cris.boxmetadata.label.title
Tibolone attenuates inflammatory response by palmitic acid and preserves mitochondrial membrane potential in astrocytic cells through estrogen receptor beta
cris.boxmetadata.label.dateissued
15 browse.startsWith.months.april 2019
cris.boxmetadata.label.accesslevel
metadata only access
cris.boxmetadata.label.resourcetype
journal article
cris.boxmetadata.label.authors
Pontificia Universidad Javeriana
cris.boxmetadata.label.publisher
Elsevier Ireland Ltd
cris.boxmetadata.label.abstract
Palmitic acid (PA) induces several metabolic and molecular changes in astrocytes, and, it is involved in pathological conditions related to neurodegenerative diseases. Previously, we demonstrated that tibolone, a synthetic steroid with estrogenic, progestogenic and androgenic actions, protects cells from mitochondrial damage and morphological changes induced by PA. Here, we have evaluated which estrogen receptor is involved in protective actions of tibolone and analyzed whether tibolone reverses gene expression changes induced by PA. Tibolone actions on astrocytic cells were mimicked by agonists of estrogen receptor α (ERα) and β (ERβ), but the blockade of both ERs suggested a predominance of ERβ on mitochondria membrane potential. Expression analysis showed a significant effect of tibolone on genes associated with inflammation such as IL6, IL1B and miR155-3p. It is noteworthy that tibolone attenuated the increased expression of TERT, TERC and DNMT3B genes induced by palmitic acid. Our results suggest that tibolone has anti-inflammatory effects and can modulate pathways associated with DNA methylation and telomeric complex. However, future studies are needed to elucidate the role of epigenetic mechanisms and telomere-associated proteins on tibolone actions.
cris.boxmetadata.label.citationstartpage
65
cris.boxmetadata.label.citationendpage
78
cris.boxmetadata.label.volume
486
cris.boxmetadata.label.language
English
cris.boxmetadata.label.ocdeknowledgeArea
Biotecnología médica
Endocrinología, Metabolismo (incluyendo diabetes, hormonas)
cris.boxmetadata.label.doi
cris.boxmetadata.label.scopusidentifier
2-s2.0-85062430500
cris.boxmetadata.label.pubmedidentifier
cris.boxmetadata.label.source
Molecular and Cellular Endocrinology
cris.boxmetadata.label.containerissn
03037207
cris.boxmetadata.label.sponsor
YG-G is supported by a PhD fellowship from Centro de Estudios Interdisciplinarios Básicos y Aplicados CEIBA (Rodolfo Llinás Program). VE was supported by the Fondecyt 1150194 . This study was supported by a research grant from COLCIENCIAS (Grant No. 824-2017 ).
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