Dopamine Problems? Blame the Hippocampus
13 November 2007. The dopamine hypothesis of schizophrenia, which proposes that dysfunction in the brain’s dopamine (DA) system causes some of the symptoms of schizophrenia, is one of the most venerable and influential biological theories of the disease (see Current Hypothesis by A. Abi-Dargham). In recent years it has been proposed that the dysregulation of the DA system observed in schizophrenia is due not to abnormalities in the system itself, but is the result of aberrant regulation of the system by other networks (see e.g., Grace, 2000; Abi-Dargham, 2004). In a new study employing a rat model of schizophrenia, Anthony Grace and Daniel Lodge at the University of Pittsburgh provide electrophysiological and behavioral evidence that disruptions in the ventral hippocampus can cause abnormal signaling in DA pathways that ascend from the ventral tegmental area (VTA) to subcortical and cortical targets in the forebrain. The subcortical (mesolimbic) and cortical (mesocortical) DA pathways have each been implicated in symptoms of schizophrenia.
MAM to dams
Grace’s group has argued that hippocampal dysfunction, which has been reported in schizophrenia, could impact dopamine neurotransmission via a multisynaptic pathway from the output center of the hippocampus—the ventral hippocampus (vHipp), or subiculum—to the VTA. (The full pathway is vHipp to nucleus accumbens to ventral pallidum to VTA.) In a report in the October 17 issue of The Journal of Neuroscience, the researchers examine this circuit in the methylazoxymethanol acetate (MAM) model of schizophrenia, in which a DNA methylating agent is administered to pregnant rat dams on the seventeenth day of gestation. As reviewed by Lodge and Grace, this technique has been shown to cause anatomical, behavioral, and electrophysiological abnormalities in adult offspring that are reminiscent of those seen in human patients with schizophrenia.
When Lodge and Grace made in vivo extracellular recordings from DA neurons in the ventral tegmental area (VTA), the adult rats that had been exposed to MAM in utero showed almost twice as much spontaneous neural activity as control rats. In parallel, the authors indeed found that the average firing rate in neurons of the vHipp of MAM-treated rats was more than twice as high as that seen in controls. When they chemically inactivated the vHipp with tetrodotoxin (TTX), the researchers found that they had abolished the increased spontaneous VTA activity in MAM-treated rats. The TTX treatment had no effect on DA neuron activity in control animals. These results were supported by experiments in which the rats were injected with D-amphetamine, an indirect dopamine agonist that is known to cause abnormally large responses in animal models of schizophrenia and in human schizophrenia patients. The MAM-treated rats showed considerably more locomotor activity than controls after amphetamine treatment, but their behavior fell within normal range after TTX inactivation of the vHipp.
Taken together, Lodge and Grace write, these results indicate that the baseline activity of dopaminergic neurons in the VTA are regulated by the ventral hippocampus, and that the disruptions in dopamine signaling associated with schizophrenia may be caused by the hippocampal abnormalities reported in the disease. The authors are circumspect about the limitations of the animal model they used in these experiments. “Nonetheless,” they write, “we posit that at the core of this disorder is a disruption of systems interactions that can be modeled in animals, but when placed in the context of complex human brain and behavioral patterns, yields the complex pattern of psychopathology recognized as schizophrenia.”—Peter Farley.
Lodge DJ, Grace AA. Aberrant hippocampal activity underlies the dopamine dysregulation in an animal model of schizophrenia. J Neurosci. 2007 Oct 17;27(42):11424-30. Abstract
Comments on News and Primary Papers
Comment by: Anissa Abi-Dargham, SRF Advisor
Submitted 29 November 2007
Posted 29 November 2007
What struck me most about the paper of Lodge and Grace is the overall consistency of the body of work between the preclinical and clinical observations, even down to the effect size for the dopaminergic alteration. Dopamine release in schizophrenia is at least double that in controls; whether measured after amphetamine (on average 17 percent displacement of the benzamide radiotracer versus 7 percent in controls) (Laruelle et al., 1999) or at baseline (19 percent D2 occupancy by dopamine in patients versus 9 percent in controls) (Abi-Dargham et al., 2000), the increase in dopamine activity in VTA of the MAM rats reported here is also a doubling of what is measured in saline-treated rats.
This work presents an important contribution to the field because it clarifies the role of the hippocampus in one of the cardinal features of the disorder as modeled in MAM rats. The fact that MAM treatment is one of the most valid animal models of schizophrenia—it replicates many of the disturbances, neurochemical, cellular, dendritic, morphometric, and behavioral, observed in schizophrenia—makes the finding very compelling.
The role of an abnormal hippocampal node in an important circuit central to the pathophysiology of schizophrenia has face validity: there are now many converging lines of evidence in patients with schizophrenia for alterations in hippocampal volume, cytoarchitecture, function, and neurochemical indices. What this paper presents that is unique is evidence, in a valid model of schizophrenia, for an etiological link between the faulty hippocampus and the faulty VTA. The next step will be to test an association between pathology of the hippocampus and that of the VTA and related striatal output in patients with schizophrenia. This is a study we currently are conducting, and is an example of translational research where a theory gets support and contributions by going back and forth between preclinical and clinical testing. If there is an association in the same patients between the hippocampal pathology and dopamine dysregulation, it will suggest that what is described for the MAM model here may be true for schizophrenia, too, i.e., that the pathology of the dopamine system is driven by a faulty hippocampal input.
