The method of cellular immobilization and perfusion was applied to adi
pocytes. The lipolytic effect of isoprenaline, whose action is produce
d as a result of receptor-drug interaction, was followed. An agarose s
olution kept at at 37 degrees C was mixed 1:1 with the cell suspension
. Thereafter, adipocytes were immobilized in the agarose threads. The
lipolytic effect of 0.1 mi of isoprenaline (1x10(-4) mol/l), that was
rapidly introduced to the cell perfusion inlet in a non-recirculating
system, was monitored by assessing glycerol production. The immobilize
d and perfused adipocytes exhibited significant lipolytic activity. Af
ter reaching the maximum effect, 0.1 mi of propranol (1x10(-3) mol/l)
that was applied to the bioreactor inlet, abolished the isoprenaline e
ffect. The present data demonstrate the potential applicability of imm
obilized perfused adipocytes For various kinds of studies.