Abstract

Objective To observe the effects of different energy of extracorporeal shock waves(ECSWs)on diabetic neuralgia in rats. Methods Fifty clean-grade healthy male Sprague-Dawley rats of both sexes, aged 8 weeks, weighing 180-200 g, were divided into 5 groups (n=10 each) using a random number table method: control group (group C), diabetic neuralgia group (group DN), low-energy ECSW group (group L+ DN), medium-energy ECSW group (group M+ DN), and high-energy ECSW group (group H+ DN). Diabetic neuralgia models were established by intraperitoneally injecting streptozotocin (60 mg/kg) in DN, L+ DN, M+ DN and H+ DN groups.ECSWs at 1, 2 and 3 bar were applied during 4 consecutive weeks after successful establishment of the model once a week (T1-T4) in L+ DN, M+ DN and H+ DN groups, respectively.The mechanical paw withdrawal threshold (MWT), thermal paw withdrawal latency (TWL) and motor nerve conduction velocity (MNCV) were measured at T1-T4.Animals were sacrificed after the last measurement, and the sciatic nerve samples were obtained for determination of the expression of tumor necrosis factor-alpha(TNF-α) and interluekin-6(IL-6) (by Western blot) and expression of TNF-α and IL-6 mRNA (by real-time polymerase chain reaction). Results Compared with group C, MWT, TWL and MNCV were significantly decreased at T1-T4, and the expression of TNF-α and IL-6 protein and mRNA was up-regulated in the other groups (P<0.05). Compared with group DN, MWT at T2-4 and TWL and MNCV at T3, 4 were significantly increased, and the expression of TNF-α and IL-6 protein and mRNA was down-regulated in L+ DN, M+ DN and H+ DN groups (P<0.05). Compared with group H+ DN, MWT at T2-4 and TWL and MNCV at T3, 4 were significantly increased, and the expression of TNF-α and IL-6 protein and mRNA was down-regulated in L+ DN and M+ DN groups, and the expression of IL-6 mRNA was significantly down-regulated in group L+ DN (P<0.05). Conclusion ECSWs can mitigate diabetic neuralgia in rats, and the low- and medium-energy ECSWs produce better efficacy, and the mechanism is related to inhibiting inflammatory responses. Key words: High-energy shock waves; Diabetic neuropathies

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