Optogenetic fMRI reveals distinct, frequency-dependent networks recruited by dorsal and intermediate hippocampus stimulations

Although the connectivity of hippocampal circuits has been extensively studied, the way in which these connections give rise to large-scale dynamic network activity remains unknown. Here, we used optogenetic fMRI to visualize the brain network dynamics evoked by different frequencies of stimulation of two distinct neuronal populations within dorsal and intermediate hippocampus. Stimulation of excitatory cells in intermediate hippocampus caused widespread cortical and subcortical recruitment at high frequencies, whereas stimulation in dorsal hippocampus led to activity primarily restricted to hippocampus across all frequencies tested. Sustained hippocampal responses evoked during high-frequency stimulation of either location predicted seizure-like afterdischarges in video-EEG experiments, while the widespread activation evoked by high-frequency stimulation of intermediate hippocampus predicted behavioral seizures. A negative BOLD signal observed in dentate gyrus during dorsal, but not intermediate, hippocampus stimulation is proposed to underlie the mechanism for these differences. Collectively, our results provide insight into the dynamic function of hippocampal networks and their role in seizures.

[1]  R. S. Sloviter,et al.  Permanently altered hippocampal structure, excitability, and inhibition after experimental status epilepticus in the rat: The “dormant basket cell” hypothesis and its possible relevance to temporal lobe epilepsy , 1991, Hippocampus.

[2]  Hiroyuki Ohsaki,et al.  Opto-fMRI analysis for exploring the neuronal connectivity of the hippocampal formation in rats , 2012, Neuroscience Research.

[3]  P. Boesiger,et al.  GABA concentrations in the human anterior cingulate cortex predict negative BOLD responses in fMRI , 2007, Nature Neuroscience.

[4]  S. Ogawa,et al.  Biophysical and Physiological Origins of Blood Oxygenation Level-Dependent fMRI Signals , 2012, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[5]  Hong-wei Dong,et al.  Are the Dorsal and Ventral Hippocampus Functionally Distinct Structures? , 2010, Neuron.

[6]  G. Glover,et al.  Retinotopic organization in human visual cortex and the spatial precision of functional MRI. , 1997, Cerebral cortex.

[7]  Jan Sijbers,et al.  Estimation of signal and noise from Rician distributed data , 1998 .

[8]  F. Hyder,et al.  Remote Effects of Focal Hippocampal Seizures on the Rat Neocortex , 2008, The Journal of Neuroscience.

[9]  O. Sporns,et al.  Complex brain networks: graph theoretical analysis of structural and functional systems , 2009, Nature Reviews Neuroscience.

[10]  Seong-Gi Kim,et al.  Neural and hemodynamic responses elicited by forelimb- and photo-stimulation in channelrhodopsin-2 mice: insights into the hemodynamic point spread function. , 2014, Cerebral cortex.

[11]  R. Buckner,et al.  Mapping brain networks in awake mice using combined optical neural control and fMRI. , 2011, Journal of neurophysiology.

[12]  H. Ladinsky,et al.  Differences between rat dorsal and ventral hippocampus in muscarinic receptor agonist binding and interaction with phospholipase C. , 1993, European journal of pharmacology.

[13]  Roland Willems,et al.  Dorsal-ventral gradient in vulnerability of CA1 hippocampus to ischemia: a combined histological and electrophysiological study , 1989, Brain Research.

[14]  T. van Groen,et al.  Extrinsic projections from area CA1 of the rat hippocampus: Olfactory, cortical, subcortical, and bilateral hippocampal formation projections , 1990, The Journal of comparative neurology.

[15]  J. P. Flynn,et al.  Differential effects of electrical stimulation and lesions of the hippocampus and adjacent regions upon attack behavior in cats. , 1968, Brain research.

[16]  F. Helmchen,et al.  Simultaneous BOLD fMRI and fiber-optic calcium recording in rat neocortex , 2012, Nature Methods.

[17]  Frank Angenstein,et al.  Variations in the temporal pattern of perforant pathway stimulation control the activity in the mesolimbic pathway , 2013, NeuroImage.

[18]  Feng Zhang,et al.  An optical neural interface: in vivo control of rodent motor cortex with integrated fiberoptic and optogenetic technology , 2007, Journal of neural engineering.

[19]  B. McNaughton,et al.  Comparison of spatial firing characteristics of units in dorsal and ventral hippocampus of the rat , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[20]  G H Glover,et al.  Motion Artifacts in fMRI: Comparison of 2DFT with PR and Spiral Scan Methods , 1995, Magnetic resonance in medicine.

[21]  Jin Hyung Lee,et al.  High-throughput optogenetic functional magnetic resonance imaging with parallel computations , 2013, Journal of Neuroscience Methods.

[22]  Jin Hyung Lee,et al.  Tracing Activity Across the Whole Brain Neural Network with Optogenetic Functional Magnetic Resonance Imaging , 2011, Front. Neuroinform..

[23]  N. Logothetis,et al.  Electric stimulation fMRI of the perforant pathway to the rat hippocampus. , 2008, Magnetic resonance imaging.

[24]  Elfar Adalsteinsson,et al.  Simple analytic variable density spiral design , 2003, Magnetic resonance in medicine.

[25]  Ana I. Domingos,et al.  Leptin regulates the reward value of nutrient , 2011, Nature Neuroscience.

[26]  Paul Leonard Gabbott,et al.  Morphological evidence that CA1 hippocampal afferents monosynaptically innervate PV-containing neurons and NADPH-diaphorase reactive cells in the medial prefrontal cortex (Areas 25/32) of the rat , 2002, Brain Research.

[27]  N. Logothetis,et al.  Functional MRI Evidence for LTP-Induced Neural Network Reorganization , 2009, Current Biology.

[28]  A. Macovski,et al.  Selection of a convolution function for Fourier inversion using gridding [computerised tomography application]. , 1991, IEEE transactions on medical imaging.

[29]  Alan P. Koretsky,et al.  3D mapping of somatotopic reorganization with small animal functional MRI , 2010, NeuroImage.

[30]  Y. Hirabayashi,et al.  Sevoflurane Is Equivalent to Isoflurane for Attenuating Bupivacaine-Induced Arrhythmias and Seizures in Rats , 1996, Anesthesia and analgesia.

[31]  Jack A. Wells,et al.  fMRI response to blue light delivery in the naïve brain: Implications for combined optogenetic fMRI studies , 2013, NeuroImage.

[32]  Andrew L Rivard,et al.  Rat Intubation and Ventilation for Surgical Research , 2006, Journal of investigative surgery : the official journal of the Academy of Surgical Research.

[33]  Reinhold Ludwig,et al.  Corticothalamic Modulation during Absence Seizures in Rats: A Functional MRI Assessment , 2003, Epilepsia.

[34]  L Forsgren,et al.  Incidence and Clinical Characterization of Unprovoked Seizures in Adults: A Prospective Population‐Based Study , 1996, Epilepsia.

[35]  Itamar Kahn,et al.  Characterization of the Functional MRI Response Temporal Linearity via Optical Control of Neocortical Pyramidal Neurons , 2011, The Journal of Neuroscience.

[36]  Ryan Chamberlain,et al.  Simultaneous fMRI and local field potential measurements during epileptic seizures in medetomidine‐sedated rats using raser pulse sequence , 2010, Magnetic resonance in medicine.

[37]  R. S. Sloviter,et al.  The functional organization of the hippocampal dentate gyrus and its relevance to the pathogenesis of temporal lobe epilepsy , 1994, Annals of neurology.

[38]  K. Deisseroth,et al.  Tuning arousal with optogenetic modulation of locus coeruleus neurons , 2010, Nature Neuroscience.

[39]  Lief E. Fenno,et al.  Principles for applying optogenetic tools derived from direct comparative analysis of microbial opsins , 2011, Nature Methods.

[40]  E C Wong,et al.  Processing strategies for time‐course data sets in functional mri of the human brain , 1993, Magnetic resonance in medicine.

[41]  D. Kleinfeld,et al.  Suppressed Neuronal Activity and Concurrent Arteriolar Vasoconstriction May Explain Negative Blood Oxygenation Level-Dependent Signal , 2007, The Journal of Neuroscience.

[42]  R. S. Sloviter,et al.  Decreased hippocampal inhibition and a selective loss of interneurons in experimental epilepsy. , 1987, Science.

[43]  L. Swanson,et al.  A direct projection from Ammon's horn to prefrontal cortex in the rat , 1981, Brain Research.

