Neurotransmitter and intracellular mechanisms of bipolar disorder; an explanation of Kato's theory of mood-stabilising neurons
References
- Kato T. Molecular neurobiology of bipolar disorder: a disease of ‘mood-stabilizing neurons’? Trends Neurosci. 2008 Oct;31 (10):495-503. https://doi.org/10.1016/j.tins.2008.07.007
- Peet M. Induction of mania with selective serotonin re-uptake inhibitors and tricyclic antidepressants. Br. J. Psychiatry 1994;164:549–550. https://doi.org/10.1192/bjp.164.4.549
- Valentini V et al. Noradrenaline transporter blockers raise extracellular dopamine in medial prefrontal but not parietal and occipital cortex: differences with mianserin and clozapine. J.Neurochem. 2004;88:917–927. https://doi.org/10.1046/j.1471-4159.2003.02238.x
- Zhou QY, Palmiter RD. Dopamine-deficient mice are severely hypoactive, adipsic, and aphagic. Cell 1995;83:1197–1209. https://doi.org/10.1016/0092-8674(95)90145-0
- Nishii K et al. Motor and learning dysfunction during postnatal development in mice defective in dopamine neuronal transmission. J. Neurosci. Res. 1998;54:450–464. https://doi.org/10.1002/(sici)1097-4547(19981115)54:4<450::aid-jnr3>3.0.co;2-b
- Torack RM, Morris, JC. The association of ventral tegmental area histopathology with adult dementia. Arch. Neurol. 1988;’45:497–501. https://doi.org/10.1001/archneur.1988.00520290025008
- Goodwin FK, Jamison KR. Manic-Depressive Illness. 2nd edn. Oxford University Press; 2007.
- Mahmood T, Silverstone T. Serotonin and bipolar disorder. J. Affect. Disord. 2001;66:1–11.
- Kato T. Role of mitochondrial DNA in calcium signalling abnormality in bipolar disorder. Cell Calcium 2008;44:92–102. https://doi.org/10.1016/j.ceca.2007.11.005
- Warsh JJ et al. Role of intracellular calcium signaling in the pathophysiology and pharmacotherapy of bipolar disorder: current status. Clin.Neurosci. Res. 2004;4:201–213. https://doi.org/10.1016/j.cnr.2004.09.012
- Hough C et al. Elevated basal and thapsigargin-stimulated intracellular calcium of platelets and lymphocytes from bipolar affective disorder patients measured by a fluorometric microassay. Biol. Psychiatry 1999;46:247–255. https://doi.org/10.1016/s0006-3223(98)00308-4
- Kato T et al. Mechanisms of altered Ca2+ signalling in transformed lymphoblastoid cells from patients with bipolar disorder. Int. J. Neuropsychopharmacol. 2003;6:379–389. https://doi.org/10.1017/s1461145703003717
- Belmaker RH et al. Reduced inositol content in lymphocyte derived cell lines from bipolar patients. Bipolar Disord. 2002;4:67–69. https://doi.org/10.1034/j.1399-5618.2002.00108.x
- Nemanov L et al. Effect of bipolar disorder on lymphocyte inositol monophosphatase mRNA levels. Int. J.Neuropsychopharmacol. 1999;2:25–29. https://doi.org/10.1017/s1461145799001315
- Yoon IS et al. Altered IMPA2 gene expression and calcium homeostasis in bipolar disorder. Mol. Psychiatry 2001;6:678–683. https://doi.org/10.1038/sj.mp.4000901
- Shamir A et al. Inositol monophosphatase in immortalized lymphoblastoid cell lines indicates susceptibility to bipolar disorder and response to lithium therapy. Mol. Psychiatry 1998;3:481–482. https://doi.org/10.1038/sj.mp.4000470
- Friedman E et al. Altered platelet protein kinase C activity in bipolar affective disorder, manic episode. Biol. Psychiatry 1993;33:520–525. https://doi.org/10.1016/0006-3223(93)90006-y
- Wang HY et al. Increased membrane-associated protein kinase C activity and translocation in blood platelets from bipolar affective disorder patients. J. Psychiatr. Res. 1999;33:171–179. https://doi.org/10.1016/s0022-3956(98)90057-7
- Hahn CG et al. Lithium and valproic acid treatments reduce PKC activation and receptor-G protein coupling in platelets of bipolar manic patients. J. Psychiatr. Res. 2005;39:355–363. https://doi.org/10.1016/j.jpsychires.2004.10.007
