Phytoestrogens genistein and daidzin enhance the acetylcholinesterase activity of the rat pheochromocytoma cell line PC12 by binding to the estrogen receptor

• Published in: Cytotechnology (Dordrecht) Vol. 40; no. 1-3; pp. 117 - 123
• Main Authors: ISODA, Hiroko, TALORETE, Terence P. N, KIMURA, Momoko, MAEKAWA, Takaaki, INAMORI, Yuhei, NAKAJIMA, Nobuyoshi, SEKI, Humitake
• Format: Conference Proceeding Journal Article
• Language: English
• Published: Dordrecht Springer 01-11-2002; Springer Nature B.V; Kluwer Academic Publishers
• Subjects: 17β-Estradiol; Acetylcholinesterase; Biological and medical sciences; Cell proliferation; Estrogen receptors; Estrogens; Fundamental and applied biological sciences. Psychology; Genistein; Pheochromocytoma cells; Phytoestrogens; Tamoxifen; Xenoestrogens; PC12; daidzin; genistein; acetylcholinesterase activity
• ISSN: 0920-9069; 1573-0778
• DOI: 10.1023/A:1023903220539

Some compounds derived from plants have been known to possess estrogenic properties and can thus alter the physiology of higher organisms. Genistein and daidzin are examples of these phytoestrogens, which have recently been the subject of extensive research. In this study, genistein and daidzin were found to enhance the acetylcholinesterase (AChE) activity of the rat neuronal cell line PC12 at concentrations as low as 0.08 muM by binding to the estrogen receptor (ER). Results have shown that this enhancement was effectively blocked by the known estrogen receptor antagonist tamoxifen, indicating the involvement of the ER in AChE induction. That genistein and daidzin are estrogenic were confirmed in a cell proliferation assay using the human breast cancer cell line MCF7. This proliferation was also blocked by tamoxifen, again indicating the involvement of the ER. On the other hand, incubating the PC12 cells in increasing concentrations of 17 beta-estradiol (E2) did not lead to enhanced AChE activity, even in the presence of genistein or daidzin. This suggests that mere binding of an estrogenic compound to the ER does not necessarily lead to enhanced AChE activity. Moreover, the effect of the phytoestrogens on AChE activity cannot be expressed in the presence of E2 since they either could not compete with the natural ligand in binding to the ER or that E2 down-regulates its own receptor. This study clearly suggests that genistein and daidzin enhance AChE activityin PC12 cells by binding to the ER; however, the actual mechanism of enhancement is not known.