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Human Primary Trophoblast Cell Culture Model to Study the Protective Effects of Melatonin Against Hypoxia/reoxygenation-induced Disruption
Published on: July 30, 2016
The rat oocyte synthesises melatonin
Kenichiro Sakaguchi1, Masanori T Itoh, Noriyuki Takahashi
1Department of Obstetrics and Gynaecology, St. Marianna University School of Medicine, Sugao, Miyamae-ku, Kawasaki 216-8511, Japan.
Melatonin is synthesized in rat ovaries, specifically within oocytes, from serotonin. This ovarian melatonin may play a role in oocyte growth and maturation.
Area of Science:
- Reproductive Biology
- Endocrinology
- Molecular Biology
Background:
- Melatonin, an indoleamine, is primarily known for its synthesis in the pineal gland.
- Previous research suggests potential melatonin synthesis within the ovary.
- The enzymes arylalkylamine N-acetyltransferase (AANAT) and acetylserotonin O-methyltransferase (ASMT) are crucial for melatonin production.
Purpose of the Study:
- To investigate the expression of AANAT and ASMT in the adult rat ovary.
- To determine if melatonin is synthesized within ovarian cells, particularly oocytes.
Main Methods:
- Reverse transcription-polymerase chain reaction (RT-PCR) to detect AANAT and ASMT mRNA.
- Western blotting to confirm the presence of AANAT protein.
- Immunohistochemistry to localize AANAT protein within ovarian tissues.
- Incubation of isolated oocytes with serotonin to assess melatonin production.
Main Results:
- Both AANAT and ASMT mRNAs were detected in the adult rat ovary.
- AANAT protein (24kDa) was identified in the ovary, similar to the pineal gland.
- AANAT protein was localized to oocytes, corpus luteum, medulla, and mast cells.
- Oocytes exhibited increasing AANAT levels during follicular development and metabolized serotonin to melatonin.
Conclusions:
- The enzymes necessary for melatonin synthesis are present and active in the adult rat ovary.
- Melatonin is synthesized directly from serotonin within oocytes.
- Oocyte-derived melatonin may influence oocyte growth, maturation, and function, potentially via antioxidant or calmodulin antagonist mechanisms.
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