| Autor: |
Xiao-fen He, Yu-rong Kang, Xue-yu Fei, Lu-hang Chen, Xiang Li, Yi-qi Ma, Qun-qi Hu, Si-ying Qu, Han-zhi Wang, Xiao-mei Shao, Bo-yi Liu, null Yi-Liang, Jun-Ying Du, Jian-qiao Fang, Yong-liang Jiang |
| Rok vydání: |
2021 |
| Předmět: |
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| Zdroj: |
Purinergic signalling. |
| ISSN: |
1573-9546 |
| Popis: |
Diabetic neuropathic pain (DNP) is frequent among patients with diabetes. We previously showed that P2X3 upregulation in dorsal root ganglia (DRG) plays a role in streptozotocin (STZ)-induced DNP but the underlying mechanism is unclear. Here, a rat model of DNP was established by a single injection of STZ (65 mg/kg). Fasting blood glucose was significantly elevated from the 1st to 3rd week. Paw withdrawal thresholds (PWTs) and paw withdrawal latencies (PWLs) in diabetic rats significantly reduced from the 2nd to 3rd week. Western blot analysis revealed that elevated p-CaMKIIα levels in the DRG of DNP rats were accompanied by pain-associated behaviors while CaMKIIα levels were unchanged. Immunofluorescence revealed significant increase in the proportion of p-CaMKIIα immune positive DRG neurons (stained with NeuN) in the 2nd and 3rd week and p-CaMKIIα was co-expressed with P2X3 in DNP rats. KN93, a CaMKII antagonist, significantly reduce mechanical hyperalgesia and thermal hyperalgesia and these effects varied dose-dependently, and suppressed p-CaMKIIα and P2X3 upregulation in the DRGs of DNP rats. These results revealed that the p-CaMKIIα upregulation in DRG is involved in DNP, which possibly mediated P2X3 upregulation, indicating CaMKIIα may be an effective pharmacological target for DNP management. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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