Detalles del proyecto
Description
Hormone-receptor interactions and the role of these interactions in the
endocrine regulation of ion fluxes in target tissues will continue to be
examined in both the avian erythrocyte and in mammalian liver and muscle
with specific reference to the catecholamine and thyroid hormones. Studies
in the turkey erythrocyte are designed to further characterize the
mechanism by which low concentrations of beta-adrenergic agents induce a
very large and virtually instantaneous increase in bi-directional sodium
and potassium fluxes; the nature of the pathway by which these changes in
fluxes are mediated; and the means by which changes in thyroid status
induce their demonstrated effects on the catecholamine responsiveness of
the normal cell. Other studies will continue work begun during the present
project period on rat liver and diaphragm with the objective of defining
the physiologic role of the catecholamine and thyroid hormones in the
regulation of cation fluxes in these more complex mammalian tissues.
Objectives of these latter studies will include a detailed characterization
of the mechanism by which beta-adrenergic agents induce prompt and striking
changes in both the uptake and release of monovalent cations in vitro; an
examination of the physiologic role of these hormonally induced changes
with particular regard to their modulation of the extracellular potassium
ion concentration; and a detailed investigation of mechanisms of thyroid
thermogenesis with special reference to the possibility that the
thermogenic effect of the thyroid hormones, rather than being attributable
to a primary induction of an increased number of active cation pump units
per se, instead results from a more proximal hormone-induced increase in
the permeability of the cell to the passive leak of sodium and potassium
ions. The recent demonstration that a marked increase in cell permeability
is demonstrable in rat liver as early as six hours after a single injection
of T3, and that this change actually precedes any reported change in active
pump unit number, now makes it possible to test such an hypothesis directly.
Estado | Finalizado |
---|---|
Fecha de inicio/Fecha fin | 9/1/85 → 1/1/90 |
Financiación
- Eunice Kennedy Shriver National Institute of Child Health and Human Development
- National Institute of Child Health and Human Development
Keywords
- Biología celular
Huella digital
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