Antinociceptive interaction of gabapentin with minocycline in murine diabetic neuropathy

被引:15
|
作者
Miranda, H. F. [1 ,2 ]
Sierralta, F. [2 ,3 ]
Jorquera, V. [1 ]
Poblete, P. [1 ]
Prieto, J. C. [1 ,4 ]
Noriega, V. [1 ,4 ]
机构
[1] Andres Bello Univ, Sch Pharm, Fac Med, Republica 590, Santiago, Chile
[2] Univ Chile, Pharmacol Program, ICBM, Fac Med, Independencia 1027, Santiago, Chile
[3] Finis Terrae Univ, Fac Odontol, Pedro de Valdivia 1509, Providencia, Chile
[4] Univ Chile, Cardiovasc Dept, Clin Hosp, Santos Dumont 999, Santiago, Chile
关键词
Neuropathy; Diabetes; Streptozocin; Minocycline; Gabapentin; Synergism; PAIN; STREPTOZOTOCIN; MECHANISMS; SYNERGISM;
D O I
10.1007/s10787-017-0308-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Diabetic neuropathy (DN) is the most common complication of diabetes and pain is one of the main symptoms of diabetic neuropathy, however, currently available drugs are often ineffective and complicated by adverse events. The purpose of this research was to evaluate the antinociceptive interaction between gabapentin and minocycline in a mice experimental model of DN by streptozocin (STZ). The interaction of gabapentin with minocycline was evaluated by the writhing and hot plate tests at 3 and 7 days after STZ injection or vehicle in male CF1 mice. STZ (150 mg/kg, i.p.) produced a marked increase in plasma glucose levels on day 7 (397.46 +/- 29.65 mg/dL) than on day 3 (341.12 +/- 35.50 mg/dL) and also developed neuropathic pain measured by algesiometric assays. Gabapentin produced similar antinociceptive activity in both writhing and hot plate tests in mice pretreated with STZ. However, minocycline was more potent in the writhing than in the hot plate test in the same type of mice. The combination of gabapentin with minocycline produced synergistic interaction in both test. The combination of gabapentin with minocycline in a 1:1 proportion fulfills all the criteria of multimodal analgesia and this finding suggests that the combination provide a therapeutic alternative that could be used for human neuropathic pain management.
引用
收藏
页码:91 / 97
页数:7
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