- Klein PS, Melton, DA. A molecular mechanism for the effect of lithium on development. Proc. Natl. Acad. Sci. U. S. A. 1996;93:8455–8459. https://doi.org/10.1073/pnas.93.16.8455
- Chen G et al. The mood-stabilizing agent valproate inhibits the activity of glycogen synthase kinase-3. J. Neurochem. 1999;72:1327–1330. https://doi.org/10.1046/j.1471-4159.2000.0721327.x
- Yin L et al. Nuclear receptor Rev-erba is a critical lithium sensitive component of the circadian clock. Science 2006;311:1002–1005. https://doi.org/10.1126/science.1121613
- Kato T et al. Reduction of brain phosphocreatine in bipolar II disorder detected by phosphorus-31 magnetic resonance spectroscopy. J. Affect. Disord. 1994;31:125–133. https://doi.org/10.1016/0165-0327(94)90116-3
- Kato T et al. Alterations in brain phosphorous metabolism in bipolar disorder detected by in vivo 31P and 7Li magnetic resonance spectroscopy. J. Affect. Disord. 1993;27:53–59. https://doi.org/10.1016/0165-0327(93)90097-4
- Dager SR et al. Brain metabolic alterations in medication free patients with bipolar disorder. Arch. Gen. Psychiatry 2004;61:450–458.
- Hamakawa H et al. Quantitative proton magnetic resonance spectroscopy of the bilateral frontal lobes in patients with bipolar disorder. Psychol. Med. 1999;29:639–644. https://doi.org/10.1017/s0033291799008442
- Port JD et al. Metabolic alterations in medication-free patients with bipolar disorder: a 3T CSF- corrected magnetic resonance spectroscopic imaging study. Psychiatry Res. 2008;162:113–121. https://doi.org/10.1016/j.pscychresns.2007.08.004
- Frey BN et al. Abnormal cellular energy and phospholipid metabolism in the left dorsolateral prefrontal cortex of medication free individuals with bipolar disorder: an in vivo 1H MRS study. Bipolar Disord. 2007;9 (Suppl. 1):119–127. https://doi.org/10.1111/j.1399-5618.2007.00454.x
- Suomalainen A et al. Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia. J. Clin. Invest. 1992;90:61–66. https://doi.org/10.1172/jci115856
- Siciliano G et al. Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene. Neuromuscul.Disord. 2003;13:162–165. https://doi.org/10.1016/s0960-8966(02)00221-3
- Fattal O et al. Psychiatric comorbidity in 36 adults with mitochondrial cytopathies. CNS Spectr. 2007;12:429–438. https://doi.org/10.1017/s1092852900015303
- Kato T, Kato, N. Mitochondrial dysfunction in bipolar disorder. Bipolar Disord. 2000;2:180–190. https://doi.org/10.1034/j.1399-5618.2000.020305.x
- Kato T et al. Increased levels of a mitochondrial DNA deletion in the brain of patients with bipolar disorder. Biol. Psychiatry 1997;42:871–875. https://doi.org/10.1016/s0006-3223(97)00012-7
- Konradi C et al. Molecular evidence for mitochondrial dysfunction in bipolar disorder. Arch. Gen. Psychiatry 2004;61:300–308.
- Naydenov AV et al. Differences in lymphocyte electron transport gene expression levels between subjects with bipolar disorder and normal controls in response to glucose deprivation stress. Arch. Gen. Psychiatry 2007;64:555–564. https://doi.org/10.1001/archpsyc.64.5.555
- Van Goethem G et al. Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions. Nat. Genet. 2001;28:211–212. https://doi.org/10.1038/90034
- Kasahara T et al. Mice with neuron-specific accumulation of mitochondrial DNA mutations show mood disorder-like phenotypes. Mol. Psychiatry 2006;11:577–593. https://doi.org/10.1038/sj.mp.4001824
- Kasahara T et al. A marked effect of electroconvulsive stimulation on behavioral aberration of mice with neuron-specific mitochondrial DNA defects. PLoS ONE 2008;3:e1877. https://doi.org/10.1371/journal.pone.0001877
- Kubota M et al. Abnormal Ca2+ dynamics in transgenic mice with neuron-specific mitochondrial DNA defects. J. Neurosci. 2006;26:12314–12324. https://doi.org/10.1523/jneurosci.3933-06.2006
- Andreazza AC et al. Oxidative stress markers in bipolar disorder: a meta-analysis. J. Affect. Disord.
