The Effects of Methylene Blue on Trace Fear Memory and Proteolytic Activity in Young and Aged Rats.

Mentor 1

James R. Moyer, Jr.

Location

Union Wisconsin Room

Start Date

28-4-2017 1:30 PM

End Date

28-4-2017 4:00 PM

Description

Both humans and rats experience age-related deficits in declarative memory.Recently, plasticity-associated protein degradation in synapses has been shown to be necessaryfor memory formation. A decrease in basal proteasome activity with increasing age is evident across various species. Decreased plasticity-associated proteasome activity with normal aging could underlie age-related deficits in memory performance previously documented in aged rats. Using trace fear conditioning (TFC) to model episodic memory in rats, we attempted to rescue age-related memory decline by upregulating proteasome activity via dietary administration of the compound methylene blue (MB). MB increases chymotrypsin-and trypsin-like proteasome activity in 3xTg-AD mice. Two experiments were conducted to test the effects of MB on trace fear memory and proteolytic activity in non-transgenic F344 young (3 months) and aged (18 months) rats. In Experiment 1, 3-month-old rats were administered 50mg of MB per 100g of powdered food for 4 months.This treatment did not affect memory performance.However, therewas a significant increase in chymotrypsin-like activity insynapsesofthe retrosplenial cortex (RSC). Since MB treatment is dose dependent, we lowered the dose in Experiment 2. 3 month and 18-month-old rats were administered 25mg of MB per 100g of powdered food.MB treatment in young rats enhanced memory performance, while not affecting memory performance in aged rats.However, there was a significant increase in chymotrypsin-like activity in the synapsesof theRSC for both aged and young rats,and the cytosolic portion of the dorsal hippocampus for young rats. These results suggest a 25mg dose of MB per 100g of food has a significant effect on TFC in young rats but not aged rats. Therefore,additional research is needed to determine the optimal dose at which MB enhances TFC in aged rats.

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Apr 28th, 1:30 PM Apr 28th, 4:00 PM

The Effects of Methylene Blue on Trace Fear Memory and Proteolytic Activity in Young and Aged Rats.

Union Wisconsin Room

Both humans and rats experience age-related deficits in declarative memory.Recently, plasticity-associated protein degradation in synapses has been shown to be necessaryfor memory formation. A decrease in basal proteasome activity with increasing age is evident across various species. Decreased plasticity-associated proteasome activity with normal aging could underlie age-related deficits in memory performance previously documented in aged rats. Using trace fear conditioning (TFC) to model episodic memory in rats, we attempted to rescue age-related memory decline by upregulating proteasome activity via dietary administration of the compound methylene blue (MB). MB increases chymotrypsin-and trypsin-like proteasome activity in 3xTg-AD mice. Two experiments were conducted to test the effects of MB on trace fear memory and proteolytic activity in non-transgenic F344 young (3 months) and aged (18 months) rats. In Experiment 1, 3-month-old rats were administered 50mg of MB per 100g of powdered food for 4 months.This treatment did not affect memory performance.However, therewas a significant increase in chymotrypsin-like activity insynapsesofthe retrosplenial cortex (RSC). Since MB treatment is dose dependent, we lowered the dose in Experiment 2. 3 month and 18-month-old rats were administered 25mg of MB per 100g of powdered food.MB treatment in young rats enhanced memory performance, while not affecting memory performance in aged rats.However, there was a significant increase in chymotrypsin-like activity in the synapsesof theRSC for both aged and young rats,and the cytosolic portion of the dorsal hippocampus for young rats. These results suggest a 25mg dose of MB per 100g of food has a significant effect on TFC in young rats but not aged rats. Therefore,additional research is needed to determine the optimal dose at which MB enhances TFC in aged rats.