Acute Anemia Elicits Cognitive Dysfunction and Evidence of Cerebral Cellular Hypoxia in Older Rats with Systemic Hypertension

Background:Postoperative cognitive dysfunction occurs frequently after cardiac, major vascular, and major orthopedic surgery. Aging and hypertensive cerebrovascular disease are leading risk factors for this disorder. Acute anemia, common to major surgery, has been identified as a possible contributor to postoperative cognitive dysfunction. The effect of hypoxia upon cognition and the cellular and molecular processes involved in learning and memory has been well described. Cerebrovascular changes related to chronic hypertension may expose cells to increased hypoxia with anemia. Methods:Young to aged spontaneously hypertensive rats underwent testing for visuospatial memory and learning in the Morris water maze, measurement of cerebral tissue oxygenation via tissue oxygen probe, and measurement of hypoxia-sensitive genes and proteins, under conditions of sham and experimental isovolemic anemia. Results:Acute isovolemic anemia elicited evidence of aging-dependent visuospatial working memory and learning impairment. Isovolemic anemia did not result in cerebral tissue hypoxia, when measured via tissue oxygen probe. Evidence of cellular hypoxia was, however, identified in response to the anemic challenge, as hypoxia-sensitive genes and proteins were up-regulated. Importantly, cellular hypoxic gene responses were increased with anemia in an age-dependent manner in this model of aging with chronic hypertension. Conclusions:In a translational model of chronic hypertension, clinically relevant levels of acute anemia were associated with an age-dependent visuospatial working memory and learning impairment that was matched by an age-dependent cellular sensitivity to anemic hypoxia. These data offer support for a possible link between anemic hypoxia and postoperative cognitive dysfunction in humans.

[1]  I. Sora,et al.  Impaired spatial working memory and decreased frontal cortex BDNF protein level in dopamine transporter knockout mice. , 2010, European journal of pharmacology.

[2]  D. Kleinfeld,et al.  The glial cell response is an essential component of hypoxia-induced erythropoiesis in mice. , 2009, The Journal of clinical investigation.

[3]  J. LaManna,et al.  Increased prolyl 4-hydroxylase expression and differential regulation of hypoxia-inducible factors in the aged rat brain. , 2009, American journal of physiology. Regulatory, integrative and comparative physiology.

[4]  Pingyuan Gong,et al.  Effect of BDNF Val66Met Polymorphism on Digital Working Memory and Spatial Localization in a Healthy Chinese Han Population , 2009, Journal of Molecular Neuroscience.

[5]  Michael X. Cohen,et al.  Interference of working memory load with long‐term memory formation , 2009, The European journal of neuroscience.

[6]  C. Callaghan,et al.  Deficits in LTP and recognition memory in the genetically hypertensive rat are associated with decreased expression of neurotrophic factors and their receptors in the dentate gyrus , 2009, Behavioural Brain Research.

[7]  M. Georgieff,et al.  Early-life iron deficiency anemia alters neurotrophic factor expression and hippocampal neuron differentiation in male rats. , 2008, The Journal of nutrition.

[8]  Nikolai Axmacher,et al.  Interaction of working memory and long-term memory in the medial temporal lobe. , 2008, Cerebral cortex.

[9]  M. Escobar,et al.  In vivo BDNF modulation of adult functional and morphological synaptic plasticity at hippocampal mossy fibers , 2008, Neuroscience Letters.

[10]  F. Wolf,et al.  Erythropoietin enhances hippocampal long-term potentiation and memory , 2008, BMC Biology.

[11]  W. Kaelin,et al.  Oxygen sensing by metazoans: the central role of the HIF hydroxylase pathway. , 2008, Molecular cell.

[12]  S. Zeger,et al.  Cognition 6 years after surgical or medical therapy for coronary artery disease , 2008, Annals of neurology.

[13]  M. Simon,et al.  Hypoxia-induced signaling in the cardiovascular system. , 2008, Annual review of physiology.

[14]  D. Wijeysundera,et al.  Risk Associated With Preoperative Anemia in Cardiac Surgery: A Multicenter Cohort Study , 2008, Circulation.

[15]  Olli Gröhn,et al.  Coupling between simultaneously recorded BOLD response and neuronal activity in the rat somatosensory cortex , 2008, NeuroImage.

[16]  C. Garvan,et al.  Type and Severity of Cognitive Decline in Older Adults after Noncardiac Surgery , 2008, Anesthesiology.

[17]  J. Blumenthal,et al.  Effects of Extreme Hemodilution during Cardiac Surgery on Cognitive Function in the Elderly , 2007, Anesthesiology.

[18]  I. C. Tudor,et al.  Impact of Preoperative Anemia on Outcome in Patients Undergoing Coronary Artery Bypass Graft Surgery , 2007, Circulation.

[19]  Philip D. Harvey,et al.  Postoperative Cognitive Dysfunction in Patients with Preoperative Cognitive Impairment: Which Domains Are Most Vulnerable? , 2007, Anesthesiology.

[20]  M. Maze,et al.  Postoperative Cognitive Dysfunction after Noncardiac Surgery: A Systematic Review , 2007, Anesthesiology.

