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Published in: Metabolic Brain Disease 4/2013

01-12-2013 | Original Paper

Altered expression of histone and synaptic plasticity associated genes in the hippocampus of streptozotocin-induced diabetic mice

Authors: Jency Thomas, Manohar L. Garg, Doug W. Smith

Published in: Metabolic Brain Disease | Issue 4/2013

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Abstract

Accumulating evidence indicates that hyper-glycaemia is deleterious to brain function, in particular to the hippocampus. It is thought this hippocampal dysfunction may contribute to hyperglycaemia related cognitive impairment, such as that which manifests with diabetes. In the present study, we investigated the effects of diabetes-related hyperglycaemia on hippocampal gene expression, in order to identify potential mechanisms that might be associated with the cognitive dysfunction that develops with diabetes mellitus. Genome-wide gene expression profiling was carried out on the hippocampi from streptozotocin (STZ)-induced diabetic mice, and from vehicle treated control mice. Genes of interest that satisfied expression fold-change and statistical criteria, and that were considered to be potentially associated with cognitive function, were further tested by real time, quantitative polymerase chain reaction (qPCR) analysis. We found that STZ-induced diabetes resulted in decreased hippocampal expression of genes involved in epigenetic regulation and synaptic plasticity, for example, histone deacetylases and glycogen synthase kinase 3 beta (HDACs and GSK3β). We also found increased expression of genes involved in signalling cascades related to cell growth, cell survival and energy metabolism, such as neurotropic tyrosine kinase receptor type 2, apolipoprotein E, and protein tyrosine phosphatase receptor type (Ntrk2, APOE, PTPRT). To our knowledge this is the first study to demonstrate a gene expression profile implicating epigenetic modifications and alterations of synaptic plasticity associated genes in diabetes mellitus. The present study will improve our understanding of the neural mechanisms that might underpin diabetes-related cognitive dysfunction.
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Literature
go back to reference Abdul-Rahman O et al (2012) Altered gene expression profiles in the hippocampus and prefrontal cortex of type 2 diabetic rats. BMC Genomics 13:81PubMedCrossRef Abdul-Rahman O et al (2012) Altered gene expression profiles in the hippocampus and prefrontal cortex of type 2 diabetic rats. BMC Genomics 13:81PubMedCrossRef
go back to reference Agis-Balboa RC et al (2012) Loss of HDAC5 impairs memory function: implications for Alzheimer’s disease. J Alzheimers Dis 33(1):35–44 Agis-Balboa RC et al (2012) Loss of HDAC5 impairs memory function: implications for Alzheimer’s disease. J Alzheimers Dis 33(1):35–44
go back to reference Alberini CM et al (2012) Memory enhancement: consolidation, reconsolidation and insulin-like growth factor 2. Trends Neurosci 35(5):274–283PubMedCrossRef Alberini CM et al (2012) Memory enhancement: consolidation, reconsolidation and insulin-like growth factor 2. Trends Neurosci 35(5):274–283PubMedCrossRef
go back to reference Alipio Z et al (2010) Reversal of hyperglycemia in diabetic mouse models using induced-pluripotent stem (iPS)-derived pancreatic beta-like cells. Proc Natl Acad Sci U S A 107(30):13426–13431PubMedCrossRef Alipio Z et al (2010) Reversal of hyperglycemia in diabetic mouse models using induced-pluripotent stem (iPS)-derived pancreatic beta-like cells. Proc Natl Acad Sci U S A 107(30):13426–13431PubMedCrossRef
go back to reference Alvarez EO et al (2009) Cognitive dysfunction and hippocampal changes in experimental type 1 diabetes. Behav Brain Res 198(1):224–230PubMedCrossRef Alvarez EO et al (2009) Cognitive dysfunction and hippocampal changes in experimental type 1 diabetes. Behav Brain Res 198(1):224–230PubMedCrossRef
go back to reference Beauquis J et al (2009) Neuronal plasticity and antidepressants in the diabetic brain. Ann N Y Acad Sci 1153:203–208PubMedCrossRef Beauquis J et al (2009) Neuronal plasticity and antidepressants in the diabetic brain. Ann N Y Acad Sci 1153:203–208PubMedCrossRef
