Establishment and Validation of a Rat Model of Pulmonary Arterial Hypertension Associated with Pulmonary Fibrosis

Summary

Here, the method of inducing pulmonary arterial hypertension associated with pulmonary fibrosis (PF-PH) rat model by injecting bleomycin into the airway is introduced. We also provide a step-by-step approach to validate this animal model.

Abstract

Patients with pulmonary fibrosis are at a higher risk of developing pulmonary hypertension, a complication with poor prognosis. At present, the mechanism of this link is still poorly understood. A major obstacle to progress in this area is the lack of a reliable animal model to replicate PF-PH. This study aimed to establish a stable PF-PH rat model. Rats were fasted overnight prior to intervention. Under sodium pentobarbital anesthesia (45 mg/kg), the trachea was intubated with a PE50 tube inserted to a depth of 3 cm (the distance from the glottis to the tube). Bleomycin (BLM) was administered intratracheally as a single dose (5 mg/kg, dissolved in 0.2 mL of 0.9% NaCl). Following the injection, the rats were immediately rotated to ensure even distribution of the BLM. At 35 days after the BLM injection, the rats exhibited progressive impairment of lung function and increased right ventricular systolic pressure and right ventricular hypertrophy, revealing the pathological characteristics of pulmonary hypertension. We provide a general and reliable method to establish a rat model of PF-PH.

Introduction

Pulmonary hypertension (PH) due to interstitial lung disease (ILD) is common clinically, with an estimated prevalence of 10% to 80% in patients with idiopathic pulmonary fibrosis (IPF), and it is also frequently seen in other fibrotic ILDs^1,2. Numerous studies have shown that the development of PH is linked to substantial morbidity and reduced survival^3,4,5. Compared to Group 1 pulmonary arterial hypertension (PAH), the pathogenesis of pulmonary arterial hypertension associated with pulmonary fibrosis (PF-PH) remains poorly understood⁶. The purpose of establishing an animal model of PF-PH in rats is to provide a reliable framework for scientific research on pulmonary fibrosis associated with pulmonary hypertension and to explore potential avenues for clinical therapeutic applications.

Bleomycin is a classic inducer of pulmonary fibrosis widely used in animal models⁷. Further research by Blackburn et al.⁸ and our laboratory⁹ has revealed that bleomycin can also trigger typical pathological features of pulmonary hypertension, such as increased right ventricular systolic pressure (RVSP) and right ventricular hypertrophy. Mechanistically, bleomycin induces pulmonary parenchymal fibrosis, hypoxic vasoconstriction, and a reduction in pulmonary vascular bed density, thereby leading to the development of pulmonary hypertension⁶. Additionally, we observed a significant loss of pulmonary vascular endothelial cells starting from day 7 of bleomycin treatment, with this loss progressively worsening over the course of the experiment⁹. This phenomenon suggests that bleomycin-induced pulmonary vascular endothelial dysfunction may play a potential role in the initiation and progression of pulmonary hypertension.

Due to pulmonary interstitial fibrosis, IPF patients are in a state of hypoxia for a long time, and compensatory changes occur in cardiopulmonary vessels, which leads to pulmonary hypertension⁶. The use of animal models can help us further understand the underlying mechanisms of human idiopathic pulmonary fibrosis associated with pulmonary hypertension. Although this model cannot fully simulate the pathological features of human disease, this model can still provide valuable insights. There are many experimental models simulating pulmonary fibrosis, such as single-dose airway infusion of bleomycin, viral vector delivery of transforming growth factors, and exposure to silica^8,10. At present, the BLM model is the most widely used and characterized model because it can be easily induced in a short time and has high reproducibility. In addition, temporal changes in pulmonary fibrosis have been evaluated in a bleomycin mouse model, where increased expression of fibrosis markers and genes associated with disease pathology, such as Col1A1 and Col1A2, were observed from days 15-21⁸. Cardiovascular changes, such as right ventricular hypertrophy and a significant increase in RVSP, were detected on or after day 33¹¹. At the same time, our laboratory has previously evaluated the changes in PH and PF parameters of rat models induced by bleomycin⁹. We found that in addition to pulmonary fibrosis (PF) characteristics such as progressive lung function impairment and collagen deposition in rats, typical features of pulmonary hypertension (PH) gradually emerged within 7 to 35 days after a single airway instillation of bleomycin. RVSP and Fulton index showed an increase in time dependence. Currently, various animals with pulmonary fibrosis have been reported in the literature. Some experts have suggested that rat models exhibited a more pronounced fibrotic response than the mouse models¹². Therefore, in order to better study the progression of pulmonary fibrosis combined with pulmonary hypertension, a bleomycin-induced rat model is the key.

