Prianishnikova E N, Zhulanova Z I, Romantsev E F, Bakhova A V
Vopr Med Khim. 1982 Sep-Oct;28(5):115-8.
After intraperitoneal administration of beta-mercaptoethylamine (MEA) into mice of F1 strain (CBA XC57B1) at a radioprotective dose, activity of PGE2 and PGF2 alpha-synthetases was decreased in liver microsomes, testicular and brain supernatants (16,000xg) within 15 min, which corresponded to period of the highest radioprotector activity. Amount of newly synthesized prostaglandins was increased in liver tissue within the subsequent periods. Within 3 hrs after the radioprotector administration these amounts constituted for PGE2 246% and for PGF2 alpha 262% as compared with controls; at the same time, activity of PG-synthetases in testes was normalized. In the brain tissue within 1 hr the newly synthesized prostaglandins amounted to 121% for PGE2 and 125% for PGF2 alpha, within 3 hrs they decreased to control values. Decrease in activity of PGE2 and PGF2 alpha-synthetases was shown to depend on MEA concentration in vitro. Possible mechanisms of the radioprotector effect at various steps of the prostaglandins biosynthesis are discussed.
以辐射防护剂量向F1品系(CBA×C57B1)小鼠腹腔注射β-巯基乙胺(MEA)后,肝微粒体、睾丸和脑上清液(16,000xg)中PGE2和PGF2α合成酶的活性在15分钟内降低,这与辐射防护剂活性最高的时期相对应。在随后的时间段内,肝组织中新合成的前列腺素量增加。在给予辐射防护剂后3小时内,与对照组相比,这些量的PGE2为246%,PGF2α为262%;同时,睾丸中PG合成酶的活性恢复正常。在脑组织中,1小时内新合成的前列腺素量PGE2为121%,PGF2α为125%,3小时内降至对照值。结果表明,PGE2和PGF2α合成酶活性的降低取决于体外MEA的浓度。讨论了前列腺素生物合成各个步骤中辐射防护剂作用的可能机制。