Share:
Share this content in WeChat
X
Clinical Article
Heterogeneous neural pathways underlying acupuncture revealed by multivariate granger causality analyses
SUN Chuan-zhu  BAI Li-jun  NIU Xuan  CHEN Hong-yan  CHEN Peng  ZHANG Ming  LAO Li-xing 

DOI:10.3969/j.issn.1674-8034.2014.06.004.


[Abstract] Objectives: Although accumulating evidence has demonstrated a wide range of cortico-subcortical networks underlying acute effects of acupuncture, less is understood regarding how and by what neural pathways these brain areas interact. We have recently proposed that acupuncture is a slow-acting agent and can induce specific patterns of dynamic CNS activities. Implicit in this evidence was the prediction that the reconfiguration of brain networks underlying both acute and sustained effects of acupuncture may elucidate its overall functional specificity.Materials and Methods: We address the idea directly by adopting a non-repeated event-related design paradigm and multivariate Granger causality analysis (mGCA).Results: We found that brain areas were only sparsely causal connected at early acupuncture needling stage, mainly including ascending path from the thalamus as well as top-down control signals from frontal cortices to nociceptive information processing areas. As time prolonged (sustained effect), more extensive regions integrated into a dense, causally interconnected network only following acupuncture at ST36 but not nonacupoint. Additionally, this reorganization of wide brain networks seemed to be evolved from the resting state.Conclusions: These findings highlighted that the specific effect of acupuncture may involve the integration of recurrent information flow among multi-levels of brain networks.
[Keywords] Acupuncture;Time-dependent activities;Heterogeneous neural pathways;Magnetic resonance imaging

SUN Chuan-zhu The Key Laboratory of Biomedical Information Engineering, Ministry of Education, Department of Biomedical Engineering, School of Life Science and Technology, Xi’an Jiaotong University, Xi’an 710049, China

BAI Li-jun * The Key Laboratory of Biomedical Information Engineering, Ministry of Education, Department of Biomedical Engineering, School of Life Science and Technology, Xi’an Jiaotong University, Xi’an 710049, China

NIU Xuan Department of Imaging, the First Affiliated Hospital of Medical College, Xi’an Jiaotong University, Xi’an 710061, China

CHEN Hong-yan Department of Radiology, Capital University of Medical Science, Beijing 100050, China

CHEN Peng Acupuncture Center, Beijing TCM Hospital Affiliated to Capital Medical University, Beijing 100010, China

ZHANG Ming Acupuncture Center, Beijing TCM Hospital Affiliated to Capital Medical University, Beijing 100010, China

LAO Li-xing School of Chinese Medicine, University of Hongkong, Hongkong, China; Center for Integrative Medicine, University of Maryland Baltimore, School of Medicine, Baltimore 21201, U S A

*Correspondence to: Bai LJ, E-mail: bailj4152615@gmail.com

Conflicts of interest   None.

Received  2014-09-16
Accepted  2014-10-20
DOI: 10.3969/j.issn.1674-8034.2014.06.004
DOI:10.3969/j.issn.1674-8034.2014.06.004.

