A new method for evaluating regional cerebral blood flow changes: Laser speckle contrast imaging in a C57BL/6J mouse model of photothrombotic ischemia

Zhan-Dong Qiu , Gang Deng , Jia Yang , Zhe Min , Da-yong Li , Yu Fang , Su-ming Zhang

Current Medical Science ›› 2016, Vol. 36 ›› Issue (2) : 174 -180.

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Current Medical Science ›› 2016, Vol. 36 ›› Issue (2) : 174 -180. DOI: 10.1007/s11596-016-1562-2
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A new method for evaluating regional cerebral blood flow changes: Laser speckle contrast imaging in a C57BL/6J mouse model of photothrombotic ischemia

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Abstract

The present study aimed to improve the processing of data acquired from laser speckle contrast imaging (LSCI) to provide a standardization method to explore changes in regional cerebral blood flow (rCBF) and to determine the correlations among rCBF, cerebral ischemic lesion volume and microvascular density over time in a focal ischemic region. C57BL/6J mice were subjected to focal photothrombotic (PT) ischemia. rCBF was measured using LSCI at different time points before and after PT ischemia through an intact skull. Standardized rCBF (SrCBF), defined as the ratio of rCBF measured in the ipsilateral region of interest (ROI) to that in the corresponding contralateral region, was calculated to evaluate potential changes. In addition, the volume of the ischemic lesion and the microvascular density were determined using Nissl staining and immunofluorescence, respectively. The relationships among the ischemic lesion volume, microvascular density and SrCBF were analyzed over time. The results showed that the cortical rCBF measured using LSCI following PT ischemia in the C57BL/6J mice gradually increased. Changes in the cerebral ischemic lesion volume were negatively correlated with SrCBF in the ischemic region. Changes in the microvascular density were similar to those observed in SrCBF. Our findings indicate that LSCI is a practical technique for observing changes in murine cortical rCBF without skull opening and for analyzing the relationships among the ischemic lesion volume, microvascular density and SrCBF following focal cerebral ischemia. Preliminary results also suggest that the use of LSCI to observe the formation of collateral circulation is feasible.

Keywords

cerebral blood flow / collateral circulation / laser speckle contrast imaging / photothrombotic ischemia

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Zhan-Dong Qiu, Gang Deng, Jia Yang, Zhe Min, Da-yong Li, Yu Fang, Su-ming Zhang. A new method for evaluating regional cerebral blood flow changes: Laser speckle contrast imaging in a C57BL/6J mouse model of photothrombotic ischemia. Current Medical Science, 2016, 36(2): 174-180 DOI:10.1007/s11596-016-1562-2

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References

[1]

LoEH, DalkaraT, MoskowitzMA. Mechanisms, challenges and opportunities in stroke. Nat Rev Neurosci, 2003, 4(5): 399-415 PMID: 12728267

[2]

BasakK, ManjunathaM, DuttaPK. Review of laser speckle-based analysis in medical imaging. Med Biol Eng Comput, 2012, 50(6): 547-558 PMID: 22476712

[3]

ZhangP, YuH, ZhouN, et al. . Early exercise improves cerebral blood flow through increased angiogenesis in experimental stroke rat model. J Neuroeng Rehabil, 2013, 10: 43 PMID: 23622352 PMCID: 3648391

[4]

HechtN, WoitzikJ, DreierJP, et al. . Intraoperative monitoring of cerebral blood flow by laser speckle contrast analysis. Neurosurg Focus, 2009, 27(4): E11 PMID: 19795950

[5]

ParthasarathyAB, WeberEL, RichardsLM, et al. . Laser speckle contrast imaging of cerebral blood flow in humans during neurosurgery: a pilot clinical study. J Biomed Opt, 2010, 15(6): 066030 PMID: 21198204

[6]

RuaroB, SulliA, AlessandriE, et al. . Laser speckle contrast analysis: a new method to evaluate peripheral blood perfusion in systemic sclerosis patients. Ann Rheum Dis, 2014, 73(6): 1181-1185 PMID: 23956248

[7]

ParthasarathyAB, TomWJ, GopalA, et al. . Robust flow measurement with multi-exposure speckle imaging. Opt Express, 2008, 16(3): 1975-1989 PMID: 18542277

[8]

HechtN, HeJ, KremenetskaiaI, et al. . Cerebral hemodynamic reserve and vascular remodeling in C57/BL6 mice are influenced by age. Stroke, 2012, 43(11): 3052-3062 PMID: 22923448

[9]

DomokiF, Zolei-SzenasiD, OlahO, et al. . Comparison of cerebrocortical microvascular effects of different hypoxic-ischemic insults in piglets: a laser-speckle imaging study. J Physiol Pharm, 2014, 65(4): 551-558

[10]

RosenblumWI, El-SabbanF. Effects of combined parenchymal and vascular injury on platelet aggregation in pial arterioles of living mice: evidence for release of aggregate-inhibiting materials. Stroke, 1977, 8(6): 691-693 PMID: 929658

[11]

WatsonBD, DietrichWD, BustoR, et al. . Induction of reproducible brain infarction by photochemically initiated thrombosis. Ann Neurol, 1985, 17(5): 497-504 PMID: 4004172

[12]

MaxwellKA, DyckRH. Induction of reproducible focal ischemic lesions in neonatal mice by photothrombosis. Dev Neurosci-Basel, 2005, 27(2): 121-126

[13]

DingS, FellinT, ZhuY, et al. . Enhanced astrocytic Ca2+ signals contribute to neuronal excitotoxicity after status epilepticus. J Neurosci, 2007, 27(40): 10674-10684 PMID: 17913901 PMCID: 2917229

