The age-related changes in lipogenic enzymes: the role of dietary factors and thyroid hormone responsiveness

• Published in: Mechanisms of ageing and development Vol. 108; no. 2; pp. 139 - 149
• Main Authors: Mooradian, Arshag D., Albert, Stewart G.
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier Ireland Ltd 03.05.1999
• Subjects: Aging; Aging - metabolism; Animals; Blood Glucose; Body Weight; Eating; Energy Intake; Fatty Acid Synthases - metabolism; Fructose - administration & dosage; Fructose - physiology; Glucosephosphate Dehydrogenase - metabolism; Lipogenesis; Malate Dehydrogenase - metabolism; Male; Phosphogluconate Dehydrogenase - metabolism; Rats; Rats, Inbred F344; Thyroid hormone; Triiodothyronine - administration & dosage; Triiodothyronine - physiology; Aging; Lipogenesis; Thyroid hormone
• ISSN: 0047-6374; 1872-6216
• DOI: 10.1016/S0047-6374(99)00007-X

To determine whether resistance to insulin or to thyroid hormones rather than an inherent defect in enzyme activity expression account for the age-related changes in lipogenic enzymes, the activities of malic enzymes (ME), fatty acid synthase (FAS), glucose-6-phosphate dehydrogenase (G-6PD) and 6-phosphogluconate dehydrogenase (6-PGD) were assayed in hepatic, retroperitoneal fat and epididymal fat cytosol of male Fischer 344 rats at 3.5, 12 and 25 months of age. The rats were maintained on either regular rat chow with 62% of calories as complex carbohydrates or were given either high glucose or fructose diet with 65.7% of calories provided by glucose or fructose respectively. Additional groups of young and aged rats were treated with l-triiodothyronine (T 3) (15 μg/100 g body weight) for 10 days. Treatment with T 3 resulted in higher levels of hepatic ME activity regardless of the diet consumed or the age of the rats. T 3 had no consistent effect on FAS, G-6PD or 6-PGD activities. ME response to T 3 in young rats was significantly greater than that found in aged rats regardless of diet. The age-related decrease in basal hepatic ME activity was not apparent in rats maintained on the high glucose or the high fructose diets, yet the T 3 responsiveness of ME in rats maintained on these diets was not normalized. In adipose tissue, with the exception of the age-related changes in basal activity of the lipogenic enzymes, neither T 3 nor the feeding of the test diets had any consistent effects. Since insulin resistance induced by high fructose feeding did not reduce hepatic lipogenic enzymes, it is unlikely that the age-related increase in insulin resistance explains the reduced lipogenic enzyme activity in aged rats. However, resistance to thyroid hormone action found in aged rats may partly account for the reduced hepatic lipogenic enzyme activity.