A Doxorubicin-Induced Murine Model of Dilated Cardiomyopathy In Vivo

Summary

Described is a protocol to establish a Doxorubicin-induced dilated cardiomyopathy (DCM) model in mice via long-term intraperitoneal injection of Doxorubicin.

Abstract

Dilated cardiomyopathy (DCM) refers to a spectrum of heterogeneous myocardial disorders characterized by ventricular dilation and depressed cardiac performance in the absence of hypertension, valvular, congenital, or ischemic heart diseases, and which may be related to infection, autoimmune or metabolic abnormalities, or family inheritance. It can progress into congestive heart failure with a poor prognosis. Doxorubicin (Dox) is widely employed as a chemotherapeutic drug, but its use is limited because it causes DCM-like changes of the myocardium. Its myocardial toxicity is attributed to oxidative stress, chronic inflammation, and cardiomyocyte apoptosis. A model of DCM exploiting these Dox-induced DCM symptoms has not been established.

Introduction

One of the most common causes of heart failure, DCM is characterized by ventricular dilatation and decreased cardiac function and is the most common reason for heart transplantation worldwide¹. In order to further investigate its pathogenesis and find effective treatments, access to mature animal models is especially important. The purpose of the described experiments is to establish a stable mouse model of DCM that resembles human DCM.

Due to the complex pathogenesis of DCM, there are many different methods to make corresponding animal models. Spontaneous DCM models² are relatively stable, but they are expensive and not easily available. Genetically modified animal models³ are not well-established and require more experimental use. DCM animal models induced by viral infection⁴ or autoimmune defects⁵ are easy to obtain, but they are not wholly representative of DCM. Models associated with myocardial toxicity include alcohol-induced DCM models and Dox-induced DCM animal models.

The Dox-induced cardiomyopathy model is obtained by intraperitoneal injection of Dox⁶. The model exploits the most severe chronic side effect of Dox: After Dox exposure, patients develop late onset DCM symptoms with clinical uniformity⁷. Dox-induced oxidative stress⁸ and mitochondrial damage⁹, which lead to cardiomyocyte apoptosis, are symptoms in the pathogenesis of DCM. There are acute and chronic Dox treatment models: a single high dose of Dox (15 mg/kg) induces a short-term model for cardiomyopathy¹⁰, while repetitive low-dose Dox injections (six weekly, 3 mg/kg) induce a long-term model for cardiomyopathy¹¹. Based on the presented study, wild type mice intraperitoneally injected once a week for a month at a dose of 5 mg/kg display morphology and histology of the heart consistent with the characteristics of DCM by the end of the treatment, providing an ideal way to establish a DCM model.

Protocol

Animal experiments were approved by Institutional Animal Care and Use Committee (IACUC) of Nanjing Drum Tower Hospital.

1. Preparation of the reagents and animals

1. Dissolve doxorubicin hydrochloride (Pfizer, USA) in sterilized water. Vortex to obtain a Dox solution of 1 mg/mL and keep at 4 °C.
2. Use C57BL/6 mice (8–10 weeks old; 25–30 g weight). For this study, mice were purchased from the Model Animal Research Center of Nanjing University and kept in the animal room of Nanjing Drum Tower Hospital.
3. Pathogen-free mouse cages were maintained under a 12 h light/dark cycle at a constant temperature of 23 °C. All animals were fed on a normal chow diet and got food and water ad libitum.

2. Establishment of DCM animal model

1. Randomize mice into a normal (n = 5) group and Dox (n = 5) group.
2. Administer the Dox solution intraperitoneally at a dose of 5 mg/kg using a 1 mL sterilized syringe 1x a week for the Dox group. Treat the control mice in the same way with the same amount of saline solution.
3. Measure the body weight of the two groups weekly. Accordingly, adjust the injection dose based on body weight weekly for a total of 4 weeks, with a cumulative dose of 20 mg/kg (Figure 1).
   NOTE: A time period of 4 weeks was chosen because echocardiography at 4 weeks showed a significant difference in cardiac function between the two groups.

3. Echocardiographic examination

1. At the end of the fourth week, conduct an echocardiographic examination of the mice.
2. Anesthetize the mice with 2% isoflurane intranasally. If the mice do not respond to a pinch of the skin with a toothed tweezer or stimulating the toes and tails, continue with the protocol.
3. Place the mouse on an animal-handling platform in the supine position. To maintain the anesthesia, cover the animal's nose and mouth with a nose cone and deliver 2% isoflurane.
   NOTE: For IP anesthesia, inject 4% chloral hydrate at a dose of 0.2 mL/20 g.
4. Remove chest fur carefully with an electric shaver. Assess cardiac function in vivo using transthoracic echocardiography.
5. Perform the LV echocardiogram in both the parasternal long-axis and short-axis views at a frame rate of 233 Hz. End-systolic and end-diastolic dimensions were defined as the phases corresponding to the ECG T wave and to the R wave, respectively.
6. On the M-mode tracings, measure the average LV end-systolic diameter (LVIDd), LV end-diastolic diameter (LVIDs), interventricular septal thickness (IVS), and LV posterior wall thickness (LVPW) from 3–5 heart beats. Also calculate the ejection fraction (EF) and fraction shortening (FS) based on echocardiography.

4. Histological staining

1. After the echocardiographic analysis, sacrifice the mice by intraventricular injection of 10% potassium chloride.
2. Perfuse the heart with about 30 mL of saline after dissection until the liver and lung become pale.
3. Excise the heart and thoroughly wash it in phosphate buffer solution to extrude blood.
4. Fix the heart in 4% formalin at room temperature for 24 h and treat the tissue in a paraffin box so that the paraffin wax cools down and solidifies.
5. Cut the hearts into 5 μm thick slices for pathological staining.
6. Dewax and rehydrate sections containing papillary muscle.
   1. Incubate slides at 55 °C for 30 min. Then, incubate in xylene 2x for 2 min each; 100% ethanol 2x for 2 min each; 95% ethanol 2x for 2 min each; 80% ethanol for 2 min; 75% ethanol for 2 min; and 50% ethanol for 2 min.
7. Stain using hematoxylin and eosin (H&E) as well as Masson’s stain.

Results

Cardiac function
Dilated cardiomyopathy is characterized by progressive ventricular dilatation and contractile dysfunction. Figure 2 shows representative echocardiographic images of the two groups. Dox-treated mice showed markedly reduced left ventricular ejection fraction and left ventricular fractional shortening (Figure 3A,B). The LV diameter also increased in both the diastolic and systolic phases (

Discussion

Dox is a nonspecific periodic antitumor chemotherapy drug commonly used in clinical practice¹². Its main side effect is cardiotoxicity, characterized by cardiomyopathy and subsequent heart failure¹³. The underlying mechanism includes damage of myocardial lipid peroxidation, inhibition of myocardial sarcoplasmic reticulum Ca²⁺-ATPase activity, and activation of the myocardial local renin-angiotensin system, resulting in increased AT II production and intracellular...

Materials

Name	Company	Catalog Number	Comments
4% paraformaldehyde	servicebio	CAS30525-89-4
C57BL/6 mice	Model Animal Research Center of Nanjing University	\
Doxorubicin hydrochloride	Pfizer	CAS25316-40-9
echocardiography	Visualsonics	\
Hematoxylin and Eosin staining kit	Solarbio	G1120
Masson staining kit	Solarbio	G1343
phosphate buffer solution	Sigma	P5368
potassium chloride	Sigma	CAS7447-40-7
sterilized syringe	Millipore	SLGP033RB