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      Characteristic Distribution Pattern of Lysophosphatidylcholine in Fibromuscular Dysplasia-Associated Visceral Artery Aneurysms Compared with Atherosclerotic Visceral Artery Aneurysms

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          Abstract

          Aim: Asymptomatic visceral artery aneurysms (VAAs) have increasingly been found, with most being either atherosclerotic VAAs or fibromuscular dysplasia (FMD)-associated VAAs. However, little is known about the pathogenesis of both diseases. We aimed to identify the differences in the distribution pattern of lipid molecules between atherosclerotic VAAs and FMD-associated VAAs.

          Methods: We conducted a histological study of VAAs using imaging mass spectrometry (IMS) to assess the accumulation of lipid molecules in both the aneurysmal sac and the adjacent arteries without aneurysmal changes in 17 VAA samples, which were resected during the surgery.

          Results: IMS revealed characteristic distributions of cholesterol ester in intima and media in the atherosclerotic VAAs, which was hardly detected in FMD-associated VAAs. However, lysophosphatidylcholine (lysoPC), a proinflammatory and proapoptotic lipid mediator, was accumulated in the medial ridge of the adventitia of FMD-associated in the aneurysmal sac, and it was also diffusely accumulated in the adjacent arteries. In contrast, lysoPC was accumulated in the area of intimal hyperplasia in atherosclerotic VAAs and the adjacent arteries.

          Conclusion: The distribution patterns of lipid molecules were different between the FMD-associated and atherosclerotic VAAs. The diffuse accumulation of lysoPCs in the visceral arteries may be a predisposition for the formation of FMD-associated VAAs.

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          Author and article information

          Journal
          J Atheroscler Thromb
          J. Atheroscler. Thromb
          jat
          jat
          Journal of Atherosclerosis and Thrombosis
          Japan Atherosclerosis Society
          1340-3478
          1880-3873
          1 June 2016
          : 23
          : 6
          : 673-680
          Affiliations
          [1 ] Division of Vascular Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan
          [2 ] Department of Cell Biology and Anatomy, Hamamatsu University School of Medicine, Hamamatsu, Japan
          [3 ] Second Department of Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan
          [4 ] Department of Medical Physiology, Hamamatsu University School of Medicine, Hamamatsu, Japan
          [5 ] Department of Anatomy and Neuroscience, Hamamatsu University School of Medicine, Hamamatsu, Japan
          [6 ] Department of Applied Biological Chemistry, Graduate School of Agriculture, Kinki University, Nara, Japan
          [7 ] Department of Anatomy, Hong Kong University, Pokfulam, Hong Kong
          Author notes

          Hiroki Tanaka and Nobuhiro Zaima contributed equally to this work.

          Address for correspondence: Naoki Unno, Division of Vascular Surgery, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu 431-3192, Japan E-mail: unno@ 123456hama-med.ac.jp
          Article
          PMC7399278 PMC7399278 7399278
          10.5551/jat.32318
          7399278
          26666464
          38e42fdb-29a3-4c7e-ad7f-0362b02aa16f
          2016 Japan Atherosclerosis Society
          History
          : 13 September 2015
          : 27 October 2015
          Page count
          Figures: 3, Tables: 1, References: 15, Pages: 8
          Categories
          Original Article

          Fibromuscular dysplasia,Imaging mass spectrometry,Atherosclerosis,Lysophosphatidylcholine,Visceral artery aneurysm

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