The triglyceride-free fatty acid (TG-FFA) cycle was studied in
white adipose tissue. The major aims of the study were 1) to see if the
rate of TG-FFA cycling (i.e. FFA reesterification) and the sensitivity
properties (see Newsholme and Crabtree, 1976, Biochem. Soc. Symp. 41,
61-109) were affected by various treatments, and 2) to measure the
rate of cycling in vivo and assess its contribution to the metabolic
rate of an animal.
There are two ways of estimating the rate of TG-FFA cycling; the
first is based on the release of glycerol and FFA from the tissue, and
the second on the synthesis of the glycerol and FFA moieties of triglyceride.
Experimental agreement between the two methods is very
good. It is shown that the rate of TG glycerol synthesis can be
estimated by measuring the incorporation of tritium from tritiated
water into the TG-glycerol moiety; this method is used to study the
TG-FFA cycle in vivo.
Experimental results indicated that the rate of TG-FFA cycling
in white adipose tissue in vitro and in vivo is affected by various
short- and long-term treatments. However, the reesterification of
FFA in adipose tissue can only account for perhaps ~1% of the basal
metabolic rate of a mouse, and perhaps 4% of the increase in osygen
consumption observed in fenoterol-treated mice.
The equations of Newsholme and Crabtree (1976) describing the
sensitivity properties of substrate cycles are extended and used
to show that the TG-FFA cycle increases the sensitivity of control of
FFA release from adipose tissue. The degree of sensitivity attainable
is variable depending on the treatment used.
The use of tritiated water for estimating TG-FFA cycling is
tentatively extended to brown adipose tissue. It is suggested that
the rate of cycling could be used as an indicator of sympathetic
activity in brown and white adipose tissue.</p