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Effect of cannabidiol as a neuroprotective agent on neurodevelopmental impairment in rats with neonatal hypoxia.
Hernández-Suárez, Ángela; Marin-Castañeda, Luis A; Rubio, Carmen; Romo-Parra, Héctor.
Affiliation
  • Hernández-Suárez Á; Centro de Investigación en Ciencias de la Salud, Facultad de Ciencias de la Salud, Universidad Anáhuac, Mexico City, Mexico.
  • Marin-Castañeda LA; Neurophysiology Department, Instituto Nacional de Neurología y Neurocirugía "Manuel Velasco Suarez", Mexico City, Mexico.
  • Rubio C; Neurophysiology Department, Instituto Nacional de Neurología y Neurocirugía "Manuel Velasco Suarez", Mexico City, Mexico. Electronic address: macaru4@yahoo.com.mx.
  • Romo-Parra H; Neurophysiology Department, Instituto Nacional de Neurología y Neurocirugía "Manuel Velasco Suarez", Mexico City, Mexico; Centro Anáhuac de Investigación en Psicología, Facultad de Psicología, Universidad Anáhuac, Mexico City, Mexico. Electronic address: hector.romo.parra@gmail.com.
Brain Dev ; 46(9): 294-301, 2024 Oct.
Article in En | MEDLINE | ID: mdl-39068045
ABSTRACT

OBJECTIVE:

This study aims to investigate the neuroprotective effects of cannabidiol (CBD) on neurodevelopmental impairments in rats subjected to neonatal hypoxia, specifically examining its potential to mitigate motor and sensory deficits without the confounding effects of ischemia.

METHODS:

Neonatal Sprague-Dawley rats were allocated to one of four groups Control, Control-CBD, Hypoxia, and Hypoxia-CBD. Hypoxia was induced on postnatal days 0 and 1. CBD (50 mg/kg) was administered orally for 14 days starting at postnatal day 0. Neurodevelopmental outcomes were assessed using the Neurodevelopmental Reflex Testing in Neonatal Rat Pups scale and the Revised Neurobehavioral Severity Scale for rodents. Statistical analyses were conducted using two-way and one-way ANOVA, with Tukey's post-hoc tests for group comparisons.

RESULTS:

Pup weights were recorded on specified postnatal days, with no significant differences observed across the groups (p = 0.1834). Significant neurological impairments due to hypoxia were noted in the Control group compared to the Hypoxia group, particularly in hindlimb grasping on postnatal day 3 (p = 0.0025), posture on postnatal day 12 (p = 0.0073), and in general balance and sound reflex on postnatal day 20 (p = 0.0016 and p = 0.0068, respectively). Additionally, a statistically significant improvement in posture was observed in the Hypoxia-CBD group compared to the Hypoxia group alone (p = 0.0024).

CONCLUSION:

Our findings indicate that CBD possesses neuroprotective properties that significantly counteract the neurodevelopmental impairments induced by neonatal hypoxia in rats. This study not only supports the therapeutic potential of CBD in managing conditions characterized by neurodevelopmental challenges due to hypoxia but also underscores the necessity for further investigation into the specific molecular mechanisms driving CBD's neuroprotective effects. Further research is essential to explore CBD's clinical applications and its potential role in treating human neurodevelopmental disorders.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cannabidiol / Rats, Sprague-Dawley / Neuroprotective Agents / Animals, Newborn Limits: Animals Language: En Journal: Brain Dev Year: 2024 Document type: Article Affiliation country: Mexico Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cannabidiol / Rats, Sprague-Dawley / Neuroprotective Agents / Animals, Newborn Limits: Animals Language: En Journal: Brain Dev Year: 2024 Document type: Article Affiliation country: Mexico Country of publication: Netherlands