Table 4.
In Vitro and in Vivo Models | CBD Dose | Treatments | Biological/Pharmacological Effect | Neurological Diseases | Ref. |
---|---|---|---|---|---|
Male Wistar rats | 10 mg/kg | 2 h after the induction of model | CBD inhibited the carrageenan-induced hyperalgesia through the desensitization of the TRPV1 receptor | Hyperalgesia | [31] |
hPBMECs and hCMEC/D3 Cells | 0.1, 0.3, 1, 3, 10 and 15 μM | 7 or 24 h of incubation | CBD, in a dose-dependent manner, led a last-lasting increase in intracellular Ca2+ level, through activation of TRPV2. In this way, CBD, enhanced cell proliferation, cell migration and tubulogenesis in human brain endothelial cells. | - | [109] |
U87MG glioma cell line | 10 µM | Cells were treated with different doses of CBD for 1 day or co-treated with CBD 10 µM and chemotherapeutic drugs for 6 h. | CBD, through activation of TRPV2 and the consequent entry of Ca2+, improved the action of chemotherapy drugs enhancing drug absorption and ameliorated cytotoxic activity in human glioma cells. | - | [110] |
human Gingival Mesenchymal Stem Cells | 5 μM | 24 h of incubation | CBD, through TRPV1 desensitization, promoted the PI3K/Akt pathway signaling, which can reduce Alzheimer’s hallmarks. | Alzheimer’s disease | [37] |
CBD, cannabidiol; hPBMECs, human primary brain microvascular endothelial cell.