Sabell I, Morata P, Quesada J, Morell M
Enzyme. 1985;34(1):27-32. doi: 10.1159/000469356.
The glycolytic metabolism through the key enzymes, hexokinase, phosphofructokinase, pyruvate kinase and lactate dehydrogenase, have been studied in the brain areas: anterior cortex, amygdala, hypothalamus, septum and hippocampus in adult rats with pharmacologically induced hyperthyroidism. The oxidative metabolism of glucose is accelerated in most brain areas by treatment with high doses of T3, as is shown by the increase in HK activity, approaching normality on reducing the dose. This decrease can also by observed in the PFK activity through the effect of assayed doses of thyroxine. The anterior cortex is the only brain area that does not show significant variations of PK activity through the effects of treatment with thyroid hormones. On the other hand, a general inhibition of the glycolytic anaerobic pathway by treatment with T3 was observed.
通过关键酶己糖激酶、磷酸果糖激酶、丙酮酸激酶和乳酸脱氢酶的糖酵解代谢,已在成年大鼠经药物诱导甲状腺功能亢进后的脑区进行了研究,这些脑区包括前额叶皮质、杏仁核、下丘脑、隔区和海马体。高剂量T3治疗可加速大多数脑区的葡萄糖氧化代谢,这表现为HK活性增加,在降低剂量时接近正常水平。通过测定剂量的甲状腺素的作用,也可观察到PFK活性的这种降低。前额叶皮质是唯一未通过甲状腺激素治疗而显示PK活性有显著变化的脑区。另一方面,观察到T3治疗对糖酵解无氧途径有普遍抑制作用。