Abstract
Duration and extent of penumbra determine the window and brain volume in which interventions may save injured tissue after stroke. Understanding the penumbra in animals is necessary in order to design models that translate to effective clinical therapies. New Zealand white rabbits were embolized with aged autologous clot () or insoluble microspheres (). To examine effects of treatment on penumbra, sphere-stroked animals were treated with 3 μm microbubbles plus ultrasound (). Rabbits were euthanized at 4 or 24 hr. Infarct volume was measured following triphenyltetrazolium chloride (TTC) staining of brain sections. Penumbra was visualized using immunostaining of pimonidazole injected fifteen minutes prior to euthanasia. Potentially reversible penumbra was present in 14.3% stroked rabbits at 4 hours and 15.7% at 24 hours after embolic stroke and represented up to 35% of total lost tissue. Intervention at up to 24 hours may benefit a significant patient population.
1. Introduction
The degree of neurologic impairment following a stroke depends to a large extent on the volume of brain tissue lost and the specific anatomic structures involved. Following local ischemia, a core population of neurons in a region with extremely low cerebral blood flow is terminally injured within a relatively short period of time. Because average time to hospitalization for stroke is greater than 90 minutes [1], this central ischemic core cannot, in general, be saved. The region around the ischemic core with blood flow that is significantly reduced, but not below levels compatible with cell life, is extremely vulnerable to further insult from oxidative damage, hemorrhage, and inflammation during reperfusion. This sublethally injured penumbra, or area at risk, is eventually subsumed into the ischemic core, unless perfusion improves, and may comprise up to 70% of the total infarct volume. Stroke therapies that encourage survival of cells in this region result in better functional outcomes for patients.
Hypoxia within the penumbra may persist for 48 hours after stroke [2–5]. Whether or not injured cells in the penumbra progress to irreparable damage and cell death is dependent on small perfusion pressure change [6], and stroke therapy interventions to increase cerebral microvascular perfusion may have marked clinical impact through reduction of the amount of hypoxic penumbral tissue that progresses to cell death. Following reduced blood flow in stroke, cerebral microvessels undergo adaptations to increase perfusion, including active dilation to increase blood flow [7]. Other responses may be maladaptive for the penumbra, including the release of adhesion molecules and focal loss of blood-brain barrier to permit influx of inflammatory cells and fibrin [8, 9]. Exposure to tissue factor with resultant thrombosis can occur where vascular flow is decreased, as in small vessels in the distribution bed of a large artery [9]. Ultrasound- (US-) facilitated thrombolysis with microbubbles (MBs) has been demonstrated to lyse clots in animal models with and without exogenous thrombolytics such as tissue plasminogen activator (tPA) [10–13]. Thrombolytic therapies may improve perfusion in small vessels, restoring cerebral blood flow to the penumbra even when recanalization of the blocked artery does not occur.
In acute human stroke, clinical imaging with CT perfusion studies or MRI diffusion studies provide some measures of penumbra which are of use in patient selection for therapy. Patients with visible penumbra may respond well to therapy hours beyond the standard temporal guidelines for thrombolytic treatment [14].
It is therefore of the utmost importance to determine the duration of the penumbra in preclinical models of stroke therapy, as this time represents the window of opportunity for intervention. Understanding possible differences in the development and duration of the penumbra in animal models is necessary in order to design meaningful animal models that translate to effective clinical therapies. Pimonidazole (Hypoxyprobe) has been demonstrated to accurately label hypoxic regions in the brain [15]. The objectives of this study were to examine the incidence and histologic features of penumbra in rabbits at 24 hours after infarction using Hypoxyprobe staining in two models of thromboembolic stroke and to determine effects of treatment with microbubbles and ultrasound on penumbra.
2. Materials and Methods
2.1. Preparation of Embolus
Emboli were prepared by obtaining an arterial blood sample (2 mL) from a donor rabbit. The blood was immediately transferred directly into a 30.5 cm length of Butterfly pediatric infusion set (no. 4506; Abbot Hospitals, Inc.; North Chicago, Ill, USA) tubing and allowed to clot at 37°C for 3 hours. Following incubation, but prior to embolization, the clot was expelled from the tubing into a dish containing physiological saline and subsequently cut into several pieces of 1.0 mm in length with an approximate diameter of 0.6 mm. A single clot piece was drawn into a 3.0 mL syringe containing physiological saline for injection into the ICA with 0.7 to 2.0 mL of saline flush. Care was taken during each flush to ensure that no air bubbles were present in the syringe.
