Depression of the radioprotective effect of isoproterenol on mammalian cells in vitro after desensitization of the cAMP system.

A short (5 min) incubation of cultured Chinese hamster fibroblasts with the specific beta-agonist isoproterenol (1 microM) leads to an increase in the intracellular content of cAMP and a decrease in radiosensitivity of the cells. Prolonged (up to 1 h) incubation induces a desensitization of the cAMP system to isoproterenol and causes a decrease both in the cAMP-stimulating and radioprotective effect of isoproterenol. There were no detectable changes in the beta-adrenoreceptor number or binding affinity of beta-receptors to the radiolabelled beta-antagonist dihydroalprenolol in desensitized cells; cAMP-phosphodiesterase activity was also the same as in intact cells. It is proposed that a 1 h incubation of the cells with isoproterenol induces the first step of desensitization, i.e. the functional "uncoupling' of beta-receptors from adenylate cyclase. Thus, the presence of beta-receptors in cells is not enough for the realization of the radioprotective potency of isoproterenol; an intact, non-desensitized, state of the cAMP system is obligatory.

Selective protection of cells against X-irradiation. Isoproterenol protects only those cells that possess beta-adrenoreceptors.

In mixed culture of Chinese hamster fibroblasts, clone 431, and transformed murine L fibroblasts, clone B-82, isoproterenol was found to protect only 431 cells against ionizing radiation. It was shown that 431 cells, in contrast to B-82 cells, possess beta-adrenoreceptors, and the radioprotective effect of isoproterenol can be realized only if this agent interacts with beta-adrenoreceptors coupled with the cAMP system. Since malignization often causes the disappearance of beta-adrenergic and other hormone receptors, the combined culturing and irradiation of the cells studied can be regarded as a model of the growth of malignant cells (B-82) among normal tissue cells (431 cells) under conditions of radiation therapy. A possibility of selective protection against radiation damage of normal tissue cells, with retention of the former radiosensitivity of tumor cells, is discussed.

[Modification of radiosensitivity and the cyclic AMP system]. / Modifikatsiia radiochuvstvitel'nosti i sistema tsiklicheskogo AMF.

The results of the experimental papers of the Soviet and foreign investigators concerning the role of cyclic AMP in modification of radiosensitivity of biological objects and the participation of cAMP system in the realization of radioprotective effect of various radioprotectants have been summarized. The action of radioprotectors on the cAMP level in cells and tissues of organism and their effect on the proteins activity of cAMP system has been considered. Particular attention has been given to the mechanisms of the radio-protective action of catecholamines on mammalian cells in vitro. On the grounds of the authors' own and literary data has been supposed that beta-adrenergic receptors and cAMP system, coupled with them, are obligatory for the performance of the radioprotective potency of catecholamines. The methodological problems of radiobiological experiments and adequate interpretation of results in compliance with terms of biochemistry and molecular endocrinology is discussed.

[Radioprotective action of catecholamines on a Chinese hamster fibroblast culture]. / Radiozashchitnoe deistvie katekholaminov na kul'turu fibroblastov kitaiskogo khomiachka.

The radioprotective ability of adrenaline, noradrenaline and isoproterenol in various concentrations has been studied in experiments on cultured Chinese hamster fibroblasts in vitro. Radioprotective effect of isoproterenol is pronounced at 10(-8)M concentration; adrenaline and especially noradrenaline are effective at higher concentrations. The antagonist of beta-adrenergic receptors propranolol blocks the radioprotective effect of catecholamines on cells. The beta-adrenergic mechanism of catecholamines radioprotective action on the mammals cells is under discussion.

[Desensitization of beta-adrenoreceptors and its influence on manifestations of the antiradiation effect of isoproterenol]. / Desensibilizatsiia beta-adrenoretseptorov i ee vliianie na proiavlenie protivoluchevogo éffekta izoproterenola.

A study was made of the function of beta-adrenoreceptors and Chinese hamster fibroblast cAMP during their desensitization to isoproterenol. Desensitization of adenylate cyclase was demonstrated to lead to the reduction of both the cAMP response to isoproterenol and isoproterenol capacity to protect the cells from ionizing radiation. This did not entail any changes in the number of beta-adrenoreceptors or in the dissociation constant of the beta-antagonist. It is assumed that desensitization provokes functional dissociation of the beta-receptor and adenylate cyclase. Intact adenylate cyclase is an absolute must for realization of the antiradiation potency of isoproterenol.

[Effect of prostaglandin E1 on the cyclic adenosine-3',5'--monophosphate system and radiosensitivity of B-82 cells cultured in vitro]. / Vliianie prostaglandina E1 na sistemu tsiklicheskogo adenozin--3',5'-monofosfata i radiochuvstvitel'nost' kletok B-82, kul'tiviruemykh in vitro.

The cyclic AMP (cAMP) system of mice fibroblasts L, clone B-82 has been studied. B-82 cells possess receptors to prostaglandin E1 (PGE1) and are deficient in beta-adrenoreceptors. It has been shown that 10 mM NaF, 1.10(-4) M GTP and 1.10(-5) M PGE1 stimulate adenylate cyclase of B-82 cells. PGE1 causes increase in the intracellular content of cAMP and protects B-82 cells against irradiation. Specifict beta-agonist isoproterenol fails to modulate adenylate cyclase activity and does not change cAMP content in B-82 cells. Isoproterenol has no effect on the B-82 cells radiosensitivity, although it is known to be a potent radioprotector. It is presumed that the stimulation of cAMP system by radioprotector is necessary for the performance of radioprotective effect.