| Literature DB >> 1634534 |
L Aguilar-Bryan1, C G Nichols, A S Rajan, C Parker, J Bryan.
Abstract
Cell membranes isolated from hamster insulinoma (HIT T15) cells at passages 65-74 contain high and low affinity receptors for a sulfonylurea derivative, 5-[125I]iodo,2-hydroxyglyburide (KD values of approximately 7 nM and 16 microM). Between passages 75 and 85, the estimated B(max) for the high affinity receptor decreases approximately 10-fold from approximately 1.6 to 0.16 pmol/mg membrane protein. By contrast, the density of low affinity binding sites, 800-1000 pmol/mg, is unaltered. The drop in high affinity receptors is paralleled by a decrease in the density of KATP channels assessed using patch-clamp and 86Rb(+)-efflux techniques. These results strongly support the idea that the high affinity sulfonylurea receptor is an integral part of the KATP channel.Entities:
Mesh:
Substances:
Year: 1992 PMID: 1634534
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157