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Hisakazu Kimura

Sapporo Medical University

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Toshihiro Mitaka

Sapporo Medical University

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Akira Yamaguchi

Sapporo Medical University

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Haruo Takemura

Sapporo Medical University

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Kenshi Imoto

Sapporo Medical University

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Tetsuyo Odajima

Sapporo Medical University

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