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. 1998 Jun 23;95(13):7385–7390. doi: 10.1073/pnas.95.13.7385

Table 3.

Effects of leptin treatment in vivo on the activities of glycogen synthase, glycogen phosphorylase, and ACC in ob/ob mouse liver

Enzyme Control, units/glww Leptin, units/glww
GSa 0.19  ±  0.05 (7) 0.58  ±  0.11 (8) P = 0.01
GST 0.62  ±  0.10 (7) 1.15  ±  0.18 (8) P < 0.05
GSa/GST 0.30  ±  0.05 (7) 0.50  ±  0.05 (8) P < 0.05
GPa* 12.5  ±  2.0 (7) 11.3  ±  1.5 (8) NS
ACC(−cit) 0.37  ±  0.02 (8) 0.27  ±  0.04 (8) P < 0.05
ACC(+cit) 0.72  ±  0.03 (8) 0.51  ±  0.05 (8) P < 0.005
ACC(−/+) 0.52  ±  0.02 (8) 0.53  ±  0.02 (8) NS
FAS 0.52  ±  0.04 (10) 0.29  ±  0.03 (10) P < 0.001

Leptin treatment as given in Table 1. Units/glww is defined as the conversion of 1 μmol of substrate per min at 30°C per glww. Number of experiments is in parentheses. GPa, the a-form of glycogen phosphorylase. NS, not significant. 

*

For comparison, GPa for lean mouse liver (N = 4) was 7.2 ± 4.2 units/glww. 

ACC activity was measured in the absence (−cit) or presence (+cit) of 4 mM citrate. ACC(−/+) is the ratio of activity at 0 and 4 mM citrate. 

For FAS activity is defined as the synthesis of 1 nmol of palmitic acid per min at 30°C per mg of liver protein.