Patients with ESRD are exposed to a constantly increasing plasma osmolality as urea accumulates in extracellular fluids. ESRD, particularly in children, can also commonly be associated with a variety of serious and usually episodic electrolyte and osmolality disorders such as hypernatremia. Plasma hyperosmolality and its correction can lead to serious central nervous system (CNS) complications including brain damage, coma, brain developmental disorders and even death. The underlying causes of these complications are not well understood, but changes In brain osmoregulatory metabolism are likely to play an important role. Effective treatments for the CNS complications of hyperosmolality are lacking. The brain adapts to plasma hyperosmolality by activating volume regulatory mechanisms. For example, hypernatremia results in brain shrinkage which is followed by return of the brain to its original volume. This behavior, termed regulatory volume increase (RVI), is mediated initially by uptake of electrolytes from the extracellular fluids. With chronic exposure to hypernatremia, electrolytes are replaced by organic solutes (""""""""organic osmolytes"""""""") such as inositol and amino acids. Correction of hypernatremia results in brain swelling and volume regulatory loss of electrolytes and organic solutes. Remarkably, the cellular and molecular mechanisms by which the brain adapts to hyperosmolality and its correction are largely unknown. Recently, however, we developed the first CNS cell culture models that exhibit a pattern of hyperosmolar volume regulation similar to that seen in vivo. We will utilize these models to 1) elucidate the mechanisms and control of volume regulatory electrolyte uptake and organic osmolyte loss and accumulation pathways in glial and neuronal cells 2) determine the mechanisms by which Na-dependent inositol transport is upregulated by hypernatremia, 3) characterize the osmoregulatory role of methylamine compounds in uremic brain cells, and 4) determine how volume regulatory electrolyte and organic osmolyte accumulation pathways are temporally coordinated. Studies outlined in this grant will provide the first detailed understanding of the cellular and molecular mechanisms by which cells of the CNS adapt to acute and chronic hyperosmolar disturbances and to the clinical correction of the hyperosmotic state. Investigations such as these are essential for. understanding the CNS complications of osmolality disturbances and in the development of more effective therapies to treat plasma hyperosmolality and ESRD. As such, our proposed investigations address directly several of the major objectives of the RFA.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
1R01DK045628-01
Application #
3247122
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Project Start
1992-09-30
Project End
1997-09-29
Budget Start
1992-09-30
Budget End
1993-09-29
Support Year
1
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Children's Hospital Boston
Department
Type
DUNS #
076593722
City
Boston
State
MA
Country
United States
Zip Code
02115
Kirk, K; Strange, K (1998) Functional properties and physiological roles of organic solute channels. Annu Rev Physiol 60:719-39
Ibsen, L; Strange, K (1996) In situ localization and osmotic regulation of the Na(+)-myo-inositol cotransporter in rat brain. Am J Physiol 271:F877-85
Churchwell, K B; Wright, S H; Emma, F et al. (1996) NMDA receptor activation inhibits neuronal volume regulation after swelling induced by veratridine-stimulated Na+ influx in rat cortical cultures. J Neurosci 16:7447-57
Strange, K; Emma, F; Jackson, P S (1996) Cellular and molecular physiology of volume-sensitive anion channels. Am J Physiol 270:C711-30
Jackson, P S; Strange, K (1996) Single channel properties of a volume sensitive anion channel: lessons from noise analysis. Kidney Int 49:1695-9
Strange, K; Jackson, P S (1995) Swelling-activated organic osmolyte efflux: a new role for anion channels. Kidney Int 48:994-1003
McManus, M L; Churchwell, K B; Strange, K (1995) Regulation of cell volume in health and disease. N Engl J Med 333:1260-6
Jackson, P S; Strange, K (1995) Single-channel properties of a volume-sensitive anion conductance. Current activation occurs by abrupt switching of closed channels to an open state. J Gen Physiol 105:643-60
Jackson, P S; Strange, K (1995) Characterization of the voltage-dependent properties of a volume-sensitive anion conductance. J Gen Physiol 105:661-76
Strange, K (1993) Maintenance of cell volume in the central nervous system. Pediatr Nephrol 7:689-97

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