Metabolite changes in the ipsilateral and contralateral cerebral hemispheres in rats with middle cerebral artery occlusion

Cerebral ischemia not only causes pathological changes in the ischemic areas but also induces a series of secondary changes in more distal brain regions (such as the contralateral cerebral hemisphere). The impact of supratentorial lesions, which are the most common type of lesion, on the contralateral cerebellum has been studied in patients by positron emission tomography, single photon emission computed tomography, magnetic resonance imaging and diffusion tensor imaging. In the present study, we investigated metabolite changes in the contralateral cerebral hemisphere after supratentorial unilateral ischemia using nuclear magnetic resonance spectroscopy-based metabonomics. The permanent middle cerebral artery occlusion model of ischemic stroke was established in rats. Rats were randomly divided into the middle cerebral artery occlusion 1-, 3-, 9- and 24-hour groups and the sham group. 1H nuclear magnetic resonance spectroscopy was used to detect metabolites in the left and right cerebral hemispheres. Compared with the sham group, the concentrations of lactate, alanine, γ-aminobutyric acid, choline and glycine in the ischemic cerebral hemisphere were increased in the acute stage, while the concentrations of N-acetyl aspartate, creatinine, glutamate and aspartate were decreased. This demonstrates that there is an upregulation of anaerobic glycolysis (shown by the increase in lactate), a perturbation of choline metabolism (suggested by the increase in choline), neuronal cell damage (shown by the decrease in N-acetyl aspartate) and neurotransmitter imbalance (evidenced by the increase in γ-aminobutyric acid and glycine and by the decrease in glutamate and aspartate) in the acute stage of cerebral ischemia. In the contralateral hemisphere, the concentrations of lactate, alanine, glycine, choline and aspartate were increased, while the concentrations of γ-aminobutyric acid, glutamate and creatinine were decreased. This suggests that there is a difference in the metabolite changes induced by ischemic injury in the contralateral and ipsilateral cerebral hemispheres. Our findings demonstrate the presence of characteristic changes in metabolites in the contralateral hemisphere and suggest that they are most likely caused by metabolic changes in the ischemic hemisphere.

[1]  Hongchang Gao,et al.  Glutamine synthetase plays a role in d-galactose-induced astrocyte aging in vitro and in vivo , 2014, Experimental Gerontology.

[2]  A. Bjørnerud,et al.  Diaschisis after thalamic stroke: a comparison of metabolic and structural changes in a patient with amnesic syndrome , 2007, Acta neurologica Scandinavica. Supplementum.

[3]  R G Shulman,et al.  Proton Magnetic Resonance Spectroscopy of Cerebral Lactate and Other Metabolites in Stroke Patients , 1992, Stroke.

[4]  T. Sugawara,et al.  Direct Correlation Between Ischemic Injury and Extracellular Glycine Concentration in Mice With Genetically Altered Activities of the Glycine Cleavage Multienzyme System , 2007, Stroke.

[5]  J. Phillis,et al.  Characterization of modes of release of amino acids in the ischemic/reperfused rat cerebral cortex , 2003, Neurochemistry International.

[6]  P. Weinstein,et al.  Reversible middle cerebral artery occlusion without craniectomy in rats. , 1989, Stroke.

[7]  Ying Xia,et al.  GABA and glycine are protective to mature but toxic to immature rat cortical neurons under hypoxia , 2005, The European journal of neuroscience.

[8]  M. Corbetta,et al.  Resting interhemispheric functional magnetic resonance imaging connectivity predicts performance after stroke , 2009, Annals of neurology.

[9]  S. Oja,et al.  GABA Release Modified by Adenosine Receptors in Mouse Hippocampal Slices under Normal and Ischemic Conditions , 2005, Neurochemical Research.

[10]  T. Nakada,et al.  Predicting the pathological fate of focal cerebral ischemia using 1H-magnetic resonance spectroscopic imaging , 2003 .

[11]  J. Reggia Neurocomputational models of the remote effects of focal brain damage. , 2004, Medical engineering & physics.

[12]  Tsutomu Nakada,et al.  1H magnetic resonance spectroscopic imaging of permanent focal cerebral ischemia in rat: longitudinal metabolic changes in ischemic core and rim , 2001, Brain Research.

[13]  E. Skinhøj,et al.  TRANSNEURAL DEPRESSION OF THE CEREBRAL HEMISPHERIC METABOLISM IN MAN , 1964, Acta neurologica Scandinavica.

[14]  O. Sporns,et al.  Dynamical consequences of lesions in cortical networks , 2008, Human brain mapping.

[15]  M. Lauritzen,et al.  Impaired Neurovascular Coupling by Transhemispheric Diaschisis in Rat Cerebral Cortex , 2004, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[16]  O. Haraldseth,et al.  In Vivo Injection of [1-13C]Glucose and [1,2-13C]Acetate Combined with Ex Vivo 13C Nuclear Magnetic Resonance Spectroscopy: A Novel Approach to the Study of Middle Cerebral Artery Occlusion in the Rat , 1998, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[17]  Ann Marie Craig,et al.  NMDA Receptor Subunits Have Differential Roles in Mediating Excitotoxic Neuronal Death Both In Vitro and In Vivo , 2007, The Journal of Neuroscience.

