Literature DB >> 14575315

Revisiting the surgical creation of volume load by aorto-caval shunt in rats.

Catherina Ocampo1, Paul Ingram, Michel Ilbawi, Rene Arcilla, Madhu Gupta.   

Abstract

Cardiac hypertrophy is an early landmark during the clinical course of heart failure, and is an important risk factor for subsequent morbidity and mortality. The hypertrophy response to different types of cardiac overload is distinguished both at the molecular and cellular levels. These changes have been extensively characterized for pressure load hypertrophy; however, similar information for volume load hypertrophy is still needed. This study was undertaken to improve the existing method of producing experimental cardiac volume load. Previous investigators have employed surgical aorto-caval shunt (ACS) as a model for volume load hypertrophy (VO) in rats. The procedure is relatively simple and involves glue to seal the aortic hole after ACS. However, it has several limitations mostly related to the use of glue e.g. poor visualization due to hardening of tissues, imperfect sealing of the puncture site and glue seeping through the aortic hole resulting in shunt occlusion. We have modified the procedure using aortic adventitial suture instead of glue and 18G angiocatheter instead of 16G needle, which eliminated the technical difficulties from the former method. The ACS was visually confirmed at sacrifice, and the VO demonstrated by time-related changes in the heart weight/body weight ratio which increased from 78% at 4 weeks to 87% at 10 weeks and increased liver/body weight ratio by 22% at 10 weeks of post aorto-caval shunt. Cardiac expression of atrial natriuretic peptide (ANF) also demonstrated time-related increase in ANF mRNA (+275% increase at 4 weeks, p < 0.05, and +370% increase at 10 weeks, p < 0.001). This modified technique of aorto-caval shunt offers simpler, reproducible and consistent model for VO hypertrophy in rats.

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Year:  2003        PMID: 14575315

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  5 in total

1.  Morphometry and ultrastructure of heart hypertrophy induced by chronic volume overload (aorto-caval fistula in the rat).

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Journal:  J Mol Cell Cardiol       Date:  1979-10       Impact factor: 5.000

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Journal:  J Mol Cell Cardiol       Date:  1999-10       Impact factor: 5.000

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Authors:  R Garcia; S Diebold
Journal:  Cardiovasc Res       Date:  1990-05       Impact factor: 10.787

5.  Pressure- and volume-induced left ventricular hypertrophies are associated with distinct myocyte phenotypes and differential induction of peptide growth factor mRNAs.

Authors:  A Calderone; N Takahashi; N J Izzo; C M Thaik; W S Colucci
Journal:  Circulation       Date:  1995-11-01       Impact factor: 29.690

  5 in total
  7 in total

1.  Contribution of calcium-activated chloride channel to elevated pulmonary artery pressure in pulmonary arterial hypertension induced by high pulmonary blood flow.

Authors:  Kai Wang; Chuansi Chen; Jianfa Ma; Jinquan Lao; Yusheng Pang
Journal:  Int J Clin Exp Pathol       Date:  2015-01-01

Review 2.  Surgical and physiological challenges in the development of left and right heart failure in rat models.

Authors:  Michael G Katz; Anthony S Fargnoli; Sarah M Gubara; Elena Chepurko; Charles R Bridges; Roger J Hajjar
Journal:  Heart Fail Rev       Date:  2019-09       Impact factor: 4.214

3.  A cardiac-enriched microRNA, miR-378, blocks cardiac hypertrophy by targeting Ras signaling.

Authors:  Raghu S Nagalingam; Nagalingam R Sundaresan; Mahesh P Gupta; David L Geenen; R John Solaro; Madhu Gupta
Journal:  J Biol Chem       Date:  2013-02-27       Impact factor: 5.157

4.  Sodium hydrosulfide alleviates pulmonary artery collagen remodeling in rats with high pulmonary blood flow.

Authors:  Xiaohui Li; Junbao Du; Hongfang Jin; Bin Geng; Chaoshu Tang
Journal:  Heart Vessels       Date:  2008-11-27       Impact factor: 2.037

5.  Hydrogen sulfide upregulates heme oxygenase-1 expression in rats with volume overload-induced heart failure.

Authors:  Chao-Ying Zhang; Xiao-Hui Li; Ting Zhang; Jin Fu; Xiao-Dai Cui
Journal:  Biomed Rep       Date:  2013-03-26

6.  Hydrogen sulfide suppresses the expression of MMP-8, MMP-13, and TIMP-1 in left ventricles of rats with cardiac volume overload.

Authors:  Chao-Ying Zhang; Xiao-Hui Li; Ting Zhang; Jin Fu; Xiao-Dai Cui
Journal:  Acta Pharmacol Sin       Date:  2013-08-26       Impact factor: 6.150

7.  Prevention of bronchial hyperreactivity in a rat model of precapillary pulmonary hypertension.

Authors:  Walid Habre; Gergely Albu; Tibor Z Janosi; Fabienne Fontao; Britta S von Ungern-Sternberg; Maurice Beghetti; Ferenc Petak
Journal:  Respir Res       Date:  2011-04-27
  7 in total

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