- Reimold AM et al. Plasma cell differentiation requires the transcription factor XBP-1. Nature 2001;412:300–307.
- So J et al. Impaired endoplasmic reticulum stress response in B-lymphoblasts from patients with bipolar-I disorder. Biol. Psychiatry 2007;62:141–147. https://doi.org/10.1016/j.biopsych.2006.10.014
- Hayashi A et al. The role of brain-derived neurotrophic factor (BDNF)-induced XBP1 splicing during brain development. J. Biol.Chem. 2007;282:34525–34534. https://doi.org/10.1074/jbc.m704300200
- Hayashi A et al. Attenuated BDNF-induced upregulation of GABAergic markers in neurons lacking Xbp1. Biochem Biophys Res Commun. 2008;376:758-63. https://doi.org/10.1016/j.bbrc.2008.09.059
- Shim J et al. The unfolded protein response regulates glutamate receptor export from the endoplasmic reticulum. Mol.Biol. Cell 2004;15:4818–4828. https://doi.org/10.1091/mbc.e04-02-0108
- Kuratomi G et al. Aberrant DNA methylation associated with bipolar disorder identified from discordant monozygotic twins. Mol.Psychiatry 2008;13:429–441. https://doi.org/10.1038/sj.mp.4002001
- Videbech P. MRI findings in patients with affective disorder: a meta-analysis. Acta Psychiatr. Scand. 1997;96:157–168. https://doi.org/10.1111/j.1600-0447.1997.tb10146.x
- Manji HK, Duman RS. Impairments of neuroplasticity and cellular resilience in severe mood disorders: implications for the development of novel therapeutics. Psychopharmacol. Bull. 2001;35:5–49. https://doi.org/10.64719/pb.4260
- Benes FM et al. The density of pyramidal and nonpyramidal neurons in anterior cingulate cortex of schizophrenic and bipolar subjects. Biol. Psychiatry 2001;50:395–406. https://doi.org/10.1016/s0006-3223(01)01084-8
- Bouras C et al. Anterior cingulate cortex pathology in schizophrenia and bipolar disorder. Acta Neuropathol. 2001;102:373–379. https://doi.org/10.1007/s004010100392
- Cotter D et al. The density and spatial distribution of GABAergic neurons, labelled using calcium binding proteins, in the anterior cingulate cortex in major depressive disorder, bipolar disorder, and schizophrenia. Biol. Psychiatry 2002;51:377–386. https://doi.org/10.1016/s0006-3223(01)01243-4
- Rajkowska G et al. Reductions in neuronal and glial density characterize the dorsolateral prefrontal cortex in bipolar disorder. Biol. Psychiatry 2001;49:741–752. https://doi.org/10.1016/s0006-3223(01)01080-0
- Beasley CL et al. Selective deficits in prefrontal cortical GABAergic neurons in schizophrenia defined by the presence of calcium-binding proteins. Biol. Psychiatry 2002;52:708–715. https://doi.org/10.1016/s0006-3223(02)01360-4
- Benes FM et al. A reduction of nonpyramidal cells in sector CA2 of schizophrenics and manic depressives. Biol. Psychiatry 1998;44:88–97. https://doi.org/10.1016/s0006-3223(98)00138-3
- Kromkamp M et al. Decreased thalamic expression of the homeobox gene DLX1 in psychosis. Arch. Gen. Psychiatry 2003;60:869–874. https://doi.org/10.1001/archpsyc.60.9.869
- Manaye KF et al. Selective neuron loss in the paraventricular nucleus of hypothalamus in patients suffering from major depression and bipolar disorder. J. Neuropathol. Exp. Neurol. 2005;64: 224–229. https://doi.org/10.1093/jnen/64.3.224
- Nonaka S et al. Chronic lithium treatment robustly protects neurons in the central nervous system against excitotoxicity by inhibiting N-methyl-D-aspartate receptor-mediated calcium influx. Proc. Natl. Acad. Sci. U. S. A. 1998;95:2642–2647. https://doi.org/10.1073/pnas.95.5.2642
- Chen G et al. The mood-stabilizing agents lithium and valproate robustly increase the levels of the neuroprotective protein bcl-2 in the CNS. J. Neurochem. 1999;72:879–882. https://doi.org/10.1046/j.1471-4159.1999.720879.x
- Williams RS et al. A common mechanism of action for three mood-stabilizing drugs. Nature 2002;417:292–295.
