Intrathecal leptin inhibits expression of the P2X2/3 receptors and alleviates neuropathic pain induced by chronic constriction sciatic nerve injury.
Intrathecal leptin inhibits expression of the P2X2/3 receptors and alleviates neuropathic pain induced by chronic constriction sciatic nerve injury.
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鞘内注射瘦素抑制 P2X2/3 受体的表达并减轻慢性收缩性坐骨神经损伤引起的神经性疼痛
DOI:
10.1186/1744-8069-9-65
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发表时间:
2013-12-10
期刊:
影响因子:
3.3
通讯作者:
Chen H
中科院分区:
文献类型:
--
作者:
Li X;Kang L;Li G;Zeng H;Zhang L;Ling X;Dong H;Liang S;Chen H
Background Leptin, an adipocytokine produced mainly by white adipose tissue, has a broad role in the regulation of neuronal functions. Accumulating evidence has revealed that leptin plays an important role in influencing neuropathic pain, shown recently by the finding that chronic administration of leptin induced thermal hyperalgesia and mechanical allodynia in naïve rats. Chronic constriction sciatic nerve injury (CCI) is a well characterized model used for studying neuropathic pain. The present study was designed to investigate whether leptin plays a role in neuropathic pain in rats induced by CCI by examining particular pain behaviors. Results After sciatic nerve injury in rats, endogenous levels of leptin and leptin receptor (OB-Rb) were increased in a time dependent manner within the ipsilateral dorsal root ganglion (DRG). Intrathecal administration of leptin once daily for 6 days, beginning 7 days after CCI, alleviated neuropathic pain and decreased the expression of IL-6, TNFα, and the P2X2 and P2X3 receptors. Attenuation of endogenous OB-Rb in the DRG by intrathecal administration of OB-Rb antisense oligonucleotides did not change thermal hyperalgesia or mechanical allodynia induced by CCI. Conclusions Our findings suggest that exogenous leptin can alleviate the chronic neuropathic pain caused by CCI. The leptin effect may be mediated by attenuated expression of IL-6, TNFα, and the P2X2 and P2X3 receptors in the DRG of CCI rats.
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影响因子:
3.3
作者:
Quarta S;Vogl C;Constantin CE;Üçeyler N;Sommer C;Kress M
通讯作者:
Kress M
影响因子:
9.3
作者:
Dubový P;Brázda V;Klusáková I;Hradilová-Svíženská I
通讯作者:
Hradilová-Svíženská I
影响因子:
3.3
作者:
Sakurai E;Kurihara T;Kouchi K;Saegusa H;Zong S;Tanabe T
通讯作者:
Tanabe T
影响因子:
3.8
作者:
Gao, Yun;Liu, Han;Liang, Shangdong
通讯作者:
Liang, Shangdong
DOI:
10.1006/bbrc.1999.0382
发表时间:
1999-03-24
影响因子:
3.1
作者:
Steppan, CM;Swick, AG
通讯作者:
Swick, AG