共 81 条
Identification and development of specific inhibitors for insulin-regulated aminopeptidase as a new class of cognitive enhancers
被引:74
作者:

Albiston, Anthony L.
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h-index: 0
机构:
Univ Melbourne, Florey Neurosci Inst, Howard Florey Inst, Parkville, Vic 3052, Australia Monash Univ, Dept Physiol, Clayton, Vic 3800, Australia

Diwakarla, Shanti
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Melbourne, Florey Neurosci Inst, Howard Florey Inst, Parkville, Vic 3052, Australia Monash Univ, Dept Physiol, Clayton, Vic 3800, Australia

Fernando, Ruani N.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Melbourne, Florey Neurosci Inst, Howard Florey Inst, Parkville, Vic 3052, Australia
Monash Inst Pharmaceut Sci, Parkville, Vic, Australia Monash Univ, Dept Physiol, Clayton, Vic 3800, Australia

Mountford, Simon J.
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h-index: 0
机构: Monash Univ, Dept Physiol, Clayton, Vic 3800, Australia

Yeatman, Holly R.
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h-index: 0
机构:
Univ Melbourne, Florey Neurosci Inst, Howard Florey Inst, Parkville, Vic 3052, Australia Monash Univ, Dept Physiol, Clayton, Vic 3800, Australia

Morgan, Broden
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h-index: 0
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Univ Melbourne, Florey Neurosci Inst, Howard Florey Inst, Parkville, Vic 3052, Australia Monash Univ, Dept Physiol, Clayton, Vic 3800, Australia

Vi Pham
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h-index: 0
机构:
Monash Univ, Dept Physiol, Clayton, Vic 3800, Australia
Univ Melbourne, Florey Neurosci Inst, Howard Florey Inst, Parkville, Vic 3052, Australia Monash Univ, Dept Physiol, Clayton, Vic 3800, Australia

Holien, Jessica K.
论文数: 0 引用数: 0
h-index: 0
机构:
St Vincents Inst Med Res, Fitzroy, Vic 3065, Australia Monash Univ, Dept Physiol, Clayton, Vic 3800, Australia

Parker, Michael W.
论文数: 0 引用数: 0
h-index: 0
机构:
St Vincents Inst Med Res, Fitzroy, Vic 3065, Australia
Univ Melbourne, Mol Sci & Biotechnol Inst Bio21, Dept Biochem & Mol Biol, Parkville, Vic 3052, Australia Monash Univ, Dept Physiol, Clayton, Vic 3800, Australia

Thompson, Philip E.
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h-index: 0
机构:
Monash Inst Pharmaceut Sci, Parkville, Vic, Australia Monash Univ, Dept Physiol, Clayton, Vic 3800, Australia

Chai, Siew Yeen
论文数: 0 引用数: 0
h-index: 0
机构:
Monash Univ, Dept Physiol, Clayton, Vic 3800, Australia
Univ Melbourne, Florey Neurosci Inst, Howard Florey Inst, Parkville, Vic 3052, Australia Monash Univ, Dept Physiol, Clayton, Vic 3800, Australia
机构:
[1] Monash Univ, Dept Physiol, Clayton, Vic 3800, Australia
[2] Univ Melbourne, Florey Neurosci Inst, Howard Florey Inst, Parkville, Vic 3052, Australia
[3] Monash Inst Pharmaceut Sci, Parkville, Vic, Australia
[4] St Vincents Inst Med Res, Fitzroy, Vic 3065, Australia
[5] Univ Melbourne, Mol Sci & Biotechnol Inst Bio21, Dept Biochem & Mol Biol, Parkville, Vic 3052, Australia
基金:
英国医学研究理事会;
关键词:
memory;
angiotensin IV;
GLUT4;
peptidomimetic;
vasopressin;
oxytocinase;
glucose;
drug development;
PLACENTAL LEUCINE AMINOPEPTIDASE/OXYTOCINASE;
CLASS-I MHC;
ANGIOTENSIN-IV;
MEMBRANE AMINOPEPTIDASE;
PASSIVE-AVOIDANCE;
AT(4) RECEPTOR;
ALZHEIMERS-DISEASE;
DOPAMINE-RECEPTORS;
GENE-EXPRESSION;
POTENTIAL ROLE;
D O I:
10.1111/j.1476-5381.2011.01402.x
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Two structurally distinct peptides, angiotensin IV and LVV-haemorphin 7, both competitive high-affinity inhibitors of insulin-regulated aminopeptidase (IRAP), were found to enhance aversion-associated and spatial memory in normal rats and to improve performance in a number of memory tasks in rat deficits models. These findings provide compelling support for the development of specific, high-affinity inhibitors of the enzyme as new cognitive enhancing agents. Different classes of IRAP inhibitors have been developed including peptidomimetics and small molecular weight compounds identified through in silico screening with a homology model of the catalytic domain of IRAP. The proof of principal that inhibition of IRAP activity results in facilitation of memory has been obtained by the demonstration that the small-molecule IRAP inhibitors also exhibit memory-enhancing properties.
引用
收藏
页码:37 / 47
页数:11
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Vrije Univ Brussel, Dept Mol & Biochem Pharmacol, B-1050 Brussels, Belgium Uppsala Univ, Dept Med Chem, SE-75123 Uppsala, Sweden