go back to reference Chen DY et al (2011) A critical role for IGF-II in memory consolidation and enhancement. Nature 469(7331):491–497PubMedCrossRef Chen DY et al (2011) A critical role for IGF-II in memory consolidation and enhancement. Nature 469(7331):491–497PubMedCrossRef
go back to reference Deng W et al (2010) New neurons and new memories: how does adult hippocampal neurogenesis affect learning and memory? Nat Rev Neurosci 11(5):339–350PubMedCrossRef Deng W et al (2010) New neurons and new memories: how does adult hippocampal neurogenesis affect learning and memory? Nat Rev Neurosci 11(5):339–350PubMedCrossRef
go back to reference Eldar-Finkelman H (2002) Glycogen synthase kinase 3: an emerging therapeutic target. Trends Mol Med 8(3):126–132PubMedCrossRef Eldar-Finkelman H (2002) Glycogen synthase kinase 3: an emerging therapeutic target. Trends Mol Med 8(3):126–132PubMedCrossRef
go back to reference Ferguson SC et al (2003) Apolipoprotein-e influences aspects of intellectual ability in type 1 diabetes. Diabetes 52(1):145–148PubMedCrossRef Ferguson SC et al (2003) Apolipoprotein-e influences aspects of intellectual ability in type 1 diabetes. Diabetes 52(1):145–148PubMedCrossRef
go back to reference Garrido JJ et al (2007) GSK3 alpha and GSK3 beta are necessary for axon formation. FEBS Lett 581(8):1579–1586PubMedCrossRef Garrido JJ et al (2007) GSK3 alpha and GSK3 beta are necessary for axon formation. FEBS Lett 581(8):1579–1586PubMedCrossRef
go back to reference Gatto G et al (2013) Protein tyrosine phosphatase receptor type O inhibits trigeminal axon growth and branching by repressing TrkB and Ret signaling. J Neurosci 33(12):5399–5410PubMedCrossRef Gatto G et al (2013) Protein tyrosine phosphatase receptor type O inhibits trigeminal axon growth and branching by repressing TrkB and Ret signaling. J Neurosci 33(12):5399–5410PubMedCrossRef
go back to reference Gispen WH et al (2000) Cognition and synaptic plasticity in diabetes mellitus. Trends Neurosci 23(11):542–549PubMedCrossRef Gispen WH et al (2000) Cognition and synaptic plasticity in diabetes mellitus. Trends Neurosci 23(11):542–549PubMedCrossRef
go back to reference Greenwood PM et al (2010) Neuronal and cognitive plasticity: a neurocognitive framework for ameliorating cognitive aging. Front Aging Neurosci 2:150PubMedCrossRef Greenwood PM et al (2010) Neuronal and cognitive plasticity: a neurocognitive framework for ameliorating cognitive aging. Front Aging Neurosci 2:150PubMedCrossRef
go back to reference Guo JT et al (2002) Inflammation-dependent cerebral deposition of serum amyloid a protein in a mouse model of amyloidosis. J Neurosci 22(14):5900–5909PubMed Guo JT et al (2002) Inflammation-dependent cerebral deposition of serum amyloid a protein in a mouse model of amyloidosis. J Neurosci 22(14):5900–5909PubMed
go back to reference Guo J et al (2010) Impaired neural stem/progenitor cell proliferation in streptozotocin-induced and spontaneous diabetic mice. Neurosci Res 68(4):329–336PubMedCrossRef Guo J et al (2010) Impaired neural stem/progenitor cell proliferation in streptozotocin-induced and spontaneous diabetic mice. Neurosci Res 68(4):329–336PubMedCrossRef
go back to reference Jackson-Guilford J et al (2000) The effect of streptozotocin-induced diabetes on cell proliferation in the rat dentate gyrus. Neurosci Lett 293(2):91–94PubMedCrossRef Jackson-Guilford J et al (2000) The effect of streptozotocin-induced diabetes on cell proliferation in the rat dentate gyrus. Neurosci Lett 293(2):91–94PubMedCrossRef
go back to reference Jafari Anarkooli I et al (2008) Evaluation of Bcl-2 family gene expression and Caspase-3 activity in hippocampus STZ-induced diabetic rats. Exp Diabetes Res 2008:638467PubMedCrossRef Jafari Anarkooli I et al (2008) Evaluation of Bcl-2 family gene expression and Caspase-3 activity in hippocampus STZ-induced diabetic rats. Exp Diabetes Res 2008:638467PubMedCrossRef
go back to reference Jope RS et al (2004) The glamour and gloom of glycogen synthase kinase-3. Trends Biochem Sci 29(2):95–102PubMedCrossRef Jope RS et al (2004) The glamour and gloom of glycogen synthase kinase-3. Trends Biochem Sci 29(2):95–102PubMedCrossRef
