Literature DB >> 17357492

Influence of transplantation of allogenic bone marrow mononuclear cells on the left ventricular remodeling of rat after acute myocardial infarction.

Ruicheng Zhang1, Nianguo Dong, Jianfeng Hou, Xian'en Fa.   

Abstract

To probe into the influence of transplantation of allogenic bone marrow mononuclear cells (BM-MNCs) on the left ventricular remodeling of rat after acute myocardial infarction (AMI), 60 male Wistar rats were evenly divided into three groups at random: control group 1, control group 2 and transplantation group. In control group 1, chest was opened without ligation of coronary artery; in control group 2 and transplantation group, the left anterior descending branch of coronary artery was ligated to establish AMI model. Prepared culture medium and allogenic BM-MNCs suspension were respectively implanted the surrounding area of infarcted cardiac muscle via epicardium of control group 2 and transplantation group. Four weeks after the operation, the osteopontin gene (OPN mRNA, P<0.01), type I collagen (P<0.01) and angiotensin II (AngII, P<0.01) content in the left ventricular non-infarcted myocardium, and the Ang II density in blood plasma (P<0.05) of transplantation group and control group 2 were all significantly higher than that of control group 1. In the transplantation group, the myocardial OPN mRNA, type I collagen and Ang II content of non-infarcted zone in left ventricle, and the Ang II concentration in blood plasma were all significantly lower than those of control group 2 (P<0.05 for all). It is concluded that allogenic BM-MNCs transplantation may ease left ventricular remodeling after AMI by inhibiting the synthesis of type I collagen in the cardiac muscle and down-regulating the expression of Ang II and OPN gene.

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Year:  2006        PMID: 17357492     DOI: 10.1007/s11596-006-0618-0

Source DB:  PubMed          Journal:  J Huazhong Univ Sci Technolog Med Sci        ISSN: 1672-0733


  9 in total

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2.  Biological characteristics of human bone marrow mesenchymal stem cell cultured in vitro.

Authors:  Xian'en Fa; Wang Lixia; Jianfeng Hou; Ruicheng Zhang; Haiyong Wang; Chenyuan Yang
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2005

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Authors:  N A Trueblood; Z Xie; C Communal; F Sam; S Ngoy; L Liaw; A W Jenkins; J Wang; D B Sawyer; O H Bing; C S Apstein; W S Colucci; K Singh
Journal:  Circ Res       Date:  2001-05-25       Impact factor: 17.367

4.  Alterations of arterial physiology in osteopontin-null mice.

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Journal:  Arterioscler Thromb Vasc Biol       Date:  2003-04-24       Impact factor: 8.311

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Authors:  S Wassmann; U Laufs; A T Bäumer; K Müller; C Konkol; H Sauer; M Böhm; G Nickenig
Journal:  Mol Pharmacol       Date:  2001-03       Impact factor: 4.436

6.  AP-1 is involved in UTP-induced osteopontin expression in arterial smooth muscle cells.

Authors:  M-A Renault; S Jalvy; I Belloc; S Pasquet; S Sena; M Olive; C Desgranges; A-P Gadeau
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7.  Transplantation of mesenchymal stem cells improves cardiac function in a rat model of dilated cardiomyopathy.

Authors:  Noritoshi Nagaya; Kenji Kangawa; Takefumi Itoh; Takashi Iwase; Shinsuke Murakami; Yoshinori Miyahara; Takafumi Fujii; Masaaki Uematsu; Hajime Ohgushi; Masakazu Yamagishi; Takeshi Tokudome; Hidezo Mori; Kunio Miyatake; Soichiro Kitamura
Journal:  Circulation       Date:  2005-08-15       Impact factor: 29.690

8.  ERK1/2 and JNKs, but not p38 kinase, are involved in reactive oxygen species-mediated induction of osteopontin gene expression by angiotensin II and interleukin-1beta in adult rat cardiac fibroblasts.

Authors:  Zhonglin Xie; Mahipal Singh; Krishna Singh
Journal:  J Cell Physiol       Date:  2004-03       Impact factor: 6.384

9.  Angiotensin-converting enzyme inhibitor helps prevent late remodeling after left ventricular aneurysm repair in rats.

Authors:  Takuya Nomoto; Takeshi Nishina; Senri Miwa; Hiroshi Tsuneyoshi; Izumi Maruyama; Kazunobu Nishimura; Masashi Komeda
Journal:  Circulation       Date:  2002-09-24       Impact factor: 29.690

  9 in total

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