# Protocol for intraventricular injection of retinoids and hypothalamic application of viral vectors in the rat and mouse brain

**Authors:** Peter I. Imoesi, Cristian M. Olarte-Sánchez, Lora Heisler, Peter McCaffery

PMC · DOI: 10.1016/j.xpro.2025.104329 · STAR Protocols · 2026-01-31

## TL;DR

This paper describes a protocol for studying vitamin A balance in rodents by injecting retinoids and using viral vectors in the brain.

## Contribution

The novel contribution is a detailed protocol for intraventricular retinoid injection and viral vector application in rodent brains to study vitamin A homeostasis.

## Key findings

- A protocol for intraventricular retinoid injection in rat brains is presented.
- Steps for viral vector application in the mouse arcuate nucleus to knock down vitamin A homeostatic genes are described.
- The approach is applicable for studying vitamin A homeostasis in rodents.

## Abstract

The brain, specifically the hypothalamus, is a key regulator of the homeostatic balance of numerous biomolecules in the body via its control of the neuroendocrine system. Here, we present a protocol to study body vitamin A balance by injecting synthetic retinoids into the third ventricle of the rat brain. We also describe steps for the intraventricular application of viral vectors to the arcuate nucleus of a mouse brain to knock down vitamin A homeostatic genes. This approach is applicable to the study of vitamin A homeostasis.

For complete details on the use and execution of this protocol, please refer to Imoesi et al.1

•Protocol to study vitamin A homeostasis in the rodent body•Steps for injecting synthetic retinoids into the third ventricle of the rat brain•Procedures for the intraventricular application of viral vectors

Protocol to study vitamin A homeostasis in the rodent body

Steps for injecting synthetic retinoids into the third ventricle of the rat brain

Procedures for the intraventricular application of viral vectors

Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics.

The brain, specifically the hypothalamus, is a key regulator of the homeostatic balance of numerous biomolecules in the body via its control of the neuroendocrine system. Here, we present a protocol to study body vitamin A balance by injecting synthetic retinoids into the third ventricle of the rat brain. We also describe steps for the intraventricular application of viral vectors to the arcuate nucleus of a mouse brain to knock down vitamin A homeostatic genes. This approach is applicable to the study of vitamin A homeostasis.

## Linked entities

- **Species:** Rattus norvegicus (taxon 10116), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Aldh1a1 (aldehyde dehydrogenase 1 family, member A1) [NCBI Gene 24188] {aka Ahd2, Aldh1, Aldh2}, Rbp4 (retinol binding protein 4, plasma) [NCBI Gene 19662] {aka Rbp-4}, Rbp4 (retinol binding protein 4) [NCBI Gene 25703] {aka RBPA}
- **Diseases:** skin irritation (MESH:D012871), hypothermia (MESH:D007035), eating and drinking difficulty (MESH:D020920), reflux (MESH:D005764), vitamin A deficiency (MESH:D014802), weight loss (MESH:D015431), sleepiness (MESH:D000077260), sinus damage (MESH:D012852), Bleeding (MESH:D006470), infection (MESH:D007239), sagittal sinus rupture (MESH:D020225), brain damage (MESH:D001925)
- **Chemicals:** aluminum (MESH:D000535), iodine (MESH:D007455), hydrogen peroxide (MESH:D006861), water (MESH:D014867), saline (MESH:D012965), RA (MESH:D014212), isoflurane (MESH:D007530), ethanol (MESH:D000431), polystyrene (MESH:D011137), DMSO (MESH:D004121), ROL (MESH:D014801), Cresyl violet (MESH:C028911), ice (MESH:D007053), oxygen (MESH:D010100), retinoid (MESH:D012176), Ethilon  Polyamide 6 (-), nitrogen (MESH:D009584), lipid (MESH:D008055), Carprofen (MESH:C007005), meloxicam (MESH:D000077239), retinyl palmitate (MESH:C014794)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** W1616T
- **Cell lines:** AAV9 — Homo sapiens (Human), Transformed cell line (CVCL_6871)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12877797/full.md

## References

6 references — full list in the complete paper: https://tomesphere.com/paper/PMC12877797/full.md

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Source: https://tomesphere.com/paper/PMC12877797