Pharmacological Interaction Between Cannabidiol and Tramadol on Experimental Diabetic Neuropathic Pain: An Isobolographic Analysis

被引:2
|
作者
Evans, Allan Arnold [1 ]
Jesus, Carlos Henrique Alves [1 ]
Martins, Lucas Latchuk [1 ]
Fukuyama, Alisson Hideki [1 ]
Gasparin, Alexia Thamara [1 ]
Crippa, Jose Alexandre [2 ,3 ]
Zuardi, Antonio Waldo [2 ,3 ]
Hallak, Jaime Eduardo Cecilio [2 ,3 ]
Genaro, Karina [4 ]
de Castro, Celio Jose [5 ]
Zanoveli, Janaina Menezes [1 ]
Cunha, Joice Maria da [1 ,6 ]
机构
[1] Univ Fed Parana, Dept Pharmacol, Lab Pharmacol Pain, Curitiba, PR, Brazil
[2] Natl Inst Translat Med INCT TM, CNPq, Ribeirao Preto, SP, Brazil
[3] Univ Sao Paulo, Dept Neurosci & Behav, Ribeirao Preto, SP, Brazil
[4] Univ Calif Irvine, Dept Anesthesiol, Irvine, CA USA
[5] Inst Educ & Res St Casa, Belo Horizonte, MG, Brazil
[6] Univ Fed Parana, Dept Pharmacol, Lab Pharmacol Pain, POB 19031,Biol Sci Bldg, BR-81540990 Curitiba, Brazil
关键词
diabetes; neuropathic pain; streptozotocin; isobologram; mechanical allodynia; pharmacological interaction; ALLOSTERIC MODULATOR; RAT MODEL; IN-VIVO; COMBINATION; RECEPTORS; DIAGNOSIS; SAFETY; THC;
D O I
10.1089/can.2021.0242
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Diabetic neuropathies are the most prevalent chronic complications of diabetes, characterized by pain and substantial morbidity. Although many drugs have been approved for the treatment of this type of pain, including gabapentin, tramadol (TMD), and classical opioids, it is common to report short-term results or potentially severe side effects. TMD, recommended as a second-line treatment can lead to unwanted side effects. Cannabidiol (CBD) has been gaining attention recently due to its therapeutic properties, including pain management. This study aimed to characterize the pharmacological interaction between CBD and TMD over the mechanical allodynia associated with experimental diabetes using isobolographic analysis.Materials and Methods: After diabetes induction by streptozotocin (STZ), diabetic rats were systemically treated with CBD or TMD alone or in combination (doses calculated based on linear regression of effective dose 40% [ED40]) and had the mechanical threshold evaluated using the electronic Von Frey apparatus. Both experimental and theoretical additive ED40 values (Z(mix) and Z(add), respectively) were determined for the combination of CBD plus TMD in this model.Results: Acute treatment with CBD (3 or 10 mg/kg) or TMD (2.5, 5, 10, or 20 mg/kg) alone or in combination (0.38+1.65 or 1.14+4.95 mg/kg) significantly improved the mechanical allodynia in STZ-diabetic rats. Isobolographic analysis revealed that experimental ED40 of the combination (Z(mix)) was 1.9 mg/kg (95% confidence interval [CI]=1.2-2.9) and did not differ from the theoretical additive ED40 2.0 mg/kg (95% CI=1.5-2.8; Z(add)), suggesting an additive antinociceptive effect in this model.Conclusions: Using an isobolographic analysis, these results provide evidence of additive pharmacological interaction between CBD and TMD over the neuropathic pain associated with experimental diabetes induced by STZ.
引用
收藏
页码:728 / 739
页数:12
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