血红素加氧酶系统在缓解糖尿病相关激素和代谢紊乱方面的作用

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochimica et biophysica acta. Molecular basis of disease Pub Date : 2024-10-25 DOI:10.1016/j.bbadis.2024.167552
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引用次数: 0

摘要

血红素加氧酶(HO)是一种催化血红素降解的酶。HO 功能障碍与包括糖尿病在内的多种病理情况有关。动物研究结果表明,在实验诱导的糖尿病中,HO 的表达和活性都会下调。这与严重的激素和代谢紊乱有关。然而,使用 HO 激活剂治疗后,这些病理变化被逆转。在实验性糖尿病动物中,通过基因操作或药物激活剂(如hemin和原卟啉钴)可上调HO。诱导 HO 可缓解血糖水平升高,改善胰岛素作用等效果。这种效应来自主要胰岛素敏感组织(即骨骼肌、肝脏和脂肪组织)的有益变化。HO 激活剂的作用是由于关键信号分子和调节酶发生了积极变化。此外,由于HO的诱导作用,与糖尿病相关的氧化应激和炎症应激得以减轻。HO上调对各种1型和2型糖尿病动物模型都有效。这些数据表明,有可能将HO激活剂作为缓解糖尿病患者荷尔蒙和新陈代谢紊乱的潜在工具进行测试。
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The relevance of the heme oxygenase system in alleviating diabetes-related hormonal and metabolic disorders
Heme oxygenase (HO) is an enzyme that catalyzes heme degradation. HO dysfunction is linked to various pathological conditions, including diabetes. Results of animal studies indicate that HO expression and activity are downregulated in experimentally induced diabetes. This is associated with severe hormonal and metabolic disturbances. However, these pathological changes have been shown to be reversed by therapy with HO activators. In animals with experimentally induced diabetes, HO was upregulated by genetic manipulation or by pharmacological activators such as hemin and cobalt protoporphyrin. Induction of HO alleviated elevated blood glucose levels and improved insulin action, among other effects. This effect resulted from beneficial changes in the main insulin-sensitive tissues, i.e., the skeletal muscle, the liver, and the adipose tissue. The action of HO activators was due to positive alterations in pivotal signaling molecules and regulatory enzymes. Furthermore, diabetes-related oxidative and inflammatory stress was reduced due to HO induction. HO upregulation was effective in various animal models of type 1 and type 2 diabetes. These data suggest the possibility of testing HO activators as a potential tool for alleviating hormonal and metabolic disorders in people with diabetes.
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来源期刊
CiteScore
12.30
自引率
0.00%
发文量
218
审稿时长
32 days
期刊介绍: BBA Molecular Basis of Disease addresses the biochemistry and molecular genetics of disease processes and models of human disease. This journal covers aspects of aging, cancer, metabolic-, neurological-, and immunological-based disease. Manuscripts focused on using animal models to elucidate biochemical and mechanistic insight in each of these conditions, are particularly encouraged. Manuscripts should emphasize the underlying mechanisms of disease pathways and provide novel contributions to the understanding and/or treatment of these disorders. Highly descriptive and method development submissions may be declined without full review. The submission of uninvited reviews to BBA - Molecular Basis of Disease is strongly discouraged, and any such uninvited review should be accompanied by a coverletter outlining the compelling reasons why the review should be considered.
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