# Lutein administration during gestation protects morphine withdrawal-induced on reflexive motor behavior in mice offspring's

**Authors:** Sahand Sariaslani, Shahin Hassanpour, Bita Vazir

PMC · DOI: 10.1016/j.heliyon.2025.e42394 · Heliyon · 2025-01-31

## TL;DR

Giving lutein during pregnancy may help protect offspring from motor behavior issues caused by morphine withdrawal.

## Contribution

The study shows lutein's protective effect on morphine-induced motor behavior issues in offspring, specifically in females.

## Key findings

- Prenatal morphine exposure reduced reflexive motor behaviors in offspring.
- Lutein reduced the negative effects of morphine on female offspring's motor behaviors.
- Lutein improved antioxidant levels in morphine-exposed mice.

## Abstract

Exposure to morphine during gestation period has vital effect on infants’ neurodevelopmental growth pattern. Lutein shows protective qualities regarding neurodegeneration and the development of the brain. This study aimed to investigate effect of parental exposure to lutein on adverse effect of the morphine withdrawal syndrome on reflexive motor behavior in mice offspring. Fourteen male mice and 56 adult female mice were randomly assigned to seven groups: the control group containing male and female mice that refrained from morphine; group 2 was morphine-abstinent male mice and female mice with no prior drug exposure; group 3 including morphine-abstinent female mice and male mice without drug experience; and group 4 of drug-naïve male and female mice. Groups 5–7 were similar to groups 2–4, but drug-naïve subjects received injections of lutein (10 mg/kg). Following delivery, offspring from each group were chosen to assess behavior and reflexive motor behaviors. Also, blood samples were collected to measure serum antioxidant activity. Based on the findings, reflexive motor behaviors significantly decreased following prenatal exposure to morphine (P < 0.05), however, no significant difference was seen between morphine exposed male with male and female morphine exposed mice (P > 0.05). Lutein administration had no effect on reflexive motor behaviors in male morphine exposed group (P > 0.05) but lutein administration significantly decreased adverse effect of the morphine on reflexive motor behaviors in female exposed group (P < 0.05). No significant difference was seen between male and females received morphine (P > 0.05). Lutein administration decreased serum malondialdehyde (MDA) production and increased superoxide dismutase (SOD), glutathione peroxidase (GPx) and total antioxidant status (TAS) levels in morphine exposed mice. It seems, maternal exposure to lutein had protective role on adverse effect of the morphine on reflexive motor behaviors in offspring.

## Linked entities

- **Chemicals:** lutein (PubChem CID 181579), morphine (PubChem CID 5288826), malondialdehyde (PubChem CID 10964)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}
- **Diseases:** neurodegeneration (MESH:D019636), morphine withdrawal syndrome (MESH:D009021)
- **Chemicals:** morphine (MESH:D009020), MDA (MESH:D008315), Lutein (MESH:D014975)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11840480/full.md

## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC11840480/full.md

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Source: https://tomesphere.com/paper/PMC11840480