Mechanism of cholecystokinin-A-receptor antagonist on human pancreatic exocrine secretion - Localization of CCK-A receptor in the human duodenum

被引:23
作者
Funakoshi, A
Fukamizu, Y
Miyasaka, K
机构
[1] Kyushu Natl Canc Ctr, Dept Gastroenterol, Minami Ku, Fukuoka 8111395, Japan
[2] Kaken Pharmaceut Co Ltd, Dev Res Lab, Kyoto, Japan
[3] Tokyo Metropolitan Inst Gerontol, Dept Clin Physiol, Tokyo, Japan
关键词
cholecystokinin-A receptor; cholecystokinin; gene expression; pancreas; duodenum;
D O I
10.1159/000051459
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Expressions of the cholecystokinin (CCK)-A and -B receptor genes in human duodenum, pancreas and gallbladder were examined by Northern blot analysis and reverse transcriptase polymerase chain reaction (RT-PCR) followed by Southern blot hybridization. The autoradiographic study of CCK-A and -B receptors in the human duodenum and pancreas was examined in vitro. To determine the subtypes to CCK receptors in the pancreas or duodenum, we studied the abilities of CCK-A and -B receptor agonists (CCK-8 and gastrin) and antagonists (loxiglumide, L-364,718 and L-365,260) to inhibit binding of I-125-CCK-8. CCK-A receptor mRNA was not expressed in the human pancreas, but was expressed in the gallbladder and duodenum, although it was expressed in the pancreas by RT-PCR. CCK-B receptor mRNA was expressed in the pancreas, but not in gallbladder and duodenum, Using autoradiography, high concentrations of CCK-A receptors were detected in the duodenal mucosa, although in the pancreas only CCK-B receptors were detected by this method. These results suggest that localization of CCK-A receptor in human duodenum provides a biochemical and morphological basis for some physiological functions of CCK.
引用
收藏
页码:75 / 80
页数:6
相关论文
共 17 条
[1]   NEUROHORMONAL CONTROL OF HUMAN PANCREATIC EXOCRINE SECRETION [J].
ADLER, G ;
NELSON, DK ;
KATSCHINSKI, M ;
BEGLINGER, C .
PANCREAS, 1995, 10 (01) :1-13
[2]   INTERACTION OF THE CHOLINERGIC SYSTEM AND CHOLECYSTOKININ IN THE REGULATION OF ENDOGENOUS AND EXOGENOUS STIMULATION OF PANCREATIC-SECRETION IN HUMANS [J].
ADLER, G ;
BEGLINGER, C ;
BRAUN, U ;
REINSHAGEN, M ;
KOOP, I ;
SCHAFMAYER, A ;
ROVATI, L ;
ARNOLD, R .
GASTROENTEROLOGY, 1991, 100 (02) :537-543
[3]   EFFECTS OF CHOLECYSTOKININ (CCK-8) ON 2 CLASSES OF GASTRODUODENAL VAGAL AFFERENT FIBER [J].
BLACKSHAW, LA ;
GRUNDY, D .
JOURNAL OF THE AUTONOMIC NERVOUS SYSTEM, 1990, 31 (03) :191-202
[4]   INHIBITION OF CHOLECYSTOKININ-STIMULATED PANCREATICOBILIARY OUTPUT IN MAN BY THE CHOLECYSTOKININ RECEPTOR ANTAGONIST MK-329 [J].
CANTOR, P ;
OLSEN, O ;
GERTZ, BJ ;
GJORUP, I ;
WORNING, H .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1991, 26 (06) :627-637
[5]   MOLECULAR-CLONING, FUNCTIONAL EXPRESSION AND CHROMOSOMAL LOCALIZATION OF THE HUMAN CHOLECYSTOKININ TYPE-A RECEPTOR [J].
DEWEERTH, A ;
PISEGNA, JR ;
HUPPI, K ;
WANK, SA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 194 (02) :811-818
[6]   IMMUNOCHEMICAL EVIDENCE OF CHOLECYSTOKININ-LIKE PEPTIDES IN BRAIN [J].
DOCKRAY, GJ .
NATURE, 1976, 264 (5586) :568-570
[7]   AN ANIMAL-MODEL OF CONGENITAL DEFECT OF GENE-EXPRESSION OF CHOLECYSTOKININ (CCK)-A RECEPTOR [J].
FUNAKOSHI, A ;
MIYASAKA, K ;
SHINOZAKI, H ;
MASUDA, M ;
KAWANAMI, T ;
TAKATA, Y ;
KONO, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 210 (03) :787-796
[8]   MODULATION OF PANCREATIC-SECRETION BY CAPSAICIN-SENSITIVE SENSORY NEURONS IN THE RAT [J].
GICQUEL, N ;
NAGAIN, C ;
CHARIOT, J ;
TSOCAS, A ;
LEVENEZ, F ;
CORRING, T ;
ROZE, C .
PANCREAS, 1994, 9 (02) :203-211
[9]   INTERACTION OF CCK WITH PANCREATIC ACINAR-CELLS [J].
JENSEN, RT ;
WANK, SA ;
ROWLEY, WH ;
SATO, S ;
GARDNER, JD .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1989, 10 (10) :418-423
[10]   VAGAL AFFERENT PATHWAY MEDIATES PHYSIOLOGICAL ACTION OF CHOLECYSTOKININ ON PANCREATIC-ENZYME SECRETION [J].
LI, Y ;
OWYANG, C .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (01) :418-424