Establishment of a rat model of myocardial infarction with a high survival rate: A suitable model for evaluation of efficacy of stem cell therapy

被引:1
作者
Srikanth, Garikipati Venkata Naga [1 ]
Prakash, Prem [2 ]
Tripathy, Inaresh Kumar [1 ]
Dikshit, Madhu [2 ]
Nityanand, Soniya [1 ]
机构
[1] Sanjay Gandhi Postgrad Inst Med Sci, Dept Hematol, Stem Cell Res Facil, Raebareli Rd, Lucknow 226014, Uttar Pradesh, India
[2] Cent Drug Res Inst, Div Pharmacol, Cardio Vasc Unit, Lucknow 226001, Uttar Pradesh, India
关键词
Rat Model; Myocardial Infarction; Innovations in LAD Ligation; High Survival Rate; Stem Cell Therapy;
D O I
暂无
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The most common rat model of myocardial infarction (MI) is by ligation of left anterior descending (LAD) coronary artery but it is associated with high mortality and large variations in the infarct size. We evolved certain innovations/modifications in the existing technique including immobilization of the heart without exteriorization, identification of the LAD by pressing it proximal to the site of ligation by an ear-bud, and subsequently its ligation 8 mm from its origin, no touch technique of the lungs during surgery, removal of air from the chest cavity prior to its closure using an in-house tubing, and deflation of the lungs before extubation. We induced MI in 24 Sprague-Dawley (SD) rats using these modifications and carried out post-MI evaluation of hemodynamic parameters, serum cardiac enzymes and histological studies upto 90 days using 13 sham operated and 3 healthy SD rats as controls. Three of the 24 rats (13%) died <24 hours of MI, but thereafter no mortality was observed till the follow-up period of 90 days. The infarct size was consistent in all the rats (21 +/- 4% of left ventricular area). This model with low early and no long-term mortality may be suitable for studying efficacy of stem cell therapy in MI, where a follow-up of at least 13 weeks is required to assess myocardial regeneration.
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页码:30 / 36
页数:7
相关论文
共 16 条
[1]   Rat models of myocardial infarction - Pathogenetic insights and clinical relevance [J].
Bhindi, Ravinay ;
Whiting, Paul K. ;
McMahon, Aisling C. ;
Khachigian, Levon M. ;
Lowe, Harry C. .
THROMBOSIS AND HAEMOSTASIS, 2006, 96 (05) :602-610
[2]   Is stem cell therapy ready for patients? Stem cell therapy for cardiac repair - Ready for the next step [J].
Boyle, Andrew J. ;
Schulman, Steven P. ;
Hare, Joshua M. .
CIRCULATION, 2006, 114 (04) :339-352
[3]  
BRADFIELD JF, 1992, LAB ANIM SCI, V42, P572
[4]   Right ventricular contractile protein function in rats with left ventricular myocardial infarction [J].
deTombe, PP ;
Wannenburg, T ;
Fan, DS ;
Little, WC .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1996, 271 (01) :H73-H79
[5]  
DIKSHIT M, 1992, ARCH INT PHARMACOD T, V318, P55
[6]  
DIKSHIT M, 1987, INDIAN J MED RES, V85, P85
[7]   HISTOPATHOLOGIC EVOLUTION OF MYOCARDIAL-INFARCTION [J].
FISHBEIN, MC ;
MACLEAN, D ;
MAROKO, PR .
CHEST, 1978, 73 (06) :843-849
[8]   EXPERIMENTAL MYOCARDIAL INFARCTION .1. A METHOD OF CORONARY OCCLUSION IN SMALL ANIMALS [J].
JOHNS, TNP ;
OLSON, BJ .
ANNALS OF SURGERY, 1954, 140 (05) :675-682
[9]   Surgical animal models of heart failure related to coronary heart disease [J].
Klocke, Rainer ;
Tian, Wen ;
Kuhlmann, Michael T. ;
Nikol, Sgrid .
CARDIOVASCULAR RESEARCH, 2007, 74 (01) :29-38
[10]   Time course studies on the functional evaluation of experimental chronic myocardial infarction in rats [J].
Manikandan, P ;
Sumitra, M ;
Nayeem, M ;
Manohar, BM ;
Lokanadam, B ;
Vairamuthu, S ;
Subramaniam, S ;
Puvanakrishnan, R .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2004, 267 (1-2) :47-58