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One-Year Treatment with Olanzapine Depot in Female Rats: Metabolic Effects

BACKGROUND: Antipsychotic drugs can negatively affect the metabolic status of patients, with olanzapine as one of the most potent drugs. While patients are often medicated for long time periods, experiments in rats typically run for 1 to 12 weeks, showing olanzapine-related weight gain and increased...

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Autores principales: Ersland, Kari M, Myrmel, Lene S, Fjære, Even, Berge, Rolf K, Madsen, Lise, Steen, Vidar M, Skrede, Silje
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6499254/
https://www.ncbi.nlm.nih.gov/pubmed/30854556
http://dx.doi.org/10.1093/ijnp/pyz012
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author Ersland, Kari M
Myrmel, Lene S
Fjære, Even
Berge, Rolf K
Madsen, Lise
Steen, Vidar M
Skrede, Silje
author_facet Ersland, Kari M
Myrmel, Lene S
Fjære, Even
Berge, Rolf K
Madsen, Lise
Steen, Vidar M
Skrede, Silje
author_sort Ersland, Kari M
collection PubMed
description BACKGROUND: Antipsychotic drugs can negatively affect the metabolic status of patients, with olanzapine as one of the most potent drugs. While patients are often medicated for long time periods, experiments in rats typically run for 1 to 12 weeks, showing olanzapine-related weight gain and increased plasma lipid levels, with transcriptional upregulation of lipogenic genes in liver and adipose tissue. It remains unknown whether metabolic status will deteriorate with time. METHODS: To examine long-term metabolic effects, we administered intramuscular long-acting injections of olanzapine (100 mg/kg BW) or control substance to female rats for up to 13 months. RESULTS: Exposure to olanzapine long-acting injections led to rapid weight gain, which was sustained throughout the experiment. At 1, 6, and 13 months, plasma lipid levels were measured in separate cohorts of rats, displaying no increase. Hepatic transcription of lipid-related genes was transiently upregulated at 1 month. Glucose and insulin tolerance tests indicated insulin resistance in olanzapine-treated rats after 12 months. CONCLUSION: Our data show that the continuous increase in body weight in response to long-term olanzapine exposure was accompanied by surprisingly few concomitant changes in plasma lipids and lipogenic gene expression, suggesting that adaptive mechanisms are involved to reduce long-term metabolic adverse effects of this antipsychotic agent in rats.
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spelling pubmed-64992542019-05-07 One-Year Treatment with Olanzapine Depot in Female Rats: Metabolic Effects Ersland, Kari M Myrmel, Lene S Fjære, Even Berge, Rolf K Madsen, Lise Steen, Vidar M Skrede, Silje Int J Neuropsychopharmacol Regular Research Articles BACKGROUND: Antipsychotic drugs can negatively affect the metabolic status of patients, with olanzapine as one of the most potent drugs. While patients are often medicated for long time periods, experiments in rats typically run for 1 to 12 weeks, showing olanzapine-related weight gain and increased plasma lipid levels, with transcriptional upregulation of lipogenic genes in liver and adipose tissue. It remains unknown whether metabolic status will deteriorate with time. METHODS: To examine long-term metabolic effects, we administered intramuscular long-acting injections of olanzapine (100 mg/kg BW) or control substance to female rats for up to 13 months. RESULTS: Exposure to olanzapine long-acting injections led to rapid weight gain, which was sustained throughout the experiment. At 1, 6, and 13 months, plasma lipid levels were measured in separate cohorts of rats, displaying no increase. Hepatic transcription of lipid-related genes was transiently upregulated at 1 month. Glucose and insulin tolerance tests indicated insulin resistance in olanzapine-treated rats after 12 months. CONCLUSION: Our data show that the continuous increase in body weight in response to long-term olanzapine exposure was accompanied by surprisingly few concomitant changes in plasma lipids and lipogenic gene expression, suggesting that adaptive mechanisms are involved to reduce long-term metabolic adverse effects of this antipsychotic agent in rats. Oxford University Press 2019-03-03 /pmc/articles/PMC6499254/ /pubmed/30854556 http://dx.doi.org/10.1093/ijnp/pyz012 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of CINP. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Regular Research Articles
Ersland, Kari M
Myrmel, Lene S
Fjære, Even
Berge, Rolf K
Madsen, Lise
Steen, Vidar M
Skrede, Silje
One-Year Treatment with Olanzapine Depot in Female Rats: Metabolic Effects
title One-Year Treatment with Olanzapine Depot in Female Rats: Metabolic Effects
title_full One-Year Treatment with Olanzapine Depot in Female Rats: Metabolic Effects
title_fullStr One-Year Treatment with Olanzapine Depot in Female Rats: Metabolic Effects
title_full_unstemmed One-Year Treatment with Olanzapine Depot in Female Rats: Metabolic Effects
title_short One-Year Treatment with Olanzapine Depot in Female Rats: Metabolic Effects
title_sort one-year treatment with olanzapine depot in female rats: metabolic effects
topic Regular Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6499254/
https://www.ncbi.nlm.nih.gov/pubmed/30854556
http://dx.doi.org/10.1093/ijnp/pyz012
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