Investigation of the BOLD and CBV fMRI responses to somatosensory stimulation in awake marmosets (Callithrix jacchus)

被引:16
|
作者
Hirano, Yoshiyuki [1 ,2 ]
Yen, Cecil C. [1 ]
Liu, Junjie V. [1 ]
Mackel, Julie B. [1 ]
Merkle, Hellmut [1 ]
Nascimento, George C. [1 ,3 ]
Stefanovic, Bojana [1 ,4 ]
Silva, Afonso C. [1 ]
机构
[1] NINDS, Cerebral Microcirculat Sect, Lab Funct & Mol Imaging, NIH, 49 Convent Dr,MSC 1065,Bldg 49,Room 3A72, Bethesda, MD 20892 USA
[2] Chiba Univ, Res Ctr Child Mental Dev, Chuo Ku, 1-8-1 Inohana, Chiba 2608670, Japan
[3] Univ Fed Rio Grande do Norte, Dept Engn Biomed, BR-59075000 Natal, RN, Brazil
[4] Sunnybrook Hlth Sci Ctr, Imaging Res, 2075 Bayview Ave,Rm S6 50, Toronto, ON M4N 3M5, Canada
基金
美国国家卫生研究院;
关键词
bold; cerebral blood volume; functional neuroimaging; neurovascular coupling; non-human primate; somatosensory cortex; BLOOD OXYGENATION; FUNCTIONAL MRI; PARALLEL ORGANIZATION; CEREBRAL-CORTEX; VISUAL-CORTEX; HUMAN-BRAIN; ISOFLURANE; RAT; CONNECTIVITY; ANESTHESIA;
D O I
10.1002/nbm.3864
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Understanding the spatiotemporal features of the hemodynamic response function (HRF) to brain stimulation is essential for the correct application of neuroimaging methods to study brain function. Here, we investigated the spatiotemporal evolution of the blood oxygen level-dependent (BOLD) and cerebral blood volume (CBV) HRF in conscious, awake marmosets (Callithrix jacchus), a New World non-human primate with a lissencephalic brain and with growing use in biomedical research. The marmosets were acclimatized to head fixation and placed in a 7-T magnetic resonance imaging (MRI) scanner. Somatosensory stimulation (333-s pulses; amplitude, 2mA; 64Hz) was delivered bilaterally via pairs of contact electrodes. A block design paradigm was used in which the stimulus duration increased in pseudo-random order from a single pulse up to 256 electrical pulses (4s). For CBV measurements, 30mg/kg of ultrasmall superparamagnetic ironoxide particles (USPIO) injected intravenously, were used. Robust BOLD and CBV HRFs were obtained in the primary somatosensory cortex (S1), secondary somatosensory cortex (S2) and caudate at all stimulus conditions. In particular, BOLD and CBV responses to a single 333-s-long stimulus were reliably measured, and the CBV HRF presented shorter onset time and time to peak than the BOLD HRF. Both the size of the regions of activation and the peak amplitude of the HRFs grew quickly with increasing stimulus duration, and saturated for stimulus durations greater than 1s. Onset times in S1 and S2 were faster than in caudate. Finally, the fine spatiotemporal features of the HRF in awake marmosets were similar to those obtained in humans, indicating that the continued refinement of awake non-human primate models is essential to maximize the applicability of animal functional MRI studies to the investigation of human brain function.
引用
收藏
页数:11
相关论文
共 29 条
  • [11] Study of the Spatial Correlation Between Neuronal Activity and BOLD fMRI Responses Evoked by Sensory and Channelrhodopsin-2 Stimulation in the Rat Somatosensory Cortex
    Li, Nan
    van Zijl, Peter
    Thakor, Nitish
    Pelled, Galit
    JOURNAL OF MOLECULAR NEUROSCIENCE, 2014, 53 (04) : 553 - 561
  • [12] Early fMRI responses to somatosensory and optogenetic stimulation reflect neural information flow
    Jung, Won Beom
    Im, Geun Ho
    Jiang, Haiyan
    Kim, Seong-Gi
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2021, 118 (11)
  • [13] Mapping of the brain hemodynamic responses to sensorimotor stimulation in a rodent model: A BOLD fMRI study
    Boussida, Salem
    Traore, Amidou S.
    Durif, Franck
    PLOS ONE, 2017, 12 (04):
  • [14] Effects of the a2-adrenergic receptor agonist dexmedetomidine on neural, vascular and BOLD fMRI responses in the somatosensory cortex
    Fukuda, Mitsuhiro
    Vazquez, Alberto L.
    Zong, Xiaopeng
    Kim, Seong-Gi
    EUROPEAN JOURNAL OF NEUROSCIENCE, 2013, 37 (01) : 80 - 95
  • [15] Activated areas found by BOLD, CBF, CBV and changes in CMRO2 during somatosensory stimulation do not co-localize in rat cortex
    Schwindt, W
    Burke, M
    Hoehn, M
    BRAIN ACTIVATION AND CBF CONTROL, PROCEEDINGS, 2002, 1235 : 49 - 56
  • [16] Assessment of brain responses to innocuous and noxious electrical forepaw stimulation in mice using BOLD fMRI
    Bosshard, Simone C.
    Baltes, Christof
    Wyss, Matthias T.
    Mueggler, Thomas
    Weber, Bruno
    Rudin, Markus
    PAIN, 2010, 151 (03) : 655 - 663
  • [17] Facilitation of electric forepaw stimulation-induced somatosensory activation in rats by additional acoustic stimulation: An fMRI investigation
    Burke, M
    Schwindt, W
    Ludwig, U
    Hennig, J
    Hoehn, M
    MAGNETIC RESONANCE IN MEDICINE, 2000, 44 (02) : 317 - 321
  • [18] BOLD fMRI and somatosensory evoked potentials are well correlated over a broad range of frequency content of somatosensory stimulation of the rat forepaw
    Goloshevsky, Artem G.
    Silva, Afonso C.
    Dodd, Stephen J.
    Koretsky, Alan P.
    BRAIN RESEARCH, 2008, 1195 : 67 - 76
  • [19] Characteristics of fMRI responses to visual stimulation in anesthetized vs. awake mice
    Thi Ngoc Anh Dinh
    Jung, Won Beom
    Shim, Hyun-Ji
    Kim, Seong-Gi
    NEUROIMAGE, 2021, 226
  • [20] Spatial correlations of laminar BOLD and CBV responses to rat whisker stimulation with neuronal activity localized by Fos expression
    Lu, HB
    Patel, S
    Luo, F
    Li, SJ
    Hillard, CJ
    Ward, BD
    Hyde, JS
    MAGNETIC RESONANCE IN MEDICINE, 2004, 52 (05) : 1060 - 1068