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Long-term Effects of Early Postnatally Administered Interleukin-1-beta on the Hypothalamic-Pituitary-Adrenal (HPA)
1Institute of Experimental Endocrinology, Humboldt University Medical School (Charite, Berlin, Germany.
Insights
Neonatal exposure to Interleukin-1 (IL-1) in rats permanently alters the hypothalamic-pituitary-adrenal (HPA) axis. This early stress can lead to structural brain changes and long-term functional disturbances in stress response.
Area of Science:
- Neuroscience
- Endocrinology
- Developmental Biology
Background:
- Perinatal stress significantly impacts the hypothalamic-pituitary-adrenal (HPA) axis.
- Interleukin-1 (IL-1) is a key mediator of stress responses and immune activation.
Purpose of the Study:
- To investigate the long-term effects of early postnatal IL-1 exposure on the HPA axis in rats.
- To determine if neonatal IL-1 administration causes lasting structural and functional changes in the HPA axis.
Main Methods:
- Wistar rats received daily injections of human recombinant IL-1 from postnatal day 1 to 4.
- Control groups received vehicle injections.
- HPA axis function and paraventricular nucleus (PVN) morphology were assessed at different ages.
Main Results:
- Neonatal IL-1 exposure led to thymus atrophy and adrenal enlargement.
- Plasma corticosterone levels were significantly elevated immediately after IL-1 treatment.
- Adult rats exposed to neonatal IL-1 showed blunted corticosterone responses to acute stress.
- Morphological analysis revealed reduced neuronal density and enlarged nuclei in the PVN of IL-1 treated rats.
Conclusions:
- Early postnatal IL-1 exposure can induce permanent structural malorganization of the PVN.
- This structural damage results in functional malprogramming of the HPA axis.
- IL-1, as part of an infection-induced stress response, may permanently affect neurodevelopmental trajectories.
Abstract:
OBJECTIVE: Since perinatal stress events are well known to exert long-term influences on the function of hypothalamic-pituitary-adrenal (HPA) axis in rats, to investigate the consequences of exposure to IL-1, a potent stimulator of this axis, during early postnatal life. METHODS: Wistar rats were treated twice a day with 0.02 ug human recombinant IL-1 from day 1-4 of age, while controls received the vehicle only. RESULTS: IL-1 -treatment had no significant influence on the mortality and body weight. However, at the end of treatment period on the 4th day of life, the thymus weight was decreased in the IL-1 -treated group (P<0.01), while the adrenals were clearly enlarged (P<0.0002). These responses were associated with a nearly 4-fold elevation of the plasma corticosterone (CS) level as compared to vehicle-treated controls (P<0.001). At the age of seven months the stimulated CS levels induced by an acute stress (novel environment) were lower in rats treated neonatally with IL-1 than in controls (P<0.01). This functional disturbance was associated with morphological alterations in the parvicellular part of the paraventricular nucleus (PVN) which is the main hypothalamic regulation centre of the HPA axis. A strong reduction of the numerical density of neurons was found in the neonatally IL-1 -treated rats (P<0.005) while the neuronal nuclei were clearly enlarged (P<0.0005). CONCLUSION: As a part of an infection-induced stress response during critical periods of development, IL-1 might be capable of inducing a permanent structural malorganization of the PVN and, consequently, functional malprogramming of the HPA axis in rats.
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