Rescue of cortical neurovascular functions during the hyperacute phase of ischemia by peripheral sensory stimulation

Neurobiology of Disease

Volumn 75, Issue , 2015, Pages 53-63

  Liao, Lun De ^a   Liu, Yu Hang ^a   Lai, Hsin Yi ^b   Bandla, Aishwarya ^a   Shih, Yen Yu Ian ^c   Chen, You Yin ^d   Thakor, Nitish V ^a,e  

^a NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

^b CHANG GUNG MEMORIAL HOSPITAL   (Taiwan)

^c UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^d NATIONAL YANG MING UNIVERSITY   (Taiwan)

^e Johns Hopkins University   (United States)

Author keywords

Collateral circulation; Electrocorticography (ECoG); Functional photoacoustic microscopy (fPAM); Ischemia; Peripheral somatosensory stimulation; Photothrombotic ischemia

Indexed keywords

ALPHA RHYTHM; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN BLOOD VOLUME; BRAIN INFARCTION SIZE; BRAIN ISCHEMIA; CONTROLLED STUDY; DELTA RHYTHM; ELECTROCORTICOGRAPHY; ELECTROSTIMULATION; EVOKED SOMATOSENSORY RESPONSE; FUNCTIONAL STATUS; MALE; NERVE STIMULATOR; NONHUMAN; OXYGEN SATURATION; PERIPHERAL SENSORY STIMULATION; PHOTOACOUSTIC MICROSCOPY; PRIMARY SOMATOSENSORY CORTEX; RAT; RESTING STATE NETWORK; ACOUSTIC MICROSCOPY; ANIMAL; BLOOD VOLUME; BRAIN CIRCULATION; CONVALESCENCE; DEVICES; DISEASE MODEL; ELECTROENCEPHALOGRAPHY; ELECTROSTIMULATION THERAPY; FORELIMB; PATHOLOGY; PATHOPHYSIOLOGY; PHYSIOLOGY; PROCEDURES; SOMATOSENSORY CORTEX; TIME; WISTAR RAT;

ANIMALS; BLOOD VOLUME; BLOOD VOLUME DETERMINATION; BRAIN ISCHEMIA; CEREBROVASCULAR CIRCULATION; DISEASE MODELS, ANIMAL; ELECTRIC STIMULATION THERAPY; ELECTROENCEPHALOGRAPHY; EVOKED POTENTIALS, SOMATOSENSORY; FORELIMB; MALE; MICROSCOPY, ACOUSTIC; RATS, WISTAR; RECOVERY OF FUNCTION; SOMATOSENSORY CORTEX; TIME FACTORS;

EID: 84921372139     PISSN: 09699961     EISSN: 1095953X     Source Type: Journal    
DOI: 10.1016/j.nbd.2014.12.022     Document Type: Article

References (49)

