Differentiating hemodynamic responses in rat primary somatosensory cortex during non-noxious and noxious electrical stimulation by optical imaging

Brain Research

Volumn 1133, Issue 1, 2007, Pages 67-77

  Luo, Weihua ^a   Li, Pengcheng ^a   Chen, Shangbin ^a   Zeng, Shaoqun ^a   Luo, Qingming ^a  

^a HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

Cerebral blood volume; Intrinsic signal; Nociception; Optical imaging; Somatosensory cortex

Indexed keywords

ANIMAL TISSUE; ARTICLE; BRAIN BLOOD VOLUME; CONTROLLED STUDY; ELECTROSTIMULATION; EVOKED RESPONSE; HEMODYNAMICS; MALE; MUSCLE TWITCH; NOCICEPTION; NONHUMAN; OPTICAL INSTRUMENTATION; PAIN THRESHOLD; PRIORITY JOURNAL; RAT; SOMATOSENSORY CORTEX;

AFFERENT PATHWAYS; ANALGESICS, OPIOID; ANIMALS; CEREBROVASCULAR CIRCULATION; ELECTRIC STIMULATION; EVOKED POTENTIALS, SOMATOSENSORY; FENTANYL; MALE; NOCICEPTORS; OPTICS AND PHOTONICS; PAIN; PAIN THRESHOLD; RATS; RATS, SPRAGUE-DAWLEY; SOMATOSENSORY CORTEX;

RATTUS;

EID: 33846316304     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2006.09.111     Document Type: Article

References (51)

