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a new large animal model of focal cerebral a new large animal model of focal cerebral ischemia ischemia Results Results Material and Methods Material and Methods Fig. 3 Behavioral data of neurological examinations, presented as means ± SD (A). Absent medial hopping reaction of right forelimb after MCAO (B). also poster: Correlation between Behavioural Improvement, Reactive Gliosis and Lesioned Area in a Stem Cell Therapy of Stroke). However, transplantation to clinical application requires close-to-practice models, i.e. large animal models of focal cerebral ischemia. Existing primate models are cost intensive, restricted to highly specialized breeding facilities and limited by ethical considerations. Therefore, we developed a new, cost effective stroke model in sheep including reproducible neurological dysfunctions and reproducible lesion size, variable by proximal or distal occlusion of the middle cerebral artery (MCAO) according to its origin. ecause of the rete mirabile (rm, Fig. 1), a network of small arteries supplied by afferent rete branches (rb) of the maxillary artery (ma), intraluminal occlusion of the MCAO via catheter blockage or artificial thrombus is not possible. Hence, we performed a transcranial exposure of middle cerebral artery (MCA). 17 Merino sheep weighting 35 to 48 kg were randomly assigned to one of four groups: proximal (n=5) and distal (n=2) MCAO, sham operation (n=5) and control (n=5). Animals undergoing the surgical procedure were deeply anaesthetised. Following exposure of the MCA, the vessel was occluded or touched (sham) by high frequency bipolar forceps. After suture, animals underwent an analgetic and antibiotic treatment. Control animals did not underwent a surgical procedure. Neurological investigation was performed before surgery and at days 1, 4, 7, 10, 16, 25, and 32 following MCAO (Fig. 3) according to a score point system (table). Further, effects of MCAO were evaluated by magnetic resonance imaging (MRI) including T1-, T2-, T2*- sequences, diffusion weighted (DW) imaging (Fig. 2A-G) and magnetic resonance angiography (MRA, Fig. 1B/C) using a Philips 1,5T clinical scanner. Animals were killed at day 35 post op. and brains were removed for neuropathological investigation (Fig. 2H). roximal MCAO results in a large cortical lesion and neurological dysfunctions including absent/delayed startle reflexes, atactic movement, circling and torticollis. Distal MCAO causes a smaller cortical lesion and reduced functional Uwe Gille 1 , Johannes Boltze 2 , Daniela Waldmin 1 , Annette Förschler 3 , Jean-Claude Ionita 4 , Kerstin Gerlach 4 , Dietmar Schneider 5 , Dietmar Egger 6 , James Ferguson 4 , Frank Emmrich 2 and Claus Zimmer 3 1 Institute of Veterinary Anatomy, An den Tierkliniken 43, 04103 Leipzig , Germany; telephone: +49 341 / 97-38057; eMail: [email protected] leipzig.de 2 Institute of Clinical Immunology and Transfusion Medicine, Johannisallee 30, 04103 Leipzig , Germany; telephone: +49 341 / 97-25820; eMail: [email protected] 3 Department of Neuroradiology, Clinic of Diagnostic Radiology, Liebigstrasse 20, 04103 Leipzig , Germany; telephone: +49 341 / 97-17410; eMail: [email protected] 4 Clinic of Large Animal Surgery, An den Tierkliniken 21, 04103 Leipzig , Germany; telephone: +49 341 / 97-38250; eMail: [email protected] leipzig.de 5 Clinic of Neurology, Liebigstrasse 22a, 04103 Leipzig , Germany; telephone: +49 341 / 97-24221; eMail: [email protected] leipzig.de 6 VITA34 AG, BBZ, Deutscher Platz 5a, 04103 Leipzig , Germany; telephone: +49 341 / 48792-0; eMail: [email protected] B PERMANENT MCAO IN SHEEP PERMANENT MCAO IN SHEEP EXPERIMENTAL CELL THERAPY OF STROKE EXPERIMENTAL CELL THERAPY OF STROKE P T Introduction Introduction he efficiency of experimental umbilical cord blood (UCB) and bone marrow (BM) cell therapies has been shown in stroke models by using rodents (see Table neurological examination score point Table neurological examination score point system system Item Item score points score points (max. (max. 14) 14) 1. food debris remaining in mouth corner no 0 yes 1 2. torticollis no 0 yes 1 3. paretic right limbs / atactic movement no 0 yes 1 4. circlic movement no 0 occasionally 1 permanently 2 5. disturbed right hemistanding reaction no disturbance 0 immediate adjustment using left limbs 1 delayed adjustment using left limbs 2 delayed adjustment using right limbs 3 delayed using right hindlimb / no using right forelimb 4 no adjustment Summary Summary • MCAO in sheep results in reproducible behavioral reproducible behavioral consequences consequences and reproducible size of ischemic lesion • to our knowledge, this is the the first first described model of model of focal focal cerebral ischemia in cerebral ischemia in sheep sheep • the model will allow to study efficiency of study efficiency of autologous cell and autologous cell and pharmaceutical therapies pharmaceutical therapies upon stroke deficits (data not shown). The MCA was clearly occluded as to be seen in MRA (Fig. 1 B). Further, sheep with occluded left MCA showed neurofunctional disabilities (Fig. 3A/B), as well as clear signs of ischemic brain tissue in MRI (Fig. 2E/F) and after brain removal (Fig. 2H). Sham operated animals showed very mild, transient dysfunctions (Fig. 3A) while controls did not show sensomotoric disabilities. Indications of ischemia in sham operated animals was not observed using MRI (Fig. 2B/C). Although a small contusion damage could be observed in some cases (Fig. 2B/C, red dotted circle), this damage only results in slight, non permanent behavioral consequences. In the ongoing study, we will investigate the efficiency of autologous UCB and BM cell therapy in sheep to prepare a clinical trial in humans. A B C A D G B E F C H day 0, T2 day 7, T2 day 7, DW sha m MCAO day 0, DWI brain, removed 35 days upon MCAO Fig. 2 B A Fig. 1 Corrosion cast (A, basal view) and MRA images of cerebral arteries in sheep (B and C). Arrows in (A) and (B) indicate occlusion of the MCA. Cerebral arteries of a sham operated animal are shown in (C).

