The paraventricular nucleus of the thalamus: a hub in the neural network for fear and anxiety

dc.contributor.authorDong, Xinwen
dc.contributor.examiningcommitteeBhullar, Rajinder (Oral Biology) Jackson, Michael (Pharmacology and Therapeutics) Ghia, Jean-Eric (Immunology) McNally, Gavan (University of New South Wales)en_US
dc.contributor.supervisorKirouac, Gilbert (Oral Biology)en_US
dc.date.accessioned2020-06-10T18:46:20Z
dc.date.available2020-06-10T18:46:20Z
dc.date.copyright2020-06-07
dc.date.issued2020-06en_US
dc.date.submitted2020-06-08T03:17:49Zen_US
dc.degree.disciplineOral Biologyen_US
dc.degree.levelDoctor of Philosophy (Ph.D.)en_US
dc.description.abstractThe paraventricular nucleus of the thalamus (PVT) is a part of a group of the midline and intralaminar thalamic nuclei. The PVT receives and sends projections to brain regions essential for fear and anxiety indicating that the PVT may be a critical hub in the brain's fear and anxiety network. This thesis presents a series of studies investigating the involvement of the PVT and its projection in fear and anxiety. The first study showed that lesions of the PVT attenuated the expression of conditioned fear while blocking orexin receptors in the PVT had no effect on fear but reduced anxiety. These findings can be potentially viewed as evidence that the PVT regulates different defensive responses independently via unique groups of neurons that project to different basal forebrain nuclei. The second study used a dual-retrograde-tracing strategy to determine whether the PVT contains distinct subpopulations of neurons that project to the shell of the nucleus accumbens (NAcSh), the dorsolateral part of the bed nucleus of the stria terminalis (BSTDL), and the lateral part of the central nucleus of the amygdala (CeL). This study revealed that most neurons in the PVT innervate the NAcSh and that many neurons project to more than one brain region. In addition, PVT neurons that project to the NAcSh, BSTDL, or CeL did not appear to be activated differentially when rats were exposed to footshocks or an open field. These results suggest that the PVT may contribute to stress-induced fear and anxiety through its projection to the NAcSh. The third study examined the involvement of the PVT-NAcSh projection in fear and anxiety using an intersectional chemogenetic technique. The result showed that selective inhibition of PVT neurons that innervate NAcSh reduced footshock-induced social anxiety in susceptible rats but not conditioned fear. In summary, experiments in this thesis demonstrate that the PVT contributes to conditioned fear and stress-induced anxiety and point to the possibility that the PVT may coordinate defensive responses by acting on the NAcSh, BSTDL, and CeL.en_US
dc.description.noteOctober 2020en_US
dc.identifier.citationDong, X., Li, Y., & Kirouac, G. J. (2015). Blocking of orexin receptors in the paraventricular nucleus of the thalamus has no effect on the expression of conditioned fear in rats. Frontiers in Behavioral Neuroscience, 9(June), 161. https://doi.org/10.3389/fnbeh.2015.00161en_US
dc.identifier.citationDong, X., Li, S., & Kirouac, G. J. (2017). Collateralization of projections from the paraventricular nucleus of the thalamus to the nucleus accumbens, bed nucleus of the stria terminalis, and central nucleus of the amygdala. Brain Structure and Function, 222(9), 3927–3943. https://doi.org/10.1007/s00429-017-1445-8en_US
dc.identifier.citationLi, Y., Dong, X., Li, S., & Kirouac, G. J. (2014). Lesions of the posterior paraventricular nucleus of the thalamus attenuate fear expression. Frontiers in Behavioral Neuroscience, 8(March), 94. https://doi.org/10.3389/fnbeh.2014.00094en_US
dc.identifier.urihttp://hdl.handle.net/1993/34711
dc.language.isoengen_US
dc.rightsopen accessen_US
dc.subjectParaventricular nucleus of the thalamusen_US
dc.subjectAnxietyen_US
dc.subjectFearen_US
dc.subjectEmotionen_US
dc.subjectNucleus accumbensen_US
dc.subjectChemogeneticen_US
dc.titleThe paraventricular nucleus of the thalamus: a hub in the neural network for fear and anxietyen_US
dc.typedoctoral thesisen_US
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