[1]
Mayer DJ, Price DD, Rafii A. Antagonism of acupuncture analgesia in man by the narcotic antagonist naloxone. Brain research, 1977, 121(2): 368.
[2]
Pomeranz B, Chiu D. Naloxone blockade of acupuncture analgesia: endorphin implicated. Life Scien, 1977, 19(11): 1757.
[3]
Price DD, Rafii A, Watkins LR, et al. A psychophysical analysis of acupuncture analgesia. Pain, 1984, 19(1): 27-42.
[4]
Bai L, Qin W, Liang J, et al. Spatiotemporal modulation of central neural pathway underlying acupuncture action: a systematic review. Current Med Imaging Review, 2009, 5(3): 167-173.
[5]
Bai L, Qin W, Tian J, et al. Detection of dynamic brain networks modulated by acupuncture using a graph theory model. Prog Nat Sci, 2009,19(7): 827-835.
[6]
Bai L, Qin W, Tian J, et al. Acupuncture modulates spontaneous activities in the anticorrelated resting brain networks. Brain Res, 2009, 1279: 37-49.
[7]
Bai L, Qin W, Tian J, et al. Time-varied characteristics of acupuncture effects in fMRI studies. Hum Brain Mapp, 2009, 30(11): 3445-3460.
[8]
Dhond RP, Yeh C, Park K, et al. Acupuncture modulates resting state connectivity in default and sensorimotor brain networks. Pain, 2008, 136(3): 407-418.
[9]
Stilla R, Deshpande G, LaConte S, et al. Posteromedial parietal cortical activity and inputs predict tactile spatial acuity. J Neurosci, 2007, 27(41): 11091-11102.
[10]
Dhamala M, Rangarajan G, Ding M. Analyzing information flow in brain networks with nonparametric Granger causality. Neuroimage, 2008, 41(2): 354-362.
[11]
Wang X, Chen Y, Ding M. Estimating Granger causality after stimulus onset: a cautionary note. Neuroimage, 2008, 41(3): 767-776.
[12]
Zhou Z, Chen Y, Ding M, et al. Analyzing brain networks with PCA and conditional Granger causality. Hum Brain Mapp, 2009, 30(7): 2197-2206.
[13]
Hui KK, Liu J, Marina O, et al. The integrated response of the human cerebro-cerebellar and limbic systems to acupuncture stimulation at ST 36 as evidenced by fMRI. Neuroimage, 2005, 27(3): 479-496.
[14]
Talaraich J, Tournoux P. Co-planar stereotactic atlas of the human brain. Thieme Medical Publishers, Weinheim: Wiley-VCH, 1988: 437-460.
[15]
Deshpande G, LaConte S, James GA, et al. Multivariate Granger causality analysis of fMRI data. Hum Brain Mapp, 2009, 30(4): 1361-1373.
[16]
Kus R, Kaminski M, Blinowska KJ. Determination of EEG activity propagation: pair-wise versus multichannel estimate. IEEE Trans Biomed Eng., 2004, 51(9): 1501-1510.
[17]
Fox MD, Snyder AZ, Vincent JL, et al. The human brain is intrinsically organized into dynamic, anticorrelated functional networks. Proc Natl Acad Sci U S A, 2005, 102(27): 9673-9678.
[18]
Treede RD, Kenshalo DR, Gracely RH, et al. The cortical representation of pain. Pain, 1999, 79(2): 105-111.
[19]
Schoenbaum G, Saddoris MP, Stalnaker TA. Reconciling the roles of orbitofrontal cortex in reversal learning and the encoding of outcome expectancies. Ann N Y Acad Sci, 2007, 1121: 320-335.
[20]
Tolle TR, Kaufmann T, Siessmeier T, et al. Region-specific encoding of sensory and affective components of pain in the human brain: a positron emission tomography correlation analysis. Ann Neurol, 1999, 45(1): 40-47.
[21]
Wu MT, Hsieh JC, Xiong J, et al. Central nervous pathway for acupuncture stimulation: localization of processing with functional MR Imaging of the brain-preliminary experience. Radiology, 1999, 212(1): 133-141.
[22]
Yu LC, Han JS. Involvement of arcuate nucleus of hypothalamus in the descending pathway from nucleus accumbens to periaqueductal grey subserving an antinociceptive effect. Internat J Neuroscien, 1989, 48(1-2): 71-78.
[23]
陈凤英,沈智威,关计添,等.手法针刺合谷穴得气与脑功能激活关系的探讨.磁共振成像, 2011, 2(2): 112-117.
[24]
Vanegas H, Schaible HG. Descending control of persistent pain: inhibitory or facilitatory? Brain Res Brain Res Rev, 2004, 46(3): 295-309.
[25]
Peets JM, Pomeranz B. CXBK mice deficient in opiate receptors show poor electroacupuncture analgesia. Nature, 1978, 273(5664): 675-676.
[26]
Ren K, Dubner R. Descending modulation in persistent pain: an update. Pain, 2002, 100(1-2): 1-6.
[27]
Takeshige C, Oka K, Mizuno T, et al. The acupuncture point and its connecting central pathway for producing acupuncture analgesia. Brain Res Bull, 1993, 30(1-2): 53-67.

PREV Brain response to transcutaneous electronical stimulation on auricular concha of the healthy subjects using fMRI
NEXT Cerebral regional homogeneity of peripheral facial paralysis treated by acupuncture: a resting-state fMRI study
  



Tel & Fax: +8610-67113815    E-mail: editor@cjmri.cn