Protocol

The animal experiments described in this study were approved by the Animal Care and Use Committee of The First Affiliated Hospital of Guangzhou Medical University (ethical approval number: 2018-456).

1. Procurement of experimental rats

1. Divide rats into two groups: the normal control group and the model group, with 7 rats in each group. Use 10-week-old male Sprague-Dawley (SD) rats weighing 200 ± 20 g for the study

2. Induction of PF-PH rat model

1. In order to prevent regurgitating aspirations during the procedure, fast the rats overnight prior to modeling.
2. Anesthetize rats by intraperitoneal injection of pentobarbital sodium (45 mg/kg) to ensure procedural accuracy and safety and minimize animal pain and stress. Confirm surgical anesthesia levels by a lack of response to toe pinching. At the same time, apply an ointment to the rats' eyes to prevent dryness.
3. Intubate the trachea of the rat with a PE50 tube inserted to a depth of 3 cm (the distance from the glottis to the tube).
4. Using a 1 mL syringe (26G), draw 0.2 mL of Bleomycin (5 mg/kg, dissolved in 0.2 mL of 0.9% NaCl). Inject the syringe containing BLM into the airway through a cannula as a single dose. For rats in the control group, perform intratracheal administration of sterile normal saline (0.2 mL). During this process, rats do not need pain relief.
5. To ensure even distribution of bleomycin, place the rat in a supine position, gently hold, and slowly rotate. The recommended rotation angle is 30°-45°, alternating between sides. Each rotation should be maintained for 10-15 s, repeated 3x-4x.
6. Place the rats on heating pads to help maintain body temperature and closely monitor their status. Observe when the rats begin to move on their own and transfer the animals from the heating pad to a separate cage for recovery.
7. After 5 weeks of BLM injection, evaluate the rats to determine whether the PF-PH model could be successfully established using methods such as echocardiographic monitoring, hemodynamic measurements, and histological analysis.

3. Echocardiographic monitoring

1. Anesthetize rats using 4% isoflurane. Remove the rat's fur with a hair removal cream and apply ultrasonic gel to its chest.
2. Evaluate the functional and structural parameters of the right heart in rats with a 250 MHz ultrasonic probe. To obtain the best long-axis view of the ventricle, place the probe on the left side of the median line of the animal's chest.
3. According to the individual anatomy, rotate the probe 15° counterclockwise relative to the left parasternal line, with the incisor pointing towards its right shoulder, and adjust the x and y axes in B-Mode so that the entire heart is in the center of the visual field.
4. Select Color to display the blood flow color to distinguish the pulmonary artery (the pulmonary artery blood flow signal in this position is blue).
5. Select PW (PW Doppler) mode, place the sampling line under the pulmonary valve, and rotate the PW angle knob to adjust the direction of the sampling line so that the sampling direction is parallel to the direction of pulmonary artery blood flow (about 25°). Press PW key again and obtain the pulmonary artery blood flow acceleration time/ejection time (PAT/PET). Measure at least five cardiac cycles and average. Use Cine to save the image.
6. Adjust the animal to a low head and a high foot, place the ultrasonic probe at the apex of the animal's heart, and drive the ultrasound along the apex of the heart to obtain the four-chamber incisal surface. Adjust the x and y axes in B mode to ensure that the four heart chambers are visible.
7. Display the measurement line 2x by holding down the M mode and place it at the junction of the tricuspid valve ring and the right ventricular free wall. Measure the tricuspid valve displacement distance (TAPSE) within at least three cardiac cycles and preserve it in Cine.
8. Place the probe at the midline of the right clavicle of the animal's chest and adjust the angle between the probe and the animal's chest notch to about 45°. Adjust the image in B-Mode so the right ventricular ventricle and interventricular septum are visible.
9. Select M-Mode to display measurement line 2x and place the measurement line in the middle of the interventricular septum. The sampling line was perpendicular to the right ventricular free wall. Save the image to obtain the thickness of the right ventricular free wall.

