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TSH 通过 PI3K/AKT/CREB 通路调控 CYP4B1 助力攻克亚临床甲减性心肌肥厚难题
为探究亚临床甲减(SCH)与心力衰竭、心肌肥厚的潜在机制,研究人员开展了相关研究。体外实验用促甲状腺激素(TSH)处理心肌细胞,体内实验用心脏特异性 TSHR 基因敲除小鼠诱导心肌肥厚。结果表明 TSH/TSHR 影响心肌细胞肥大,CYP4B1 有望成为治疗靶点,为 SCH ...
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