トミダ タイチロウ
Tomida Taichiro
冨田 太一郎 所属 東邦大学 医学部 医学科 職種 講師 |
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論文種別 | 原著 |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | Compensatory role of neuregulin-1 in diabetic cardiomyopathy |
掲載誌名 | 正式名:Journal of Pharmacological Sciences 略 称:J Pharmacol Sci ISSNコード:1347-8613/1347-8648 |
掲載区分 | 国外 |
出版社 | Elsevier |
巻・号・頁 | 153(3),pp.130-141 |
総ページ数 | 12 |
著者・共著者 | Mikami Y†, Iwase F†, Ohshima D†, Tomida T†, Adachi-Akahane S*† |
発行年月 | 2023/09/01 |
概要 | Diabetes mellitus is a prevalent risk factor for congestive heart failure. Diabetic cardiomyopathy patients present with left ventricular (LV) diastolic dysfunction at an early stage, then systolic dysfunction as the disease progresses. The mechanism underlying the development of diabetic cardiomyopathy has not yet been fully understood. This study aimed to elucidate the mechanisms by which diastolic dysfunction precedes systolic dysfunction at the early stage of diabetic cardiomyopathy. We hypothesized that the downregulation of cardioprotective factors is involved in the pathogenesis of diabetic cardiomyopathy. LV diastolic dysfunction, but not systolic dysfunction, was observed in type-1 diabetes mellitus model mice 4 weeks after STZ administration (STZ-4W), mimicking the early stage of diabetic cardiomyopathy. Counter to expectations, neuregulin-1 (NRG1) was markedly upregulated in the vascular endothelial cell in the ventricles of STZ-4W mice. To clarify the functional significance of the upregulated NRG1, we blocked its receptor ErbB2 with trastuzumab (TRZ). In STZ-4W mice, TRZ significantly reduced the systolic function without affecting diastolic function and caused a more prominent reduction in Akt phosphorylation levels. These results indicate that the compensatory upregulated NRG1 contributes to maintaining the LV systolic function, which explains why diastolic dysfunction precedes systolic dysfunction at the early stage of diabetic cardiomyopathy. |
DOI | 10.1016/j.jphs.2023.08.009 |
文献番号 | 37770154/PubMedID |