Biphasic dose responses induced by prostaglandins are documented and assess
ed with respect to quantitative features of their dose-response functions,
mechanistic foundation, and biological generalizability. Biphasic responses
were seen for multiple endpoints, including DNA synthesis, neutrophil migr
ation, corticosterone production, fibroblast proliferation, and other param
eters. In addition, numerous nonsteroidal antiinflammatory agents and other
drugs alter prostaglandin concentrations and/or transport in a biphasic do
se-response manner. These findings have considerable implications for the u
nderstanding of basic biological regulatory processes as well as clinical p
ractices.