Intracranial Pressure Monitoring In Nontraumatic Intraventricular Hemorrhage Rodent Model

Summary

Monitoring intracranial pressure in rodent models of nontraumatic intraventricular hemorrhage is not common in the current literature. Herein, we demonstrate a technique for measuring intracranial pressure, mean arterial pressure, and cerebral perfusion pressure during intraventricular hemorrhage in a rat animal model.

Abstract

Survivors of intraventricular hemorrhage are often left with significant long-term memory impairment; thus, research utilizing intraventricular hemorrhage animal models is essential. In this study, we sought out ways to measure intracranial pressure, mean arterial pressure, and cerebral perfusion pressure during nontraumatic intraventricular hemorrhage in rats. The experimental design included three Sprague Dawley groups: sham, standard 200 µl intraventricular hemorrhage, and vehicle control groups. By introducing an intraparenchymal fiberoptic pressure sensor, precise intracranial pressure measurements were obtained in all groups. Cerebral perfusion pressures were calculated with the knowledge of intracranial pressure and mean arterial pressure values. As expected, the intraventricular hemorrhage and vehicle control groups both experienced a rise in the intracranial pressure and subsequent decline in cerebral perfusion pressure during intraventricular injection of autologous blood and artificial cerebrospinal fluid, respectively. The addition of an intraparenchymal fiberoptic pressure sensor is beneficial in monitoring precise intracranial pressure changes.

Introduction

Intraventricular hemorrhage (IVH), a type of intracranial hemorrhage (ICH), is a devastating disease that carries significant mortality and morbidity. IVH is characterized as the accumulation of blood products inside the intracranial ventricles. Isolated IVH in uncommon and typically occurs in adults¹. It may be associated with hypertensive hemorrhage, ruptured intracranial aneurysm or another vascular malformation, tumors, or trauma¹. IVH leads to secondary brain injury as well as the development of hydrocephalus². Survivors of IVH are often left with significant functional, memory, and cognitive impairments following their injury. These long-term cognitive and memory deficits are reported in as high as 44% of survivors of ICH³. In subarachnoid hemorrhage (SAH), another type of ICH, it is well known that approximately half of the survivors will have memory deficits, and for those who have IVH in addition to SAH, outcomes tend to be significantly worse^4,5,6.

Underlying mechanisms of memory dysfunction following IVH remain to be elucidated. In vivo research utilizing nontraumatic IVH animal models with functional and memory dysfunction is essential in order to discover potential therapeutic targets for such patients. Animal models with more severe memory and functional dysfunction following IVH would be the best to study these changes. The senior author's lab has also been investigating specifically the role of high intracranial pressure (ICP) in the development of memory deficits in IVH rat models. Hence, methods to precisely measure ICPs during IVH were important to investigate. Herein, we report on methods of precisely measuring ICPs in an IVH rat model. Although ICP monitoring has previously been used in traumatic ICH as well as subarachnoid hemorrhage animal models, ICP monitoring in spontaneous IVH rodent models is not as commonly reported in the literature^7,8. Hence, the experimental design presented herein included three groups of Sprague Dawley rats: sham, standard 200 µl intraventricular hemorrhage, and vehicle control. For IVH group, an autologous intraventricular blood injection model was used. For vehicle control animals, intraventricular injection of sterile Lactated Ringer's solution was used. ICPs, mean arterial pressures (MAPs), and cerebral perfusion pressures (CPPs) were recorded intraoperatively, and results are reported herein.

Protocol

All research methods and animal care/maintenance were performed in compliance with the institutional guidelines at the University of California, Davis. The Institutional Animal Care and Use Committee (IACUC) of the University of California, Davis, approved all animal use protocols and experimental procedures (IACUC protocol #21874).

1. Animal housing

1. Obtain Sprague-Dawley rats of age 8-10 months old. Prior to any experimental procedure, house the rats in a vivarium and allow at least 1 week for general adaptation in their cages following a 12-h light/dark cycle with food and water ad libitum.

