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Detection of impaired cognitive function in rat with hepatosteatosis model and improving effect of GLP-1 analogs (exenatide) on cognitive function in hepatosteatosis.

ScientificWorldJournal · 2014

Last updated 2026-05-28

In a study of 18 rats fed fructose to induce liver fat (hepatosteatosis), those with the condition showed worse memory performance than 6 control rats with normal diets. However, rats with hepatosteatosis given the GLP-1 drug exenatide directly into the brain had improved memory performance compared to those given a salt solution.

AI summary of the abstract below.

JournalScientificWorldJournal, 2014
Citations7
Relative citation ratio0.27
NIH percentile17
Molecules exenatide
Conditions studied Mash

Abstract

The aims of the study were to evaluate (1) detection of cognitive function changing in rat with hepatosteatosis model and (2) evaluate the effect of GLP-1 analog (exenatide) on cognitive function in hepatosteatosis. In the study group, 30% fructose was given in nutrition water to perform hepatosteatosis for 8 weeks to 18 male rats. Six male rats were chosen as control group and had normal nutrition. Fructose nutrition group were stratified into 3 groups. In first group (n = 6), intracerebroventricular (ICV) infusion of exenatide (n = 6) was given. ICV infusion of NaCl (n = 6) was given to second group. And also, the third group had no treatment. And also, rats were evaluated for passive avoidance learning (PAL) and liver histopathology. Mean levels of latency time were statistically significantly decreased in rats with hepatosteatosis than those of normal rats (P < 0.00001). However, mean level of latency time in rats with hepatosteatosis treated with ICV exenatide was statistically significantly increased than that of rats treated with ICV NaCl (P < 0.001). Memory performance falls off in rats with hepatosteatosis feeding on fructose (decreased latency time). However, GLP-1 ameliorates cognitive functions (increased latency time) in rats with hepatosteatosis and releated metabolic syndrome.

Verbatim abstract via PubMed 24741367 ↗

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