Cannabidiol Reduces Short- and Long-Term High Glutamate Release after Severe Traumatic Brain Injury and Improves Functional Recovery

This study aimed to determine if orally administered cannabidiol (CBD) lessens the cortical over-release of glutamate induced by a severe traumatic brain injury (TBI) and facilitates functional recovery. The short-term experiment focused on identifying the optimal oral pretreatment of CBD. Male Wist...

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Main Authors: Cindy Santiago-Castañeda (Author), Saúl Huerta de la Cruz (Author), Christopher Martínez-Aguirre (Author), Sandra Adela Orozco-Suárez (Author), Luisa Rocha (Author)
Format: Book
Published: MDPI AG, 2022-08-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Cindy Santiago-Castañeda  |e author 
700 1 0 |a Saúl Huerta de la Cruz  |e author 
700 1 0 |a Christopher Martínez-Aguirre  |e author 
700 1 0 |a Sandra Adela Orozco-Suárez  |e author 
700 1 0 |a Luisa Rocha  |e author 
245 0 0 |a Cannabidiol Reduces Short- and Long-Term High Glutamate Release after Severe Traumatic Brain Injury and Improves Functional Recovery 
260 |b MDPI AG,   |c 2022-08-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics14081609 
500 |a 1999-4923 
520 |a This study aimed to determine if orally administered cannabidiol (CBD) lessens the cortical over-release of glutamate induced by a severe traumatic brain injury (TBI) and facilitates functional recovery. The short-term experiment focused on identifying the optimal oral pretreatment of CBD. Male Wistar rats were pretreated with oral administration of CBD (50, 100, or 200 mg/kg) daily for 7 days. Then, extracellular glutamate concentration was estimated by cortical microdialysis before and immediately after a severe TBI. The long-term experiment focused on evaluating the effect of the optimal treatment of CBD (pre- vs. pre- and post-TBI) 30 days after trauma. Sensorimotor function, body weight, and mortality rate were evaluated. In the short term, TBI induced a high release of glutamate (738% ± 173%; <i>p</i> < 0.001 vs. basal). Oral pretreatment with CBD at all doses tested reduced glutamate concentration but with higher potency at when animals received 100 mg/kg (222 ± 33%, <i>p</i> < 0.01 vs. TBI), an effect associated with a lower mortality rate (22%, <i>p</i> < 0.001 vs. TBI). In the long-term experiment, the TBI group showed a high glutamate concentration (149% <i>p</i> < 0.01 vs. SHAM). In contrast, animals receiving the optimal treatment of CBD (pre- and pre/post-TBI) showed glutamate concentrations like the SHAM group (<i>p</i> > 0.05). This effect was associated with high sensorimotor function improvement. CBD pretreatment, but not pre-/post-treatment, induced a higher body weight gain (39% ± 2.7%, <i>p</i> < 0.01 vs. TBI) and lower mortality rate (22%, <i>p</i> < 0.01 vs. TBI). These results support that orally administered CBD reduces short- and long-term TBI-induced excitotoxicity and facilitated functional recovery. Indeed, pretreatment with CBD was sufficient to lessen the adverse sequelae of TBI. 
546 |a EN 
690 |a traumatic brain injury 
690 |a cannabidiol 
690 |a glutamate 
690 |a sensorimotor function 
690 |a body weight 
690 |a mortality 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 14, Iss 8, p 1609 (2022) 
787 0 |n https://www.mdpi.com/1999-4923/14/8/1609 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/e4c6938ee68b4d9993a2fa47f470a295  |z Connect to this object online.