HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Metformin attenuates antipsychotic-induced metabolic dysfunctions in MK801-induced schizophrenia-like rats.

AbstractRATIONALE:
Second-generation antipsychotics are the first-line medications prescribed for schizophrenic patients; however, some of them, such as olanzapine and risperidone, may induce metabolic dysfunctions during short-term treatment. Metformin is an effective adjuvant that attenuates antipsychotic-induced metabolic dysfunctions (AIMD) in clinical practice. Whether metformin can reverse AIMD and whether metformin affects the therapeutic effects of antipsychotics in animal models of schizophrenia are questions that still need to be investigated.
METHODS:
In this study, an animal model of schizophrenia was established by consecutive injections of MK801 during the neurodevelopmental period. In adulthood, different dosages of olanzapine or risperidone treatment were administered to the schizophrenia model animals for 14 days. Both therapeutic effects and metabolic adverse effects were measured by behavioral tests, histopathological tests, and biochemical tests. The coadministration of different doses of metformin with olanzapine or risperidone was used to evaluate the effects of metformin on both AIMD and the therapeutic effect of those antipsychotics.
RESULTS:
The MK801-treated rats showed schizophrenia-like behavior and variations in the shape and volume of the hippocampus. Both olanzapine and risperidone reversed the MK801-induced behavioral abnormalities as the dosage increased; however, they degenerated the hepatocytes in the liver and influenced the blood lipid levels and blood glucose levels. The coadministration of metformin did not affect the therapeutic effects of olanzapine or risperidone on behavioral abnormalities but attenuated the metabolic dysfunctions induced by those antipsychotics.
CONCLUSION:
Metformin attenuated the olanzapine- and risperidone-induced metabolic dysfunctions in MK801-induced schizophrenia-like rats without reducing the therapeutic effects of the antipsychotics.
AuthorsChao Luo, Xu Wang, Xiaoyuan Mao, Hanxue Huang, Yong Liu, Jingping Zhao, Honghao Zhou, Zhaoqian Liu, Xiangping Li
JournalPsychopharmacology (Psychopharmacology (Berl)) Vol. 237 Issue 8 Pg. 2257-2277 (Aug 2020) ISSN: 1432-2072 [Electronic] Germany
PMID32588080 (Publication Type: Journal Article)
Chemical References
  • Antipsychotic Agents
  • Excitatory Amino Acid Antagonists
  • Dizocilpine Maleate
  • Metformin
Topics
  • Animals
  • Animals, Newborn
  • Antipsychotic Agents (toxicity)
  • Dizocilpine Maleate (toxicity)
  • Dose-Response Relationship, Drug
  • Excitatory Amino Acid Antagonists (toxicity)
  • Female
  • Metabolic Diseases (chemically induced, drug therapy, psychology)
  • Metformin (therapeutic use)
  • Rats
  • Rats, Sprague-Dawley
  • Schizophrenia (chemically induced, drug therapy)
  • Schizophrenic Psychology

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: