AI Article Synopsis

  • The study investigated how Multi-component Chinese Medicine Jinzhida (JZD) affects cognitive decline in diabetic rats, aiming to confirm that JZD helps cognitive function by reducing endoplasmic reticulum stress (ERS) and enhancing insulin signaling.
  • After inducing type 2 diabetes in rats, researchers evaluated cognitive performance through various behavioral tests and assessed changes in insulin signaling pathways after JZD treatment.
  • Results showed that JZD treatment improved memory and learning in diabetic rats by suppressing ERS and enhancing insulin signaling in the hippocampus, suggesting a potential therapeutic role for JZD in cognitive decline associated with diabetes.

Article Abstract

Background: To investigate the effects of treatment with Multi component Chinese Medicine Jinzhida (JZD) on behavioral deficits in diabetes-associated cognitive decline (DACD) rats and verify our hypothesis that JZD treatment improves cognitive function by suppressing the endoplasmic reticulum stress (ERS) and improving insulin signaling transduction in the rats' hippocampus.

Methods: A rat model of type 2 diabetes mellitus (T2DM) was established using high fat diet and streptozotocin (30 mg/kg, ip). Insulin sensitivity was evaluated by the oral glucose tolerance test and the insulin tolerance test. After 7 weeks, the T2DM rats were treated with JZD. The step-down test and Morris water maze were used to evaluate behavior in T2DM rats after 5 weeks of treatment with JZD. Levels of phosphorylated proteins involved in the ERS and in insulin signaling transduction pathways were assessed by Western blot for T2DM rats' hippocampus.

Results: Compared to healthy control rats, T2DM rats initially showed insulin resistance and had declines in acquisition and retrieval processes in the step-down test and in spatial memory in the Morris water maze after 12 weeks. Performance on both the step-down test and Morris water maze tasks improved after JZD treatment. In T2DM rats, the ERS was activated, and then inhibited the insulin signal transduction pathways through the Jun NH2-terminal kinases (JNK) mediated. JZD treatment suppressed the ERS, increased insulin signal transduction, and improved insulin resistance in the rats' hippocampus.

Conclusions: Treatment with JZD improved cognitive function in the T2DM rat model. The possible mechanism for DACD was related with ERS inducing the insulin signal transduction dysfunction in T2DM rats' hippocampus. The JZD could reduce ERS and improve insulin signal transduction and insulin resistance in T2DM rats' hippocampus and as a result improved the cognitive function.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3735391PMC
http://dx.doi.org/10.1186/1472-6882-13-161DOI Listing

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