ArticleJournal of animal science2020
Presence of Clock genes in equine full-term placenta.
Article in Journal of animal science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed, 4 citations in OpenAlex.
- SARS-CoV-2 Rapidly Infects Peripheral Sensory and Autonomic Neurons, Contributing to Central Nervous System Neuroinvasion before Viremia.International journal of molecular sciences · 2024Article
- Equine Placentitis in Mares Induces the Secretion of Pro-Inflammatory CytokineVeterinary sciences · 2023Article
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Mammals have a circadian rhythm that is synchronized by a master clock located in the hypothalamic suprachiasmatic nucleus (SCN). The SCN regulates additional clocks located in peripheral tissues, including some involved in endocrine or reproductive functions. Studies in humans and mice report that molecular clocks also exist in the placenta. However, little is known about the presence of "Clock genes," namely Circadian Locomotor Output Cycles Kaput (CLOCK), Brain and Muscle Arnt-Like 1 (BMAL1), Period 1 (PER1), Period 2 (PER2), Cryptochrome 1 (CRY1), and Cryptochrome 2 (CRY2), in equine placenta. Pregnancy length in mares varies and shows fluctuations in hormone concentrations throughout pregnancy. We postulate that similar to humans and mice, Clock genes are present in the horse placentas. Our goal was to determine if relative levels of clock genes were different between placentas associated with males and female fetuses or correlated with gestational length. We used polymerase chain reaction and immunofluorescence to study the presence of CLOCK, BMAL1, PER1, PER2, CRY1, and CRY2 in full-term mare placentas. Clock genes were present in all placentas, with significant lower levels of CRY2 and CLOCK in placentas that were associated with male fetuses. There was no association between relative levels of Clock genes and gestational length. These data provide the stage for future studies aimed at uncovering a function for Clock genes in the horse placenta.
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Registered trials
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