Implantation of an Isoproterenol Mini-Pump to Induce Heart Failure in Mice

Summary

The chronic administration of isoproterenol via an implanted osmotic pump has been used widely to mimic advanced heart failure in mice. Here, we describe detailed methods in surgical mini-pump implantation for the continuous isoproterenol administration over 3 weeks, as well as, echocardiographic assessment for the successful model creation.

Abstract

Isoproterenol (ISO), is a non-selective beta-adrenergic agonist, that is used widely to induce cardiac injury in mice. While the acute model mimics stress-induced cardiomyopathy, the chronic model, administered through an osmotic pump, mimics advanced heart failure in humans. The purpose of the described protocol is to create the chronic ISO-induced heart failure model in mice using an implanted mini-pump. This protocol has been used to induce heart failure in 100+ strains of inbred mice. Techniques on surgical pump implantation are described in detail and may be relevant to anyone interested in creating a heart failure model in mice. In addition, the weekly cardiac remodeling changes based on echocardiographic parameters for each strain and expected time to model development are presented. In summary, the method is simple and reproducible. Continuous ISO administered via the implanted mini-pump over 3 to 4 weeks is sufficient to induce cardiac remodeling. Finally, the success for ISO model creation may be assessed in vivo by serial echocardiography demonstrating hypertrophy, ventricular dilation, and dysfunction.

Introduction

Heart failure with reduced ejection fraction (HFrEF) is accompanied by a well-recognized compensatory response of the sympathetic nervous system to maintain cardiovascular homeostasis¹. Hemodynamic stress and deleterious effects on the heart and circulation were observed with chronic activation. These have become the cornerstone of contemporary pharmacotherapy for heart failure and are important mechanisms in the progression of heart failure and therapeutic antagonism of neurohormonal systems¹.

Several mouse models are available for basic investigations of heart failure. Genetic models are attractive for exploring molecular therapies and investigating signaling pathways. However, these models may not be relevant to common forms of heart failure. Other common models include left anterior descending (LAD) artery ligation, transaortic constriction (TAC), and isoproterenol (ISO), each aiming at a different pathological etiology^2,3,4,5,6. LAD artery ligation induces an anterior wall myocardial infarction thus creating a model specific for ischemic cardiomyopathy. TAC induces acute pressure overload to create a hypertensive model of heart failure. Although the pressure gradient can be measured, allowing for the stratification of hypertrophy, the acute onset of hypertension lacks direct clinical relevance⁴. Both LAD and TAC models require a high level of surgical expertise to execute. Acute ISO model of heart failure mimics stress-induced cardiomyopathy, also known as Takotsubo disease, which is characterized by a marked increase in catecholamines and activity in the left ventricle that mimics acute myocardial infarction^7,8. In contrast, chronic ISO models of heart failure present symptoms characteristics of advanced heart failure, with chronically elevated levels of catecholamines¹. The advantages of the chronic ISO model are that it provides chronic adrenergic stimulation that mimics advanced heart failure and that it is relatively easy to create. The investigator should choose a model that best recapitulates their pathology of interest.

The overall goal of this method is to induce heart failure in mice using an implanted mini pump that releases ISO continuously to mimic chronic sympathetic activation found in heart failure patients¹. The method is simple and reproducible. Although there is clear variation among mouse strains, ISO administered over 3 to 4 weeks at 30 mg/kg/day is sufficient to induce cardiac remodeling in most mice. Specifically, ISO leads to a pro-hypertrophic compensatory phase during week 1 followed by wall thinning, ventricular dilation and decrease in systolic function by week 2 and 3². Success for the ISO model creation can be assessed in vivo by serial echocardiography demonstrating hypertrophy, dilation, and ventricular dysfunction, as well as ex vivo via histological and molecular assessment of harvested cardiac tissue for intramyocardial lipid accumulation, fibrosis, ER stress, apoptosis, and gene expression^9,10,11,12.

Protocol

This protocol adheres to the animal care guidelines of the University of California, Los Angeles (ARC protocol #2010-075). Readers are advised to adhere to their own IACUC-approved protocol, as peri-procedure mouse care and analgesia management may be institution-specific.

