Expression of a novel angiotensin II receptor subtype in gerbil brain

被引:21
作者
deOliveira, AM [1 ]
Viswanathan, M [1 ]
Heemskerk, FMJ [1 ]
Saavedra, JM [1 ]
机构
[1] NIMH,CLIN SCI LAB,PHARMACOL SECT,BETHESDA,MD 20892
关键词
hippocampus; circumventricular organ; guanine nucleotide; brain angiotensin system; receptor pharmacology; quantitative autoradiography;
D O I
10.1016/0006-8993(95)01158-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Angiotensin II receptors are highly localized in adult gerbil brain. Apparent receptor number is high in subfornical organ, vascular organ of the lamina terminalis, nucleus of the solitary tract, hippocampus, and in the anterior pituitary gland. In the hippocampus, binding is localized to the stratum oriens, radiatum, the lacunar molecular layers of the CA1 subfield, and the molecular layer of the gyrus dentatus, with a medial to lateral and anterior to posterior gradient in receptor expression. Binding is absent from the pyramidal layer of the CA1 subfield and from the granular cell layer of the gyrus dentatus, areas rich in angiotensin IV binding. Characterization in the hippocampus revealed the presence of a high affinity receptor, sensitive to incubation with the guanine nucleotide GTP gamma S, and displaced by angiotensin II = angiotensin III < Sar(1)-Ile(8)-angiotensin II, but not by angiotensin IV or other angiotensin fragments, the AT(1) receptor antagonist losartan, or the AT(2) ligands CGP 42112 or PD 123177. In other brain areas, binding was equally insensitive to displacement by AT(1) or AT(2) ligands, with the exception of binding in the olfactory bulb, which was totally displaced by CGP 42112 and PD 123177, but not by losartan. In the gerbil, most of the brain and pituitary angiotensin II receptors are different from the AT(1), AT(2) and AT(4) subtypes, and should be considered 'atypical' until further characterization.
引用
收藏
页码:177 / 187
页数:11
相关论文
共 25 条
  • [1] ANGIOTENSIN-II RECEPTOR SUBTYPES - CHARACTERIZATION, SIGNALING MECHANISMS, AND POSSIBLE PHYSIOLOGICAL IMPLICATIONS
    BOTTARI, SP
    DEGASPARO, M
    STECKELINGS, UM
    LEVENS, NR
    [J]. FRONTIERS IN NEUROENDOCRINOLOGY, 1993, 14 (02) : 123 - 171
  • [2] NOMENCLATURE FOR ANGIOTENSIN RECEPTORS - A REPORT OF THE NOMENCLATURE-COMMITTEE OF THE COUNCIL-FOR-HIGH-BLOOD-PRESSURE-RESEARCH
    BUMPUS, FM
    CATT, KJ
    CHIU, AT
    DEGASPARO, M
    GOODFRIEND, T
    HUSAIN, A
    PEACH, MJ
    TAYLOR, DG
    TIMMERMANS, PBMWM
    [J]. HYPERTENSION, 1991, 17 (05) : 720 - 721
  • [3] IDENTIFICATION AND CHARACTERIZATION OF A NEW BINDING-SITE FOR ANGIOTENSIN-II IN MOUSE NEUROBLASTOMA NEURO-2A CELLS
    CHAKI, S
    INAGAMI, T
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 182 (01) : 388 - 394
  • [4] RODENT MODELS OF CEREBRAL-ISCHEMIA
    GINSBERG, MD
    BUSTO, R
    [J]. STROKE, 1989, 20 (12) : 1627 - 1642
  • [5] IDENTIFICATION OF AN AII(3-8) [AIV] BINDING-SITE IN GUINEA-PIG HIPPOCAMPUS
    HARDING, JW
    COOK, VI
    MILLERWING, AV
    HANESWORTH, JM
    SARDINIA, MF
    HALL, KL
    STOBB, JW
    SWANSON, GN
    COLEMAN, JKM
    WRIGHT, JW
    HARDING, EC
    [J]. BRAIN RESEARCH, 1992, 583 (1-2) : 340 - 343
  • [6] THE DISTRIBUTION OF ANGIOTENSIN-II BINDING-SITES IN RODENT BRAIN
    HARDING, JW
    STONE, LP
    WRIGHT, JW
    [J]. BRAIN RESEARCH, 1981, 205 (02) : 265 - 274
  • [7] COEXPRESSION OF C-FOS AND HSP70 MESSENGER-RNA IN GERBIL BRAIN AFTER ISCHEMIA - INDUCTION THRESHOLD, DISTRIBUTION AND TIME-COURSE EVALUATED BY IN-SITU HYBRIDIZATION
    IKEDA, J
    NAKAJIMA, T
    OSBORNE, OC
    MIES, G
    NOWAK, TS
    [J]. MOLECULAR BRAIN RESEARCH, 1994, 26 (1-2): : 249 - 258
  • [8] Inagami T., 1994, J HYPERTENS, V12, P583
  • [9] JI H, 1991, MOL PHARMACOL, V39, P120
  • [10] LOSKOTA WJ, 1973, STEREOTAXIC ATLAS MO