[21]  D. Grobbee,et al.  Cognitive and cardiac outcomes 5 years after off-pump vs on-pump coronary artery bypass graft surgery. , 2007, JAMA.

[22]  S. Neggers,et al.  Brain areas involved in spatial working memory , 2006, Neuropsychologia.

[23]  M. Nikinmaa,et al.  Oxygen availability regulates metabolism and gene expression in trout hepatocyte cultures. , 2006, American journal of physiology. Regulatory, integrative and comparative physiology.

[24]  Jun Shen,et al.  Increased oxygen consumption in the somatosensory cortex of α-chloralose anesthetized rats during forepaw stimulation determined using MRS at 11.7 Tesla , 2006, NeuroImage.

[25]  T Hoshi,et al.  Oxygen sensing in the body. , 2006, Progress in biophysics and molecular biology.

[26]  M. López-Lázaro HIF‐1: hypoxia‐inducible factor or dysoxia‐inducible factor? , 2006, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[27]  E. Gordon,et al.  Brain function in obstructive sleep apnea: results from the Brain Resource International Database. , 2006, Journal of integrative neuroscience.

[28]  A. Brzecka Brain preconditioning and obstructive sleep apnea syndrome. , 2005, Acta neurobiologiae experimentalis.

[29]  M. Cacchio,et al.  Oxygen and life span: chronic hypoxia as a model for studying HIF-1α, VEGF and NOS during aging , 2005, Respiratory Physiology & Neurobiology.

[30]  G. Mundy,et al.  The effect of iron supplementation on the level of haemoglobin after lower limb arthroplasty. , 2005, The Journal of bone and joint surgery. British volume.

[31]  D. Gozal,et al.  Effect of intermittent hypoxia on long-term potentiation in rat hippocampal slices , 2004, Brain Research.

[32]  E. Procyk,et al.  The primate working memory networks , 2004, Cognitive, affective & behavioral neuroscience.

[33]  J. LaManna,et al.  Structural and functional adaptation to hypoxia in the rat brain , 2004, Journal of Experimental Biology.

[34]  E. Bacha,et al.  The influence of hemodilution on outcome after hypothermic cardiopulmonary bypass: results of a randomized trial in infants. , 2003, The Journal of thoracic and cardiovascular surgery.

[35]  Sang Chul Park,et al.  Analysis of the effect of aging on the response to hypoxia by cDNA microarray , 2003, Mechanisms of Ageing and Development.

[36]  C. Mazer,et al.  Hemodilutional anemia is associated with increased cerebral neuronal nitric oxide synthase gene expression. , 2003, Journal of applied physiology.

[37]  G. Cable In-flight hypoxia incidents in military aircraft: causes and implications for training. , 2003, Aviation, space, and environmental medicine.

[38]  Hymie Anisman,et al.  Conceptual, Spatial, and Cue Learning in the Morris Water Maze in Fast or Slow Kindling Rats: Attention Deficit Comorbidity , 2002, The Journal of Neuroscience.

[39]  J. Kramer,et al.  Oxygen Reverses Deficits of Cognitive Function and Memory and Increased Heart Rate Induced by Acute Severe Isovolemic Anemia , 2002, Anesthesiology.

[40]  F. Amenta,et al.  Microanatomical changes of intracerebral arteries in spontaneously hypertensive rats: a model of cerebrovascular disease of the elderly , 2001, Mechanisms of Ageing and Development.

[41]  Y. Arai,et al.  Magnetic resonance imaging findings and postoperative neurologic dysfunction in elderly patients undergoing coronary artery bypass grafting. , 2001, The Annals of thoracic surgery.

[42]  Guiquan Chen,et al.  A learning deficit related to age and β-amyloid plaques in a mouse model of Alzheimer's disease , 2000, Nature.

[43]  R. Wenger Mammalian oxygen sensing, signalling and gene regulation. , 2000, The Journal of experimental biology.

[44]  A. Levy,et al.  The function of hypoxia‐inducible factor 1 (HIF‐1) is impaired in senescent mice , 1999, FEBS letters.

[45]  P. Rabbitt,et al.  Long-term postoperative cognitive dysfunction in the elderly: ISPOCD1 study , 1998, The Lancet.

[46]  P. S. Wang,et al.  Effect of aging on erythropoietin secretion in male rats. , 1996, The journals of gerontology. Series A, Biological sciences and medical sciences.

[47]  G. Semenza,et al.  Hypoxia-inducible factor 1 is a basic-helix-loop-helix-PAS heterodimer regulated by cellular O2 tension. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[48]  F. Powell,et al.  Oxygen sensing in the brain--invited article. , 2009, Advances in experimental medicine and biology.

[49]  F. Torrealba,et al.  The parietal association cortex of the rat. , 2008, Biological research.

[50]  B. Row,et al.  Intermittent hypoxia and cognitive function: implications from chronic animal models. , 2007, Advances in experimental medicine and biology.

[51]  D. Stewart,et al.  Increased expression of HIF-1alpha, nNOS, and VEGF in the cerebral cortex of anemic rats. , 2007, American journal of physiology. Regulatory, integrative and comparative physiology.

[52]  R. Becker,et al.  Rats Late Treatment With Ramipril Increases Survival in Old Spontaneously Hypertensive , 1999 .