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Neurosteriod enhancement of glutamatergic transmission via transient receptor potential melastatin 3 chanels in the developing cerebellum

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Please use this identifier to cite or link to this item: http://hdl.handle.net/1928/13190

Neurosteriod enhancement of glutamatergic transmission via transient receptor potential melastatin 3 chanels in the developing cerebellum

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dc.contributor.author Zamudio-Bulcock, Paula
dc.date.accessioned 2011-08-31T16:52:17Z
dc.date.available 2012-07-31T10:00:07Z
dc.date.issued 2011-08-31
dc.date.submitted July 2011
dc.identifier.uri http://hdl.handle.net/1928/13190
dc.description.abstract Neurosteroids are compounds synthesized de novo within the central nervous system and affect brain function via genomic and non-genomic mechanisms. Sulfated neurosteroids modulate synaptic neurotransmission via interactions with various membrane receptors located at pre- and/ or postsynaptic sites, including metabotropic and ionotropic neurotransmitter receptors and ion permeable channels. The interactions of sulfated neurosteroids with these types of targets can induce rapid changes in neurotransmitter release and/or in postsynaptic responses. Since the 1940's, pregnenolone sulfate (PregS), the sulfated version of the steroid precursor, pregnenolone, has been suggested to have anti-stress, anti-aging, antidepressive, neuroprotective and memory enhancing effects in the mature brain. However, little is known on the physiological role of PregS in the development of the brain. Previous studies from our laboratory have postulated PregS as a novel enhancer of excitatory neurotransmission in the hippocampus, a brain area important for learning and memory. In the work presented here, we evaluated the effects of PregS in the developing rat cerebellum. The cerebellum is a brain region essential for motor coordiation, balance and equilibrium, muscle tone, and cognitive and language functions. We found that PregS potently and reversibly enhanced the release of the excitatory neurotransmitter, glutamate, onto neonatal Purkinje cells (PCs), which provide the sole output from the cerebellar cortex. This effect of PregS was present at the climbing-fiber-to-PC synapse, a powerful glutamatergic synapse important for the timing of conditioned reflexes. Interestingly, the mechanism responsible for this effect of PregS is mediated by a Ca2+ permeable cation channel, the transient receptor potential melastatin 3 (TRPM3) channel. This channel was recently shown to be sensitive to PregS and to be involved in a number of physiological events in the periphery. However, its role in brain physiology is unknown. Thus, the studies presented here postulate TRPM3 channels as novel modulators of excitatory neurotransmission in the immature brain. In addition, we found that TRPM3 channels are highly expressed in all layers of the developing cerebellar cortex. This finding suggests that these steroid-sensitive channels play a major role in the development of this brain region. Lastly, we found that pharmacologically-induced increases in endogenous PregS-like neurosteroids potentiate glutamatergic transmission at PCs in organotypic hindbrain cultures. This finding sets up the stage for future experiments that will investigate the effect of TRPM3 channels and endogenous PregS in the development of the cerebellar cortex. en_US
dc.description.sponsorship National Insitutes of Health Grants MH70386 and AA14973 en_US
dc.language.iso en_US en_US
dc.subject developing cerebellum en_US
dc.subject neurosteroid en_US
dc.subject pregnenolone sulfate en_US
dc.subject transient receptor potential melastatin 3 en_US
dc.subject.lcsh Cerebellum--Growth.
dc.subject.lcsh Ion channels.
dc.subject.lcsh Neurotransmitters--Receptors.
dc.subject.lcsh Pregnenolone.
dc.subject.lcsh Purkinje cells.
dc.subject.lcsh Glutamic acid.
dc.title Neurosteriod enhancement of glutamatergic transmission via transient receptor potential melastatin 3 chanels in the developing cerebellum en_US
dc.type Dissertation en_US
dc.description.degree Biomedical Sciences en_US
dc.description.level Doctoral en_US
dc.description.department University of New Mexico. Biomedical Sciences Graduate Program en_US
dc.description.advisor Valenzuela, Carlos Fernando
dc.description.committee-member Partridge, Donald
dc.description.committee-member Zhao, Xinyu
dc.description.committee-member Mueller, Wolfgang
emb.embargo.terms 2012-07-31


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