8-(N,N-DIETHYLAMINO)OCTYL 3,4,5-TRIMETHOXYBENZOATE (TMB-8) ACTS AS A MUSCARINIC RECEPTOR ANTAGONIST IN THE EPITHELIAL-CELL LINE HT29
Citation
J. Leipziger et al., 8-(N,N-DIETHYLAMINO)OCTYL 3,4,5-TRIMETHOXYBENZOATE (TMB-8) ACTS AS A MUSCARINIC RECEPTOR ANTAGONIST IN THE EPITHELIAL-CELL LINE HT29, Naunyn-Schmiedeberg's archives of pharmacology, 353(3), 1996, pp. 295-301
Categorie Soggetti
Pharmacology & Pharmacy
SICI code
0028-1298(1996)353:3<295:83(AAA>2.0.ZU;2-9
Abstract
8-(N, N-diethylamino)octyl-3,4,5-trimethoxybenzoate (TMB-8) is a widel
y used pharmacological tool to investigate the involvement of intracel
lular Ca2+ stores in cellular responses. In this study we investigate
the effect of TMB-8 as a putative inhibitor of ''Ca2+ signalling'' in
single fura-2 loaded HT29 colonic epithelial cells stimulated by ATP,
carbachol (CCH) and neurotensin (NT). TMB-8 effectively inhibited the
CCH-induced (100 mu mol/l intracellular Ca2+ ([Ca2+](i)) transient wit
h an IC50 of 20 mu mol/l. However, [Ca2+](i), transients induced by ot
her phospholipase C coupled agonists ATP (10 mu mol/l, n = 4) and NT (
10 nmol/l, n = 4) remained unaffected by TMB-8 (50 mu mol/l). The agon
ist-induced [Ca2+](i) transients remained equally unaffected by 100 mu
mol/l TMB-8 when the stimulatory concentration was reduced to 0.5 mu
mol/l for ATP (n = 4) or 1 nmol/l for NT (n = 4). The competitive natu
re of the TMB-8-induced inhibition of the CCH-induced [Ca2+](i) transi
ent was demonstrated by examining the agonist at various concentration
s in absence and presence of the antagonist. High TMB-8 concentrations
(100 mu mol/l) alone induced a small [Ca2+](i) increase (Delta[Ca2+](
i): 40 +/- 5 nmol/l, n = 7). We assume that this increase is a consequ
ence of a TMB-8 induced intracellular alkalinization (Delta pH: 0.1 +/
- 0.02, n = 7) occurring simultaneously with the increase in [Ca2+](i)
. From these results we draw the following conclusions: (1) In sharp c
ontrast to a large number of other studies, but in agreement with stud
ies in other types of cells, these results substantially challenge the
value of the ''tool'' TMB-8 as an ''intracellular Ca2+ antagonist'';
(2) TMB-8 acts a muscarinic receptor antagonist at the M(3) receptor;
(3) TMB-8 does not influence the release of Ca2+ from intracellular st
ores when IP3 signal transduction is activated by ATP or NT; (4) TMB-8
as a weak organic base alkalinizes the cytosol at high concentrations
; and (5) TMB-8 induces small [Ca2+](i) transients at higher concentra
tions.