» Articles » PMID: 24747816

The Role of 1.5 Tesla MRI and Anesthetic Regimen Concerning Cardiac Analysis in Mice with Cardiomyopathy

Overview
Journal PLoS One
Date 2014 Apr 22
PMID 24747816
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Accurate assessment of left ventricular function in rodent models is essential for the evaluation of new therapeutic approaches for cardiac diseases. In our study, we provide new insights regarding the role of a 1.5 Tesla (T) magnetic resonance imaging (MRI) device and different anesthetic regimens on data validity. As dedicated small animal MRI and echocardiographic devices are not broadly available, we evaluated whether monitoring cardiac function in small rodents with a clinical 1.5 T MRI device is feasible. On a clinical electrocardiogram (ECG) synchronized 1.5 T MRI scanner we therefore studied cardiac function parameters of mice with chronic virus-induced cardiomyopathy. Thus, reduced left ventricular ejection fraction (LVEF) could be verified compared to healthy controls. However, our results showed a high variability. First, anesthesia with medetomidine, midazolam and fentanyl (MMF) led to depressed cardiac function parameters and more variability than isoflurane gas inhalation anesthesia, especially at high concentrations. Furthermore, calculation of an average ejection fraction value from sequenced scans significantly reduced the variance of the results. To sum up, we introduce the clinical 1.5 T MRI device as a new tool for effective analysis of left ventricular function in mice with cardiomyopathy. Besides, we suggest isoflurane gas inhalation anesthesia at high concentrations for variance reduction and recommend calculation of an average ejection fraction value from multiple sequenced MRI scans to provide valid data and a solid basis for further clinical testing.

Citing Articles

Mouse Cardiovascular Imaging.

Phoon C, Aristizabal O, Farhoud M, Turnbull D, Wadghiri Y Curr Protoc. 2024; 4(9):e1116.

PMID: 39222027 PMC: 11371386. DOI: 10.1002/cpz1.1116.


Functional Cardiovascular Characterization of the Common Marmoset ().

Klosener L, Samolovac S, Barnekow I, Konig J, Moussavi A, Boretius S Biology (Basel). 2023; 12(8).

PMID: 37627007 PMC: 10452209. DOI: 10.3390/biology12081123.


Medetomidine/midazolam/fentanyl narcosis alters cardiac autonomic tone leading to conduction disorders and arrhythmias in mice.

Tomsits P, Volz L, Xia R, Chivukula A, Schuttler D, Clauss S Lab Anim (NY). 2023; 52(4):85-92.

PMID: 36959339 PMC: 10063441. DOI: 10.1038/s41684-023-01141-0.


Non-invasive assessment of HFpEF in mouse models: current gaps and future directions.

Villalba-Orero M, Garcia-Pavia P, Lara-Pezzi E BMC Med. 2022; 20(1):349.

PMID: 36229816 PMC: 9563110. DOI: 10.1186/s12916-022-02546-3.


Activation of the MET receptor attenuates doxorubicin-induced cardiotoxicity in vivo and in vitro.

Gallo S, Spilinga M, Albano R, Ferrauto G, Di Gregorio E, Casanova E Br J Pharmacol. 2020; 177(13):3107-3122.

PMID: 32133617 PMC: 7280013. DOI: 10.1111/bph.15039.


References
1.
Wagenhaus B, Pohlmann A, Dieringer M, Els A, Waiczies H, Waiczies S . Functional and morphological cardiac magnetic resonance imaging of mice using a cryogenic quadrature radiofrequency coil. PLoS One. 2012; 7(8):e42383. PMC: 3411643. DOI: 10.1371/journal.pone.0042383. View

2.
Kania G, Blyszczuk P, Valaperti A, Dieterle T, Leimenstoll B, Dirnhofer S . Prominin-1+/CD133+ bone marrow-derived heart-resident cells suppress experimental autoimmune myocarditis. Cardiovasc Res. 2008; 80(2):236-45. DOI: 10.1093/cvr/cvn190. View

3.
Protti A, Dong X, Sirker A, Botnar R, Shah A . MRI-based prediction of adverse cardiac remodeling after murine myocardial infarction. Am J Physiol Heart Circ Physiol. 2012; 303(3):H309-14. PMC: 3423156. DOI: 10.1152/ajpheart.00208.2012. View

4.
Nakamura Y, Asakura Y, Piras B, Hirai H, Tastad C, Verma M . Increased angiogenesis and improved left ventricular function after transplantation of myoblasts lacking the MyoD gene into infarcted myocardium. PLoS One. 2012; 7(7):e41736. PMC: 3404994. DOI: 10.1371/journal.pone.0041736. View

5.
Zaruba M, Theiss H, Vallaster M, Mehl U, Brunner S, David R . Synergy between CD26/DPP-IV inhibition and G-CSF improves cardiac function after acute myocardial infarction. Cell Stem Cell. 2009; 4(4):313-23. DOI: 10.1016/j.stem.2009.02.013. View