-transparent.png){kind=logo}
The activities of four glycolytic enzymes were measured in the lung homogenate of CFLP mice treated with a variety of carcinogens and non-carcinogens for mouse lung. The carcinogenic urethane, dimethylnitrosamine (DMNA), 3-methylcholanthrene (MCA), benzo[a]pyrene (BP), 7,12-dimethylbenz[a]anthracene (DMBA) and aflatoxin B1 enhanced the activity of hexokinase (HK), phosphofructokinase (PFK), pyruvate kinase (PK) and lactate dehydrogenase (LDH) 28 days after a single intraperitoneal administration. These carcinogens also altered the ratio of LDH H and M subunits. In contrast, under the same conditions the non-carcinogenic phenylurethane, ethylformate, chrysene, perylene and pyrene, as well as the pulmonarily toxic Paraquat, butylated hydroxytoluene (BHT) and cadmium chloride (CdCl2), did not influence either the activities of the enzymes tested or the isozyme pattern of LDH.
P Rády, and
I Arany, and
F Boján, and
P Kertai
October 1992,
Indian journal of biochemistry & biophysics,
P Rády, and
I Arany, and
F Boján, and
P Kertai
September 1985,
Archives of toxicology,
P Rády, and
I Arany, and
F Boján, and
P Kertai
August 1984,
Applied and environmental microbiology,
P Rády, and
I Arany, and
F Boján, and
P Kertai
November 1978,
Chemico-biological interactions,
P Rády, and
I Arany, and
F Boján, and
P Kertai
August 1980,
FEBS letters,
P Rády, and
I Arany, and
F Boján, and
P Kertai
November 1981,
Molecular pharmacology,
P Rády, and
I Arany, and
F Boján, and
P Kertai
March 1982,
British journal of haematology,
P Rády, and
I Arany, and
F Boján, and
P Kertai
January 1955,
Zeitschrift fur die gesamte experimentelle Medizin,
P Rády, and
I Arany, and
F Boján, and
P Kertai
May 1981,
British journal of industrial medicine,
P Rády, and
I Arany, and
F Boján, and
P Kertai
November 1969,
The Biochemical journal,