[18]  G. Donnan,et al.  Contralesional Thalamic Surface Atrophy and Functional Disconnection 3 Months after Ischemic Stroke , 2015, Cerebrovascular Diseases.

[19]  Maurizio Corbetta,et al.  The role of impaired neuronal communication in neurological disorders , 2007, Current opinion in neurology.

[20]  M. Castillo,et al.  Clinical applications of proton MR spectroscopy. , 1996, AJNR. American journal of neuroradiology.

[21]  Huiru Tang,et al.  NMR analysis of the rat neurochemical changes induced by middle cerebral artery occlusion. , 2012, Talanta.

[22]  C. Arango-Dávila,et al.  Assessment transcallosal Diaschisis in a model of focal cerebral ischemia in rats , 2016, Colombia medica.

[23]  G. Berlucchi Two hemispheres but one brain , 1983, Behavioral and Brain Sciences.

[24]  W. Kempinsky Experimental study of distant effects of acute focal brain injury; a study of diaschisis. , 1958, A.M.A. archives of neurology and psychiatry.

[25]  Leif Hertz,et al.  Bioenergetics of cerebral ischemia: A cellular perspective , 2008, Neuropharmacology.

[26]  M. Tanabe,et al.  Neuroprotection via strychnine-sensitive glycine receptors during post-ischemic recovery of excitatory synaptic transmission in the hippocampus. , 2010, Journal of pharmacological sciences.

[27]  Na Wang,et al.  Systemic Perturbations of Key Metabolites in Diabetic Rats During the Evolution of Diabetes Studied by Urine Metabonomics , 2013, PloS one.

[28]  Changhan Ouyang,et al.  Enhanced activity of GABA receptors inhibits glutamate release induced by focal cerebral ischemia in rat striatum , 2007, Neuroscience Letters.

[29]  R. Caselli Bilateral impairment of somesthetically mediated object recognition in humans. , 1991, Mayo Clinic proceedings.

[30]  B. Anuncibay-Soto,et al.  Neuroprotection by salubrinal treatment in global cerebral ischemia , 2016, Neural regeneration research.

[31]  Jan Sobesky,et al.  Crossed cerebellar diaschisis after stroke: Can perfusion-weighted MRI show functional inactivation? , 2011, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[32]  D. Saunders,et al.  MR spectroscopy in stroke. , 2000, British medical bulletin.

[33]  B. Miller A review of chemical issues in 1H NMR spectroscopy: N‐acetyl‐l‐aspartate, creatine and choline , 1991, NMR in biomedicine.

[34]  David Y B Deng,et al.  Hypoxia-inducible factor 1-α-AA-modified bone marrow stem cells protect PC12 cells from hypoxia-induced apoptosis, partially through VEGF/PI3K/Akt/FoxO1 pathway. , 2012, Stem cells and development.

[35]  A E Hillis,et al.  Crossed Cerebellar Diaschisis in Acute Stroke Detected by Dynamic Susceptibility Contrast MR Perfusion Imaging , 2009, American Journal of Neuroradiology.

[36]  Y. Michotte,et al.  Neurochemical changes and laser Doppler flowmetry in the endothelin-1 rat model for focal cerebral ischemia , 2000, Brain Research.

[37]  W. Lu,et al.  Glycine Exerts Dual Roles in Ischemic Injury Through Distinct Mechanisms , 2012, Stroke.

[38]  Y. Nishizawa,et al.  Glutamate release and neuronal damage in ischemia. , 2001, Life sciences.

[39]  Geirmund Unsgård,et al.  Differences in Neurotransmitter Synthesis and Intermediary Metabolism between Glutamatergic and GABAergic Neurons during 4 Hours of Middle Cerebral Artery Occlusion in the Rat: The Role of Astrocytes in Neuronal Survival , 2001, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[40]  R. Vanninen,et al.  Crossed Cerebellar Diaschisis in Acute Ischemic Stroke: A Study with Serial SPECT and MRI , 2007, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[41]  Neuronal mechanisms underlying transhemispheric diaschisis following focal cortical injuries , 2014, Brain Structure and Function.

[42]  A. Akaike,et al.  Contribution of endogenous glycine and d-serine to excitotoxic and ischemic cell death in rat cerebrocortical slice cultures. , 2007, Life sciences.

[43]  J. Yu,et al.  Effects of oxysophoridine on amino acids after cerebral ischemic injury in mice , 2014, Annals of Indian Academy of Neurology.

[44]  K. Kogure,et al.  Biochemical and Molecular Characteristics of the Brain with Developing Cerebral Infarction , 1999, Cellular and molecular neurobiology.

[45]  J. Lindon,et al.  Metabonomics: a platform for studying drug toxicity and gene function , 2002, Nature Reviews Drug Discovery.

[46]  M. Botez,et al.  Diaschisis and Neurobehavior , 1998, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

[47]  J. Baron,et al.  PET studies of cortical diaschisis in patients with motor hemi-neglect , 1991, Journal of the Neurological Sciences.

[48]  K. Herholz,et al.  Metabolic changes in acute and subacute cerebral infarctions: findings at proton MR spectroscopic imaging. , 1995, Radiology.