2019
DOI: 10.23736/s0026-4784.19.04405-8
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TNF-α effect on human delivery onset by CB1/TRPV1 crosstalk: new insights into endocannabinoid molecular signaling in preterm vs. term labor. Analysis of the EC/EV pathway and predictive biomarkers for early diagnosis of preterm delivery

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Cited by 14 publications
(11 citation statements)
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“…We hypothesise that in TLM without contractions, an abnormal level of secreted IL‐8 may contribute to early ripening of the cervix and initiate the procedure of giving birth. An investigation of cell‐signaling pathways in female reproduction found that TNFα can be a biomarker of delivery onset 21 . Other immune biomarkers in our study were not found to have independent effects on late miscarriage.…”
Section: Discussioncontrasting
confidence: 63%
“…We hypothesise that in TLM without contractions, an abnormal level of secreted IL‐8 may contribute to early ripening of the cervix and initiate the procedure of giving birth. An investigation of cell‐signaling pathways in female reproduction found that TNFα can be a biomarker of delivery onset 21 . Other immune biomarkers in our study were not found to have independent effects on late miscarriage.…”
Section: Discussioncontrasting
confidence: 63%
“…Our group examined CB 1 R and CRIP1a in human uterine and placental tissue obtained during cesarean deliveries, and we found a significant reduction in CB 1 R protein in uterine tissue obtained during labor compared to non-labor. Torrela and colleagues evaluated CB 1 R, CB 2 R, transient receptor potential vanilloid receptor type 1 (TRPV1), FAAH, NAPE-PLD, monoacylglycerol lipase (MAGL) and diacylglycerol lipase (DAGL) in human placental samples obtained after spontaneous vaginal deliveries using qPCR ( 36 ). Compared to samples obtained at 30 weeks gestation (preterm), there was a significant increase in CB 1 R mRNA at term.…”
Section: Cannabinoid Receptor Influence In Pregnancy and Labormentioning
confidence: 99%
“…However, the usage of tocolytic agents for preterm labor is disputed among obstetricians worldwide, and professional organizations have established various guidelines which vary greatly in their recommendations [ 14 ]. To emphasize, preterm birth is still a challenge to researchers studying its basic mechanisms, and though there have been some recent headways into its molecular pathways and prediction models [ 15 ], the question of when to start tocolytic therapy and for how long remains a common but difficult decision for clinicians. Currently, it is generally recommended that tocolysis be limited to the occurrence of preterm labor between the gestational ages (GA) of 24 weeks and 30 weeks or to those over 30 weeks of GA accompanied with cervical length <15 mm or 20 mm [ 4 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 , 24 ].…”
Section: Introductionmentioning
confidence: 99%