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丙硫氧嘧啶改变小鼠嗅觉黏膜中谷胱甘肽依赖性酶的表达和活性。

Propylthiouracil alters the expression and activity of glutathione-dependent enzymes in the mouse olfactory mucosa.

作者信息

Etienne Lisa A, Maruniak Joel A, Walters Eric

机构信息

Department of Genetics and Human Genetics, College of Medicine, Howard University, Washington, DC 20059, USA.

出版信息

Brain Res. 2003 Jul 11;977(2):149-56. doi: 10.1016/s0006-8993(03)02556-3.

Abstract

Propylthiouracil (PTU) is an anti-thyroid drug that reportedly can impair olfactory function in humans and mice. In the mouse, PTU treatment disrupts survival and differentiation of olfactory precursor neurons. While the mechanism responsible for this effect is not understood, it is suspected that these changes are consequent to localized toxicity due to PTU metabolism. In vitro and in vivo studies in other biological systems demonstrate that PTU can significantly alter glutathione S-transferase (GST) enzyme expression and activity. The localization of GST biotransformation enzymes in basal cells, sustentacular cells and Bowman's glands of the olfactory mucosa suggests that these cells play a significant role in olfactory physiology. This study investigated the effects of PTU treatment, T(4) replacement therapy and thyroidectomy on GST expression, GST and glutathione peroxidase (GSH-PX) activity in mouse olfactory tissue. One month treatment with PTU revealed a significant decrease in expression of GST alpha (37%) as identified by Western blot analysis. In contrast, no change in GST mu expression was observed after 1 month of treatment. Concomitant treatment with T(4) caused a significant induction of GST alpha, and mu isozymes. GST enzyme activity significantly decreased after 1 month of PTU treatment (53%) and remained suppressed, despite the presence of exogenous T(4). GSH-PX activity significantly decreased after 1 month of PTU treatment (30%) and remained at control levels with T(4) supplementation. Thyroidectomy caused a 25% reduction in olfactory GST alpha expression. Total GST and GSH-PX activity were not altered in these animals. Supplementation with T(4) in thyroidectomized animals prevented the suppression of GST alpha expression. These results suggest that the combined action of localized PTU toxicity and altered levels of circulating thyroid hormone contribute to PTU-mediated abnormalities in the olfactory system.

摘要

丙硫氧嘧啶(PTU)是一种抗甲状腺药物,据报道它会损害人类和小鼠的嗅觉功能。在小鼠中,PTU治疗会破坏嗅觉前体细胞的存活和分化。虽然导致这种效应的机制尚不清楚,但怀疑这些变化是PTU代谢引起的局部毒性所致。在其他生物系统中的体外和体内研究表明,PTU可显著改变谷胱甘肽S-转移酶(GST)的酶表达和活性。GST生物转化酶在嗅觉黏膜的基底细胞、支持细胞和鲍曼腺中的定位表明,这些细胞在嗅觉生理中发挥着重要作用。本研究调查了PTU治疗、T(4)替代疗法和甲状腺切除术对小鼠嗅觉组织中GST表达、GST和谷胱甘肽过氧化物酶(GSH-PX)活性的影响。PTU治疗1个月后,通过蛋白质印迹分析发现GSTα的表达显著降低(37%)。相比之下,治疗1个月后未观察到GSTμ表达的变化。同时给予T(4)可显著诱导GSTα和μ同工酶。PTU治疗1个月后,GST酶活性显著降低(53%),尽管存在外源性T(4),但仍保持抑制状态。PTU治疗1个月后,GSH-PX活性显著降低(30%),补充T(4)后保持在对照水平。甲状腺切除术导致嗅觉GSTα表达降低25%。这些动物的总GST和GSH-PX活性未改变。甲状腺切除术后动物补充T(4)可防止GSTα表达的抑制。这些结果表明,局部PTU毒性和循环甲状腺激素水平改变的联合作用导致了PTU介导的嗅觉系统异常。

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