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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MDPI AG,
2022-08-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_e4c6938ee68b4d9993a2fa47f470a295 | ||
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. |