Key result
Hypophysectomy and insulin increased hepatic lipogenesis in cockerels, while pituitary homogenates reduced lipid synthesis, suggesting pituitary hormones directly inhibit lipogenesis.
Hepatic lipogenesis in cockerels is increased by hypophysectomy and insulin, suggesting pituitary hormones may directly inhibit lipogenesis or modulate hepatic insulin sensitivity.
Avian findings on pituitary inhibition of lipogenesis leave open translation to mammalian insulin sensitivity or human metabolic disease.
Hypophysectomy increases hepatic lipogenesis in cockerels. In an attempt to find the possible hormonal mechanism for this we have examined the effects of hypophysectomy, insulin and pituitary homogenates on hepatic lipogenesis. Insulin (5 U/kg) injected intravenously, simultaneously with glucose-14C tracer, increased the amount of 14C found in liver lipids at 30 min after the injection. Similarly, insulin injected 5 min before killing, increased the incorporation of glucose-14C and acetate-14C by liver slices during a 30 min incubation. Hypophysectomy increased lipogenesis within 24 hours. The effect of insulin was most pronounced in hypophysectomized cockerels. The activity of the lipogenic enzyme, acetyl CoA carboxylase was similarly affected. A homogenate of chicken pituitaries added to the medium reduced lipid synthesis from glucose-14C by liver slices. This effect was larger in liver slices in which lipogenesis had been stimulated by insulin. The increased rate of hepatic lipgenesis in hypophysectomized cockerels may be caused partly by increased hepatic sensitivity to the lipogenic action of insulin or by the removal of a direct inhibition by pituitary hormones.
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Kompiang. et al. (1976) studied Hepatic lipogenesis. Hypophysectomy and insulin vs. Intact cockerels / no insulin was evaluated on Hepatic lipogenesis (incorporation of 14C into liver lipids). Hypophysectomy and insulin increased hepatic lipogenesis in cockerels, while pituitary homogenates reduced lipid synthesis, suggesting pituitary hormones directly inhibit lipogenesis.
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