go back to reference Kim WY et al (2009) GSK-3 is a master regulator of neural progenitor homeostasis. Nat Neurosci 12(11):1390–1397PubMedCrossRef Kim WY et al (2009) GSK-3 is a master regulator of neural progenitor homeostasis. Nat Neurosci 12(11):1390–1397PubMedCrossRef
go back to reference Kim MS et al (2012) An essential role for histone deacetylase 4 in synaptic plasticity and memory formation. J Neurosci 32(32):10879–10886PubMedCrossRef Kim MS et al (2012) An essential role for histone deacetylase 4 in synaptic plasticity and memory formation. J Neurosci 32(32):10879–10886PubMedCrossRef
go back to reference Koponen E et al (2004) Overexpression of the full-length neurotrophin receptor trkB regulates the expression of plasticity-related genes in mouse brain. Brain Res Mol Brain Res 130(1–2):81–94PubMedCrossRef Koponen E et al (2004) Overexpression of the full-length neurotrophin receptor trkB regulates the expression of plasticity-related genes in mouse brain. Brain Res Mol Brain Res 130(1–2):81–94PubMedCrossRef
go back to reference Lim SH et al (2009) Synapse formation regulated by protein tyrosine phosphatase receptor T through interaction with cell adhesion molecules and Fyn. EMBO J 28(22):3564–3578PubMedCrossRef Lim SH et al (2009) Synapse formation regulated by protein tyrosine phosphatase receptor T through interaction with cell adhesion molecules and Fyn. EMBO J 28(22):3564–3578PubMedCrossRef
go back to reference Lu B et al (2008) Cell biology of BDNF and its relevance to schizophrenia. Novartis Found Symp 289:119–129, discussion 129–35, 193–5PubMedCrossRef Lu B et al (2008) Cell biology of BDNF and its relevance to schizophrenia. Novartis Found Symp 289:119–129, discussion 129–35, 193–5PubMedCrossRef
go back to reference Lubin FD et al (2011) Epigenetic mechanisms: critical contributors to long-term memory formation. Neuroscientist 17(6):616–632PubMedCrossRef Lubin FD et al (2011) Epigenetic mechanisms: critical contributors to long-term memory formation. Neuroscientist 17(6):616–632PubMedCrossRef
go back to reference Ma LY et al (2011) Ghrelin-attenuated cognitive dysfunction in streptozotocin-induced diabetic rats. Alzheimer Dis Assoc Disord 25(4):352–363PubMedCrossRef Ma LY et al (2011) Ghrelin-attenuated cognitive dysfunction in streptozotocin-induced diabetic rats. Alzheimer Dis Assoc Disord 25(4):352–363PubMedCrossRef
go back to reference Malone JI et al (2008) Hyperglycemia not hypoglycemia alters neuronal dendrites and impairs spatial memory. Pediatr Diabetes 9(6):531–539PubMedCrossRef Malone JI et al (2008) Hyperglycemia not hypoglycemia alters neuronal dendrites and impairs spatial memory. Pediatr Diabetes 9(6):531–539PubMedCrossRef
go back to reference Marzluff WF et al (2002) The human and mouse replication-dependent histone genes. Genomics 80(5):487–498PubMedCrossRef Marzluff WF et al (2002) The human and mouse replication-dependent histone genes. Genomics 80(5):487–498PubMedCrossRef
go back to reference Marzluff WF et al (2008) Metabolism and regulation of canonical histone mRNAs: life without a poly(A) tail. Nat Rev Genet 9(11):843–854PubMedCrossRef Marzluff WF et al (2008) Metabolism and regulation of canonical histone mRNAs: life without a poly(A) tail. Nat Rev Genet 9(11):843–854PubMedCrossRef
go back to reference McNay EC et al (2010) Hippocampal memory processes are modulated by insulin and high-fat-induced insulin resistance. Neurobiol Learn Mem 93(4):546–553PubMedCrossRef McNay EC et al (2010) Hippocampal memory processes are modulated by insulin and high-fat-induced insulin resistance. Neurobiol Learn Mem 93(4):546–553PubMedCrossRef
go back to reference Ming GL et al (2011) Adult neurogenesis in the mammalian brain: significant answers and significant questions. Neuron 70(4):687–702PubMedCrossRef Ming GL et al (2011) Adult neurogenesis in the mammalian brain: significant answers and significant questions. Neuron 70(4):687–702PubMedCrossRef
go back to reference Minichiello L (2009) TrkB signalling pathways in LTP and learning. Nat Rev Neurosci 10(12):850–860PubMedCrossRef Minichiello L (2009) TrkB signalling pathways in LTP and learning. Nat Rev Neurosci 10(12):850–860PubMedCrossRef
go back to reference Mirnics K et al (2004) Progress in the use of microarray technology to study the neurobiology of disease. Nat Neurosci 7(5):434–439PubMedCrossRef Mirnics K et al (2004) Progress in the use of microarray technology to study the neurobiology of disease. Nat Neurosci 7(5):434–439PubMedCrossRef
