EFFECTS OF SELECTED VASOACTIVE SUBSTANCES ON ADENYLATE-CYCLASE ACTIVITY IN BRAIN, ISOLATED BRAIN MICROVESSELS, AND PRIMARY CULTURES OF BRAIN MICROVESSEL ENDOTHELIAL-CELLS

被引:15
作者
BARANCZYKKUZMA, A
AUDUS, KL
GUILLOT, FL
BORCHARDT, RT
机构
[1] UNIV KANSAS, SCH PHARM, DEPT PHARMACEUT CHEM, LAWRENCE, KS 66045 USA
[2] WARSAW ACAD MED & HOSP, INST BIOPHARM, DEPT BIOCHEM, PL-02097 WARSAW, POLAND
[3] SANDOZ LTD, DEPT BIOPHARMACEUT, CH-4002 BASEL, SWITZERLAND
关键词
BRAIN MICROVESSEL ENDOTHELIA; BLOOD-BRAIN BARRIER; ADENYLATE CYCLASE; CAMP; ANGIOTENSIN-II; HISTAMINE; CATECHOLAMINES; BRADYKININ;
D O I
10.1007/BF00966802
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The specific activity of adenylate cyclase was assayed in homogenates of gray matter, freshly isolated and primary cultured microvessel endothelial cells from bovine cerebral cortex. Specific activities for the tissues were 14.6 +/- 2.1, 15.6 +/- 2.7, and 8.4 +/- 1.5 pmol cAMP/mg protein/min +/- SD for gray matter, cultured microvessels, and freshly isolated microvessels, respectively. Adenylate cyclase associated with gray matter and cultured microvessels was sensitive to histamine and selected catecholamines. Perhaps due to metabolic deficiencies, adenylate cyclase of freshly isolated microvessels exhibited little or no response to either the catecholamines or histamine. Angiotensin II stimulated adenylate cyclase of both freshly isolated and cultured microvessels but had no effect on gray matter. Bradykinin did not stimulate cAMP generation in any of the tissues. Overall results support the role of cAMP in regulating brain microvessel functions and suggest that primary cultures of brain microvessels may be useful in examining cAMP-mediated biochemical pathways at the blood-brain barrier.
引用
收藏
页码:209 / 214
页数:6
相关论文
共 37 条
[1]   EFFECTS OF ACUTE-HYPOXIA ON THE ADENYLATE-CYCLASE AND EVANS BLUE TRANSPORT OF BRAIN MICROVESSELS [J].
ADAM, G ;
JOO, F ;
TEMESVARI, P ;
DUX, E ;
SZERDAHELYI, P .
NEUROCHEMISTRY INTERNATIONAL, 1987, 10 (04) :529-532
[2]   BOVINE BRAIN MICROVESSEL ENDOTHELIAL-CELL MONOLAYERS AS A MODEL SYSTEM FOR THE BLOOD-BRAIN-BARRIER [J].
AUDUS, KL ;
BORCHARDT, RT .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1987, 507 :9-18
[3]   THE USE OF CULTURED EPITHELIAL AND ENDOTHELIAL-CELLS FOR DRUG TRANSPORT AND METABOLISM STUDIES [J].
AUDUS, KL ;
BARTEL, RL ;
HIDALGO, IJ ;
BORCHARDT, RT .
PHARMACEUTICAL RESEARCH, 1990, 7 (05) :435-451
[4]   CHARACTERIZATION OF AN INVITRO BLOOD-BRAIN-BARRIER MODEL SYSTEM FOR STUDYING DRUG TRANSPORT AND METABOLISM [J].
AUDUS, KL ;
BORCHARDT, RT .
PHARMACEUTICAL RESEARCH, 1986, 3 (02) :81-87
[5]  
BACA GM, 1978, BLOOD VESSELS, V15, P286
[6]  
BARANCZYKKUZMA A, 1986, J NEUROCHEM, V47, P484
[7]  
BETZ A L, 1989, Cerebrovascular and Brain Metabolism Reviews, V1, P133
[8]   SEROTONIN, NOREPINEPHRINE, AND HISTAMINE MEDIATION OF ENDOTHELIAL-CELL BARRIER FUNCTION-INVITRO [J].
BOTTARO, D ;
SHEPRO, D ;
PETERSON, S ;
HECHTMAN, HB .
JOURNAL OF CELLULAR PHYSIOLOGY, 1986, 128 (02) :189-194
[9]   PERMEABILITY OF HUMAN-ENDOTHELIAL MONOLAYERS - EFFECT OF VASOACTIVE AGONISTS AND CAMP [J].
CASNOCHA, SA ;
ESKIN, SG ;
HALL, ER ;
MCINTIRE, LV .
JOURNAL OF APPLIED PHYSIOLOGY, 1989, 67 (05) :1997-2005
[10]   THE BLOOD-BRAIN-BARRIER IN HYPOXIA - ULTRASTRUCTURAL ASPECTS AND ADENYLATE-CYCLASE ACTIVITY OF BRAIN CAPILLARIES [J].
DUX, E ;
TEMESVARI, P ;
JOO, F ;
ADAM, G ;
CLEMENTI, F ;
DUX, L ;
HIDEG, J ;
HOSSMANN, KA .
NEUROSCIENCE, 1984, 12 (03) :951-958