Key result
Insulin-regulated aminopeptidase (IRAP) inhibitors enhanced aversion-associated and spatial memory in normal and memory-deficit rat models, supporting their development as cognitive enhancers.
Why the study?
Do insulin-regulated aminopeptidase (IRAP) inhibitors enhance memory in rat models?
Do insulin-regulated aminopeptidase (IRAP) inhibitors enhance memory in rat models?
Preclinical evidence suggests that specific inhibitors of insulin-regulated aminopeptidase (IRAP) may serve as a new class of cognitive enhancing agents.
Answers are grounded in this paper and cite their sources.
Merits targeted IRAP inhibitor development; leaves open clinical efficacy and safety in humans.
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.
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Albiston et al. (2011) conducted a review in Cognitive deficits. Insulin-regulated aminopeptidase (IRAP) inhibitors was evaluated on Memory enhancement. Insulin-regulated aminopeptidase (IRAP) inhibitors enhanced aversion-associated and spatial memory in normal and memory-deficit rat models, supporting their development as cognitive enhancers.
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