go back to reference Reagan LP et al (1999) Neurological changes induced by stress in streptozotocin diabetic rats. Ann N Y Acad Sci 893:126–137PubMedCrossRef Reagan LP et al (1999) Neurological changes induced by stress in streptozotocin diabetic rats. Ann N Y Acad Sci 893:126–137PubMedCrossRef
go back to reference Revsin Y et al (2005) Neuronal and astroglial alterations in the hippocampus of a mouse model for type 1 diabetes. Brain Res 1038(1):22–31PubMedCrossRef Revsin Y et al (2005) Neuronal and astroglial alterations in the hippocampus of a mouse model for type 1 diabetes. Brain Res 1038(1):22–31PubMedCrossRef
go back to reference Richter-Schmidinger T et al (2011) Influence of brain-derived neurotrophic-factor and apolipoprotein E genetic variants on hippocampal volume and memory performance in healthy young adults. J Neural Transm 118(2):249–257PubMedCrossRef Richter-Schmidinger T et al (2011) Influence of brain-derived neurotrophic-factor and apolipoprotein E genetic variants on hippocampal volume and memory performance in healthy young adults. J Neural Transm 118(2):249–257PubMedCrossRef
go back to reference Schmittgen TD et al (2008) Analyzing real-time PCR data by the comparative C(T) method. Nat Protoc 3(6):1101–1108PubMedCrossRef Schmittgen TD et al (2008) Analyzing real-time PCR data by the comparative C(T) method. Nat Protoc 3(6):1101–1108PubMedCrossRef
go back to reference Stranahan AM et al (2008) Diabetes impairs hippocampal function through glucocorticoid-mediated effects on new and mature neurons. Nat Neurosci 11(3):309–317PubMedCrossRef Stranahan AM et al (2008) Diabetes impairs hippocampal function through glucocorticoid-mediated effects on new and mature neurons. Nat Neurosci 11(3):309–317PubMedCrossRef
go back to reference Tesch GH, Allen TJ (2007) Rodent models of streptozotocin-induced diabetic nephropathy. Nephrology (Carlton) 12(3):261–266CrossRef Tesch GH, Allen TJ (2007) Rodent models of streptozotocin-induced diabetic nephropathy. Nephrology (Carlton) 12(3):261–266CrossRef
go back to reference Tolwani RJ et al (2002) BDNF overexpression increases dendrite complexity in hippocampal dentate gyrus. Neuroscience 114(3):795–805PubMedCrossRef Tolwani RJ et al (2002) BDNF overexpression increases dendrite complexity in hippocampal dentate gyrus. Neuroscience 114(3):795–805PubMedCrossRef
go back to reference Wexler EM et al (2009) Endogenous Wnt signaling maintains neural progenitor cell potency. Stem Cells 27(5):1130–1141PubMedCrossRef Wexler EM et al (2009) Endogenous Wnt signaling maintains neural progenitor cell potency. Stem Cells 27(5):1130–1141PubMedCrossRef
go back to reference Yang T et al (2006) LAR protein tyrosine phosphatase receptor associates with TrkB and modulates neurotrophic signaling pathways. J Neurobiol 66(13):1420–1436PubMedCrossRef Yang T et al (2006) LAR protein tyrosine phosphatase receptor associates with TrkB and modulates neurotrophic signaling pathways. J Neurobiol 66(13):1420–1436PubMedCrossRef
go back to reference Zhang WJ et al (2008) Impairment of hippocampal neurogenesis in streptozotocin-treated diabetic rats. Acta Neurol Scand 117(3):205–210PubMedCrossRef Zhang WJ et al (2008) Impairment of hippocampal neurogenesis in streptozotocin-treated diabetic rats. Acta Neurol Scand 117(3):205–210PubMedCrossRef
go back to reference Zhang X et al (2013) Endoplasmic reticulum stress-mediated hippocampal neuron apoptosis involved in diabetic cognitive impairment. Biomed Res Int 2013:924327PubMed Zhang X et al (2013) Endoplasmic reticulum stress-mediated hippocampal neuron apoptosis involved in diabetic cognitive impairment. Biomed Res Int 2013:924327PubMed
Metadata
Title
Altered expression of histone and synaptic plasticity associated genes in the hippocampus of streptozotocin-induced diabetic mice
Authors
Jency Thomas
Manohar L. Garg
Doug W. Smith
Publication date
01-12-2013
Publisher
Springer US
Published in
Metabolic Brain Disease / Issue 4/2013
Print ISSN: 0885-7490
Electronic ISSN: 1573-7365
DOI
https://doi.org/10.1007/s11011-013-9418-y

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