Example：10.1021/acsami.1c06204 or Chem. Rev., 2007, 107, 2411-2502
Effects of Haloperidol and Cyproheptadine on the Cytoskeleton of the Sea Urchin Embryos Biochemistry (Moscow), Supplement Series A: Membrane and Cell Biology (IF), Pub Date : 2020-07-01, DOI: 10.1134/s1990747820020087 D. A. Nikishin, L. A. Malchenko, I. Milošević, L. Rakić, Y. B. Shmukler
Abstract Early sea urchin embryos are sensitive to agonists and antagonists of transmitter receptors, both metabotropic and channel ones. In this work, we studied mechanisms of the cytostatic action of cyproheptadine and haloperidol–antagonists of serotonin 5HT 2 receptors and dopamine D 2 receptors, respectively. For this purpose, we employed the model of the blockade of the first cleavage division in sea urchin, which allows quantifying the effects of embryotoxic substances. The action of haloperidol and cyproheptadine is mediated by the effects on cytoskeleton elements. Both antagonists caused an increase in the degree of polymerization of the actin cytoskeleton, both in the cortical layer and in the cytoplasm. In addition, both antagonists affected the tubulin cytoskeleton: haloperidol predominantly disturbed spatial organization of the mitotic spindle, while cyproheptadine caused a complete depolymerization of tubulin and arrest of mitotic processes. The results indicate that cytostatic effects of dopamine and serotonin antagonists on cleavage divisions of sea urchin embryos are mediated by similar and/or crosstalk molecular mechanisms but also have significant differences that require further research.