AGONISTIC AND ANTAGONISTIC PROPERTIES OF ANGIOTENSIN ANALOGS AT THE AT2-RECEPTOR IN PC12W CELLS

被引:92
作者
BRECHLER, V [1 ]
JONES, PW [1 ]
LEVENS, NR [1 ]
DEGASPARO, M [1 ]
BOTTARI, SP [1 ]
机构
[1] CIBA GEIGY AG,CARDIOVASC RES DEPT,DIV PHARMACEUT,K125845,CH-4002 BASEL,SWITZERLAND
关键词
AT2-RECEPTOR; PARTICULATE GUANYLATE CYCLASE; PC12W CELL; CGP-42112; PD-123319;
D O I
10.1016/0167-0115(93)90244-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Despite some recent reports describing the effects of AT2 receptor selective ligands in vitro and in vivo, the physiological function of this receptor is still a matter of debate. This problem stemms amongst others from the difficulty in interpreting results from in vivo experiments with drugs of which it is not known whether they act as agonists or antagonists. We reported earlier that angiotensin II inhibits basal and atrial natriuretic peptide stimulated particulate guanylate cyclase activity through AT2 receptors in PC12W cells [1]. We have used this parameter in intact PC12W cells in order to determine the pharmacological properties of different widely used angiotensin receptor ligands. We found CGP 42112 to behave as a full agonist in this system, whereas PD 123319 and Sar1Ile8angiotensin II act as antagonists. As expected, the AT1 antagonist losartan did not affect this response.
引用
收藏
页码:207 / 213
页数:7
相关论文
共 26 条
  • [1] THE ANGIOTENSIN-AT2 RECEPTOR STIMULATES PROTEIN TYROSINE PHOSPHATASE-ACTIVITY AND MEDIATES INHIBITION OF PARTICULATE GUANYLATE-CYCLASE
    BOTTARI, SP
    KING, IN
    REICHLIN, S
    DAHLSTROEM, I
    LYDON, N
    DEGASPARO, M
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 183 (01) : 206 - 211
  • [2] BOTTARI SP, 1991, MOL PHARM SECT, V207, P157
  • [3] BOTTARI SP, 1993, IN PRESS FRONT NEURO, V14
  • [4] THE ANGIOTENSIN AT2-RECEPTOR MODULATES T-TYPE CALCIUM CURRENT IN NONDIFFERENTIATED NG108-15 CELLS
    BUISSON, B
    BOTTARI, SP
    DEGASPARO, M
    GALLOPAYET, N
    PAYET, MD
    [J]. FEBS LETTERS, 1992, 309 (02): : 161 - 164
  • [5] STIMULATION OF INOSITOL TRISPHOSPHATE FORMATION IN HEPATOCYTES BY VASOPRESSIN, ADRENALINE AND ANGIOTENSIN-II AND ITS RELATIONSHIP TO CHANGES IN CYTOSOLIC FREE CA-2+
    CHAREST, R
    PRPIC, V
    EXTON, JH
    BLACKMORE, PF
    [J]. BIOCHEMICAL JOURNAL, 1985, 227 (01) : 79 - 90
  • [6] IDENTIFICATION OF ANGIOTENSIN-II RECEPTOR SUBTYPES
    CHIU, AT
    HERBLIN, WF
    MCCALL, DE
    ARDECKY, RJ
    CARINI, DJ
    DUNCIA, JV
    PEASE, LJ
    WONG, PC
    WEXLER, RR
    JOHNSON, AL
    TIMMERMANS, PBMWM
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 165 (01) : 196 - 203
  • [7] CLARK KL, IN PRESS BR J PHARM
  • [8] COGAN MG, 1991, J PHARMACOL EXP THER, V259, P687
  • [9] BIOCHEMICAL-CHARACTERIZATION OF 2 ANGIOTENSIN-II RECEPTOR SUBTYPES IN THE RAT
    DEGASPARO, M
    WHITEBREAD, S
    MELE, M
    MOTANI, AS
    WHITCOMBE, PJ
    RAMJOUE, HP
    KAMBER, B
    [J]. JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1990, 16 : S31 - S35
  • [10] GLOSSMANN H, 1974, J BIOL CHEM, V249, P664