Cargando…
Atypical Antipsychotics and the Human Skeletal Muscle Lipidome
Atypical antipsychotics (AAPs) are a class of medications associated with significant metabolic side effects, including insulin resistance. The aim of this study was to analyze the skeletal muscle lipidome of patients on AAPs, compared to mood stabilizers, to further understand the molecular changes...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316471/ https://www.ncbi.nlm.nih.gov/pubmed/30322152 http://dx.doi.org/10.3390/metabo8040064 |
_version_ | 1783384537591447552 |
---|---|
author | Burghardt, Kyle J. Ward, Kristen M. Sanders, Elani J. Howlett, Bradley H. Seyoum, Berhane Yi, Zhengping |
author_facet | Burghardt, Kyle J. Ward, Kristen M. Sanders, Elani J. Howlett, Bradley H. Seyoum, Berhane Yi, Zhengping |
author_sort | Burghardt, Kyle J. |
collection | PubMed |
description | Atypical antipsychotics (AAPs) are a class of medications associated with significant metabolic side effects, including insulin resistance. The aim of this study was to analyze the skeletal muscle lipidome of patients on AAPs, compared to mood stabilizers, to further understand the molecular changes underlying AAP treatment and side effects. Bipolar patients on AAPs or mood stabilizers underwent a fasting muscle biopsy and assessment of insulin sensitivity. A lipidomic analysis of total fatty acids (TFAs), phosphatidylcholines (PCs) and ceramides (CERs) was performed on the muscle biopsies, then lipid species were compared between treatment groups, and correlation analyses were performed with insulin sensitivity. TFAs and PCs were decreased and CERs were increased in the AAP group relative to those in the mood stabilizer group (FDR q-value <0.05). A larger number of TFAs and PCs were positively correlated with insulin sensitivity in the AAP group compared to those in the mood stabilizer group. In contrast, a larger number of CERs were negatively correlated with insulin sensitivity in the AAP group compared to that in the mood stabilizer group. The findings here suggest that AAPs are associated with changes in the lipid profiles of human skeletal muscle when compared to mood stabilizers and that these changes correlate with insulin sensitivity. |
format | Online Article Text |
id | pubmed-6316471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63164712019-01-10 Atypical Antipsychotics and the Human Skeletal Muscle Lipidome Burghardt, Kyle J. Ward, Kristen M. Sanders, Elani J. Howlett, Bradley H. Seyoum, Berhane Yi, Zhengping Metabolites Article Atypical antipsychotics (AAPs) are a class of medications associated with significant metabolic side effects, including insulin resistance. The aim of this study was to analyze the skeletal muscle lipidome of patients on AAPs, compared to mood stabilizers, to further understand the molecular changes underlying AAP treatment and side effects. Bipolar patients on AAPs or mood stabilizers underwent a fasting muscle biopsy and assessment of insulin sensitivity. A lipidomic analysis of total fatty acids (TFAs), phosphatidylcholines (PCs) and ceramides (CERs) was performed on the muscle biopsies, then lipid species were compared between treatment groups, and correlation analyses were performed with insulin sensitivity. TFAs and PCs were decreased and CERs were increased in the AAP group relative to those in the mood stabilizer group (FDR q-value <0.05). A larger number of TFAs and PCs were positively correlated with insulin sensitivity in the AAP group compared to those in the mood stabilizer group. In contrast, a larger number of CERs were negatively correlated with insulin sensitivity in the AAP group compared to that in the mood stabilizer group. The findings here suggest that AAPs are associated with changes in the lipid profiles of human skeletal muscle when compared to mood stabilizers and that these changes correlate with insulin sensitivity. MDPI 2018-10-13 /pmc/articles/PMC6316471/ /pubmed/30322152 http://dx.doi.org/10.3390/metabo8040064 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Burghardt, Kyle J. Ward, Kristen M. Sanders, Elani J. Howlett, Bradley H. Seyoum, Berhane Yi, Zhengping Atypical Antipsychotics and the Human Skeletal Muscle Lipidome |
title | Atypical Antipsychotics and the Human Skeletal Muscle Lipidome |
title_full | Atypical Antipsychotics and the Human Skeletal Muscle Lipidome |
title_fullStr | Atypical Antipsychotics and the Human Skeletal Muscle Lipidome |
title_full_unstemmed | Atypical Antipsychotics and the Human Skeletal Muscle Lipidome |
title_short | Atypical Antipsychotics and the Human Skeletal Muscle Lipidome |
title_sort | atypical antipsychotics and the human skeletal muscle lipidome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316471/ https://www.ncbi.nlm.nih.gov/pubmed/30322152 http://dx.doi.org/10.3390/metabo8040064 |
work_keys_str_mv | AT burghardtkylej atypicalantipsychoticsandthehumanskeletalmusclelipidome AT wardkristenm atypicalantipsychoticsandthehumanskeletalmusclelipidome AT sanderselanij atypicalantipsychoticsandthehumanskeletalmusclelipidome AT howlettbradleyh atypicalantipsychoticsandthehumanskeletalmusclelipidome AT seyoumberhane atypicalantipsychoticsandthehumanskeletalmusclelipidome AT yizhengping atypicalantipsychoticsandthehumanskeletalmusclelipidome |