2. Anesthesia and pre-operative procedures

1. Anesthetize the rat with 4% isoflurane for 4 min. Hang the rat by its teeth in a supine position on an intubation platform, and intubate endotracheally using an endotracheal cannula and laryngoscope.
2. Place the anesthetized and intubated rat on a ventilator (2% isoflurane and O2/N2 carrier gas). The rat is adequately anesthetized if no response to a painful stimulus such as a hindleg pinch is observed.
3. Insert a rectal thermometer to continuously monitor the temperature.
4. Perform all operative procedures using sterile technique. Clip the hair on the head and the femoral region and prep the skin with three alternating scrubs of Betadine and 70% alcohol prior to surgery.
5. Aspirate any accumulated respiratory secretions by temporarily removing the rat from the ventilator and aspirating the secretions with PE-50 tubing connected to a 10 mL syringe.
6. Protect the rat's eyes with sterile artificial tears eye ointment.
7. Inject local bupivacaine (~0.1 mL of 0.25% solution) into the skin and subcutaneous tissues prior to the scalp incision.

3. Surgery protocol

1. Placement of intraventricular needle and intracranial pressure (ICP) monitor
   1. Place the rat in a prone position in a stereotactic frame and ear bar the rat.
   2. Make a 1.5-cm scalp incision along the midline with a 15-blade scalpel.
   3. Apply mild pressure with gauze for hemostasis.
   4. Using a sterile cotton tip applicator, separate the periosteum from the skull until the bregma landmark is visible.
   5. Locate and mark out bregma using stereotaxis and mark out the location of two bilateral burr holes, 1.4 mm lateral and 0.9 mm posterior to the bregma.
   6. Using a hand-held drill, create these two small (up to 2 mm) cranial burr holes in the right and left hemispheres. Irrigate out any excess bone chips with sterile Lactated Ringer's solution.
   7. In the right hemisphere, position a 22-G guide cannula at the level of the burr hole to insert the 28-G needle through the cannula to the depth of the right lateral ventricle (4.6 mm in relation to the bregma) in order to create IVH.
   8. Connect the fiberoptic pressure sensor to the read-out unit. Turn on the read-out unit and ensure the units selected are in mmHg. Then prime the sensor by submerging its tip into a small beaker with Lactated Ringer's solution until the read-out unit reads out zero. Once it is zeroed in the Lactated Ringers solution, it is all set to be inserted.
   9. In the left hemisphere, gently insert the pressure sensor to 2-3 mm depth into the cortex for real-time ICP monitoring.
2. Femoral artery cannulation and insertion of mean arterial pressure (MAP) monitor
   1. After insertion of the ICP monitor, turn the lower trunk of the rat for easy access to the left thigh and groin area.
   2. After sterile preparation and local bupivacaine administration, make a 1.5 cm skin incision over the hindlimb with a 15-blade scalpel.
   3. Dissect out the left femoral artery first superficially with a hemostat and then deeper layers using forceps with fine tips under a microscope. Identify the deep blue femoral vein to help locate the adjacent artery.
   4. Tie off the distal femoral artery using 3-0 silk suture and place a temporary metal clip on the proximal portion of the femoral artery.
   5. Have a second fiberoptic pressure sensor connected to the read-out unit already primed. Insert the pressure sensor into the polyethylene (PE-50) tubing, which is inserted into a Tuohy Borst that is then closed. Connect the Tuohy Borst to a 3-way-stopcock connected to a 1 mL syringe at one end and a 22-G needle with PE-50 tubing at the other end.
   6. Under the microscope, make a 2 mm femoral arteriotomy with micro scissors and cannulate it with PE-50 tubing connected to the rest of the setup.
3. Intraventricular injection
   1. Aspirate 500 µL of blood using a 1 mL syringe and turn the 3-way-stopcock to have the pressure sensor read MAP.
   2. Prime the 28-G intraventricular needle connected to PE-50 tubing with the aspirated blood for IVH animals and Lactated Ringer's for the vehicle control animals. Then insert this needle into the guide cannula to the depth of the right lateral ventricle.
   3. Using 100 µL/min rate, inject the blood or sterile Lactated Ringer's solution (200 µL) into the right lateral ventricle by pumping the 1 mL syringe with the thumb. Prior to this and during intraventricular injection, monitor and record ICP, arterial blood pressure, and rectal temperature.
   4. Monitor and record the post-injection ICP and MAP values.
4. Closure
   1. Following completion of the intraventricular injection, withdraw the PE-50 tubing containing the pressure sensor that was inserted into the femoral artery and apply the temporary clip to the femoral artery to prevent bleeding.
   2. Tie off the proximal portion of the femoral artery using the 3-0 silk suture.
   3. Close the femoral incision in an interrupted fashion using 3-0 silk.
   4. Remove the guide cannula with the intraventricular needle and the ICP monitor.
   5. Seal the burr holes with bone wax.
   6. Close the cranial incision with 3-0 silk suture in an interrupted fashion.
   7. Apply topical bupivacaine to the incision and inject 0.35 mL of carprofen (5 mg/kg) postoperatively. Do not leave animals unattended until they have regained sufficient consciousness to maintain sternal recumbency.
   8. Allow rats to fully recover after surgery under supervision and return them to their home cages with free access to food and water after recovery.

