Benelli C, Michel O, Michel R
J Steroid Biochem. 1982 Jun;16(6):755-61. doi: 10.1016/0022-4731(82)90032-2.
The effect of thyroidectomy on corticosterone and aldosterone biosynthesis, in rat adrenal cortex, were investigated in vitro. Thyroidectomy slowed down by about 30% the activity of microsomal 21 hydroxylase and mitochondrial 11 beta hydroxylase, the two stages leading to corticosterone formation from progesterone. The plasma corticosterone concentration also diminished in thyroidectomized rat. The mitochondrial enzyme system catalyzing the conversion of corticosterone into aldosterone included both 18 hydroxylase and 180H dehydrogenase. In the absence of thyroid hormone, values of both enzyme activity slowed down by about 30%. Thus thyroidectomy induced a general decrease in all mitochondrial hydroxylation processes requiring NNADPH as energetic cofactor. Mitochondrial NADPH was mainly synthesized by the activity of NADP+ malic enzyme and pyridine nucleotide transhydrogenase; the activity of both enzymes was determined in submitochondrial particles from adrenal cortex of normal and thyroidectomized rats. The activity of NADP+ malic enzyme and non energy-dependent transhydrogenase in the direction of NADPH formation dropped significantly after thyroidectomy, thus reducing the amount of NADPH available for hydroxylating mechanisms. The results should be compared to the large rise in th cytosolic malic enzyme level caused by thyroidectomy. The latter also ensured that the transhydrogenase reaction did not vary in the direction of NADP+ formation. Further, the drop in NADPH synthesis after thyroidectomy was coupled with a decrease in phosphorylation rate of added ADPH by adrenal cortex mitochondria of thyroidectomized rat. These findings might account for the general decline in the energy-dependent processes involved in steroidogenesis, a decline mainly due to the lowering of the H+ ions gradient driving ATP and NADPH synthesis through electron transfer.
本研究在体外对大鼠肾上腺皮质进行甲状腺切除,以探讨其对皮质酮和醛固酮生物合成的影响。甲状腺切除使微粒体21-羟化酶和线粒体11β-羟化酶的活性降低了约30%,这两个阶段是孕酮生成皮质酮的过程。甲状腺切除大鼠的血浆皮质酮浓度也降低。催化皮质酮转化为醛固酮的线粒体酶系统包括18-羟化酶和180H脱氢酶。在缺乏甲状腺激素的情况下,这两种酶的活性值均降低了约30%。因此,甲状腺切除导致所有需要NNADPH作为能量辅助因子的线粒体羟化过程普遍下降。线粒体NADPH主要由NADP +苹果酸酶和吡啶核苷酸转氢酶的活性合成;在正常和甲状腺切除大鼠肾上腺皮质的亚线粒体颗粒中测定了这两种酶的活性。甲状腺切除后,NADP +苹果酸酶和非能量依赖性转氢酶在NADPH形成方向上的活性显著下降,从而减少了可用于羟化机制的NADPH量。这些结果应与甲状腺切除引起的胞质苹果酸酶水平大幅升高进行比较。后者还确保转氢酶反应在NADP +形成方向上没有变化。此外,甲状腺切除后NADPH合成的下降与甲状腺切除大鼠肾上腺皮质线粒体对添加的ADPH磷酸化速率的降低有关。这些发现可能解释了类固醇生成中能量依赖过程的普遍下降,这种下降主要是由于通过电子传递驱动ATP和NADPH合成的H +离子梯度降低所致。