[14]

MuraokaK, ShingoT, YasuharaT, et al. . The high integration and differentiation potential of autologous neural stem cell transplantation compared with allogeneic transplantation in adult rat hippocampus. Exp Neurol, 2006, 199(2): 311-327 PMID: 16529744

[15]

BaroneFC, KnudsenDJ, NelsonAH, et al. . Mouse strain differences in susceptibility to cerebral ischemia are related to cerebral vascular anatomy. J Cerebr Blood F Met, 1993, 13(4): 683-692

[16]

TsujiM, OhshimaM, TaguchiA, et al. . A novel reproducible model of neonatal stroke in mice: comparison with a hypoxia-ischemia model. Exp Neurol, 2013, 247: 218-225 PMID: 23651512

[17]

WoodNI, SopesenBV, RobertsJC, et al. . Motor dysfunction in a photothrombotic focal ischaemia model. Behav Brain Res, 1996, 78(2): 113-120 PMID: 8864043

[18]

WangZ, LuoW, ZhouF, et al. . Dynamic change of collateral flow varying with distribution of regional blood flow in acute ischemic rat cortex. J Biomed Opt, 2012, 17(12): 125001 PMID: 23203323

[19]

ObrenovitchTP, ChenS, FarkasE. Simultaneous, live imaging of cortical spreading depression and associated cerebral blood flow changes, by combining voltage-sensitive dye and laser speckle contrast methods. NeuroImage, 2009, 45(1): 68-74 PMID: 19100842

[20]

LeeJK, ParkMS, KimYS, et al. . Photochemically induced cerebral ischemia in a mouse model. Surg Neurol, 2007, 67(6): 620-625 PMID: 17512331

[21]

WuLJ, WuG A, SharifMR, et al. . The voltagegated proton channel Hv1 enhances brain damage from ischemic stroke. Nat Neurosci, 2012, 15(4): 565-573 PMID: 22388960 PMCID: 3314139

[22]

LuoW, WangZ, LiP, et al. . Tracing collateral circulation after ischemia in rat cortex by laser speckle. J Innov Opt Heal Sci, 2012, 1(2): 217-226

[23]

ArmitageGA, ToddKG, ShuaibA, et al. . Laser speckle contrast imaging of collateral blood flow during acute ischemic stroke. J Cerebr Blood F Met, 2010, 30(8): 1432-1436

[24]

HeilM, EitenmullerI, Schmitz-RixenT, et al. . Arteriogenesis versus angiogenesis: similarities and differences. J Cell Mol Med, 2006, 10(1): 45-55 PMID: 16563221 PMCID: 3933101

[25]

LiY, ZhuS, YuanL, et al. . Predicting the ischemic infarct volume at the first minute after occlusion in rodent stroke model by laser speckle imaging of cerebral blood flow. J Biomed Opt, 2013, 18(7): 76024 PMID: 23887483

[26]

OhshimaM, TsujiM, TaguchiA, et al. . Cerebral blood flow during reperfusion predicts later brain damage in a mouse and a rat model of neonatal hypoxic-ischemic encephalopathy. Exp Neurol, 2012, 233(1): 481-489 PMID: 22143064

[27]

SaverJL, JohnstonKC, HomerD, et al. . Infarct volume as a surrogate or auxiliary outcome measure in ischemic stroke clinical trials. The RANTTAS Investigators. Stroke, 1999, 30(2): 293-298 PMID: 9933262

[28]

WahlF, AllixM, PlotkineM, et al. . Neurological and behavioral outcomes of focal cerebral ischemia in rats. Stroke, 1992, 23(2): 267-272 PMID: 1561657

[29]

HayasakaN, NagaiN, KawaoN, et al. . In vivo diagnostic imaging using micro-CT: sequential and comparative evaluation of rodent models for hepatic/brain ischemia and stroke. PloS One, 2012, 7(2): e32342 PMID: 22384223 PMCID: 3285673

[30]

LlewellynME, ThompsonKR, DeisserothK, et al. . Orderly recruitment of motor units under optical control in vivo. Nat Med, 2010, 16(10): 1161-1165 PMID: 20871612

[31]

LinTN, SunSW, CheungWM, et al. . Dynamic changes in cerebral blood flow and angiogenesis after transient focal cerebral ischemia in rats. Evaluation with serial magnetic resonance imaging. Stroke, 2002, 33(12): 2985-2991 PMID: 12468801

[32]

LiuJ, WangY, AkamatsuY, et al. . Vascular remodeling after ischemic stroke: mechanisms and therapeutic potentials. Prog Neurobiol, 2014, 115: 138-156 PMID: 24291532 PMCID: 4295834

[33]

ZhangS, MurphyTH. Imaging the impact of cortical microcirculation on synaptic structure and sensory-evoked hemodynamic responses in vivo. PLoS Biol, 2007, 5(5): e119 PMID: 17456007 PMCID: 1854912

[34]

Liguz-LecznarM, ZakrzewskaR, DaniszewskaK, et al. . Functional assessment of sensory functions after photothrombotic stroke in the barrel field of mice. Behav Brain Res, 2014, 261: 202-209 PMID: 24388975

[35]

SchabitzWR, BergerC, KollmarR, et al. . Effect of brain-derived neurotrophic factor treatment and forced arm use on functional motor recovery after small cortical ischemia. Stroke, 2004, 35(4): 992-997 PMID: 14988579

[36]

BoquillonM, BoquillonJP, BraletJ. Photochemically induced, graded cerebral infarction in the mouse by laser irradiation evolution of brain edema. J Pharmacol Toxicol, 1992, 27(1): 1-6

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