The purpose of this study was to determine and compare the F levels in plasma, enamel, and bones of nursing rat pups that received the same daily dose of F by continuous or periodic delivery during enamel development. The hypothesis was that F delivered continuously would result in enamel F levels higher than those attained when F was delivered periodically. For continuous delivery, copolymer devices (Southern Research Institute) that provide slow release of F were implanted in the backs of four-day-old rat pups. For periodic delivery, rat pups received F by intraperitoneal injection or gastric intubation. The doses were 0.01, 0.02, or 0.04 mg F/day. The rats were killed at 13 days of age, 24 hours after the last periodic delivery. Plasma was collected, femur and calvaria bones were removed, and enamel was scraped from developing first molars. Fluoride assay was by the microdiffusion method of Taves, with a F electrode. For the 0.02 mg F/day dose, plasma levels in control, implanted, injected, and gastric-intubated rats were 0.004, 0.020, 0.011, and 0.009 ppm, respectively. Enamel F levels were 1.1, 61.9, 54.0, and 42.3 ppm, respectively. Femur F levels were 2.2, 81.2, 84.8, and 68.1 ppm, respectively. Calvaria F levels were 2.5, 79.3, 80.1, and 67.9 ppm, respectively. The results showed that there was no significant difference in the enamel F levels or in the bone F levels in rat pups that received continuous or periodic, by injection, delivery of F at the same daily dose.(ABSTRACT TRUNCATED AT 250 WORDS)
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IBRO Neurosci Rep
June 2025
Department of Human Anatomy and Medical Physiology, Faculty of Health Sciences, University of Nairobi, P.O. Box 30197-00100, Nairobi, Kenya.
Background: Maternal folate usage is essential for neurodevelopment, but its effects on cerebellar structure are unclear. Cerebellum undergoes a protracted period of development, making it sensitive to maternal nutritional imbalances. Astrocytes are necessary for cerebellar cortex structure and function.
View Article and Find Full Text PDFIntroduction: This study designed to examine whether social/ environmental experiences can induce the epigenetic modification, and influence the associated physiology and behaviour. To test this, we have used social stress [prenatal stress (PNS)] model and then housed at environmental enrichment (EE) condition to evaluate the interaction between specific epigenetic modification and its influence on behaviour.
Methods: Pregnant rats were randomly divided into a control group, PNS group, and PNS+EE group.
Cardiovasc Toxicol
January 2025
Department of Physiology, Pharmacology and Toxicology, West Virginia University School of Medicine, Morgantown, WV, USA.
Pregnancy is a vulnerable time with significant cardiovascular changes that can lead to adverse outcomes, which can extend into the postpartum window. Exposure to emissions from electronic cigarettes (Ecig), commonly known as "vaping," has an adverse impact on cardiovascular function during pregnancy and post-natal life of offspring, but the postpartum effects on maternal health are poorly understood. We used a Sprague Dawley rat model, where pregnant dams are exposed to Ecigs between gestational day (GD)2-GD21 to examine postpartum consequences.
View Article and Find Full Text PDFCardiovasc Toxicol
January 2025
Department of Physiology, Pharmacology, and Toxicology, West Virginia University, Morgantown, WV, 26505, USA.
Engineered nanomaterials (ENM) are capable of crossing the placental barrier and accumulating in fetal tissue. Specifically, the ENM nano-titanium dioxide (nano-TiO), has been shown to accumulate in placental and fetal tissue, resulting in decreased birthweight in pups. Additionally, nano-TiO is an established cardiac toxicant and regulator of glucose homeostasis, and exposure in utero may lead to serious maladaptive responses in cardiac development and overall metabolism.
View Article and Find Full Text PDFJ Dev Orig Health Dis
January 2025
Postgraduate Program in Physiological Sciences, State University of Londrina, Londrina, Parana, Brazil.
Nutritional status during the developmental periods leads to predisposition to several diseases and comorbidities, highlighting metabolic and reproductive changes throughout adult life, and in the next generations. One of the experimental models used to induce undernutrition is litter size expansion, which decreases the availability of breast milk to pups and delays development. This work evaluated the effects of maternal undernutrition induced by litter size expansion, a maternal undernutrition preconception model, on the metabolic and reproductive alterations of the offspring.
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