[Effect of pulse electromagnetic radiation on erythrocyte ghosts]. / Vliianie impul'snogo élektromagnitnogo izlucheniia na teni éritrotsitov.

The pulse microwave radiation has been shown to increase the fluorescence intensity of 2-toluidinonaphthanene-6-sulfonate (2,6-TNS) and 1-anilinonaphthalene-8-sulfonate (1,8-ANS) built-in membranes of erythrocyte ghosts. In experiments with 2,6-TNS a frequency dependence of the effect of microwave radiation with maximum within the frequency range of 55-65 Hz has been found. It is suggested that the changes registered with fluorescent probes are induced by mechanical oscillations generated by the pulse microwave radiation.

[Inductive-resonance energy transfer between chromophores localized in different parts of irradiated and nonirradiated erythrocyte ghosts]. / Induktivno-rezonansnyi perenos énergii mezhdu khromoforami, lokalizovannymi v raznykh uchastkakh obluchennykh i neobluchennykh tenei éritrotsitov.

A study was made of the inductive-resonance energy transfer between chromophore pairs, tryptophan--pyren, tryptophan--1.8-anilinonaphthalene sulfonate (ANS), puren--1.8-ANS, diphenylhexatrien--ethidium, and 1,8-ANS--ethidium, in irradiated (250 Gy) and nonirradiated preparations of erythrocytic membranes. The radiation--induced decrease in the energy transfer was noted in the pairs in which one of the chromophores was localized in a lipid phase. On the basis of the data obtained it is suggested that irradiation of membranes causes the lesions in them which lead to a reduction of the effective thickness of a hydrophobic part of the lipid bilayer.

Effects of irradiation on the interaction of fluorescent probes with lymphocytes.

Low doses of radiation reduce the rate and magnitude of fluorescent probe interaction with spleen cells. The uptake of 8-anilino-naphthalene sulfonic acid (ANS), but not diphenyl-hexatriene (DPH), is reduced in a dose-dependent fashion in cells that receive 25-100 rads. The effects of irradiation are most evident in a "medium" fluorescent subpopulation with no effect observed for a "dim" subpopulation. Splenic lymphocytes enriched for T cells show lower uptake of ANS, compared with a B-cell-enriched population. In addition, the normal decrease in ANS fluorescence polarization that occurs during the initial 10 minutes of probe interaction is attenuated in irradiated cells. These findings are consistent with the notion that low doses of radiation limit the penetration of ANS, but not DPH, into a less restrictive microenvironment within the plasma membranes of T, but not B, cells.