2024
DOI: 10.1089/can.2021.0242
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Pharmacological Interaction Between Cannabidiol and Tramadol on Experimental Diabetic Neuropathic Pain: An Isobolographic Analysis

Allan Arnold Evans,
Carlos Henrique Alves Jesus,
Lucas Latchuk Martins
et al.
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Cited by 3 publications
(1 citation statement)
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“…In this study, the addition of JWH015 reduced the gastrointestinal side effects and conditioned place preference associated with morphine treatment [126]. In contrast, additive, but not synergistic, analgesic effects were observed with combination treatment with cannabidiol and tramadol in the streptozotocin-induced rat model of diabetic neuropathy [127] and with PhAR-DBH-Me and tramadol in a model of cisplatin-induced neuropathy [125]. Ultimately, despite preclinical evidence of the anti-nociceptive effects of cannabinoid receptor 1/2 (CB1/2) agonism and fatty acid amide hydrolase (FAAH) inhibition, translation of these preclinical findings into clinical data has been limited.…”
Section: Additional Combination Therapiesmentioning
confidence: 64%
“…In this study, the addition of JWH015 reduced the gastrointestinal side effects and conditioned place preference associated with morphine treatment [126]. In contrast, additive, but not synergistic, analgesic effects were observed with combination treatment with cannabidiol and tramadol in the streptozotocin-induced rat model of diabetic neuropathy [127] and with PhAR-DBH-Me and tramadol in a model of cisplatin-induced neuropathy [125]. Ultimately, despite preclinical evidence of the anti-nociceptive effects of cannabinoid receptor 1/2 (CB1/2) agonism and fatty acid amide hydrolase (FAAH) inhibition, translation of these preclinical findings into clinical data has been limited.…”
Section: Additional Combination Therapiesmentioning
confidence: 64%