Abstract

Depression is an independent risk factor for cardiovascular disease and is significantly associated with the prevalence of abdominal aortic aneurysm (AAA). We investigated the effect of repeated social defeat (RSD) on AAA development. Eight-week-old male wild-type mice were exposed to RSD by being housed with larger CD-1 mice in a shared cage. They were subjected to vigorous physical contact. After the confirmation of depressive-like behavior, calcium chloride was applied to the infrarenal aorta of the mice. At one week, AAA development was comparable between the defeated and control mice, without any differences being observed in the accumulated macrophages or in the matrix metalloproteinase activity. At two weeks, the maximum diameter and circumference of the aneurysm were significantly increased in the defeated mice, and a significant decrease in periaortic fibrosis was also observed. Consistently, the phosphorylation of the extracellular signal-regulated kinase and the incorporation of 5-bromo-2′-deoxyuridine in the primarily cultured aortic vascular smooth muscle cells were significantly reduced in the defeated mice, which was accompanied by a substantial increase in mitogen-activated protein kinase phosphatase-1 (MKP-1). The MKP-1 mRNA and protein expression levels during AAA were much higher in the defeated mice than they were in the control mice. Our findings demonstrate that RSD enhances AAA development by suppressing periaortic fibrosis after an acute inflammatory response and imply novel mechanisms that are associated with depression-related AAA development.

Highlights

  • Mental disorders are an important cause of debility worldwide and are a main contributor to comprehensive disease burden and represent substantial causes of death [1]

  • We showed that repeated social defeat (RSD) enhances CaCl2-induced Abdominal aortic aneurysm (AAA) development and impaired fibrotic wound healing following an acute inflammatory response

  • The platelet-derived growth factor (PDGF)-induced mitogen-activated protein kinase phosphatase-1 (MKP-1) protein expression was noticeably higher in the vascular smooth muscle cells (VSMCs) from the defeated mice than in it was in the control mice, and treatment with the phosphatase inhibitor completely restored extracellular signal-regulated kinase (ERK) phosphorylation to the same extent as seen in the control mice

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Summary

Introduction

Mental disorders are an important cause of debility worldwide and are a main contributor to comprehensive disease burden and represent substantial causes of death [1]. There is increasing evidence that depression is causally connected to the development of atherosclerotic cardiovascular disease (CVD) through the integration of various factors; the detailed mechanisms of depression-related CVD development remain to be fully elucidated [6–8]. A population-based prospective study showed that patients with depressive symptoms have a significantly higher risk of incident AAA after the adjustment of conventional risk factors [13]. A nationwide cohort study showed that the prevalence of depression was significantly higher in patients with AAA, independent of treatment modality [14]. These findings suggest that depression is significantly related to the development of AAA than was previously thought and imply that an additional mechanism other than conventional cardiovascular risk factors is implicated in depression-related AAA development

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