[44]  T. Jay,et al.  Selectivity of the hippocampal projection to the prelimbic area of the prefrontal cortex in the rat , 1989, Brain Research.

[45]  K. Deisseroth,et al.  Neural substrates of awakening probed with optogenetic control of hypocretin neurons , 2007, Nature.

[46]  Andrew J. Weitz,et al.  Progress with optogenetic functional MRI and its translational implications , 2013 .

[47]  Dae-Shik Kim,et al.  Spatial relationship between neuronal activity and BOLD functional MRI , 2004, NeuroImage.

[48]  G. Feng,et al.  Cell type–specific channelrhodopsin-2 transgenic mice for optogenetic dissection of neural circuitry function , 2011, Nature Methods.

[49]  René Hen,et al.  Serotonin receptor expression along the dorsal–ventral axis of mouse hippocampus , 2012, Philosophical Transactions of the Royal Society B: Biological Sciences.

[50]  Dae-Shik Kim,et al.  Origin of Negative Blood Oxygenation Level—Dependent fMRI Signals , 2002, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[51]  Alan P. Koretsky,et al.  BOLD fMRI and somatosensory evoked potentials are well correlated over a broad range of frequency content of somatosensory stimulation of the rat forepaw , 2008, Brain Research.

[52]  Murtaza Z Mogri,et al.  Optical Deconstruction of Parkinsonian Neural Circuitry , 2009, Science.

[53]  Frank Angenstein,et al.  Frequency-dependent activation pattern in the rat hippocampus, a simultaneous electrophysiological and fMRI study , 2007, NeuroImage.

[54]  K. Deisseroth,et al.  Millisecond-timescale, genetically targeted optical control of neural activity , 2005, Nature Neuroscience.

[55]  Dae-Shik Kim,et al.  Global and local fMRI signals driven by neurons defined optogenetically by type and wiring , 2010, Nature.

[56]  F. L. D. Silva,et al.  Septotemporal distribution of entorhinal projections to the hippocampus in the cat: Electrophysiological evidence , 1985, The Journal of comparative neurology.

[57]  Karl Deisseroth,et al.  Optogenetics in Neural Systems , 2011, Neuron.

[58]  L. Swanson,et al.  Spatial organization of direct hippocampal field CA1 axonal projections to the rest of the cerebral cortex , 2007, Brain Research Reviews.

[59]  Yul-Wan Sung,et al.  Functional magnetic resonance imaging , 2004, Scholarpedia.

[60]  Craig J. Brozinsky,et al.  Functional connectivity with the hippocampus during successful memory formation , 2005, Hippocampus.

[61]  Arthur W. Toga,et al.  Genomic–anatomic evidence for distinct functional domains in hippocampal field CA1 , 2009, Proceedings of the National Academy of Sciences.

[62]  R. Racine,et al.  Epileptiform burst responses in ventral vs dorsal hippocampal slices , 1985, Brain Research.

[63]  Toru Ishizuka,et al.  Optogenetically Induced Seizure and the Longitudinal Hippocampal Network Dynamics , 2013, PloS one.

[64]  R. Henkelman Measurement of signal intensities in the presence of noise in MR images. , 1985, Medical physics.

[65]  M. Bunsey,et al.  Differential Effects of Dorsal and Ventral Hippocampal Lesions , 1998, The Journal of Neuroscience.

[66]  L. Swanson,et al.  Analysis of direct hippocampal cortical field CA1 axonal projections to diencephalon in the rat , 2006, The Journal of comparative neurology.

[67]  Farsin Hamzei,et al.  Reduction of Excitability (“Inhibition”) in the Ipsilateral Primary Motor Cortex Is Mirrored by fMRI Signal Decreases , 2002, NeuroImage.

[68]  Jin Hyung Lee,et al.  Informing brain connectivity with optogenetic functional magnetic resonance imaging , 2012, NeuroImage.

[69]  Tanemichi Chiba,et al.  Collateral projection from the amygdalo–hippocampal transition area and CA1 to the hypothalamus and medial prefrontal cortex in the rat , 2000, Neuroscience Research.

[70]  Maria Thom,et al.  Variability of sclerosis along the longitudinal hippocampal axis in epilepsy: A post mortem study , 2012, Epilepsy Research.