Premium
Improvement of memory for context by inhibition of caspase‐1 in aged rats
Author(s) -
Gemma Carmelina,
Fister Matthew,
Hudson Charles,
Bickford Paula C.
Publication year - 2005
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1111/j.1460-9568.2005.04334.x
Subject(s) - proinflammatory cytokine , hippocampal formation , hippocampus , context (archaeology) , neuroscience , fear conditioning , caspase 1 , synaptic plasticity , psychology , medicine , inflammation , amygdala , biology , inflammasome , paleontology , receptor
Impaired learning and memory is a common pathologic feature associated with numerous neurologic disorders. There is strong evidence that central inflammation contributes significantly to the progression of several neurodegenerative diseases as well as to the ageing process. For example, in aged rats an increase in interleukin‐1β (IL‐1β) is implicated in the decline of synaptic plasticity in the hippocampus and impaired performance on cognitive tasks such as contextual fear conditioning. IL‐1β is a proinflammatory cytokine initially synthesized in an inactive precursor form that is cleaved by caspase‐1 to generate the biologically mature form. In the present study, cleavage of IL‐1β was chronically inhibited using a specific caspase‐1 inhibitor (Ac‐YVAD‐CMK; 10 pmol) in both aged (22 month) and young (4 month) rats. Both groups received Ac‐YVAD‐CMK for 28 days intracerebroventricularly through a brain infusion cannula connected to an osmotic minipump. On day 20 the animals were trained in contextual fear conditioning, and memory for context was tested on day 22. Chronic infusion of a specific caspase‐1 inhibitor in aged rats ameliorated age‐related increases in hippocampal IL‐1β and improved memory for context.