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Effect of Tangluoning on expression of TRL2 /4 in dorsal root ganglion of rats with diabetic peripheral neuropathy |
LI Yixiao1 WANG Liying1 GUO Yuxin1 LIU Qin1 CHEN Feng1 ZHANG Taojing2 |
1.The Second Clinical Medical College of Beijing University of Chinese Medicine,Beijing 100029, China;
2.Department of Endocrinology, Dongfang Hospital, Beijing University of Chinese Medicine, Beijing 100078, China |
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Abstract Objective To investigate the regulating effect of Tangluoning on Toll-like receptors 2/4 (TLR2/4) in dorsal root ganglion (DRG) of rats with diabetic peripheral neuropathy (DPN). Methods Eighty of eight-week-old male SD rats were selected. Fourteen rats were randomly selected as normal group, the rest of 66 rats were intraperitoneally injected with 60 mg/kg streptozotocin to induce DPN rat model, among which 61 rats were succeeded. They were divided into the model group (21 rats), the Western medicine group (19 rats) and the Chinese medicine group (21 rats) by random number table method. Chinese medicine group was gavaged Tangluoning with 5 g/(kg·d), the Western medicine group was gavaged α-lipoic acid with 20 mg/(kg·d), the model group and normal group were gavaged equal amount of distilled water. The drug was administered continuously for 8 weeks. After 8 weeks, the expression of TLR2 and TLR4 proteins in DRG was detected by Western blot. Results The expression levels of TLR2 and TLR4 proteins in normal group were weak, while the expression levels of TLR2 and TLR4 proteins in the model group were higher than those in normal group (P < 0.01). The expression levels of TLR2 and TLR4 proteins in the Chinese medicine group and the Western medicine group were lower than those in the model group (P < 0.05). There were no statistically significant differences in the expression levels of TLR2 and TLR4 proteins between the Chinese medicine group and the Western medicine group (P > 0.05). Conclusion Tangluoning may have impact on the signaling pathways such as the mediated NF-κB by inhibiting the expression of TLR2 and TLR4, thereby reducing inflammation and oxidative stress and reducing nerve damage.
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