4.7 Article

Evaluation of Triclosan Effects on Cultured Swine Luteal Cells

期刊

ANIMALS
卷 11, 期 3, 页码 -

出版社

MDPI
DOI: 10.3390/ani11030606

关键词

corpus luteum; progesterone; nitric oxide; superoxide anion; redox status

资金

  1. Program FIL-Quota Incentivante of University of Parma
  2. Fondazione Cariparma

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The study identified that triclosan disrupts cellular function, particularly interfering with hormone production and cell proliferation, suggesting a critical evaluation of its effects.
Simple Summary A great concern has been raised against many chemicals, both natural and man-made, that can mimic or interfere with the hormones. Among these, using swine ovarian cells, we were aimed to explore the potential effect of triclosan, an antimicrobial agent widely used in cosmetics and home products. Our results demonstrate that triclosan disrupts cellular function, in particular interfering with hormone production and proliferation, thus suggesting a critical evaluation of its effects. Triclosan is a chlorinated phenolic, used in many personal and home care products for its powerful antimicrobial effect. Several studies have shown triclosan toxicity and the American Food and Drug Administration (FDA) in 2016 has limited its use. It has been recently included in endocrine-disrupting chemicals (EDCs), a list of chemicals known for their ability to interfere with hormonal signaling with particular critical effects on reproduction both in animals and humans. In order to deepen the knowledge in this specific field, the present study was undertaken to explore the effect of different concentrations of triclosan (1, 10, and 50 mu M) on cultured luteal cells, isolated from swine ovaries, evaluating effects on growth Bromodeoxyuridine (BrDU) incorporation and Adenosine TriPhosphate (ATP) production, steroidogenesis (progesterone secretion) and redox status (superoxide and nitric oxide production, enzymatic and non-enzymatic scavenging activity). A biphasic effect was exerted by triclosan on P4 production. In fact, the highest concentration inhibited, while the others stimulated P4 production (p < 0.05). Triclosan significantly inhibited cell proliferation, metabolic activity, and enzymatic scavenger activity (p < 0.05). On the contrary, nitric oxide production was significantly increased by triclosan (p < 0.01), while superoxide anion generation and non-enzymatic scavenging activity were unaffected.

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