Lindeberg, Gunnar
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Uppsala Univ, Dept Med Chem, SE-75123 Uppsala, Sweden Uppsala Univ, Dept Med Chem, SE-75123 Uppsala, Sweden

Karlen, Anders
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Uppsala Univ, Dept Med Chem, SE-75123 Uppsala, Sweden Uppsala Univ, Dept Med Chem, SE-75123 Uppsala, Sweden

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Erdelyi, Mate
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Univ Gothenburg, Dept Chem, SE-41296 Gothenburg, Sweden Uppsala Univ, Dept Med Chem, SE-75123 Uppsala, Sweden

Hallberg, Anders
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Uppsala Univ, Dept Med Chem, SE-75123 Uppsala, Sweden Uppsala Univ, Dept Med Chem, SE-75123 Uppsala, Sweden
[10]
Small potent ligands to the insulin-regulated aminopeptidase (IRAP)/AT4 receptor
[J].
Axen, Andreas
;
Andersson, Hanna
;
Lindeberg, Gunnar
;
Ronnholm, Harriet
;
Kortesmaa, Jarkko
;
Demaegdt, Heidi
;
Vauquelin, Georges
;
Karlen, Anders
;
Hallberg, Mathias
.
JOURNAL OF PEPTIDE SCIENCE,
2007, 13 (07)
:434-444

Axen, Andreas
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机构: Univ Uppsala, Dept Pharmaceut Biosci, Div Biol Res Drug Dependence, S-75124 Uppsala, Sweden

Andersson, Hanna
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机构: Univ Uppsala, Dept Pharmaceut Biosci, Div Biol Res Drug Dependence, S-75124 Uppsala, Sweden

Lindeberg, Gunnar
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机构: Univ Uppsala, Dept Pharmaceut Biosci, Div Biol Res Drug Dependence, S-75124 Uppsala, Sweden

Ronnholm, Harriet
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机构: Univ Uppsala, Dept Pharmaceut Biosci, Div Biol Res Drug Dependence, S-75124 Uppsala, Sweden

Kortesmaa, Jarkko
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机构: Univ Uppsala, Dept Pharmaceut Biosci, Div Biol Res Drug Dependence, S-75124 Uppsala, Sweden

Demaegdt, Heidi
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机构: Univ Uppsala, Dept Pharmaceut Biosci, Div Biol Res Drug Dependence, S-75124 Uppsala, Sweden

Vauquelin, Georges
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机构: Univ Uppsala, Dept Pharmaceut Biosci, Div Biol Res Drug Dependence, S-75124 Uppsala, Sweden

Karlen, Anders
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机构: Univ Uppsala, Dept Pharmaceut Biosci, Div Biol Res Drug Dependence, S-75124 Uppsala, Sweden

Hallberg, Mathias
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机构: Univ Uppsala, Dept Pharmaceut Biosci, Div Biol Res Drug Dependence, S-75124 Uppsala, Sweden