MODULATION OF FLUOROALUMINATE-INDUCED INOSITOL PHOSPHATE FORMATION BY INCREASES IN TISSUE CYCLIC-AMP CONTENT IN BOVINE TRACHEAL SMOOTH-MUSCLE

被引:43
作者
HALL, IP [1 ]
DONALDSON, J [1 ]
HILL, SJ [1 ]
机构
[1] QUEENS MED CTR,SCH MED,DEPT PHYSIOL & PHARMACOL,CLIFTON BLVD,NOTTINGHAM NG7 2UH,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1111/j.1476-5381.1990.tb15861.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. The effect of fluoroaluminate complexes (AlCl3 plus NaF) upon smooth muscle tone, [3H]-inositol phosphate accumulation and [3H]-cyclic AMP accumulation has been investigated in slices of bovine tracheal smooth muscle. 2. Fluoroaluminate (10 μM AlCl3 + various concentrations of NaF) elicited concentration-dependent contractions of bovine tracheal smooth muscle strips at concentrations of NaF in the range 1-10 mM. The resultant contractile response was reversed by isoprenaline (50 nM) and was preserved in calcium-free medium. 3 Fluoroaluminate stimulated [3H]-inositol phosphate formation at concentrations of NaF over 1 mM. The response to 20 mM NaF + AlCl3 was 164 ± 29% of the response to 1 mM histamine. Fluoroaluminate also increased the incorporation of [3H]-myo-inositol into membrane phospholipids. 4. Fluoroaluminate produced a small rise in [3H]-cyclic AMP levels (2.1 fold increase over basal with 20 mM NaF). The response to forskolin (1 μM, 8.6 fold over basal) was reduced by fluoroaluminate in a concentration-dependent manner, but still remained significantly (P < 0.05) elevated over the response to fluoroaluminate alone. 5. The [3H]-inositol phosphate response to fluoroaluminate was inhibited by salbutamol (maximum inhibition 60%, IC50 = 0.08 μM), forskolin (1 μM, 46% inhibition) and isobutylmethylxanthine (1 mM, 73% inhibition). 6. These data suggest that inhibition of agonist-induced inositol phospholipid turnover by cyclic AMP in this tissue can occur at the post-receptor level.
引用
收藏
页码:646 / 650
页数:5
相关论文
共 29 条
[1]  
BARNES PJ, 1986, ASTHMA CLIN PHARM TH, P146
[2]  
BERRIDGE MJ, 1987, ANNU REV BIOCHEM, V56, P159, DOI 10.1146/annurev.bi.56.070187.001111
[3]  
BLACKMORE PF, 1985, J BIOL CHEM, V260, P4477
[4]   MASS CHANGES OF INOSITOL(1,4,5) TRISPHOSPHATE IN TRACHEALIS MUSCLE FOLLOWING AGONIST STIMULATION [J].
CHILVERS, ER ;
CHALLISS, RAJ ;
BARNES, PJ ;
NAHORSKI, SR .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1989, 164 (03) :587-590
[5]   CARBACHOL AND HISTAMINE STIMULATION OF GUANINE-NUCLEOTIDE-DEPENDENT PHOSPHOINOSITIDE HYDROLYSIS IN RAT-BRAIN CORTICAL MEMBRANES [J].
CLARO, E ;
GARCIA, A ;
PICATOSTE, F .
BIOCHEMICAL JOURNAL, 1989, 261 (01) :29-35
[6]   G-PROTEINS, THE INOSITOL LIPID SIGNALING PATHWAY, AND SECRETION [J].
COCKCROFT, S ;
STUTCHFIELD, J .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1988, 320 (1199) :247-265
[7]   ROLE OF GUANINE-NUCLEOTIDE BINDING-PROTEIN IN THE ACTIVATION OF POLYPHOSPHOINOSITIDE PHOSPHODIESTERASE [J].
COCKCROFT, S ;
GOMPERTS, BD .
NATURE, 1985, 314 (6011) :534-536
[8]  
DELLABIANCA V, 1986, BIOCHIM BIOPHYS ACTA, V886, P441
[9]  
DONALDSON J, 1988, MOL PHARMACOL, V33, P626
[10]  
GILMAN AG, 1987, ANNU REV BIOCHEM, V56, P615, DOI 10.1146/annurev.bi.56.070187.003151