Pioglitazone improves porcine oocyte maturation and subsequent parthenogenetic embryo development in vitro by increasing lipid metabolism.


Journal

Molecular reproduction and development
ISSN: 1098-2795
Titre abrégé: Mol Reprod Dev
Pays: United States
ID NLM: 8903333

Informations de publication

Date de publication:
09 2019
Historique:
received: 06 08 2018
accepted: 30 06 2019
pubmed: 21 8 2019
medline: 19 6 2020
entrez: 21 8 2019
Statut: ppublish

Résumé

Optimization of culture conditions is important to improve oocyte maturation and subsequent embryo development. In particular, this study analyzed the effects of increasing concentrations of PIO in the maturation medium on spindle formation and chromosome alignment, glutathione, and intracellular ROS levels and expression of selected genes related to maternal markers, apoptosis, and lipid metabolism. The percentage of oocytes displaying normal spindle formation and chromosome alignment was higher in the 1 µM PIO (1 PIO)-treated group than in the control group. The glutathione level was significantly higher in the 1 PIO-treated group than in the control group, while the reactive oxygen species level did not differ. Expression of maternal marker (MOS and GDF9), antiapoptotic (BIRC5), and lipid metabolism-related (ACADS, CPT2, SREBF1, and PPARG) genes was higher in the 1 PIO-treated group than in the control group, while expression of a proapoptotic gene (CASP3) was lower. The blastocyst formation rate and the percentage of blastocysts that reached at least the hatching stage on Days 6 and 7, and the percentage of blastocysts containing more than 128 cells were significantly higher in the 1 PIO-treated group than in the control group. These results indicate that PIO treatment during in vitro maturation improves porcine oocyte maturation and subsequent parthenogenetic embryo development mainly by enhancing lipid metabolism and antioxidant defense in oocytes.

Identifiants

pubmed: 31429176
doi: 10.1002/mrd.23252
doi:

Substances chimiques

Pioglitazone X4OV71U42S

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1245-1254

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Sang-Gi Jeong (SG)

Faculty of Biotechnology, College of Applied Life Sciences, Jeju National University, Jeju-si, Korea.
Stem Cell Research Center, Jeju National University, Jeju-si, Korea.

Seung-Eun Lee (SE)

Faculty of Biotechnology, College of Applied Life Sciences, Jeju National University, Jeju-si, Korea.
Stem Cell Research Center, Jeju National University, Jeju-si, Korea.

Won-Jae Kim (WJ)

Faculty of Biotechnology, College of Applied Life Sciences, Jeju National University, Jeju-si, Korea.
Stem Cell Research Center, Jeju National University, Jeju-si, Korea.

Yun-Gwi Park (YG)

Faculty of Biotechnology, College of Applied Life Sciences, Jeju National University, Jeju-si, Korea.
Stem Cell Research Center, Jeju National University, Jeju-si, Korea.

Jae-Wook Yoon (JW)

Faculty of Biotechnology, College of Applied Life Sciences, Jeju National University, Jeju-si, Korea.
Stem Cell Research Center, Jeju National University, Jeju-si, Korea.

Chan-Oh Park (CO)

Faculty of Biotechnology, College of Applied Life Sciences, Jeju National University, Jeju-si, Korea.
Stem Cell Research Center, Jeju National University, Jeju-si, Korea.

Hyo-Jin Park (HJ)

Faculty of Biotechnology, College of Applied Life Sciences, Jeju National University, Jeju-si, Korea.
Stem Cell Research Center, Jeju National University, Jeju-si, Korea.

Eun-Young Kim (EY)

Faculty of Biotechnology, College of Applied Life Sciences, Jeju National University, Jeju-si, Korea.
Stem Cell Research Center, Jeju National University, Jeju-si, Korea.
Mirae Cell Bio, Seoul, Korea.

Se-Pill Park (SP)

Faculty of Biotechnology, College of Applied Life Sciences, Jeju National University, Jeju-si, Korea.
Stem Cell Research Center, Jeju National University, Jeju-si, Korea.
Mirae Cell Bio, Seoul, Korea.

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