Rowe B P, Grove K L, Saylor D L, Speth R C
Department of Physiology, James H. Quillen College of Medicine, East Tennessee State University, Johnson City 37614-0002.
Regul Pept. 1991 Mar 26;33(1):45-53. doi: 10.1016/0167-0115(91)90014-8.
The non-peptidic angiotensin II receptor subtype selective antagonists, DuP 753 and PD123177, were used to characterize angiotensin II receptor binding sites in the rat brain. Competitive receptor autoradiography with 125I-Sar1-Ile8 angiotensin II defined a regional distribution of binding sites that were sensitive to either DuP 753 (designated AII alpha subtype) or PD123177 (designated AII beta subtype). Whereas most brain nuclei could be assigned to a category containing a predominant subtype, a multiple receptor subtype analysis indicated that some regions are homogeneous, while others contain a mixture of both AII alpha and AII beta subtypes.