1. Preparation of isoproterenol osmotic pump

NOTE: This procedure has been applied successfully on 9+ week-old female mice weighing 18+ g from over 100 inbred mouse strains, as well as, in male mice in a subset of strains. There is no maximum body weight limit for this procedure. Always include age-matched controls, as it is unknown whether the age of treatment affects isoproterenol-induced susceptibility to heart failure development.

1. Weigh and record the body weight for each mouse.
2. Calculate the appropriate amount and concentration of isoproterenol for each mouse (See Table 1 ; Supplemental File).
   NOTE: The osmotic pumps used in this experiment (Table of Materials) have a reservoir volume of 100 µL and are designed to deliver drugs at continuous flow rates for up to 28 days. Prepare an extra 20 µL of isoproterenol solution per pump to account for the volume loss in the filling tube during pump loading.
3. Weigh out the appropriate amount of isoproterenol (Table 1) using an analytical balance and dissolve it in 120 µL of sterile 0.9% NaCl solution. Pipette vigorously or vortex for 1 min to completely solubilize isoproterenol.
   NOTE: Prepare the osmotic pumps in a laboratory biosafety cabinet. Pumps should be handled with surgical gloves. Sterile technique is recommended throughout the preparation of the osmotic pumps and during the surgical implantation procedure.
4. Weigh and record the empty osmotic pump together with its flow moderator and then remove the flow moderator.
5. Aspirate 120 µL of isoproterenol solution into a 1.0 mL syringe and attach the 27-gauge blunt-tipped filling tube provided with the osmotic pumps.
   NOTE: Make sure the syringe and filling tube are free of air bubbles.
6. While holding the pump in the upright position, insert the filling tube through the pump opening at the top until the tip of the filling tube sits near the bottom of the pump reservoir.
7. Load the osmotic pump by pushing the syringe plunger slowly until the isoproterenol solution fills up to the pump opening.
8. Carefully remove the filling tube and wipe off the excess solution.
9. Insert back the flow moderator to close the pump and wipe off any excess solution.
10. Confirm that over 90% of the reservoir volume has been filled by reweighing the osmotic pump.
    NOTE: Control pumps are prepared in the same manner by filling the pump reservoir with sterile 0.9% NaCl solution.

2. Preparation of surgical instruments

1. Clean all surgical instruments, including fiber optic O-ring light microscope illuminator, 2 forceps, needle holder, hot bead sterilizers, glass beads, and scissors (Table of Materials).
2. Autoclave surgical instruments at 121° C for 30 min to sterilize instruments prior to surgery.

3. Isoproterenol osmotic pump surgical implantation

1. Induce anesthesia by placing the mouse in an induction chamber with 3% isoflurane in 95% O2 and 5% CO2. Maintain anesthesia with 2% isoflurane via a nosecone.
2. Administer 5 mg/kg carprofen s.c. to the scruff of the neck between the shoulder blades for analgesia.
3. Place ophthalmic ointment on the eyes to prevent corneal dehydration.
4. Check the depth of anesthesia by monitoring the respiration rate, toe pinch reflex, and color of the mucous membrane.
5. Place the mouse in a supine position on a heated pad. Remove hair from the lower abdomen and disinfect the skin with betadine or chlorhexidine.
   NOTE: To minimize post-operative infection, ensure that the surgical field is free of incident hair.
6. Use a pair of surgical scissors to cut a 1 cm-long midline skin incision. Use a pair of blunt-ended scissors to carefully dissect the skin from the underlying peritoneal walls.
   NOTE: An intraperitoneal delivery is preferred to accommodate the size of the pump.
7. Pull the peritoneal walls away from the underlying bowel with forceps and cut a 0.8 cm hole in the peritoneal walls using fine surgical scissors.
8. Insert the osmotic pump into the peritoneal cavity with the flow moderator end first.
9. Close the hold in the peritoneal walls using 5.0 absorbable sutures in an interrupted fashion. Use 6.0 non-absorbable sutures to close the skin incision in an interrupted fashion.
10. Place the mouse in a dedicated incubator to keep it warm and dry during recovery. Assess recovery from anesthesia by monitoring the mouse every 30 mins in the first two hours for return of normal breathing and movement.
11. Once the mouse has fully recovered from anesthesia, return it to routine housing. Continue to monitor the animal for complications daily up to 3 days and then every 2 to 3 days thereafter until the end of the experiment.
    NOTE: Animals should be monitored for evidence of post-operative pain or infection, signs of weight loss, lack of mobility, abnormal posture, failure to groom, and excessive licking or biting of the incision area.
12. Administer carprofen 5mg/kg s.c. every 24 h for up to 48 h and thereafter as needed.
13. Administer 0.25 mg/mL amoxicillin in drinking water for 5 days to prevent surgical site infections.
14. Remove non-absorbable sutures after 7 to 10 days.

