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锂对小鼠神经组织和垂体前叶组织中甲状腺素代谢的调节作用。

Regulatory effect of lithium on thyroxine metabolism in murine neural and anterior pituitary tissue.

作者信息

St Germain D L

出版信息

Endocrinology. 1987 Apr;120(4):1430-8. doi: 10.1210/endo-120-4-1430.

Abstract

The conversion of T4 to T3 in the brain and anterior pituitary gland contributes significantly to the T3 content of these tissues and appears to be an important modulator of thyroid hormone action. In the present study, the antimanic agent lithium was demonstrated in cultured neural and pituitary tissue to have a significant inhibitory effect on the activity of low Km (type II) iodothyronine 5'-deiodinase (I5'D), the enzyme mediating T3 formation. At medium lithium concentrations of 3.3-5 mM, 15'D activity was decreased 44 +/- 3% (P less than 0.001) in the NB41A3 mouse neuroblastoma cell line and 48 +/- 2% (P less than 0.001) in the GH3 rat pituitary tumor cell line. This inhibitory effect was only observed in intact cells. Significant inhibition of this enzymatic process was also noted in the anterior pituitary gland of thyroidectomized rats injected 3-24 h earlier with either 4 or 10 mmol/kg BW LiCl. This decrease in low Km I5'D activity was accompanied by significant decreases in the serum T3 concentration and the pituitary nuclear T3 content. Renal high Km (type I) I5'D activity was unaffected by lithium administration. These studies demonstrate that lithium, an agent of proven therapeutic benefit in patients with manic-depressive illness, can affect changes in T4 metabolism and cellular T3 content in neural and anterior pituitary tissue. Given the prominent mood changes that occur in patients with disordered thyroid function, this finding suggests that the therapeutic benefits of lithium in affective illness may be derived in part from alterations in thyroid hormone economy in the brain.

摘要

大脑和垂体前叶中甲状腺素(T4)向三碘甲状腺原氨酸(T3)的转化对这些组织的T3含量有显著贡献,并且似乎是甲状腺激素作用的重要调节因子。在本研究中,在培养的神经和垂体组织中证实,抗躁狂药物锂对低Km(II型)碘甲腺原氨酸5'-脱碘酶(I5'D)的活性具有显著抑制作用,该酶介导T3的形成。在锂的中等浓度为3.3 - 5 mM时,NB41A3小鼠神经母细胞瘤细胞系中的I5'D活性降低了44±3%(P<0.001),GH3大鼠垂体瘤细胞系中的I5'D活性降低了48±2%(P<0.001)。这种抑制作用仅在完整细胞中观察到。在3 - 24小时前注射4或10 mmol/kg体重LiCl的甲状腺切除大鼠的垂体前叶中,也注意到该酶促过程受到显著抑制。低Km I5'D活性的这种降低伴随着血清T3浓度和垂体核T3含量的显著降低。肾高Km(I型)I5'D活性不受锂给药的影响。这些研究表明,锂是一种已被证明对躁狂抑郁症患者有治疗益处的药物,可影响神经和垂体前叶组织中T4代谢和细胞T3含量的变化。鉴于甲状腺功能紊乱患者会出现明显的情绪变化,这一发现表明锂在情感性疾病中的治疗益处可能部分源于大脑中甲状腺激素代谢的改变。

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