1. Bingel U., Lorenz J., Glauche V., Knab R., Glascher J., Weiller C., and Buchel C. Somatotopic organization of human somatosensory cortices for pain: a single trial fMRI study. NeuroImage 23 (2004) 224-232
2. Blood A.J., Pouratian N., and Toga A.W. Temporally staggered forelimb stimulation modulates barrel cortex optical intrinsic signal responses to whisker stimulation. J. Neurophysiol. 88 (2002) 422-437
3. Bonhoeffer T., and Grinvald A. Iso-orientation domains in cat visual cortex are arranged in pinwheel-like patterns. Nature 353 (1991) 429-431
4. Bushnell M.C., Duncan G.H., Hofbauer R.K., Ha B., Chen J.I., and Carrier B. Pain perception: is there a role for primary somatosensory cortex?. Proc. Natl. Acad. Sci. U. S. A. 96 (1999) 7705-7709
5. Casey K.L., Svensson P., Morrow T.J., Raz J., Jone C., and Minoshima S. Selective opiate modulation of nociceptive processing in the human brain. J. Neurophysiol. 84 (2000) 525-533
6. Chang C., and Shyu B.C. A fMRI study of brain activations during non-noxious and noxious electrical stimulation of the sciatic nerve of rats. Brain Res. 897 (2001) 71-81
7. Chen-Bee C.H., Polley D.B., Brett-Green B., Prakash N., Kwon M.C., and Frostig R.D. Visualizing and quantifying evoked cortical activity assessed with intrinsic signal imaging. J. Neurosci. Methods 97 (2000) 157-173
8. Creac'h C., Henry P., Caille J.M., and Allard M. Functional MR imaging analysis of pain-related brain activation after acute mechanical stimulation. AJNR Am. J. Neuroradiol. 21 (2000) 1402-1406
9. Culver J.P., Siegel A.M., Franceschini M.A., Mandeville J.B., and Boas D.A. Evidence that cerebral blood volume can provide brain activation maps with better spatial resolution than deoxygenated hemoglobin. NeuroImage 27 (2005) 947-959
10. de Tommaso M., Guido M., Libro G., Losito L., Sciruicchio V., Monetti C., and Puca F. Abnormal brain processing of cutaneous pain in migraine patients during the attack. Neurosci. Lett. 333 (2002) 29-32
11. Derdikman D., Hildesheim R., Ahissar E., Arieli A., and Grinvald A. Imaging spatiotemporal dynamics of surround inhibition in the barrels somatosensory cortex. J. Neurosci. 23 (2003) 3100-3105
12. Devor A., Ulbert I., Dunn A.K., Narayanan S.N., Jones S.R., Andermann M.L., Boas D.A., and Dale A.M. Coupling of the cortical hemodynamic response to cortical and thalamic neuronal activity. Proc. Natl. Acad. Sci. U. S. A. 102 (2005) 3822-3827
13. Erdos B., Lacza Z., Toth I.E., Szelke E., Mersich T., Komjati K., Palkovits M., and Sandor P. Mechanisms of pain-induced local cerebral blood flow changes in the rat sensory cortex and thalamus. Brain Res. 960 (2003) 219-227
14. Erinjeri J.P., and Woolsey T.A. Spatial integration of vascular changes with neural activity in mouse cortex. J. Cereb. Blood Flow Metab. 22 (2002) 353-360
15. Favorov O.V., Whitsel B.L., Chiu J.S., and Tommerdahl M. Activation of cat SII cortex by flutter stimulation of contralateral vs. ipsilateral forepaws. Brain Res. 1071 (2006) 81-90
16. Fayuk D., Aitken P.G., Somjen G.G., and Turner D.A. Two different mechanisms underlie reversible, intrinsic optical signals in rat hippocampal slices. J. Neurophysiol. 87 (2002) 1924-1937
17. Firestone L.L., Gyulai F., Mintun M., Adler L.J., Urso K., and Winter P.M. Human brain activity response to fentanyl imaged by positron emission tomography. Anesth. Analg. 82 (1996) 1247-1251
18. Friedman R.M., Chen L.M., and Roe A.W. Modality maps within primate somatosensory cortex. Proc. Natl. Acad. Sci. U. S. A. 101 (2004) 12724-12729
19. Grinvald A., Lieke E., Frostig R.D., Gilbert C.D., and Wiesel T.N. Functional architecture of cortex revealed by optical imaging of intrinsic signals. Nature 324 (1986) 361-364
20. Hendrich K.S., Kochanek P.M., Melick J.A., Schiding J.K., Statler K.D., Williams D.S., Marion D.W., and Ho C. Cerebral perfusion during anesthesia with fentanyl, isoflurane, or pentobarbital in normal rats studied by arterial spin-labeled MRI. Magn. Reson. Med. 46 (2001) 202-206
21. Ichimi K., Kuchiwaki H., Inao S., Shibayama M., and Yoshida J. Cerebral blood flow regulation under activation of the primary somatosensory cortex during electrical stimulation of the forearm. Neurol. Res. 21 (1999) 579-584
22. Ji R.R., Kohno T., Moore K.A., and Woolf C.J. Central sensitization and LTP: do pain and memory share similar mechanisms?. Trends Neurosci. 26 (2003) 696-705
23. Kalliomaki J., Weng H.-R., Nilsson H.-J., and Schouenborg J. Nociceptive C fibre input to the primary somatosensory cortex (SI). A field potential study in the rat. Brain Res. 622 (1993) 262-270
24. Lamour Y., Willer J.C., and Guilbaud G. Rat somatosensory (SmI) cortex: I. Characteristics of neuronal responses to noxious stimulation and comparison with responses to non-noxious stimulation. Exp. Brain Res. 49 (1983) 35-45
25. Le Bars D., Gozariu M., and Cadden S.W. Animal models of nociception. Pharmacol. Rev. 53 (2001) 597-652
