TY - JOUR
T1 - Inhibitory effect of DS-4574, a mast cell stabilizer with peptidoleukotriene receptor antagonism, on gastric acid secretion in rats
AU - Tabuchi, Yoshiaki
AU - Furuhama, Kazuhisa
PY - 1994/4/1
Y1 - 1994/4/1
N2 - We examined the inhibitory effect of DS-4574 (6-(2-cyclohexylethyl)[1,3,4]thiadiazolo[3,2-a]-1,2,3-triazolo[4,5-d] py pyrimidin-9(3H)-one), a mast cell stabilizer with peptidoleukotriene receptor antagonism, on gastric acid secretion stimulated by several secretagogues in rats. In anesthetized rats with acute gastric fistulas, DS-4574 (50 mg/kg, intraduodenal) significantly inhibited gastric acid secretion induced by both carbachol (50 μg/kg, s.c.) and pentagastrin (75 μg/kg, s.c.), but not by histamine (2.5 mg/kg, s.c.). In unanesthetized pylorus-ligated rats, DS-4574 (10 and 25 mg/kg, intraduodenal) markedly suppressed increases in gastric acid output and histamine leakage into the gastric juice produced by carbachol (0.1 mg/kg, s.c.) or pentagastrin (1 mg/kg, s.c.). When the relationship between acid output and histamine leakage elicited by carbachol and pentagastrin was assessed, there was a close correlation (r = 0.84) that was highly significant (P < 0.01). In the in vitro study with rat gastric tissues, DS-4574 (10-7-10-5 M) had no effect on the K+-dependent ATPase activity or on aminopyrine uptake into mucosal preparations containing parietal cells stimulated by carbachol (10-5 M), histamine (10-4 M), or dibutyryl-cyclic AMP (10-3 M). These results suggest that the effect of DS-4574 may be mediated by inhibition of endogenous histamine from histamine-storing cells in the stomach.
AB - We examined the inhibitory effect of DS-4574 (6-(2-cyclohexylethyl)[1,3,4]thiadiazolo[3,2-a]-1,2,3-triazolo[4,5-d] py pyrimidin-9(3H)-one), a mast cell stabilizer with peptidoleukotriene receptor antagonism, on gastric acid secretion stimulated by several secretagogues in rats. In anesthetized rats with acute gastric fistulas, DS-4574 (50 mg/kg, intraduodenal) significantly inhibited gastric acid secretion induced by both carbachol (50 μg/kg, s.c.) and pentagastrin (75 μg/kg, s.c.), but not by histamine (2.5 mg/kg, s.c.). In unanesthetized pylorus-ligated rats, DS-4574 (10 and 25 mg/kg, intraduodenal) markedly suppressed increases in gastric acid output and histamine leakage into the gastric juice produced by carbachol (0.1 mg/kg, s.c.) or pentagastrin (1 mg/kg, s.c.). When the relationship between acid output and histamine leakage elicited by carbachol and pentagastrin was assessed, there was a close correlation (r = 0.84) that was highly significant (P < 0.01). In the in vitro study with rat gastric tissues, DS-4574 (10-7-10-5 M) had no effect on the K+-dependent ATPase activity or on aminopyrine uptake into mucosal preparations containing parietal cells stimulated by carbachol (10-5 M), histamine (10-4 M), or dibutyryl-cyclic AMP (10-3 M). These results suggest that the effect of DS-4574 may be mediated by inhibition of endogenous histamine from histamine-storing cells in the stomach.
KW - Carbachol
KW - DS-4574
KW - Gastric acid secretion
KW - Histamine leakage
KW - Mast cell stabilizer
KW - Pentagastrin
UR - http://www.scopus.com/inward/record.url?scp=0028327058&partnerID=8YFLogxK
U2 - 10.1016/0014-2999(94)90102-3
DO - 10.1016/0014-2999(94)90102-3
M3 - 学術論文
C2 - 8026547
AN - SCOPUS:0028327058
SN - 0014-2999
VL - 255
SP - 229
EP - 234
JO - European Journal of Pharmacology
JF - European Journal of Pharmacology
IS - 1-3
ER -