The effect of low- and high-dose levothyroxine on the expression, protein level, and function of P-glycoprotein in mice

Pub Date : 2023-10-18 DOI:10.12681/jhvms.31421
B Tras, K Uney, H Eser Faki, T Melik Parlak, Z Ozdemir Kutahya
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Abstract

The study was investigated the effect of different doses of levothyroxine on the mRNA expression, protein level and function of Pgp. Mice were divided into 6 groups as control, low dose levothyroxine, high dose levothyroxine, fexofenadine, low dose levothyroxine+fexofenadine and high dose levothyroxine+fexofenadine. Mice received levothyroxine at doses of 8 and 80 µg/kg daily for 21 days. Fexofenadine was administered at dose of 40 mg/kg at the 24 h following the last administration of levothyroxine. The mRNA levels and protein level of Pgp in liver and small intestine were determined by RT-PCR and western blot analysis, respectively. Plasma concentrations of fexofenadine were determined using HPLC. Levothyroxine at low and high doses caused an insignificant increase intestinal mRNA expression of mdr1a, while high dose levothyroxine+fexofenadine caused a significant increase. Levothyroxine caused a dose-dependent decrease in intestinal mRNA expression of mdr1b. In liver, levothyroxine caused a dose-dependent increase in the mRNA expression of mdr1a. Fexofenadine significantly reduced the effect of levothyroxine on mRNA expression of mdr1a in liver. Levothyroxine increased the protein level of Pgp in liver and decrease in intestines. Low dose levothyroxine significantly increased the plasma concentration of fexofenadine. The effects of levothyroxine on the mRNA expression of mdr1a and b in small intestine and liver and protein level of Pgp varied depending on the dose, tissue type, and fexofenadine administration.
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低、高剂量左甲状腺素对小鼠p -糖蛋白表达、蛋白水平及功能的影响
研究不同剂量左甲状腺素对大鼠Pgp mRNA表达、蛋白水平及功能的影响。将小鼠分为对照组、低剂量左甲状腺素组、高剂量左甲状腺素组、非索非那定组、低剂量左甲状腺素+非索非那定组和高剂量左甲状腺素+非索非那定组。小鼠接受左甲状腺素治疗,剂量分别为8和80µg/kg,每天21天。非索非那定在末次给药左甲状腺素后24 h给药,剂量为40 mg/kg。RT-PCR和western blot分别检测肝脏和小肠中Pgp mRNA和蛋白水平。采用高效液相色谱法测定非索非那定的血药浓度。低剂量和高剂量左甲状腺素对肠道mdr1a mRNA表达的增加不显著,而高剂量左甲状腺素+非索非那定对肠道mdr1a mRNA表达的增加显著。左旋甲状腺素引起肠道mdr1b mRNA表达呈剂量依赖性降低。在肝脏中,左旋甲状腺素引起mdr1a mRNA表达的剂量依赖性增加。非索非那定显著降低左旋甲状腺素对肝脏mdr1a mRNA表达的影响。左旋甲状腺素增加肝脏Pgp蛋白水平,降低肠道Pgp蛋白水平。低剂量左甲状腺素显著增加非索非那定血药浓度。左旋甲状腺素对大鼠小肠和肝脏mdr1a和b mRNA表达及Pgp蛋白水平的影响随给药剂量、组织类型和非索非那定的不同而不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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