26. Li P., Luo Q., Luo W., Chen S., Cheng H., and Zeng S. Spatiotemporal characteristics of cerebral blood volume changes in rat somatosensory cortex evoked by sciatic nerve stimulation and obtained by optical imaging. J. Biomed. Opt. 8 (2003) 629-635
27. Liu G.B., Zhang Y., Pettigrew J.D., Xu W.F., and Li C.-Y. Spreading and synchronization of intrinsic signals in visual cortex of macaque monkey evoked by a localized visual stimulus. Brain Res. 985 (2003) 13-20
28. Moulton E.A., Keaser M.L., Gullapalli R.P., and Greenspan J.D. Regional intensive and temporal patterns of functional MRI activation distinguishing noxious and innocuous contact heat. J. Neurophysiol. 93 (2005) 2183-2193
29. Nemoto M., Nomura Y., Sato C., Tamura M., Houkin K., Koyanagi I., and Abe H. Analysis of optical signals evoked by peripheral nerve stimulation in rat somatosensory cortex: dynamic changes in hemoglobin concentration and oxygenation. J. Cereb. Blood Flow Metab. 19 (1999) 246-259
30. Ngai A.C., Ko K.R., Morii S., and Winn H.R. Effect of sciatic nerve stimulation on pial arterioles in rats. Am. J. Physiol. 254 (1988) H133-H139
31. Norup Nielsen A., and Lauritzen M. Coupling and uncoupling of activity-dependent increases of neuronal activity and blood flow in rat somatosensory cortex. J. Physiol. 533 (2001) 773-785
32. Paxinos G., and Watson C. The Rat Brain in Stereotaxic Coordinates. 2nd ed. (1998), Academic Press, New York
33. Rubin B.D., and Katz L.C. Optical imaging of odorant representations in the mammalian olfactory bulb. Neuron 23 (1999) 499-511
34. Schuett S., Bonhoeffer T., and Hubener M. Mapping retinotopic structure in mouse visual cortex with optical imaging. J. Neurosci. 22 (2002) 6549-6559
35. Schwartz T.H., and Bonhoeffer T. In vivo optical mapping of epileptic foci and surround inhibition in ferret cerebral cortex. Nat. Med. 7 (2001) 1063-1067
36. Schwartz T.H., Chen L.M., Friedman R.M., Spencer D.D., and Roe A.W. Intraoperative optical imaging of human face cortical topography: a case study. NeuroReport 15 (2004) 1527-1531
37. Sheth S.A., Nemoto M., Guiou M., Walker M., Pouratian N., Hageman N., and Toga A.W. Columnar specificity of microvascular oxygenation and volume responses: implications for functional brain mapping. J. Neurosci. 24 (2004) 634-641
38. Sheth S.A., Nemoto M., Guiou M., Walker M., Pouratian N., and Toga A.W. Linear and nonlinear relationships between neuronal activity, oxygen metabolism, and hemodynamic responses. Neuron 42 (2004) 347-355
39. Sheth S.A., Nemoto M., Guiou M.W., Walker M.A., and Toga A.W. Spatiotemporal evolution of functional hemodynamic changes and their relationship to neuronal activity. J. Cereb. Blood Flow Metab. 25 (2005) 830-841
40. Silva A.C., Lee S.P., Yang G., Iadecola C., and Kim S.G. Simultaneous blood oxygenation level-dependent and cerebral blood flow functional magnetic resonance imaging during forepaw stimulation in the rat. J. Cereb. Blood Flow Metab. 19 (1999) 871-879
41. Simons S.B., Tannan V., Chiu J., Favorov O.V., Whitsel B.L., and Tommerdahl M. Amplitude-dependency of response of SI cortex to flutter stimulation. BMC Neurosci. 6 (2005) 43
42. Stucky C.L., Gold M.S., and Zhang X. Mechanisms of pain. Proc. Natl. Acad. Sci. U. S. A. 98 (2001) 11845-11846
43. Suh M., Bahar S., Mehta A.D., and Schwartz T.H. Temporal dependence in uncoupling of blood volume and oxygenation during interictal epileptiform events in rat neocortex. J. Neurosci. 25 (2005) 68-77
44. Takashima I., Kajiwara R., and Iijima T. Voltage-sensitive dye versus intrinsic signal optical imaging: comparison of optically determined functional maps from rat barrel cortex. NeuroReport 12 (2001) 2889-2894
45. Tommerdahl M., Delemos K.A., Vierck Jr. C.J., Favorov O.V., and Whitsel B.L. Anterior parietal cortical response to tactile and skin-heating stimuli applied to the same skin site. J. Neurophysiol. 75 (1996) 2662-2670
46. Tommerdahl M., Delemos K.A., Favorov O.V., Metz C.B., Vierck Jr. C.J., and Whitsel B.L. Response of anterior parietal cortex to different modes of same-site skin stimulation. J. Neurophysiol. 80 (1998) 3272-3283
47. Tommerdahl M., Delemos K.A., Whitsel B.L., Favorov O.V., and Metz C.B. Response of anterior parietal cortex to cutaneous flutter versus vibration. J. Neurophysiol. 82 (1999) 16-33
48. Ureshi M., Kershaw J., and Kanno I. Nonlinear correlation between field potential and local cerebral blood flow in rat somatosensory cortex evoked by changing the stimulus current. Neurosci. Res. 51 (2005) 139-145
49. Vanzetta I., Slovin H., Omer D.B., and Grinvald A. Columnar resolution of blood volume and oximetry functional maps in the behaving monkey; implications for FMRI. Neuron 42 (2004) 843-854
50. Yaksh T.L. Pharmacology and mechanisms of opioid analgesic activity. Acta Anaesthesiol. Scand. 41 (1997) 94-111
51. Zhao F., Wang P., Hendrich K., and Kim S.G. Spatial specificity of cerebral blood volume-weighted fMRI responses at columnar resolution. NeuroImage 27 (2005) 416-424