- Chen G et al. Enhancement of hippocampal neurogenesis by lithium. J. Neurochem. 2000;75: 1729–1734.
- Hao Y et al. Mood stabilizer valproate promotes ERK pathway-dependent cortical neuronal growth and neurogenesis. J. Neurosci. 2004;24:6590–6599. https://doi.org/10.1523/jneurosci.5747-03.2004
- Laeng P et al. The mood stabilizer valproic acid stimulates GABA neurogenesis from rat forebrain stem cells. J. Neurochem. 2004;91:238–251. https://doi.org/10.1111/j.1471-4159.2004.02725.x
- Klein PS, Melton DA. A molecular mechanism for the effect of lithium on development. Proc. Natl. Acad. Sci. U. S. A. 1996;93:8455–8459. https://doi.org/10.1073/pnas.93.16.8455
- Chen G et al. The mood-stabilizing agent valproate inhibits the activity of glycogen synthase kinase-3. J. Neurochem. 1999;72:1327–1330. https://doi.org/10.1046/j.1471-4159.2000.0721327.x
- Du J et al. Structurally dissimilar antimanic agents modulate synaptic plasticity by regulating AMPA glutamate receptor subunit GluR1 synaptic expression. Ann. N. Y. Acad. Sci. 2003;1003:378–380. https://doi.org/10.1196/annals.1300.031
- Zhou R et al. The anti-apoptotic, glucocorticoid receptor cochaperone protein BAG-1 is a long-term target for the actions of mood stabilizers. J. Neurosci. 2005;25:4493–4502. https://doi.org/10.1523/jneurosci.4530-04.2005
- Basta-Kaim A et al. Mood stabilizers inhibit glucocorticoid receptor function in LMCAT cells. Eur. J. Pharmacol. 2004;495:103–110. https://doi.org/10.1016/j.ejphar.2004.05.034
- Cui J et al. Role of glutathione in neuroprotective effects of mood stabilizing drugs lithium and valproate. Neuroscience 2007;144:1447–1453. https://doi.org/10.1016/j.neuroscience.2006.11.010
- Higashi M et al. Mood stabilizing drugs expand the neural stem cell pool in the adult brain through activation of notch signaling. Stem Cells 2008;26:1758–1767. https://doi.org/10.1634/stemcells.2007-1032
- Leng Y et al. Synergistic neuroprotective effects of lithium and valproic acid or other histone deacetylase inhibitors in neurons: roles of glycogen synthase kinase-3 inhibition. J. Neurosci. 2008;28:2576–2588. https://doi.org/10.1523/jneurosci.5467-07.2008
- Brennan BP et al. Rapid Enhancement of Glutamatergic Neurotransmission in Bipolar Depression Following Treatment with Riluzole. Neuropsychopharmacology 2010;35:834-846. https://doi.org/10.1038/npp.2009.191
- Post RM, Weiss SR. A speculative model of affective illness cyclicity based on patterns of drug tolerance observed in amygdala-kindled seizures. Mol. Neurobiol. 1996;13:33–60. https://doi.org/10.1007/bf02740751
- Levinson AJ et al. Cortical inhibitory dysfunction in bipolar disorder: a study using transcranial magnetic stimulation. J. Clin. Psychopharmacol. 2007;27:493–497. https://doi.org/10.1097/jcp.0b013e31814ce524
- Benes FM et al. A reduction of nonpyramidal cells in sector CA2 of schizophrenics and manic depressives. Biol. Psychiatry 1998;44:88–97. https://doi.org/10.1016/s0006-3223(98)00138-3
- Benes FM et al. Regulation of the GABA cell phenotype in hippocampus of schizophrenics and bipolars. Proc. Natl. Acad. Sci. U.S. A. 2007;104:10164–10169. https://doi.org/10.1073/pnas.0703806104
- Lewy AJ et al. Manic-depressive patients may be supersensitive to light. Lancet 1981;1:383–384. https://doi.org/10.1016/s0140-6736(81)91697-4
- Frank E et al. Interpersonal and social rhythm therapy: an intervention addressing rhythm dysregulation in bipolar disorder. Dialogues Clin.Neurosci. 2007;9:325–332. https://doi.org/10.31887/dcns.2007.9.3/efrank