Long-term goals of the proposed work are to understand controlling mechanisms involved in the normal functioning of the adult mammalian hypothalamus. Specifically, this work centers on the magnocellular neuroendocrine cells (MNCS) of the hpothalamo-neurohypophysial system (HNS), consisting chiefly of the supraoptic (SON) and paraventricular (PVN) nuclei and their axonal projections. MNCs synthesize either oxytocin or vasopressin and, in response to physiological stimuli, release these peptides from axon terminals in the pituitary neural lobe or within the CNS. Well known to play important roles in water regulation, control of blood pressure, reproductive physiology and care of the young, this model system has yielded many insights into CNS functioning. So well studied are the peripheral effects of HNS outputs that even results from in vitro experiments with the SON and PVN can often be related directly to the functioning of the intact animal. In order to further the central mission of this work, this proposal focuses on two main aspects of HNS functioning: interactions among the MNCs themselves, particularly interneuronal coupling, and extrinsic and intrinsic factors that modulate MNC excitability. The proposed studies will use electrophysiological methods, intracellular an patch-clamp recording techniques in brain slices, accompanied by immunocytochemical and biochemical approaches, all aimed at uncovering fundamental mechanisms of CNS functioning.
Specific aims are:
Aim 1. To continue our investigations of interneuronal coupling in the SON. Experiments will further define the physiological conditions that enhance or diminish coupling, define the relationships between receptor activation and coupling, and determine cellular mechanisms that modulate MNC coupling.
Aim 2. To continue investigation determining the mechanisms by which physiological changes alter MNC excitability. Specific studies will investigate the contributions of neuronal histamine, oxytocin, and intrinsic ionic mechanisms to MNC excitability and, thus, to mechanisms ultimately governing peptide release. Factors to be investigated include: depolarizing after potentials, plateau potentials, receptor-mediated conductances, and termination of bursts of phasic firing, as well as physiological state of the animal.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS016942-17
Application #
2714429
Study Section
Neurology B Subcommittee 2 (NEUB)
Program Officer
Baughman, Robert W
Project Start
1981-01-01
Project End
2001-05-31
Budget Start
1998-06-01
Budget End
1999-05-31
Support Year
17
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of California Riverside
Department
Neurosciences
Type
Schools of Earth Sciences/Natur
DUNS #
City
Riverside
State
CA
Country
United States
Zip Code
92521
Ponzio, Todd A; Hatton, Glenn I (2005) Adenosine postsynaptically modulates supraoptic neuronal excitability. J Neurophysiol 93:535-47
Hatton, Glenn I (2002) Glial-neuronal interactions in the mammalian brain. Adv Physiol Educ 26:225-37
Yang, Qin Zhao; Hatton, Glenn I (2002) Histamine H1-receptor modulation of inter-neuronal coupling among vasopressinergic neurons depends on nitric oxide synthase activation. Brain Res 955:115-22
Hatton, Glenn I; Zhao Yang, Qin (2002) Peripartum interneuronal coupling in the supraoptic nucleus. Brain Res 932:120-3
Hatton, Glenn I; Yang, Qin Zhao (2002) Synaptic potentials mediated by alpha 7 nicotinic acetylcholine receptors in supraoptic nucleus. J Neurosci 22:29-37
Hatton, G I; Yang, Q Z (2001) Ionotropic histamine receptors and H2 receptors modulate supraoptic oxytocin neuronal excitability and dye coupling. J Neurosci 21:2974-82
Li, Z; Hatton, G I (2000) Histamine suppresses non-NMDA excitatory synaptic currents in rat supraoptic nucleus neurons. J Neurophysiol 83:2616-25
Hatton, G I (1999) Astroglial modulation of neurotransmitter/peptide release from the neurohypophysis: present status. J Chem Neuroanat 16:203-21
Yang, Q Z; Hatton, G I (1999) Nitric oxide via cGMP-dependent mechanisms increases dye coupling and excitability of rat supraoptic nucleus neurons. J Neurosci 19:4270-9
Li, Z; Miyata, S; Hatton, G I (1999) Inositol 1,4,5-trisphosphate-sensitive Ca2+ stores in rat supraoptic neurons: involvement in histamine-induced enhancement of depolarizing afterpotentials. Neuroscience 93:667-74

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