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Effects of Nicotine on Early Pregnancy in the Rat
65
Citations
25
References
1979
Year
Nicotine TreatmentFertilityReproductive HealthFemale Reproductive FunctionReproductive BiologyEmbryologyPreimplantation Embryonic DevelopmentReproductive EndocrinologyReproductive PhysiologyTobacco ControlFemale InfertilityNicotineImplantation (Embryology)Public HealthDevelopmental ToxicologyPreimplantation PeriodMaternal HealthNeuropharmacologyEndocrinologyDevelopmental BiologyOogenesisPhysiologyUterine ReceptivityPregnancyHuman Embryonic DevelopmentEarly PregnancyMedicine
The effects of nicotine on preimplantation embryonic development were investigated in the rat. A high dose of nicotine (7.5 mg nicotine tartrate) was injected s.c. twice daily from the morning of proestrus (Day 0 of pregnancy) until the day of sacrifice. Rats were sacrificed at 600, 1200, 1800 or 2400 h on Days 1-5 of pregnancy and the location and stage of development of the ova were recorded. Nicotine caused a delay of approximately 12 h in ovum cleavage from the 2-cell to the 4-cell stage; each step of embryonic development after the 4-cell stage was thereby delayed. In nicotinetreated rats, ovum entry into the uterus, blastocyst formation, shedding of the zona pellucida and implantation were delayed. A single injection of 0.2 pg estradiol on Day 3 of pregnancy abolished the delay in ovum entry into the uterus. Daily injection of nicotine caused a concentration or “crowding” of implantation sites toward the tubal ends of the uterine horns. An additional injection of estrogen on the afternoon of Day 4 resulted in even greater crowding. Concentrations of progesterone (P), luteinizing hormone (LH) and prolactin (PRL) in peripheral serum during the preimplantation period were lower in nicotine-treated rats than in saline-treated rats. On the other hand, serum concentrations of estrogens and follicle stimulating hormone were higher in nicotine-treated rats as compared to those in saline-treated rats. These results suggest that delayed implantation of ova in nicotine-treated rats is due not to a decreased secretion of estrogen, but rather to a delay in the increase of P secretion which is necessary to prepare the uterus for implanting blastocysts. This disturbance in P secretion appears to be the result, at least in part, of the hormonal imbalance of the hypothalamo-pituitary axis caused by the nicotine treatment.
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