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特拉唑嗪:通过调节磷酸甘油酸酯激酶1防治帕金森病

付余 聂昊 毛如雪 郑凯

神经损伤与功能重建2024,Vol.19Issue(4):242-246,5.
神经损伤与功能重建2024,Vol.19Issue(4):242-246,5.DOI:10.16780/j.cnki.sjssgncj.20230252

特拉唑嗪:通过调节磷酸甘油酸酯激酶1防治帕金森病

Terazosin:A potential Method of Treatment and Prevention of Parkinson's Disease through Phosphoglycerate Kinase1

付余 1聂昊 1毛如雪 1郑凯1

作者信息

  • 1. 华中科技大学同济医学院附属同济医院老年医学科 武汉 430030||血管衰老教育部重点实验室 武汉 430030
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摘要

Abstract

Terazosin,as a derivative of prazosin,is a long-acting selective α 1 adrenal receptor blocker,which is widely used in the treatment of hypertension and benign prostatic hyperplasia due to its good water solubility,high bioavailability and long half-life.Recent studies have found that TZ can activate intracellular phosphoglycerate kinase1(Pgk1)in a specific dose range to protect the neurons and may be beneficial for the treatment and prevention of Parkinson's disease(PD).This effect may be related to the improvement of cell energy metabolism,the increase of intracellular ATP concentration and the activation of Hsp90 caused by the activation of Pgk1.This indicates a new clinical application prospect of terazosin.This article will review and summarize the research progress of TZ in the newly discovered pharmacological mechanism and potential clinical application prospect,and discuss the possible research direction in the future.

关键词

特拉唑嗪/帕金森病/磷酸甘油酸酯激酶1

Key words

Terazosin/Parkinson's disease/phosphoglycerate kinase1

分类

医药卫生

引用本文复制引用

付余,聂昊,毛如雪,郑凯..特拉唑嗪:通过调节磷酸甘油酸酯激酶1防治帕金森病[J].神经损伤与功能重建,2024,19(4):242-246,5.

基金项目

国家自然科学基金(丰富环境通过DNA甲基化调控Foxd3/miR-135a-5p通路改善AD小鼠学习记忆的机制研究,No.82371442) (丰富环境通过DNA甲基化调控Foxd3/miR-135a-5p通路改善AD小鼠学习记忆的机制研究,No.82371442)

神经损伤与功能重建

OACSTPCD

1001-117X

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