A TRYPSIN INHIBITOR-LIKE PEPTIDE PEC-60 REDUCES THE AFFINITY OF DOPAMINE-D2 AGONIST BINDING-SITES IN RAT NEOSTRIATAL MEMBRANES

被引：10

作者：

VONEULER, G ^{[1
]}

FERRE, S ^{[1
]}

VONEULER, M ^{[1
]}

AGERBERTH, B ^{[1
]}

MUTT, V ^{[1
]}

FUXE, K ^{[1
]}

机构：

[1] KAROLINSKA INST,DEPT BIOCHEM,S-10401 STOCKHOLM 60,SWEDEN

来源：

EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION | 1991年 / 207卷 / 04期

关键词：

D O I：

10.1016/0922-4106(91)90013-8

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

[No abstract available]

引用

收藏

页码：365 / 366

页数：2

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[3] PEC-60, A NOVEL PORCINE 60-RESIDUE INTESTINAL PEPTIDE, REDUCES DOPAMINE UTILIZATION IN DISCRETE PARTS OF THE NEOSTRIATUM OF THE MALE-RAT FOLLOWING AN INTRACEREBROVENTRICULAR INJECTION
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[J]. ACTA PHYSIOLOGICA SCANDINAVICA, 1991, 141 (01): : 139 - 140
[4] INTRAVENTRICULAR-INJECTION OF NEUROTENSIN REDUCES DOPAMINE D2 AGONIST BINDING IN RAT FOREBRAIN AND INTERMEDIATE LOBE OF THE PITUITARY-GLAND - RELATIONSHIP TO SERUM HORMONE LEVELS AND NERVE-TERMINAL COEXISTENCE
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[J]. BRAIN RESEARCH, 1990, 531 (1-2) : 253 - 262
[5] VONEULER G, 1989, ACTA PHYSIOL SCAND, V135, P443