4. Echocardiographic assessment under anesthesia

NOTE: Echocardiographic assessment can be performed repeatedly to monitor serial cardiac remodeling over several weeks. We performed echocardiographic measurements at weekly intervals over 3 weeks.

1. Induce anesthesia in an induction chamber at 1.25% to 1.5% of isoflurane. Once appropriately sedated, secure the mouse onto the echocardiography platform with tape allowing the mouse to continue receiving anesthesia through a nose cone.
2. Decrease isoflurane to a maintenance dosage of 1% to minimize negative chronotropic and inotropic effects of over-sedation. Take note of respiratory and heart rates throughout the study and adjust isoflurane dosage as needed.
3. Remove the chest hair with a depilatory lotion and wipe the chest free of hair.
4. Place the ultrasound gel on the chest and position the ultrasound probe to image the heart.
5. In B-mode, image the left ventricle (LV) in the parasternal long-axis view. Adjust the echocardiography platform to align the aortic valve and the LV apex in the plane of the ultrasound beam.
6. Tilt the echocardiography platform to place the LV long axis at 90 degrees to the ultrasound beam and the LV maximum diameter at the center of the image.
7. Image the LV short axis by turning the ultrasound probe 90 degrees.
8. In M-mode measure LV wall thickness and internal dimensions.
9. Place the mouse back into the cage. Monitor for return of normal breathing and spontaneous body movements.

Results

In our previously published study, we administered an ISO dosage of 30 mg/kg/d over 21 days via the osmotic pump across 105 Hybrid Mouse Diversity Panel (HMDP) strains^2,13. We assessed outcomes using echocardiogram performed at baseline, week 1, 2 and 3 of ISO treatment (Figure 1). Similar to a prior study where the authors studied the impact of isoproterenol among 23 mouse strains¹⁴, we observed striking inte...

Discussion

We have applied this method to over 100+ strains of inbred mice to assess cardiac outcomes due to chronic beta-adrenergic stimulation^2,13. Significant differences in susceptibility to isoproterenol are known to exist among mouse strains and may be customized to the strain of interest as needed¹⁶. This may be due to the variation in beta-adrenergic receptor function between mouse strains¹⁷, strain-dependent differenc...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Micro-Osmotic Pump System with Flow Moderator in Place	Alzet	Model 1004	Includes filling tube, flow moderator and pump body
(-)-Isoproterenol hydrochloride	Sigma-Aldrich	16504-1G	(-)-Isoproterenol hydrochloride is a powder that needs to be stored at -20°C.
1 ml sterile syringe	VWR	BD309602
30 W LED Fiber optic O-ring light microscope illuminator	AmScope	SKU: LED-30WR
5-0 COATED VICRYL (polyglactin 910) Suture	Ethicon	J303H	5-0, absorbable
Fine Scissors - Sharp	FST	14060-09
Glass beads	FST	18000-46
Hot bead sterilizers	FST	18000-50
Iris forceps	WPI	15915
Look Sharpoint 6-0, 18" Black Nylon Monofilament Suture	LOOK	AA-2176	6-0, non-absorbable
Needle holder	WPI	15926
Normal Saline, 0.9% NaCl	Fisher	89167-772