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Published on: August 25, 2014
Long-term behavioral consequences of brief, repeated neonatal isolation
1Department of Neuroscience, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Forchheimer 113, Bronx, NY 10461, USA.
Brain Research
|November 28, 2006
Summary
Neonatal isolation in rats increased anxiety-related behaviors in adulthood. However, this early-life stress did not alter hypothalamic-pituitary-adrenal (HPA) axis function or stress hormone levels.
Area of Science:
- Neuroscience
- Endocrinology
- Behavioral Science
Background:
- Early-life stress can cause long-term neuroendocrine and behavioral changes.
- The stress hyporesponsive period (SHRP) is a critical window for stress exposure effects.
Purpose of the Study:
- To investigate the effects of neonatal isolation stress on adult anxiety-related behavior and endocrine stress reactivity in rats.
- To determine if early-life stress during the SHRP alters hypothalamic-pituitary-adrenal (HPA) axis function.
Main Methods:
- Rats were isolated daily for 1 hour from postnatal day 4 to 9.
- Adult rats were assessed for anxiety-related behaviors using the elevated plus maze and open field tests.
- Endocrine stress reactivity was measured by assessing ACTH and corticosterone levels following restraint stress.
Main Results:
- Neonatal isolation significantly decreased exploration in the center of the open field and reduced entries into the open arms of the elevated plus maze, indicating enhanced anxiety-related behaviors.
- Neonatal isolation did not affect basal or restraint-induced levels of ACTH or corticosterone.
- Early-life stress enhanced anxiety-related behaviors without altering HPA axis function.
Conclusions:
- Neonatal isolation stress during the SHRP can lead to increased anxiety-like behaviors in adult rats.
- The observed behavioral changes occur independently of alterations in the HPA axis's endocrine response to stress.