4. Estimation of lung function

1. Open the PFT software and check that the device is recognized. Calibrate according to equipment instructions to ensure the accuracy of flow sensors and pressure sensors. Set test parameters in the PFT software, such as respiratory rate, tidal volume, test duration, etc.
2. The animal detection mode is the mode for rat studies. Turn the switch of the main control instrument on and ensure that the switch of each signal amplifier is in the off position.
3. Set the airflow according to the animal's body weight. Turn on the suction airflow regulating nut and set the inspiration at 5. Turn on the expiratory airflow regulating nut and set the slow expiration to -4. Set the pressure value to 60 cm H₂O and then calibrate the instrument according to the order of FRC flow, flow, high flow, and lung pressure with an error of less than 0.5%.
4. Anesthetize rats by intraperitoneal injection with pentobarbital sodium (45 mg/kg) as in step 2.2. Cut the skin along the center of the neck and remove the muscle layer by layer.
5. At the exposed upper portion of the cervical trachea, make a horizontal incision between the tracheal cartilage rings. Quickly insert the metal cannula into the tracheal incision, ensuring the cannula is correctly positioned and secure. Use 4-0 silk thread sutures to fix the cannula to the trachea, preventing it from slipping or dislodging. Place the rat in the PFT animal compartment and connect the tracheal cannula to the airflow channel interface outside the instrument.
6. Click the Start button and examine the forced vital capacity (FVC) and dynamic lung compliance. To ensure data consistency, record each indicator at least 3x.
7. After the test is complete, the data is saved and exported to the analysis software. Use statistical software to analyze the data and compare the lung function parameters of different groups.

5. Hemodynamic and histological measurements

1. Detection of Right ventricular systolic pressure (RVSP)
   1. Anesthetize rats by intraperitoneal injection with pentobarbital sodium (45 mg/kg) as in step 2.2. Confirm that the rat has been properly anesthetized by pinching the toe to ensure that the rat does not respond. Fix the abdomen of the rat upward on the experimental bench and apply eye cream to the rat's eyes to prevent dryness.
   2. Make an incision (about 4 cm) on the right side of the neck through surgical scissors and separate the external jugular vein through microsurgical forceps. Separate the veins with a length of about 1 cm gently with micro-forceps and insert two surgical lines at the distal and proximal ends.
   3. Before intubation, soak the PE50 tube in normal saline containing 1% heparin sodium or EDTA for at least 30 minutes. Adjust the physiological recorder to bring the pressure back to the 0 line and adjust the pressure range to 0-150 mmHg.
   4. Ligate the distal end of the external jugular vein with 4-0 silk thread, gently lift the proximal surgical line, and place it on the distal vein wall. Use small scissors to make a small incision (about 0.3 mm). After inserting PE50 tube into the external jugular vein, use 4-0 silk thread to ligate the catheter together with the external jugular vein to prevent blood leakage.
   5. Observe the venous pressure waveform on the recorder. Push the catheter slowly into the right atrium, and the right atrium waveform is visible, with an amplitude of about 0-5 mmHg. After the catheter continues to advance from the right atrium to the right ventricle, the right ventricle pressure waveform can be seen. When the pressure is stable, record RVP for 5 min and the data is saved and analyzed with analysis software.
2. Detection of Fulton index
   1. After detection of RVSP, following isoflurane anesthesia (5%, 2 L/min O₂), euthanize the rats through exsanguination.
   2. After thoracotomy, remove the intact heart of the rat with tweezers. Cut off the auricle and the connective tissue near the heart with scissors.
   3. Cut the free wall of the right ventricle along the pulmonary artery. This tissue is the right ventricle(RV). The remaining tissues are left ventricle plus interventricular septum(LV+S). After separation, drain the surface of the right ventricle (RV) and left ventricle plus interventricular septum (LV+S) with filter paper and weigh separately using an analytical balance. After recording the weight of the right ventricle (RV) and the left ventricle plus ventricular septum (LV+S), calculate the weight ratio of the right ventricle to the left ventricle plus ventricular septum (RV/(LV+S)).
3. Histological staining
   1. After opening the thoracic cavity, use a 10 mL syringe to draw 3 mL of saline. Insert the syringe into the pulmonary artery and slowly inject the saline to flush the lungs, removing blood and other residues.
   2. Use scissors to dissect the right accessory lobe and the right anterior lobe of the lung. Place these two lung lobes into 4% formalin for fixation to preserve tissue morphology and structure. Quickly place the remaining three lobes of the lung (such as the left lung, right middle lobe, and right posterior lobe) into liquid nitrogen for frozen storage, ready for subsequent experiments.
   3. Remove excess fat and connective tissue from the surface of the lung tissue to ensure the tissue blocks are clean and neat. Trim the lung lobes into small blocks measuring 5 mm x 5 mm x 3 mm. Place the trimmed tissue blocks into the dehydrator and gradually dehydrate them using a gradient series of alcohol (60%, 70%, 80%, 90%, 100%).
   4. Immerse the lung tissue in xylene for 2 h to achieve transparency. After removal, soak it in melted paraffin at 56-58 °C for 2 h to ensure complete infiltration. Then, place the tissue into a mold, positioning it with the cutting surface facing downward for subsequent sectioning.
   5. Slice the wax block on the microtome with a thickness of 4-8 µm¹³, and store it at room temperature for pathological staining.
   6. Perform Eosin and Masson's trichrome staining¹⁴.

