# Alterations in Nitric Oxide Production After Post-Weaning Social Isolation

**Authors:** Stanislava VRANKOVA, Zuzana GALANDAKOVA, Jana KLIMENTOVA, Olga PECHANOVA, Martina CEBOVA

PMC · DOI: 10.33549/physiolres.935723 · Physiological Research · 2025-12-01

## TL;DR

Social isolation in early life affects brain chemistry and behavior in rats, with longer isolation causing more significant changes.

## Contribution

The study reveals how prolonged social isolation alters nitric oxide signaling and lipid peroxidation in specific brain regions.

## Key findings

- 29 weeks of isolation reduced open-field exploration and impaired acoustic startle habituation.
- Isolated rats showed decreased cerebellar NOS activity and increased hippocampal nNOS and iNOS expression.
- Both 10 and 29 weeks of isolation increased lipid peroxidation markers in the brain.

## Abstract

Early-life stressful stimuli, such as social isolation, alter brain neurochemistry and lead to negative behavioral outcomes in adulthood. Isolated animals are deprived of social interactions, which results in impaired brain development. Post-weaning isolation rearing deregulates various brain processes and may affect nitric oxide (NO) signaling. The aim of our study was to determine time-dependent impact of social isolation on behavioral and biochemical parameters in Wistar Kyoto rats. At the age of 21 days, male rats were randomly assigned into four groups reared in isolation or socially for 10 or 29 weeks. At the end of the rearing, open-field and prepulse inhibition (PPI) tests were carried out. Furthermore, in several brain areas we assessed NO synthase (NOS) activity, protein expression of nNOS and iNOS isoforms and the concentration of conjugated dienes (CD), a marker of lipid peroxidation. The number of entries into the central zone of the open field test decreased significantly only after 29 weeks of isolation. Isolated rats (IR) rats exhibited impaired habituation of the acoustic startle response after prolonged social isolation. While cerebellar NOS activity and nNOS protein expression decreased significantly in IR rats after 29 weeks of isolation, the expression of nNOS and iNOS was increased in the hippocampus. 10-week and 29-week social isolation led to increased CD concentration in the brain. Our results suggest that the duration of social isolation plays an important role in the development of behavioral and biochemical changes in the brain. The decreased NO bioavailability may result from lipid peroxidation, oxidative stress, and inflammatory responses.

## Linked entities

- **Proteins:** NOS1 (nitric oxide synthase 1), NOS2 (nitric oxide synthase 2)
- **Chemicals:** nitric oxide (PubChem CID 145068)

## Full-text entities

- **Genes:** NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, Nos1 (nitric oxide synthase 1) [NCBI Gene 24598] {aka bNOS}, Sod1 (superoxide dismutase 1) [NCBI Gene 24786] {aka CuZnSOD}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, Lep (leptin) [NCBI Gene 25608] {aka OB, obese}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 24383] {aka BARS-38, Gapd}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, glyceraldehyde 3-phosphate dehydrogenase [NCBI Gene 108351137], TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, NOS1 (nitric oxide synthase 1) [NCBI Gene 4842] {aka IHPS1, N-NOS, NC-NOS, NOS, bNOS, nNOS}, GCLC (glutamate-cysteine ligase catalytic subunit) [NCBI Gene 2729] {aka CNSHA7, GCL, GCS, GLCL, GLCLC}, Nos2 (nitric oxide synthase 2) [NCBI Gene 24599] {aka Nos2a, iNos}
- **Diseases:** schizophrenia (MESH:D012559), anxiety (MESH:D001007), neurotoxic (MESH:D020258), Startle (MESH:D016750), psychosis (MESH:D011618), cognitive and behavioral disturbances (MESH:D003072), obesity (MESH:D009765), weight gain (MESH:D015430), inflammation (MESH:D007249), impaired brain development (MESH:D002658), cognitive, behavioral, and neurochemical abnormalities (OMIM:614756), anxious behavior (MESH:D001523)
- **Chemicals:** NaCl (MESH:D012965), CDs (MESH:D002104), SR (MESH:D013324), N2 (MESH:D009584), reactive oxygen species (MESH:D017382), EDTA (MESH:D004492), tetrahydrobiopterin (MESH:C003402), water (MESH:D014867), P (MESH:D010758), nitrate (MESH:D009566), cyclohexane (MESH:C506365), SDS (MESH:D012967), nitrite (MESH:D009573), Chloroform (MESH:D002725), Lipids (MESH:D008055), malondialdehyde (MESH:D008315), GSH (MESH:D005978), methanol (MESH:D000432), NO (MESH:D009569), Tris (-), calcium (MESH:D002118), Tween-20 (MESH:D011136), glutamate (MESH:D018698)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12849789/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12849789/full.md

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Source: https://tomesphere.com/paper/PMC12849789