# Early Deficient Lactation Differentially Affects Neonatal Thymic Cortical Development and Humoral Immune Responses in Rats

**Authors:** María Belén Sánchez, María Cecilia Michel Lara, María José Germanó, Flavia Judith Neira, Luciana Belén Viruel, Jacqueline Lisset Tomsich, Claudio Rodríguez-Camejo, Mariana Troncoso, Elisa Olivia Pietrobon, Marta Soaje, Ana Hernández, Evelyn L. Jara, Susana Ruth Valdez, Juan Pablo Mackern-Oberti

PMC · DOI: 10.3390/ijms27041708 · International Journal of Molecular Sciences · 2026-02-10

## TL;DR

This study shows that poor lactation in rats due to low prolactin harms neonatal thymic development and immune responses.

## Contribution

The study introduces a novel rat model to investigate lactation deficiency's impact on neonatal immune development.

## Key findings

- Early hypoPRL in rats leads to increased pup mortality and reduced body weight and weight gain.
- Thymic development is impaired with reduced thymus weight and altered lymphocyte development.
- Deficient lactation compromises passive immune transfer, reducing OVA-specific immunoglobulin levels in pups.

## Abstract

Hypoprolactinemia (hypoPRL) disrupts lactation and compromises milk production. Although maternal milk is a critical source of nutrients and bioactive compounds for newborns, the consequences of deficient lactation based on reduced milk quantity on the offspring’s immune development remain incompletely understood. Therefore, this study aimed to elucidate how deficient lactation due to hypoPRL interferes with offspring immunity and development. Female Sprague Dawley (SD) and spontaneous hypoPRL Oncins France Colony A (OFA) rats were euthanized on day 2 of lactation to assess the impact of hypoPRL on serum, milk, and tissue samples. We demonstrated that early deficient lactation in the OFA model impaired maternal performance, leading to increased pup mortality during early lactation. OFA pups exhibited reduced body weight and weight gain, decreased cerebral weight and index, and an increased cephalization index. Thymic development was markedly altered, as evidenced by reduced thymus weight, area, and cortical extension. These structural changes were accompanied by increased thymic Rag 1 expression, suggesting altered lymphocyte development. In parallel, passive immune transfer was compromised, with reduced levels of OVA-specific immunoglobulin isotypes detected in pup serum, reflecting changes in milk-derived immune support. In summary, maternal hypoPRL during early lactation adversely affects offspring growth and thymic maturation with lasting consequences for neonatal immune maturation. This study provides a novel experimental framework to investigate the consequences of lactation deficiency with potential implications for understanding lactation insufficiency and its impact on neonatal immune exposure.

## Linked entities

- **Genes:** RAG1 (recombination activating 1) [NCBI Gene 5896]

## Full-text entities

- **Genes:** PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}, Foxn1 (forkhead box N1) [NCBI Gene 287469] {aka RONU, Rnu, Whn}, Cxcl1 (C-X-C motif chemokine ligand 1) [NCBI Gene 14825] {aka Fsp, Gro1, KC, Mgsa, N51, Scyb1}, Prl (prolactin) [NCBI Gene 19109] {aka Gha1, Prl1a1}, Rag1 (recombination activating 1) [NCBI Gene 84600], Igh-6 (immunoglobulin heavy chain 6) [NCBI Gene 299357] {aka IgM, Igh-1a, Igh6, RGD1359202}, Fcgrt (Fc gamma receptor and transporter) [NCBI Gene 29558] {aka FcRn}, Pigr (polymeric immunoglobulin receptor) [NCBI Gene 25046] {aka RNPIGR2, pIgA-R}, Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}, Igg-2a (gamma-2a immunoglobulin heavy chain) [NCBI Gene 367586], Prl (prolactin) [NCBI Gene 24683] {aka Gha1, PRLB, PRLSD1, Prl1a1, Prol, RATPRLSD1}, Ccl2 (C-C motif chemokine ligand 2) [NCBI Gene 20296] {aka HC11, JE, MCAF, MCP-1, MCP1, SMC-CF}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 24383] {aka BARS-38, Gapd}
- **Diseases:** Inadequate (MESH:D012892), thymic atrophy (MESH:D013953), psychomotor retardation (MESH:D011596), malnutrition (MESH:D044342), infection (MESH:D007239), obesity (MESH:D009765), gain (MESH:D015430), diarrhea (MESH:D003967), hyperthyroidism (MESH:D006980), hyperprolactinemia (MESH:D006966), neurobehavioral disorders (MESH:D019954), herpes virus infection (MESH:D020031), injury to (MESH:D014947), acute respiratory infections (MESH:D012141), Deficient Lactation (MESH:D007775), growth impairment (MESH:D006130), PRL deficiency (MESH:C562708), lactation insufficiency (MESH:D000309)
- **Chemicals:** citrate (MESH:D019343), DNP (MESH:D019297), incomplete Freund's adjuvant (MESH:C114843), DAB (MESH:C000469), Sodium Acetate (MESH:D019346), PBS (MESH:D007854), diethyl ether (MESH:D004986), formaldehyde (MESH:D005557), dimethylsulfoxide (MESH:D004121), H2SO4 1N (-), oxytocin (MESH:D010121), H2O2 (MESH:D006861), hematoxylin (MESH:D006416), nicotine (MESH:D009538), E (MESH:D004540), bromocriptine (MESH:D001971), diazepam (MESH:D003975), progesterone (MESH:D011374), paraffin (MESH:D010232), P (MESH:D010758), xylazine (MESH:D014991), 3,3',5,5'-tetramethylbenzidine (MESH:C021758), corticosterone (MESH:D003345)
- **Species:** Moloney murine leukemia virus (no rank) [taxon 11801], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12940351/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12940351/full.md

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Source: https://tomesphere.com/paper/PMC12940351