Cyclofenil diphenol, a weak non-steroidal oestrogen, profoundly inhibits [35S]
proteoglycan synthesis in cultures of Swarm
chondrosarcoma chondrocytes under conditions in which
protein synthesis is only marginally reduced. In the present experiments it was shown that after a 40-min treatment with
Cyclofenil diphenol (90 micrograms ml-1) most of the normally abundant Golgi stacks in these cells disappeared and after 60 min they were absent. After 2-3 h treatment the cisternae of the endoplasmic reticulum (ER) were grossly distended and transformed into large ribosome-studded vesicles containing flocculent and filamentous material. These changes were dependent on the concentration of
Cyclofenil and were fully reversible within 21 h of withdrawing the
drug. The ultrastructural changes differed in some aspects if
protein synthesis was blocked with
cycloheximide for 15 min or 180 min before and during treatment with
Cyclofenil. The Golgi disappeared but the ER cisternae, though distended, formed a continuous network and swollen ribosome-studded vesicles did not develop. However, non-membrane-bounded structures containing lipid droplets and material of low electron density developed in the cytoplasm under these conditions. The ultrastructural changes induced by
Cyclofenil differ from those induced by
monensin and
diethylcarbamazine, suggesting that the
drug acts at a different point in the secretory pathway for macromolecules.