Browsing by Subject "Gz"
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Item Open Access Electrophysiology of Gαz protein as a mediator for seizure susceptibility(2016-05-06) Boms, OkechiSeizures are marked by a state of irregular, recurrent neuronal activity in the brain. Seizures are typical across a wide range of disorders including epilepsy, autism, and they are high comorbidity with anxiety disorders. In the mouse model, increased levels of brain-derived neurotrophic factor (BDNF) have been linked to increased seizure susceptibility. Gαz, a member of the G-protein family, is important for the negative regulation of BDNF; Gαz-null show more BDNF-regulated axon growth. We postulated that since Gαz-null mice have increased levels of BDNF, Gαz might play a role in mediating seizure susceptibility. A previous study from our lab showed that Gαz -null mice were in fact more susceptible to seizures than wildtype (WT) mice. This study was conducted to characterize neuronal seizure activity and progression across different brain regions for this genetic model. Electrodes were implanted into the brains of WT and Gαz -null mice to record the local field potential (LFPs), proxy for relative activity, during induced seizure by the pilocarpine (180mg/kg) drug. LFP data was recorded simultaneously from 6 brain regions: amygdala, dorsal hippocampus, motor cortex, somatosensory cortex, ventral hippocampus, and thalamus. The Gαz -null mice had more severe seizure behavior and more robust electrographic activity in comparison to the WT group. The site of seizure onset and progression for the WT group closely matches the pattern from other studies, while the Gαz -null mice showed a novel pattern. The behavioral and electrographic results confirm the role of Gαz in mediating seizure severity and susceptibility; further studies will be needed to confirm the seizure progression pattern noted for the WT and Gαz-null groups.Item Open Access The Role of Gz in Neuron Development and CNS Biology(2011) Hultman, RainboHeterotrimeric G proteins play invaluable roles in cellular processes involving transmembrane signaling, particularly at sites of neuronal connectivity within the central nervous system (CNS). Gαz is a member of the Gαi subfamily of heterotrimeric G proteins that displays unique biochemical characteristics and is primarily expressed in neuronal and neuroendocrine cells. Studies in Gz–null mice over the past decade reveal that Gz significantly impacts responses to psychoactive drugs, and is capable of coupling to D2 dopamine, 5–HT1A serotonin, μ–opioid, and α2A–adrenergic receptors. These studies have suggested that Gz may play a critical role in diseases and disorders involving disruptions of monoamine neurotransmitter signaling in the brain such as depression, anxiety, drug abuse, ADHD, schizophrenia, drug addiction, and pain sensitivity. Much is still unknown about the roles and mechanisms of action of Gz in biology.
In this thesis, I have built on what is known regarding Gαz biochemistry by conducting a series of studies that provide further understanding of its role in the CNS, particularly in neuronal development and seizure susceptibility. Gz interacts with several proteins that act as regulators and effectors: RGSZ, adenylyl cyclase, EYA2, and Rap1GAP being the best characterized. A finding regarding its impact of Gz on neurotrophin signaling through RAP1GAP in particular has led to much of the work described here. The studies presented in this thesis indicate that Gαz inhibits BDNF-stimulated axon growth in cortical neurons, establishing an endogenous role for Gαz in regulation of neurotrophin signaling in the CNS that may have important implications for development and plasticity. Furthermore, Gαz was shown to be uniquely distributed to synaptic vesicles suggesting that one mechanism underlying Gz biology may be the regulation of vesicle loading, docking, or release. Finally, I demonstrate that Gz-null mice are hypersusceptible to pilocarpine–induced seizures, and provide histology data indicating increased levels of zinc in the hippocampus. Taken together, these findings suggest that Gz plays a regulatory role at the intersection of neurotrophin and GPCR signaling in the CNS.