Me. Bizeau et al., A high-sucrose diet increases gluconeogenic capacity in isolated periportal and perivenous rat hepatocytes, AM J P-ENDO, 280(5), 2001, pp. E695-E702
Citations number
37
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
A high-sucrose (SU) diet increases gluconeogenesis (GNG) in the Liver. The
present study was conducted to determine the contribution of periportal (PP
) and perivenous (PV) cell populations to this SU-induced increase in GNG.
Male Sprague-Dawley rats were fed an SU (68% sucrose) or starch (ST, 68% st
arch) diet for 1 wk, and hepatocytes were isolated from the PP or PV region
of the liver acinus. Hepatocytes were incubated for 1 h in the presence of
various gluconeogenic substrates, and glucose release into the medium was
used to estimate GNG. When incubated in the presence of 5 mM lactate, which
enters GNG at the level of pyruvate, glucose release (nmol . h(-1) . mg(-1
)) was significantly increased by the SU diet in both PP (84.8 +/- 3.4 vs.
70.4 +/- 2.6) and PV(64.3 +/- 2.5 vs. 38.2 +/- 2.1) cells. Addition of palm
itate (0.5 mM) increased glucose release from lactate in PP cells by 11.6 /- 0.5 and 20.6 +/- 1.5% and in PV cells by 11.0 +/- 4.4 and 51.1 +/- 9.1%
in SU and ST, respectively. When cells were incubated with 5 mM dihydroxyac
etone (DHA), which enters GNG at the triosephosphate level, glucose release
was significantly increased by the SU diet in both cell types. In contrast
, glucose release from fructose (0.5 mM) was significantly increased by the
SU diet in PV cells only. These changes in glucose release were accompanie
d by significant increases in the maximal specific activities of glucose-g-
phosphatase (G-6-Pase) and phosphoenol pyruvate carboxykinase (PEPCK) in bo
th PP and PV cells. These data suggest that the SU diet influences GNG in b
oth PP and PV cell populations. It appears that SU feeding produces changes
in GNG via alterations in at least two critical enzymes, G-6-Pase and PEPC
K.