Membrane-initiated or nongenomic activities of steroids contribute to the e
ffects of steroids on a wide variety of target organs, including those with
low receptor numbers, recently discovered due to the Increased sensitivity
of new measurement techniques. Membrane-initiated responses are the cell's
rapid and first response to steroids. The responses that emanate from the
membrane can have direct functional consequences, such as secretion of othe
r peptide hormones or rapid behavioral changes. Other rapid responses are p
rerequisites for subsequent genomic responses. The wide variety of signal t
ransduction schemes employed by various tissues and hormones are summarized
and discussed in terms of the identity of proteins that mediate these resp
onses. Probable mixed binding systems for steroids in plasma membranes are
compared to similar multiple hormone-binding protein systems in extracellul
ar fluids and inside cells. These issues are related to steroid-dependent t
umor growth, developmental and therapeutic apoptosis, and the actions of en
docrine disrupters. The integration of membrane-initiated effects with geno
mic mechanisms results in the complete cellular response to steroids.