4. Postoperative management

1. Check all postoperative animals daily for seven postoperative days to monitor their recovery, neurological status, behavior, weight, and incisions.
2. Administer 0.35 mL of carprofen (5 mg/kg) by subcutaneous injection at the time of surgery and on the 1^st and 2^nd postoperative days.
3. Remove the sutures on the 7^th postoperative day in a sterile fashion.

Results

Intracranial, mean arterial, and cerebral perfusion pressures
Both ICPs and MAPs were monitored intraoperatively in all animals (Figure 1). Rats were of 8-10 months old with a mean weight of 495 ± 17 g. Real-time ICP graphs were also collected (Figure 2). Excluding the sham group, ICPs increased significantly during intraventricular injection in IVH as well as vehicle control groups (Figure 3). ICPs pea...

Discussion

This study investigated mechanisms to measure ICPs, MAPs, and CPPs in a nontraumatic IVH rat animal model. The results were recorded from the following groups: sham, VH 200 µL, and vehicle control (artificial cerebrospinal fluid intraventricular injection) animals. This experimental design was chosen to investigate how ICPs can be monitored during IVH injection as we hypothesized that the spike in ICPs may contribute to the more significant secondary brain injury and thus memory deficit in IVH animal models. Therefo...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
0.25% bupivacaine	Hospira, Inc.	409115901
1 mL syringe	Covetrus	60734
10% providine iodine solution	Aplicare	MSD093947
20 mL syringe	Covidien	8881520657
22 G needles	Becton Dickinson	305155
28 G intraventricular needles	P technologies	8IC313ISPCXC	C313I/SPC 28-Gneedles to fit 22-G guide cannula with 6 mm projection
3-0 silk suture	Henry Schein, Inc.	SP116
3-way-stopcock	Merti Medical Systems	M3SNC
4% paraformaldehyde	Fisher Chemical	30525-89-4
AnyMaze software	Any-Maze behavioral tracking software		Stoelting CO, USA
Artificial ointment	Covetrus	48272
Blood collection vials with EDTA	Becton Dickinson	367856
Bone wax	CP Medical, Inc.	CPB31A
Carprofen	Zoetis, Inc.	54771-8507-1
Centrifuge	Beckman	BE-GS6R	Model GS-6R
Cotton tip applicators	Covetrus	71214
Drill	Dremel	1600A011JA
Fiberoptic pressure sensors with readout units	Opsens Medical	OPP-M200-X-80SC- 2.0PTFE-XN-100PIT-P1 and LIS-P1-N-62SC	Opp-M200 packaged pressure sensors with LifeSens system
Forceps		11923-13, 11064-07
Gauze	Covetrus	71043
Guillotine	World Precision Instruments	51330
Heating pad with rectal thermometer	CWE, Inc.	08-13000 ,08-13014	TC1000 Temperature controller
Hemostats		13013-14,  13008-12
Isoflurane	Covetrus	29405
Lactated ringers	Baxter Healthcare Corp.	Y345583
Laryngoscope	American Diagnostic Corporation	4080
Metal clip	Fine Scientic Tools	18056-14
Micro scissors	Fine Scientic Tools	15007-08
Microscope	Leica	model L2
Needle driver		12003-15
Polyethylene tubing	Thermo Fisher Scientific	14-170-12B	PE-50 tubing
Rats	Envigo		Sprague Dawley rats 8–10 months old
Scalpel		10010-00
Scissors		14090-11
Stereotaxic instrument	Kopf instruments		Model 940 with ear bars
Syringe pump	KD Scientific	780100	Model 100 series
Tuohy Borst	Abbott	23242
Ventilator	Harvard rodent ventilator	55-0000	Model 683