A NOVEL NON-H-1, NON-H-2 HISTAMINE ANTAGONIST PROTECTS AGAINST CYSTEAMINE-INDUCED DUODENAL-ULCERS IN RATS

被引：2

作者：

GLAVIN, GB

BRANDES, LJ

机构：

[1] UNIV MANITOBA,FAC MED,DEPT SURG,WINNIPEG R3E 0W3,MANITOBA,CANADA

[2] UNIV MANITOBA,MANITOBA INST CELL BIOL,DEPT MED,WINNIPEG R3E 0W3,MANITOBA,CANADA

来源：

PHARMACOLOGY | 1988年 / 37卷 / 05期

关键词：

D O I：

10.1159/000138477

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

引用

页码：277 / 280

页数：4

共 14 条

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[2] BRANDES L, 1988, IN PRESS CANCER RES
[3] A DIPHENYLMETHANE DERIVATIVE SELECTIVE FOR THE ANTI-ESTROGEN BINDING-SITE MAY HELP DEFINE ITS BIOLOGICAL ROLE
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[J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 124 (01) : 244 - 249
[4] A DIPHENYLMETHANE DERIVATIVE SPECIFIC FOR THE ANTIESTROGEN BINDING-SITE FOUND IN RAT-LIVER MICROSOMES
BRANDES, LJ
HERMONAT, MW
[J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 123 (02) : 724 - 728
[5] THE ANTIPROLIFERATIVE PROPERTIES OF TAMOXIFEN AND PHENOTHIAZINES MAY BE MEDIATED BY A UNIQUE HISTAMINE-RECEPTOR (QUESTIONABLE-H-3) DISTINCT FROM THE CALMODULIN-BINDING SITE
BRANDES, LJ
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CAWKER, MD
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[J]. CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1986, 18 (01) : 21 - 23
[6] BRANDES LJ, 1987, CANCER RES, V47, P4025
[7] NEW EVIDENCE THAT THE ANTIESTROGEN BINDING-SITE MAY BE A NOVEL GROWTH-PROMOTING HISTAMINE-RECEPTOR (QUESTIONABLE-H-3) WHICH MEDIATES THE ANTIESTROGENIC AND ANTIPROLIFERATIVE EFFECTS OF TAMOXIFEN
BRANDES, LJ
BOGDANOVIC, RP
[J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1986, 134 (02) : 601 - 608
[8] COMPARING BINDING OF HISTAMINE AND H2-ANTAGONIST WITH THEIR EFFECTS ON GASTRIC-ACID SECRETION
EKBLAD, EBM
LICKO, V
[J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 923 (02) : 315 - 322
[9] GLAVIN G, 1988, IN PRESS CAN J PHYSL
[10] GLAVIN G, 1988, IN PRESS J PHARM PHA, V40

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