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Characteristics of Learning and Memory in Streptozocin-Induced Diabetic Mice

Flood, James F, Mooradian, Arshag D, Morley, John E·1990·Diabetes

Abstract

We demonstrated that mice with streptozocin-induced diabetes mellitus have normal acquisition for relatively simple tasks but show problems in learning more complex tasks such as shuttle box avoidance. Enhanced learning previously reported in simple passive avoidance tasks appears to be due to increased foot shock sensitivity. Diabetic mice show a marked memory retention deficit after learning an active avoidance T-maze task. This retention deficit was reversed by a single injection of insulin, suggesting that it may be related to hyperglycemia per se. Diabetic mice have a shift to the left in the inverted U-shaped dose-response curve for memory retention produced by the acetylcholine agonist arecoline. Based on a preliminary screening, responses to several other pharmacological memory enhancers are probably altered in diabetic mice. These studies suggest that this mouse model of diabetes mellitus demonstrates a deficit in memory retention and retrieval similar to that seen in humans with diabetes mellitus.

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Metadata

Authors
Flood, J. F., Mooradian, A. D., & Morley, J. E.
Venue
Diabetes
Published
1990-11-01
Volume
39
Issue
11
Pages
1391-1398
ISSN
  • 0012-1797 (ISSN-L)
  • 1939-327X
OpenAlex
W2010222033
Cited by
180
References
0
FWCI
2.52
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Characteristics of Learning and Memory in Streptozocin-Induced Diabetic Mice. https://app.cochat.ai/papers/10.2337/diab.39.11.1391
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Flood, J. F., Mooradian, A. D., & Morley, J. E. (1990). Characteristics of Learning and Memory in Streptozocin-Induced Diabetic Mice. Diabetes. https://doi.org/10.2337/diab.39.11.1391

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.