Cholecystokinin inhibits independent ingestion in neonatal rats.

This relationship has also been studied in embryonic and neonatal rats.

The research suggests that NT-4/5 prevents injuries that cause death of facial motor neurons in neonatal rats.

The parapyramidal region (PPR) in the ventral medulla is also known to produce locomotion when stimulated in neonatal rats.

The supralumbar segments of the spinal cord are the most effective site for 5-HT to induce locomotion in the neonatal rat.

Intussusception, also known as splitting angiogenesis, was first observed in neonatal rats.

The amiloride-sensitive channels responsible for salt recognition and response is functional in adult rats but not neonatal rats.

However, single very high doses of diazepam have been found to cause lifelong immunosuppression in neonatal rats.

Plucking whiskers in neonatal rats causes a long-lasting expansion of the representation of the spared whisker in layer 4.

ACPD can induce convulsions in neonatal rats.