a new large animal model of focal cerebral ischemia

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A. D. G. E. B. F. C. day 0, T2. day 7, T2. day 7, DW. sham. MCAO. H. day 0, DWI. brain, removed 35 days upon MCAO. a new large animal model of focal cerebral ischemia. PERMANENT MCAO IN SHEEP. - PowerPoint PPT Presentation

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Page 1: a new large animal model of focal cerebral ischemia

a new large animal model of focal cerebral ischemiaa new large animal model of focal cerebral ischemia

ResultsResultsResultsResultsMaterial and MethodsMaterial and MethodsMaterial and MethodsMaterial and Methods

Fig. 3 Behavioral data of neurological examinations, presented as means ± SD (A). Absent medial hopping reaction of right forelimb after MCAO (B).

also poster: Correlation between Behavioural Improvement, Reactive Gliosis and Lesioned Area in a Stem Cell Therapy of Stroke). However, transplantation to clinical application requires close-to-practice models, i.e. large animal models of focal cerebral ischemia. Existing primate models are cost intensive, restricted to highly specialized breeding facilities and limited by ethical considerations. Therefore, we developed a new, cost effective stroke model in sheep including reproducible neurological dysfunctions and reproducible lesion size, variable by proximal or distal occlusion of the middle cerebral artery (MCAO) according to its origin.

ecause of the rete mirabile (rm, Fig. 1), a network of small arteries supplied by afferent rete branches (rb) of the maxillary artery (ma), intraluminal occlusion of the MCAO via catheter blockage or artificial thrombus is not

possible. Hence, we performed a transcranial exposure of middle cerebral artery (MCA). 17 Merino sheep weighting 35 to 48 kg were randomly assigned to one of four groups: proximal (n=5) and distal (n=2) MCAO, sham operation (n=5) and control (n=5). Animals undergoing the surgical procedure were deeply anaesthetised. Following exposure of the MCA, the vessel was occluded or touched (sham) by high frequency bipolar forceps. After suture, animals underwent an analgetic and antibiotic treatment. Control animals did not underwent a surgical procedure. Neurological investigation was performed before surgery and at days 1, 4, 7, 10, 16, 25, and 32 following MCAO (Fig. 3) according to a score point system (table). Further, effects of MCAO were evaluated by magnetic resonance imaging (MRI) including T1-, T2-, T2*-sequences, diffusion weighted (DW) imaging (Fig. 2A-G) and magnetic resonance angiography (MRA, Fig. 1B/C) using a Philips 1,5T clinical scanner. Animals were killed at day 35 post op. and brains were removed for neuropathological investigation (Fig. 2H).

roximal MCAO results in a large cortical lesion and neurological dysfunctions including absent/delayed startle reflexes, atactic movement, circling and torticollis. Distal MCAO causes a smaller cortical lesion and reduced functional

Uwe Gille1, Johannes Boltze2, Daniela Waldmin1, Annette Förschler3, Jean-Claude Ionita4, Kerstin Gerlach4, Dietmar Schneider5, Dietmar Egger6, James Ferguson4, Frank Emmrich2 and Claus Zimmer3

