Biomedical subjects

J E Biaglow

Publications and source records attributed to J E Biaglow.

At least 109 records · Page 6Linked to original sources

PubMed1978

Effects of sensitizers on cell respiration: II. The effects of hypoxic cell sensitizers on oxygen utilization in cellular and chemical models.

The metabolic activity of nitroheterocyclic sensitizers could limit their usefulness in vivo. Biochemical mechanisms of drug metabolism, toxicity and effects on cell respiration have been studied in microsomes, and the kinetics of the simulated redox reactions determined by pulse radiolysis. Stimulated oxidation of coenzyme, glucose, ascorbate or glutathione substrate radicals by nitroheterocyclic sensitizers, with the concomitant appearance of the respective nitro radical anions, is observed. Under hypoxia, the nitro radical anions decay slowly by second order processes, forming reduced metabolites. In air, the nitro radical anions react with oxygen forming superoxide radical anions, peroxide and regenerating the drug. Nitro radical-anions also react with cytochrome-c indicating a possible interference with mitochondrial energy metabolism.

Animals↗

PubMed1978

Effects of sensitizers on cell respiration: III. The effects of hypoxic cell radiosensitizers on oxidative metabolism and the radiation response of an in vitro tumour model.

Physiological factors are important when considering the effects of radiosensitizers on the radiation response of complex systems such as multicellular spheroids. In this system, under conditions of unlimited nutrient supply, cells are rendered hypoxic by metabolism. Thus, using the spheroid system as an in vitro model of the tumour-cell microenvironment, we have determined the relative contribution of radiosensitization and respiratory effects of a number of electron-affinic sensitizers having potential clinical use. These studies are indicative of physiological responses at the cellular level, and suggest optimal drug administration schemes for obtaining maximal radiation response in vivo hypoxic cell sensitizers.

Cell Survival↗

PubMed1978

Respiration of mammalian cells at low concentrations of oxygen: I. Effect of hypoxic-cell radiosensitizing drugs.

Drugs which sensitize hypoxic mammalian cells to radiation damage in vitro can also affect the cellular respiration rate. This phenomenon was studied in detail to determine whether the changes in oxygen consumption occur at low oxygen concentrations and under optimal nutritional conditions. We have found that cells in tissue culture can undergo adaptive changes in respiration (electron flow) which make them insensitive to the effects of radiosensitizing drugs and even respiration uncouplers such as dinitrophenol, and the inhibitors rotenone and cyanide. At low cell densities, where nutrient depletion in the medium would be negligible, the drugs have reduced effects, particularly at low oxygen concentrations (below 40 mmHg oxygen partial pressure). Parallel cytotoxicity and growht inhibition studies indicate that most drugs are unlikely to have substantial effect on respiration at non-cytotoxic levels.

Cells, Cultured↗

PubMed1978

Nitropyrrole radiosensitizers: structure function relationships.

Nitropyrrole derivatives have been tested as hypoxic cell radiosensitizers in vitro and in vivo. Radiosensitizing potential generally increases with nitropyrrole electron affinity. N-hydroxyethyl substitution decreases toxicity relative to N--CH3, N--CH2 CH3 and N--CH2 CH2 CH3 substitution. The most effective nitropyrrole tested in vivo is N-hydroxyethyl-2-cyano-5-nitropyrrole (NP-1).

Animals↗

PubMed1977