Laruelle M, Abi-Dargham A, Gil R, Kegeles L, Innis R. Increased dopamine transmission in schizophrenia: relationship to illness phases. Biol Psychiatry. 1999;46:56-72. Abstract
Abi-Dargham A, Rodenhiser J, Printz D, Zea-Ponce Y, Gil R, Kegeles LS, Weiss R, Cooper TB, Mann JJ, Van Heertum RL, Gorman JM, Laruelle M. Increased baseline occupancy of D2 receptors by dopamine in schizophrenia. Proc Natl Acad Sci U S A. 2000;97:8104-8109. Abstract
View all comments by Anissa Abi-DarghamComment by: Elizabeth Tunbridge
Submitted 20 December 2007
Posted 20 December 2007
I recommend the Primary Papers
In their recent paper Lodge and Grace elegantly demonstrate that hyperactivity of the ventral hippocampus underlies the elevated number of spontaneously active ventral tegmental dopamine neurons, and the concomitant increase in amphetamine-induced locomotor activity, found in MAM-treated rats. Since neonatal MAM treatment recapitulates some of the neurochemical, anatomical, and behavioral abnormalities associated with schizophrenia, these findings raise the possibility that the abnormal subcortical dopamine function associated with this disorder might also result from hippocampal dysfunction.
These findings are consistent with a wealth of evidence suggesting that the hippocampus is a prominent site of dysfunction in the schizophrenic brain (reviewed in Harrison, 2004), and it will be exciting to see the results of the clinical studies described by Anissa Abi-Dargham above.
In the future, it will be important to try to integrate these findings with other models aiming to explain the subcortical dopaminergic hyperactivity seen in schizophrenia. One well-known hypothesis is that these abnormalities might result from hypofunction of the prefrontal cortex (PFC; Weinberger, 1987; Bertolino et al., 2000). Animal studies demonstrate that PFC activity impacts on striatal dopamine function (e.g., Shim et al., 1996) and vice versa (Kellendonk et al., 2006). Thus, it will be of interest to assess the relative contributions of hippocampal and prefrontal dysfunction to these subcortical abnormalities in schizophrenia. Such investigations will necessarily involve the use of both patient populations and appropriate animal model systems. A difficult question will be to establish whether any one of these three regions represents a site of a primary “lesion” in schizophrenia or, perhaps more likely, whether their dysfunction reflects abnormalities in the circuits that link them.
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Harrison PJ. The hippocampus in schizophrenia: a review of the neuropathological evidence and its pathophysiological implications.
Psychopharmacology (Berl). 2004 Jun;174(1):151-62. Epub 2004 Mar 6. Review.
Kellendonk C, Simpson EH, Polan HJ, Malleret G, Vronskaya S, Winiger V, Moore H, Kandel ER. Transient and selective overexpression of dopamine D2 receptors in the striatum causes persistent abnormalities in prefrontal cortex functioning. Neuron. 2006 Feb 16;49(4):603-15.
Shim SS, Bunney BS, Shi WX. Effects of lesions in the medial prefrontal cortex on the activity of midbrain dopamine neurons. Neuropsychopharmacology. 1996 Nov;15(5):437-41.
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View all comments by Elizabeth Tunbridge
Comments on Related News
Related News: SfN 2013—Different Roads to Dopamine Dysfunction in SchizophreniaComment by: Melkaye Melka
Submitted 5 December 2013
Posted 9 December 2013
Atypical antipsychotics have been used to treat psychiatric disorders such as schizophrenia. However, the mechanisms of action of antipsychotics remain poorly understood. On the other hand, dopamine neurons form the focus of attention in the etiology and pathophysiology of schizophrenia. As noted by Michele Solis’ snapshot from the conference, the work of Grace and colleagues showed that prenatal injections of methylazoxymethanol acetate (MAM), a DNA-methylating agent, lead to hyperactive dopamine signaling (Moore et al., 2006). Focusing on the mechanisms of action, previous studies have suggested that antipsychotic drugs may cause promoter methylation of genes involved in psychosis (Dong et al., 2009). DNA methylation changes have also been associated with major psychosis (Mill et al., 2008).
In a recent in-vivo study, we have observed organ-specific (hippocampus, cerebellum, and liver) changes in DNA methylation following a therapeutic dose of a model antipsychotic drug (olanzapine) (Melka et al., 2013, in press). In particular, we noted that the dopamine signaling pathway was one of the most significant networks affected by olanzapine-induced DNA methylation changes. Specifically, the results showed that olanzapine significantly alters promoter DNA methylation of genes involved in dopamine synthesis, transport, receptors, and metabolism. These results support a dopamine hypothesis of psychosis and a role for epigenetic mechanisms in the development of psychosis, as well as its treatment with antipsychotic drugs. Given that some of the genes affected are tissue specific and affect a variety of networks, our results could also explain the delayed therapeutic response of antipsychotics as well as their patient-specific efficacy and side effects.
Dong E, Grayson DR, Guidotti A, Costa E. Antipsychotic subtypes can be characterized by differences in their ability to modify GABAergic promoter methylation: Epigenomics 2009; 1: 201-1. Abstract
Melka MG, Castellani CA, Laufer BI, Rajakumar N, O’Reilly R and Singh SM. Olanzapine induced DNA methylation changes support the dopamine hypothesis of psychosis. J Mol Psychiatry; 2013; 1:19. (In press)
Mill J, Tang T, Kaminsky Z, Khare T, Yazdanpanah S, Bouchard L, Jia P, Assadzadeh A, Flanagan J, Schumacher A, Wang SC, Petronis A. Epigenomic profiling reveals DNA-methylation changes associated with major psychosis. Am J Hum Genet . 2008 Mar ; 82(3):696-711. Abstract
Moore H, Jentsch JD, Ghajarnia M, Geyer MA, Grace AA. A neurobehavioral systems analysis of adult rats exposed to methylazoxymethanol acetate on E17: implications for the neuropathology of schizophrenia. Biol Psychiatry . 2006 Aug 1 ; 60(3):253-64. Abstract
View all comments by Melkaye Melka