Yassin Nemat Z, El-Shenawy Siham M, Abdel-Rahman Rehab F, Yakoot Mostafa, Hassan Mohamed, Helmy Sherine
Department of Pharmacology, National Research Center, Cairo, Egypt.
Green Clinic and Research Center, Alexandria, Egypt.
Drug Des Devel Ther. 2015 Mar 12;9:1491-8. doi: 10.2147/DDDT.S79957. eCollection 2015.
We aimed to investigate the effect of topical application of a Copper indomethacin (Cu-Indo) gel preparation on monosodium iodoacetate (MIA) induced arthritis of the knee joint of rats and to test our hypothesis that copper complex of indomethacin could be a more potent anti-inflammatory agent than its parent compound.
After induction of osteoarthritis by the intracapsular injection of 50 μL with 40 mg/mL MIA, we compared the anti-inflammatory efficacy and safety of a topical application of 1% indomethacin gel in a dose of 1 g/kg of the gel (equivalent to 10 mg/kg of the active substance) daily for 3 weeks versus three decremental dose levels of Cu-Indo gel: an equivalent dose, half the dose, and 25% of the dose of indomethacin. Anti-inflammatory efficacy was assessed in all treated groups by measurement of serum inflammatory cytokines: interleukin 6, interleukin 8, and tumor necrosis factor alpha; and by the weekly assessment of knee joint swelling. Joint mobility and motor coordination were also assessed once weekly by the accelerating rotarod apparatus; histopathological examination of affected joints was also performed. Safety of topical application of Cu-Indo (0.25, 0.5, and 1 g/kg) for up to 3 months to rats' skin was determined by the estimation of a complete blood count, liver and kidney functions, and histopathologic examination for target tissues.
Cu-Indo gel at lower doses was superior to or at least as effective as its parent substance, indomethacin, in most of the studied parameters of inflammation. The lowest tested dose of Cu-Indo, corresponding to 25% of the parent substance indomethacin, exhibited the highest efficacy in reducing the elevated serum-tested interleukins and in increasing the time of duration on the rotarod test, whereas its effect on reduction of edema and tumor necrosis factor alpha was comparable to that of the others. After 3 months of daily application, there were no notable changes in studied safety parameters with the lowest Cu-Indo dose, but the group treated with the higher dose showed a small but statistically significant increase in serum-unconjugated bilirubin and a slight decrease in hemoglobin levels, red blood cells, and platelet count, with normal indices denoting a slight hemolytic effect at the highest dose.
Cu-Indo gel has potent anti-inflammatory activity against joint inflammation in the MIA-treated rat model of osteoarthritis at doses of 0.25, 0.5, and 1 g/kg. The lowest studied dose was better on both safety and efficacy parameters.
我们旨在研究局部应用铜吲哚美辛(Cu-Indo)凝胶制剂对碘乙酸钠(MIA)诱导的大鼠膝关节关节炎的影响,并验证我们的假设,即吲哚美辛的铜络合物可能是比其母体化合物更有效的抗炎剂。
通过关节腔内注射50μL 40mg/mL的MIA诱导骨关节炎后,我们比较了每日局部应用1%吲哚美辛凝胶,剂量为1g/kg凝胶(相当于10mg/kg活性物质),持续3周,与Cu-Indo凝胶的三个递减剂量水平:等效剂量、半剂量和吲哚美辛剂量的25%的抗炎效果和安全性。通过测量血清炎症细胞因子:白细胞介素6、白细胞介素8和肿瘤坏死因子α,以及每周评估膝关节肿胀,评估所有治疗组的抗炎效果。还通过加速转棒仪每周评估一次关节活动度和运动协调性;对受影响的关节进行组织病理学检查。通过估计全血细胞计数、肝肾功能以及对靶组织进行组织病理学检查,确定将Cu-Indo(0.25、0.5和1g/kg)局部应用于大鼠皮肤长达3个月的安全性。
在大多数研究的炎症参数中,较低剂量的Cu-Indo凝胶优于或至少与其母体物质吲哚美辛一样有效。Cu-Indo的最低测试剂量,相当于母体物质吲哚美辛的25%,在降低血清检测的白细胞介素升高和增加转棒试验持续时间方面表现出最高的疗效,而其对减轻水肿和肿瘤坏死因子α的作用与其他剂量相当。每日应用3个月后,最低Cu-Indo剂量组的研究安全参数没有明显变化,但高剂量治疗组的血清未结合胆红素略有但统计学上显著增加,血红蛋白水平、红细胞和血小板计数略有下降,正常指标表明最高剂量时有轻微溶血作用。
在0.25、0.5和1g/kg剂量下,Cu-Indo凝胶对MIA诱导的骨关节炎大鼠模型的关节炎症具有强大的抗炎活性。研究的最低剂量在安全性和疗效参数方面均表现更佳。