6. Detection of hydroxyproline (HYP)

1. Weigh 30-100 mg lung tissue in a glass tube. Add 2 mL of hydrochloric acid solution (6 mol/L) and digest at 110 °C in an oven for 2-6 h until no large clumps are visible.
2. After cooling, adjust the pH value to the range of 6-8 using 1 mL of NaOH solution (10 mol/L), then condense the distilled water to 4 mL solution. Finally, centrifuge at 28,620 x g at 25 °C for 20 min and take the supernatant to be.
3. Preheat the microplate reader for 30 min, adjust the wavelength to 560 nm, and zero the instrument using distilled water.
4. Dilute the standard solution with distilled water to prepare standard solutions with concentrations of 30, 15, 7.5, 3.75, 1.875, 0.938, 0.469, and 0.234 µg/mL.
5. Take 60 µL of the sample supernatant and mix it with 60 µL of Reagent A, then let it stand at room temperature for 20 min.
6. Add 60 µL of Reagent B and 120 µL of distilled water. Place the mixed solution in 60 °C water bath for 20 min. Follow the same steps for each concentration of the standard solutions (e.g., 30, 15, 7.5, 3.75, 1.875, 0.938, 0.469, 0.234 µg/mL) and perform the operations accordingly.
7. After standing at room temperature for 15 min, take 200 µL of the solution in the 96-well plate to detect the light absorption value at 560 nm. Plot the standard curve with the concentration of the standard solutions as the x-axis and the measured values as the y-axis, obtaining the equation y=kx+b. Substitute the measured value of the sample into the equation to determine the concentration of the sample.

Results

Bleomycin-induced pulmonary fibrosis in rats
Bleomycin has been reported as a classic inducer of pulmonary fibrosis in animal models⁷. Here, indexes of pulmonary fibrosis were assessed following BLM stimulation. First, after 35 days of BLM treatment, we conducted lung function tests and found that both FVC (Figure 1E) and dynamic lung compliance (Figure 1F) in the model group were significantly reduced. These result...

Discussion

Idiopathic pulmonary fibrosis is a progressive, fatal disease with a median survival of 2-3 years from diagnosis, suggesting a bleak prognosis⁹. Pulmonary hypertension is a common comorbidity of IPF, which rapidly deteriorates IPF with a worsened prognosis¹⁵. What's more, there were limited therapeutic options for IPF-PH⁷. Thus, it is essential to gain a deeper understanding of the underlying molecular mechanisms of PF-PH, which may provide a potenti...

Materials

Name	Company	Catalog Number	Comments
Bleomycin	MedChemExpress	HY-17565A
Coupling agent	HYNAUT	BX-CSRH
Formalin fixative	Biosharp)	BL401B
Hair removal cream	LUSEN	LS-B-TMG-50
Hematoxylin eosin (HE) staining kit	Beyotime	C0189S
Isoflurane	RWD Life Science(China)	R510-22-10
Masson Tri-color dyeing kit	Beyotime	C0189S
Normal saline	KERONG	SLYS-001
syringe	Beyotime	FS701-50pcs