1Institute of Veterinary Anatomy, An den Tierkliniken 43, 04103 Leipzig , Germany; telephone: +49 341 / 97-38057; eMail: [email protected]

2Institute of Clinical Immunology and Transfusion Medicine, Johannisallee 30, 04103 Leipzig , Germany; telephone: +49 341 / 97-25820; eMail: [email protected]

3Department of Neuroradiology, Clinic of Diagnostic Radiology, Liebigstrasse 20, 04103 Leipzig , Germany; telephone: +49 341 / 97-17410; eMail: [email protected]

4Clinic of Large Animal Surgery, An den Tierkliniken 21, 04103 Leipzig , Germany; telephone: +49 341 / 97-38250; eMail: [email protected]

5Clinic of Neurology, Liebigstrasse 22a, 04103 Leipzig , Germany; telephone: +49 341 / 97-24221; eMail: [email protected]

6VITA34 AG, BBZ, Deutscher Platz 5a, 04103 Leipzig , Germany; telephone: +49 341 / 48792-0; eMail: [email protected]

B

PERMANENT MCAO IN SHEEPPERMANENT MCAO IN SHEEP

EXPERIMENTAL CELL THERAPY OF STROKEEXPERIMENTAL CELL THERAPY OF STROKE

P

TIntroductionIntroductionIntroductionIntroduction

he efficiency of experimental umbilical cord blood (UCB) and bone marrow (BM) cell therapies has been shown in stroke models by using rodents (see

Table neurological examination score point systemTable neurological examination score point system ItemItem score points score points

(max. 14)(max. 14)1. food debris remaining in mouth cornerno 0yes 1

2. torticollisno 0yes 1

3. paretic right limbs / atactic movementno 0yes 1

4. circlic movementno 0occasionally 1permanently 2

5. disturbed right hemistanding reactionno disturbance 0immediate adjustment using left limbs 1delayed adjustment using left limbs 2delayed adjustment using right limbs 3delayed using right hindlimb / no using right forelimb 4no adjustment 5

6. disturbed right hopping reactionno disturbance 0delayed medial, immediate lateral adjustment 1delayed medial and lateral adjustment 2no medial adjustment, delayed lateral adjustment 3no adjustment 4

Table neurological examination score point systemTable neurological examination score point system ItemItem score points score points

(max. 14)(max. 14)1. food debris remaining in mouth cornerno 0yes 1

2. torticollisno 0yes 1

3. paretic right limbs / atactic movementno 0yes 1

4. circlic movementno 0occasionally 1permanently 2

5. disturbed right hemistanding reactionno disturbance 0immediate adjustment using left limbs 1delayed adjustment using left limbs 2delayed adjustment using right limbs 3delayed using right hindlimb / no using right forelimb 4no adjustment 5

6. disturbed right hopping reactionno disturbance 0delayed medial, immediate lateral adjustment 1delayed medial and lateral adjustment 2no medial adjustment, delayed lateral adjustment 3no adjustment 4

SummarySummarySummarySummary• MCAO in sheep results in reproducible reproducible

behavioral consequencesbehavioral consequences and reproducible size of ischemic lesion

• to our knowledge, this is thethe first first described model of model of focalfocal cerebral cerebral ischemia in sheepischemia in sheep

• the model will allow to study efficiency study efficiency of autologous cell and pharmaceutical of autologous cell and pharmaceutical therapiestherapies upon stroke

deficits (data not shown). The MCA was clearly occluded as to be seen in MRA (Fig. 1 B). Further, sheep with occluded left MCA showed neurofunctional disabilities (Fig. 3A/B), as well as clear signs of ischemic brain tissue in MRI (Fig. 2E/F) and after brain removal (Fig. 2H).Sham operated animals showed very mild, transient dysfunctions (Fig. 3A) while controls did not show sensomotoric disabilities. Indications of ischemia in sham operated animals was not observed using MRI (Fig. 2B/C). Although a small contusion damage could be observed in some cases (Fig. 2B/C, red dotted circle), this damage only results in slight, non permanent behavioral consequences.In the ongoing study, we will investigate the efficiency of autologous UCB and BM cell therapy in sheep to prepare a clinical trial in humans.

A B

C

A

D

G

B

E F

C

H

day 0, T2 day 7, T2 day 7, DW

sham

MC

AO

day 0, DWI

brain, removed 35 days upon MCAO

Fig. 2

B

A

Fig. 1 Corrosion cast (A, basal view) and MRA images of cerebral arteries in sheep (B and C). Arrows in (A) and (B) indicate occlusion of the MCA. Cerebral arteries of a sham operated animal are shown in (C).