Mc. Sugden et al., CHANGES IN LIPOPROTEIN-LIPASE ACTIVITIES IN ADIPOSE-TISSUE, HEART ANDSKELETAL-MUSCLE DURING CONTINUOUS OR INTERRUPTED FEEDING, Biochemical journal, 292, 1993, pp. 113-119
Lipoprotein lipase (LPL) activities in parametrial and interscapular a
dipose tissue, soleus and adductor longus muscles and hearts of female
rats were measured during progressive starvation, chow re-feeding aft
er 24 h starvation and throughout dark and light phases in rats permit
ted unrestricted access to chow. Adipose-tissue LPL activities decline
d by 50 % after 6 h starvation and continued to fall as the starvation
period was extended to 24 h. Skeletal-muscle LPL activities dramatica
lly increased between 9 and 12 h of starvation. Cardiac LPL activities
increased 2.5-fold within 6 h of starvation, reaching a maximum after
12 h of starvation. Adipose-tissue LPL activities increased rapidly w
ithin 2 h of re-feeding chow ad libitum after 24 h starvation, achievi
ng 'fed ad libitum' values after 6 h. Oxidative-skeletal-muscle LPL ac
tivities also increased after 2 h of re-feeding and exceeded 'fed ad l
ibitum' values throughout the 6 h re-feeding period. Cardiac LPL activ
ities remained up-regulated for the 6 h of re-feeding. Adipose-tissue
LPL activities exceeded those of cardiac or skeletal muscle throughout
both light and dark phases. The lowest adipose-tissue LPL activities
were observed at 9 h into the light phase. In contrast, cardiac LPL ac
tivity declined throughout the dark phase, with a minimum at 9 h into
the dark phase. No such variation was observed for skeletal-muscle LPL
activities. A diurnal nadir in plasma triacyl-glycerol (TG) concentra
tions coincided with the peak in cardiac LPL activities. The results d
emonstrate that, during unrestricted feeding and re-feeding after prol
onged starvation, changes in skeletal-muscle and adipose-tissue LPL ac
tivities are neither reciprocal nor co-ordinate. Regulation of cardiac
LPL activity during the diurnal cycle may be an important aspect of b
oth of cardiac fuel selection and whole-body TG metabolism.