2.2. Animal Procedure
All animal procedures were approved by the Institutional Animal Care and Use Committee. The surgical and angiographic procedures were previously described by Brown et al. [16]. Briefly, male and female New Zealand white rabbits (; mean body weight kg) were randomly assigned to stroke model groups and anesthetized. The right side of each rabbit’s head was clipped, and depilatory cream was applied. A single plane C-arm digital subtraction angiography machine (OEC 9800; GE Healthcare; Salt Lake City, Utah, USA) was utilized for all angiographic procedures. Baseline subselective internal carotid artery (ICA) magnification angiography was performed via the right femoral artery in lateral and frontal projections to assess the cerebral vasculature of each rabbit. Rabbits were embolized by injection of 1.0 mm blood clot aged for 3 to 5 hours or 700–900 μm microspheres (Embosphere; BioSphere Medical Inc.; Rockland, Mass, USA) in 0.7 to 2.0 mL of physiologic saline into the ICA, occluding branches. One minute following embolization, repeat angiography was performed, and the degree and location of the arterial occlusion were documented.
For animals in the treatment group, an intravenous catheter (Instyle-W; Becton Dickinson; Sandy, Utah, USA) placed into the left ear vein was used for administration of 3 μm MB, and transcutaneous pulsed wave (20% duty cycle) US at 1 MHz and 0.8 W/cm2 (Sonicator 716; Mettler Electronics; Anaheim, Calif, USA) was applied for one hour. Following embolization a hand-held 10 cm2 therapeutic transducer was placed in front of the ear and behind the eye and was coupled to the skin with standard US gel. Positioning of the US probe was confirmed fluoroscopically.
Rabbits exhibiting a complex origin of the internal carotid artery preventing subselection and subsequent embolization on initial angiography () and rabbits that did not undergo angiography () were used as unstroked controls for pimonidazole staining. Animals were euthanized via IV pentobarbital overdose at 4 or 24 hours after embolization.
2.3. Measurement of Infarct Volume
Brain was harvested immediately after euthanasia, chilled in physiologic saline on melting ice for 60 minutes, and sliced coronally at 0.4 cm intervals using a mold and slicing guide (Harvard Apparatus) to assure consistent sectioning. All coronal brain sections were placed in 1% 2,3,5-triphenyltetrazolium chloride (Sigma-Aldrich; St. Louis, Mo, USA) for 45 minutes at 37°C, fixed in 10% formalin, and photographed with a digital camera. Section area and area of infarction were measured using NIH ImageJ. Infarct and section volumes for each slice were calculated by multiplying each value by the slice thickness of 4 mm. Total brain percent infarct volume was calculated by dividing the sum of the infarct volumes into the sum of the section volumes and multiplying by 100%.
2.4. Histopathology
To verify infarct locations each brain section was fixed in 10% formalin, processed and embedded into paraffin, sectioned at 4 μm, and stained with hematoxylin and eosin. Each brain coronal section was evaluated by a veterinary pathologist without knowledge of treatment group.
Hypoxia in the penumbra may be evaluated using nitroimidazole compounds that are reduced in living cells to a radical anion. In hypoxic cells, this compound irreversibly binds cellular components and accumulates [16]. The compound does not bind in cells that are not hypoxic, and it is not metabolized by dead cells in infarcted areas. All rabbits received 100 mg of pimonidazole (Chemicon) IV 15 minutes prior to euthanasia. Following TTC staining, formalin fixation, and processing as described above, all sections from each brain were immunolabeled using an antibody specific for pimonidazole (Hypoxyprobe, Chemicon). Briefly, sections were deparaffinized and antigen retrieval was performed via decloaking in tris-buffered saline tween-20 (TBST) for 20 minutes. Dako peroxidase block was applied for 10 minutes, and sections were rinsed three times in TBST. 10% normal goat serum was applied for 30 minutes, and sections were blotted. Primary monoclonal antibody to bound pimonidazole (Chemicon) was applied at a 1 : 50 dilution in Dako diluent with background blocking agents for 40 minutes. Sections were rinsed three times in TBST, and secondary Vector antigoat IgG antibody (Vector) diluted at 1 : 400 in Dako diluent with background blocking agents was applied for 30 minutes. Sections were rinsed three times in TBST. Dako DAB+ was applied for 3 minutes. Sections were rinsed in TBST and lightly counterstained with hematoxylin. Brain sections from animals that did not receive pimonidazole as well as sections stained without primary antibody are used as negative controls.
