AN ANIMAL-MODEL OF CONGENITAL DEFECT OF GENE-EXPRESSION OF CHOLECYSTOKININ (CCK)-A RECEPTOR

被引:129
作者
FUNAKOSHI, A
MIYASAKA, K
SHINOZAKI, H
MASUDA, M
KAWANAMI, T
TAKATA, Y
KONO, A
机构
[1] KYUSHU NATL CANC CTR,RES INST,FUKUOKA 815,JAPAN
[2] TOKYO METROPOLITAN GERIATR HOSP & INST GERONTOL,DEPT CLIN PHYSIOL,TOKYO 173,JAPAN
[3] SOCIAL INSURANCE INATSUKI HOSP,FUKUOKA 82002,JAPAN
关键词
D O I
10.1006/bbrc.1995.1728
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
Expressions of the CCK-A and B receptor genes in fetal and adult pancreas of OLETF rats were examined by the reverse transcriptase polymerase chain reaction followed by Southern blot hybridization. The pancreatic responses to various stimulants were examined in vitro and results were compared with those of control (LETO) rats. CCK-A receptor mRNA was not expressed in the fetal pancreas of either strain or in the adult pancreas of OLETF rats, but was expressed in the adult pancreas of LETO rats. CCK-B receptor mRNA was expressed in fetal and adult pancreas in both strains. Southern blot hybridization indicated a difference in gene structure in the two strains. The maximal effective concentrations of neuromedin C, carbachol, and secretin for amylase secretion and intracellular Ca2+ movement stimulated by carbachol and neuromedin C were similar in the two strains. CCK-8 and the non-sulfated form stimulated amylase secretion only in LETO rats. These results suggest that OLETF rats are a new model of a congenital defect of the CCK-A receptor gene and should be useful for determining CCK receptor function. (C) 1995 Academic Press,Inc.
引用
收藏
页码:787 / 796
页数:10
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