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Updated: Aug 29, 2026

A Murine Model of Fetal Exposure to Maternal Inflammation to Study the Effects of Acute Chorioamnionitis on Newborn Intestinal Development
Published on: June 24, 2020
Inhibition of amniotic interleukin-6 and prostaglandin E2 release by ampicillin
Fortunato Vesce1, Barbara Pavan, Laura Lunghi
1Department of Biochemical Sciences and Advanced Therapy, Section of Obstetrics and Gynaecology, University of Ferrara, Ferrara, Italy. ves@dns.unife.it
Objective:
To test the effect of ampicillin on amniotic interleukin-6 (IL-6) and prostaglandin E2 (PGE2) release.
Methods:
In an in vitro study, IL-6 and PGE2 release from amnion-like Wistar Institute Susan Hayflick cells was assayed under basal conditions, as well as after incubation with ampicillin. In an in vivo study, amniotic fluid IL-6 was assayed in a total of 212 patients submitted to genetic amniocentesis during the 17th week of their singleton physiological pregnancy. The study population was subdivided as follows: 92 patients sampled before ampicillin administration, 70 patients sampled 4 hours after administration of 1 g ampicillin, and 50 patients sampled 12 hours after administration of 1 g ampicillin.
Results:
At doses ranging from 10-7 to 10-4 M, ampicillin decreased IL-6 release from Wistar Institute Susan Hayflick cells. The drug effect was already statistically significant (-30%; P <.05) at the lowest concentration tested (10-7 M), reaching the maximum (-50%) at 10-6 M after 4 hours of incubation. Moreover, ampicillin concentrations ranging from 10-7 to 10-4 M decreased PGE2 release from Wistar Institute Susan Hayflick cells; maximal inhibition was reached at 10-6 M after 4 hours (-40%; P <.05). Finally, IL-6 levels measured in amniotic fluid of patients sampled 4 hours after ampicillin administration proved strongly and significantly reduced when compared with those sampled either before or 12 hours after treatment (P <.001).
Conclusion:
The capacity of ampicillin to directly decrease amniotic IL-6 and PGE2 release should be considered in the management of bacterial and nonbacterial inflammatory complications of pregnancy mediated by the cytokine and prostanoid interaction.
Insights
Ampicillin effectively reduces amniotic interleukin-6 (IL-6) and prostaglandin E2 (PGE2) release in vitro and in vivo. This suggests ampicillin
Area of Science:
- Obstetrics and Gynecology
- Pharmacology
- Immunology
Background:
- Interleukin-6 (IL-6) and prostaglandin E2 (PGE2) play critical roles in pregnancy complications.
- Understanding the impact of commonly used antibiotics on these mediators is crucial for clinical management.
Purpose of the Study:
- To investigate the direct effects of ampicillin on the release of IL-6 and PGE2 from amniotic cells.
- To evaluate the in vivo impact of ampicillin administration on amniotic fluid IL-6 levels in pregnant patients.
Main Methods:
- In vitro assays using Wistar Institute Susan Hayflick cells to measure IL-6 and PGE2 release after ampicillin incubation.
- In vivo study involving genetic amniocentesis in 212 pregnant patients, measuring amniotic fluid IL-6 before and after ampicillin administration.
Main Results:
- Ampicillin significantly decreased both IL-6 and PGE2 release from amnion cells in a dose-dependent manner in vitro.
- In vivo, amniotic fluid IL-6 levels were significantly reduced 4 hours after ampicillin administration compared to baseline and 12-hour post-administration levels.
Conclusions:
- Ampicillin demonstrates a direct inhibitory effect on amniotic IL-6 and PGE2 production.
- These findings support considering ampicillin's anti-inflammatory properties in managing pregnancy complications involving cytokine and prostanoid pathways.
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