PMID- 23831946 OWN - NLM STAT- MEDLINE DCOM- 20140128 LR - 20130812 IS - 1879-3169 (Electronic) IS - 0378-4274 (Linking) VI - 221 IP - 3 DP - 2013 Aug 29 TI - Synergistic effects of pyrrolizidine alkaloids and lipopolysaccharide on preterm delivery and intrauterine fetal death in mice. PG - 212-8 LID - S0378-4274(13)01110-7 [pii] LID - 10.1016/j.toxlet.2013.06.238 [doi] AB - Preterm birth is the leading cause of death for newborn infants, and lipopolysaccharide (LPS) is commonly used to induce preterm delivery in experimental animals. Pyrrolizidine alkaloids (PAs) are widespread and occur in foods, herbs, and other plants. This study was to investigate the synergistic effects of LPS and two representative PAs, retrorsine (RTS) and monocrotaline (MCT), on preterm delivery and fetal death. Pregnant Kunming mice were divided into seven groups: control, RTS, MCT, LPS, RTS+LPS and two MCT+LPS groups. Animals in PAs and PAs+LPS groups were dosed intragastrically with RTS (10mg/kg) or MCT (20 mg/kg or 60 mg/kg) from gestational day (GD) 9 to GD16; mice given LPS were injected intraperitoneally with 150 mug/kg on GD15.5. Latencies to delivery, numbers of pups live and dead at birth were recorded, and livers of live neonates were collected. The incidence of LPS-induced preterm birth was enhanced in dams pretreated with MCT, and combination of PAs and LPS increased fetal mortality from PAs. The enhancement of LPS-induced preterm delivery and fetal demise in animals exposed chronically to PAs and other substances found in foods and beverages consumed widely by humans merits further focused investigation. CI - Copyright (c) 2013 Elsevier Ireland Ltd. All rights reserved. FAU - Guo, Yu AU - Guo Y AD - Department of Pharmacology, School of Basic Medical Science, Wuhan University, Wuhan 430071, China. FAU - Ma, Zhenguo AU - Ma Z FAU - Kou, Hao AU - Kou H FAU - Sun, Rongze AU - Sun R FAU - Yang, Hanxiao AU - Yang H FAU - Smith, Charles Vincent AU - Smith CV FAU - Zheng, Jiang AU - Zheng J FAU - Wang, Hui AU - Wang H LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20130704 PL - Netherlands TA - Toxicol Lett JT - Toxicology letters JID - 7709027 RN - 0 (Lipopolysaccharides) RN - 0 (Pyrrolizidine Alkaloids) RN - 0 (Thiobarbituric Acid Reactive Substances) SB - IM MH - Animals MH - Animals, Newborn MH - Female MH - Fetal Death/*chemically induced MH - Lipopolysaccharides/*toxicity MH - Liver/drug effects/enzymology/metabolism/pathology MH - Male MH - Mice MH - Pregnancy MH - Premature Birth/*chemically induced MH - Pyrrolizidine Alkaloids/*toxicity MH - Specific Pathogen-Free Organisms MH - Statistics, Nonparametric MH - Thiobarbituric Acid Reactive Substances/metabolism OTO - NOTNLM OT - Fetal death OT - GD OT - IUGR OT - LPS OT - Lipopolysaccharide OT - MCT OT - Oxidative injury OT - PAs OT - Preterm delivery OT - Pyrrolizidine alkaloids OT - ROS OT - RTS OT - TBARS OT - gestational day OT - intrauterine growth retardation OT - lipopolysaccharide OT - monocrotaline OT - pyrrolizidine alkaloids OT - reactive oxygen species OT - retrorsine OT - thiobarbituric acid reactive substances EDAT- 2013/07/09 06:00 MHDA- 2014/01/29 06:00 CRDT- 2013/07/09 06:00 PHST- 2012/05/20 00:00 [received] PHST- 2013/06/22 00:00 [revised] PHST- 2013/06/27 00:00 [accepted] PHST- 2013/07/09 06:00 [entrez] PHST- 2013/07/09 06:00 [pubmed] PHST- 2014/01/29 06:00 [medline] AID - S0378-4274(13)01110-7 [pii] AID - 10.1016/j.toxlet.2013.06.238 [doi] PST - ppublish SO - Toxicol Lett. 2013 Aug 29;221(3):212-8. doi: 10.1016/j.toxlet.2013.06.238. Epub 2013 Jul 4.