1. Abu Fanne R., et al. Blood-brain barrier permeability and tPA-mediated neurotoxicity. Neuropharmacology 2010, 58:972-980.
2. Armitage G.A., et al. Laser speckle contrast imaging of collateral blood flow during acute ischemic stroke. J. Cereb. Blood Flow Metab. 2010, 30:1432-1436.
3. Azizi S.N., et al. Determination of epinephrine in pharmaceutical formulation by an optimized novel luminescence method using CdS quantum dots as sensitizer. J. Fluoresc. 2013, 23:227-235.
4. Claassen J., et al. Quantitative continuous EEG for detecting delayed cerebral ischemia in patients with poor-grade subarachnoid hemorrhage. Clin. Neurophysiol. 2004, 115:2699-2710.
5. Culver J.P., et al. Diffuse optical tomography of cerebral blood flow, oxygenation, and metabolism in rat during focal ischemia. J. Cereb. Blood Flow Metab. 2003, 23:911-924.
6. Dehghani H., et al. Numerical modelling and image reconstruction in diffuse optical tomography. Philosophical transactions. Ser. A Math. Phys. Eng. Sci. 2009, 367:3073-3093.
7. Di S., Barth D.S. Topographic analysis of field potentials in rat vibrissa barrel cortex. Brain Res. 1991, 546:106-112.
8. Di S., et al. Laminar analysis of extracellular field potentials in rat vibrissa barrel cortex. J. Neurophysiol. 1990, 63:832-840.
9. Finnigan S.P., et al. Correlation of quantitative EEG in acute ischemic stroke with 30-day NIHSS score: comparison with diffusion and perfusion MRI. Stroke 2004, 35:899-903.
10. Fisher M., et al. Update of the stroke therapy academic industry roundtable preclinical recommendations. Stroke 2009, 40:2244-2250.
11. Frostig R.D., et al. Cortical functional architecture and local coupling between neuronal activity and the microcirculation revealed by in vivo high-resolution optical imaging of intrinsic signals. Proc. Natl. Acad. Sci. 1990, 87:6082-6086.
12. Frostig R.D., et al. A rat's whiskers point the way toward a novel stimulus-dependent, protective stroke therapy. Neuroscientist 2013, 19:313-328.
13. Gibson A., Dehghani H. Diffuse optical imaging. Philosophical transactions. Ser. A Math. Phys. Eng. Sci. 2009, 367:3055-3072.
14. Go A.S., et al. Heart disease and stroke statistics-2013 update: a report from the American Heart Association. Circulation 2013, 127:6-245.
15. Hu S., et al. Functional transcranial brain imaging by optical-resolution photoacoustic microscopy. J. Biomed. Opt. 2009, 14:1-3.
16. Jablonka J.A., et al. Remapping of the somatosensory cortex after a photothrombotic stroke: dynamics of the compensatory reorganization. Neuroscience 2010, 165:90-100.
17. Kao Y.C., et al. Dynamic perfusion and diffusion MRI of cortical spreading depolarization in photothrombotic ischemia. Neurobiol. Dis. 2014, 71:131-139.
18. Kingwell K. Stroke: improving the management of patients at risk of haemorrhagic stroke. Nat. Rev. Neurol. 2014, 10:1.
19. Knecht S., et al. Reorganizational and perceptional changes after amputation. Brain 1996, 119:1213-1219.
20. Lai H.Y., et al. Design, simulation and experimental validation of a novel flexible neural probe for deep brain stimulation and multichannel recording. J. Neural Eng. 2012, 9:1-15.
21. Lay C.C., et al. Mild sensory stimulation completely protects the adult rodent cortex from ischemic stroke. PLoS ONE 2010, 5:11270.
22. Lay C.C., et al. Mild sensory stimulation reestablishes cortical function during the acute phase of ischemia. J. Neurosci. 2011, 31:11495-11504.
23. Liao L.D., et al. Imaging brain hemodynamic changes during rat forepaw electrical stimulation using functional photoacoustic microscopy. Neuroimage 2010, 52:562-570.
24. Liao L.-D., et al. Investigation of the cerebral hemodynamic response function in single blood vessels by functional photoacoustic microscopy. J. Biomed. Opt. 2012, 17:1-10.
25. Liao L.D., et al. Transcranial imaging of functional cerebral hemodynamic changes in single blood vessels using in vivo photoacoustic microscopy. J. Cereb. Blood Flow Metab. 2012, 32:938-951.
26. Liao L.D., et al. Neurovascular coupling: in vivo optical techniques for functional brain imaging. Biomed. Eng. Online 2013, 12:38.
27. Liepert J., et al. Treatment-induced cortical reorganization after stroke in humans. Stroke 2000, 31:1210-1216.
28. Liu H.H., et al. Functional electrical stimulation increases neural stem/progenitor cell proliferation and neurogenesis in the subventricular zone of rats with stroke. Chin. Med. J. 2013, 126:2361-2367.
29. Lo E.H. Experimental models, neurovascular mechanisms and translational issues in stroke research. Br. J. Pharmacol. 2008, 153(Suppl. 1):S396-S405.
30. Lo E.H., et al. Mechanisms, challenges and opportunities in stroke. Nat. Rev. Neurosci. 2003, 4:399-415.
31. Luckl J., et al. The biological effect of contralateral forepaw stimulation in rat focal cerebral ischemia: a multispectral optical imaging study. Front. Neuroenerg. 2010, 2:1-9.
32. Luo W.H., et al. Tracing collateral circulation after ischemia in rat cortex by laser speckle imaging. J. Innov. Opti. Health Sci. 2008, 1:217-226.
33. Miao P., et al. Random process estimator for laser speckle imaging of cerebral blood flow. Opt. Express 2010, 18:218-236.
34. Molnár L., et al. A new model for inducing transient cerebral ischemia and subsequent reperfusion in rabbits without craniectomy. Stroke 1988, 19:1262-1266.
35. Muir K.W., et al. Imaging of acute stroke. Lancet Neurol. 2006, 5:755-768.
36. Nemoto M., et al. Functional signal- and paradigm-dependent linear relationships between synaptic activity and hemodynamic responses in rat somatosensory cortex. J. Neurosci. 2004, 24:3850-3861.
37. Paxinos G., Watson Charles The rat brain in stereotaxic coordinates 2007, Academic Press, San Diego.
38. Sakatani K., et al. Somatosensory evoked potentials in rat cerebral cortex before and after middle cerebral artery occlusion. Stroke 1990, 21:124-132.
39. Schaffer C.B., et al. Two-photon imaging of cortical surface microvessels reveals a robust redistribution in blood flow after vascular occlusion. PLoS Biol. 2006, 4:258-270.
40. Shih A.Y., et al. Active dilation of penetrating arterioles restores red blood cell flux to penumbral neocortex after focal stroke. J. Cereb. Blood Flow Metab. 2009, 29:738-751.
41. Sims N.R., Muyderman H. Mitochondria, oxidative metabolism and cell death in stroke. Biochim. Biophys. Acta (BBA) Bioenerg. 2010, 1802:80-91.
42. Tatlisumak T. Is CT or MRI the method of choice for imaging patients with acute stroke? Why should men divide if fate has united?. Stroke 2002, 33:2144-2145.
43. Tolonen U., Sulg I.A. Comparison of quantitative EEG parameters from 4 different analysis techniques in evaluation of relationships between EEG and CBF in brain infarction. Electroencephalogr. Clin. Neurophysiol. 1981, 51:177-185.
44. Tsytsarev V., et al. Living brain optical imaging: technology, methods and applications. J. Neurosci. Neuroeng. 2012, 1:180-192.
45. Vymazal J., et al. Comparison of CT and MR imaging in ischemic stroke. Insights Imaging 2012, 3:619-627.
46. Watson B.D., et al. Induction of reproducible brain infarction by photochemically initiated thrombosis. Ann. Neurol. 1985, 17:497-504.
47. Zhang H.F., et al. Functional photoacoustic microscopy for high-resolution and noninvasive in vivo imaging. Nat. Biotechnol. 2006, 24:848-851.
48. Zhang H., et al. Wide genetic variation in the native pial collateral circulation is a major determinant of variation in severity of stroke. J. Cereb. Blood Flow Metab. 2010, 30:923-934.
49. Zhang S.J., et al. EEG patterns from acute to chronic stroke phases in focal cerebral ischemic rats: correlations with functional recovery. Physiol. Meas. 2013, 34:423-435.