Hypoxyprobe- stained slides were digitally scanned using the Aperio ScanScope T2 (Aperio, Vista, Calif, USA). The Scanscope produces high resolution slides which may be viewed and analyzed at magnifications up to 200x. Scanned slides were examined to detect penumbral staining. Penumbra was defined as strong staining (within the upper 90% of staining intensity) immediately adjacent to and contiguous with regions of necrosis. Sections were analyzed using morphometrics (ImageScope, Aperio) for area of penumbra, area of infarct, and area of penumbra plus infarct. Lesion size was measured as the area of the penumbra and the associated infarct. Penumbral area was measured, and relative size was given as the percent of total lesion. When multiple infarcted regions were present within a section, areas for penumbra and infarcts were summed to give a total area.
2.5. Statistical Analysis
Incidence of penumbra among groups was compared using Fisher’s exact test as implemented in the statistical software package StatXact. The relationship between penumbra size and percent infarct volume was assessed using both Pearson and Spearman correlation coefficients, because of the potential for a nonlinear association. A t-test was used to compare the mean percent stroke volumes between those rabbits with and without penumbra. Stroke volumes are presented as mean ± standard deviation.
3. Results
Repeat angiography (Figures 1(a) and 1(b)) demonstrated occlusion in 56 animals. Location of occlusion and numbers of animals affected are given in the table of Figure 1. The most common type of occlusion on repeat angiography was single occlusion in the middle cerebral artery (MCA, 26/63). Additional 18 animals had occlusion of both the ACA and the middle cerebral artery (MCA). Triple occlusions involving the cerebral arteries occurred in 3 animals, and the occipital artery (OA) was occluded in one animal. No visible occlusion was noted in 7/63 animals, all from the clot control group, although measurable stroke volume was noted with TTC stain for these animals, and all had histologic infarction. Clot model was also associated with fewer MCA and ACA occlusions (, , resp.). No other significant differences were noted for occlusion location and model or treatment group.
Infarct volume in stroked animals ranged from 0.1% to 18.4%. Unstroked staining control rabbits had stroke volume of 0, as expected. Penumbra was evident in Hypoxyprobe-stained sections as intense staining adjacent to and contiguous with infarct (Figure 2). Brain sections from all animals exhibited diffuse mild hypoxia as demonstrated by weak to moderate cellular pimonidazole staining, and necrotic tissue (infarct) was not labeled by pimonidazole (Figure 2(c)). No labeling was observed in control sections from rabbits which were not given pimonidazole (Figure 2(d)) and sections stained without primary antibody (data not shown). Penumbra was observed in 1/7 rabbits (14.3%) at 4 hours and in 8/51 (15.7%) rabbits at 24 h (Table 1).
(a)
(b)
(c)
(d)
Incidence of penumbra did not differ with stroke model (; clot control versus sphere control) or with treatment at 24 hours (; treated versus sphere control, Table 1). Penumbral staining occurred around both large and small infarcts, and penumbra size was not significantly correlated with percent infarct volume () at 24 hours. Mean stroke volume percent did not differ between rabbits with or without penumbra at 24 hours (4.43 ± 4.97 versus 3.60 ± 4.56, resp.; ). The average size of penumbra as a percentage of total lesion (infarct plus penumbra) at 24 hours was 14% ± 4%. Penumbra ranged from 0.96% to 35% of the total lesion. Rarely, hypoxic tissue encircled the ischemic core, but penumbra was more often eccentric, encompassing only a portion of the circumference of the ischemic core.
4. Discussion
Preclinical animal models are an important tool in evaluation of potential stroke therapies. It is of vital importance to understand the pathogenesis of brain loss in these models and to determine what the optimal window of treatment therapy is for each model as well as the optimal time for evaluation of cerebral damage. As stroke develops, hypoxic tissue peripheral to the ischemic core (penumbra) undergoes progressive damage culminating in cell death if perfusion does not improve. This tissue represents the area of the brain most amenable to stroke therapies and most vulnerable to reperfusion injury. The volume of the penumbra may be equal to or greater than the volume of the ischemic core on CT perfusions or MRI diffusion imaging [17]; therefore, treatments that protect this vulnerable region from further injury may result in significantly reduced final stroke volume and improved clinical outcome.
In contrast to studies to determine the optimal window of therapy, studies designed to examine cerebral injury and effects of treatment on total stroke volume should be evaluated at a time point when hypoxic penumbra is no longer evident and stroke is maximally developed. For these reasons, it is vitally important to determine the duration of penumbra in preclinical animal models. Although penumbra has been documented in humans at 48 hours after infarction [2, 3], no penumbra was evident in a rat model at 48 hours [18, 19]. Using in vivo PET imaging of F-fluoromisonidazole in a rat carotid artery occlusion model, Takasawa et al. [18] demonstrated that significant penumbra is not present at 48 hours after occlusion. However, this study did not examine time points between 180 minutes and 48 hours. Saita et al. [4] found negligible uptake of F-fluoromisonidazole in 4 rats at 22 hours after infarction. Noto et al. [21] used a similar compound, pimonidazole (Hypoxyprobe, Chemicon), to evaluate the penumbra in a rat model of focal cerebral ischemia and found increased Hypoxyprobe labeling in 5/5 animals at 24 hours after infarction [20, 21]. The objective of this study was to determine the incidence of hypoxic penumbra in two rabbit thromboembolic stroke models and to examine the effects of thrombolytic therapy on penumbra at 24 hours after infarction.
Penumbra was easily distinguished as clearly defined regions of very intense staining adjacent to and contiguous with infarcts. This staining pattern was observed in 15.7% of animals at 24 hours. There is convincing evidence that the penumbra is likely to succumb to cell death over time and therefore contribute up to 50% of the total brain loss in stroke [6, 19]. In the rabbits of this study, the penumbra represented on average approximately 14% of the total lesion. This result is consistent with previously published findings in humans and rats [19, 22]. Penumbra was occasionally circumferential but more often did not completely encircle infarct. This pattern is consistent with reperfusion gradients that depend on available collateral blood supply. The penumbra was very similar in size and shape to penumbra imaged using 18F fluoromisonidazole PET [18], a compound that accumulates in hypoxic tissue using the same mechanism as pimonidazole, and 2-deoxyglucose PET [19] in rats. Despite some differences in location of occlusion between groups on postembolization angiography, no significant differences were found in incidence of penumbra. This suggests that persistence of penumbra is independent of type of occlusion.
The observed differences in location of occlusion between clot and sphere models may be explained by functional differences in type of embolus It is of particular interest that all animals without visible occlusion in major arteries but histologic evidence of stroke were embolized with aged clot. This suggests that clot may be partially lysed by endogenous processes during and immediately following embolization, at least in some animals, resulting in fragmentation and blockage of smaller vessels downstream.
Although penumbra persisted for 24 hours in some animals, no effect of treatment with 3 μm microbubbles and ultrasound on the incidence of penumbra was noted. This indicates that this treatment exerts protective effects, if any, on penumbra at early time points. However, other treatments may have more significant effect on penumbra, and further study is warranted. Currently in the United States, approximately 3% of strokes are treated using IV thrombolytic therapy applying a 4.5-hour window or using intra- arterial clot removal applying a 6-hour window [23]. With accurate penumbra imaging, much later interventions may be successfully applied [14]. In this rabbit model 15.7% had significant penumbra, potentially curable areas of brain damage even at 24 hours. This suggests that clinical tests for penumbra, CT perfusion, or MRI diffusion studies should be performed regardless of stroke duration to select these patients who can still profit from intervention at much later times than currently is the standard of care [24–26]. Our results suggest that therapy could potentially benefit a much greater patient population.
Diffuse mild cerebral hypoxia, characterized by weak to moderate, diffuse staining with pimonidazole, was evident in all animals. This staining was not present in control sections from animals not given pimonidazole or controls stained without the primary antibody, and it most likely represents binding of pimonidazole in hypoxic brain induced by the euthanasia process, which involves sedation followed by intravenous injection of pentobarbital. To avoid mischaracterization of this background hypoxia as penumbra, threshold for penumbra was set at the upper 90% of staining intensity and included only staining contiguous with infarcts. Certainly brain swelling can compromise blood flow in areas away from the primary infarct. This may have excluded some areas of actual penumbra by generally underestimating its volume or presence.
Hypoxic penumbra remained in 15.7% of rabbits at 24 hours. This suggests that a significant number of patients may benefit from additional imaging at 24 hours, with continued intervention if residual penumbra is present.
Acknowledgments
This work was supported by NIH Grant 1R01HL082481-01 for W. C. Culp (PI). The authors wish to thank Jennifer James and Shirley Mullins of the Experimental Pathology Core Laboratory, UAMS, for histology services.