The effect of CA1 administration of orexin-A on hippocampal expression of COX-2 and BDNF in a rat model of orofacial pain

被引:0
|
作者
Kooshki, Razieh [1 ]
Abbasnejad, Mehdi [1 ]
Esmaeili-Mahani, Saeed [1 ]
Raoof, Maryam [2 ,3 ]
机构
[1] Shahid Bahonar Univ Kerman, Dept Biol, Fac Sci, POB 76135133, Kerman, Iran
[2] Kerman Univ Med Sci, Inst Neuropharmacol, Neurosci Res Ctr, Lab Mol Neurosci, Kerman, Iran
[3] Kerman Univ Med Sci, Endodontol Res Ctr, Kerman, Iran
关键词
Orofacial pain; orexins; brain-derived neurotrophic factor; cyclooxygenase; 2; rats; TRIGEMINAL NUCLEUS CAUDALIS; LONG-TERM POTENTIATION; 6-HYDROXYDOPAMINE-INDUCED NEUROTOXICITY; CREB PHOSPHORYLATION; MEMORY IMPAIRMENT; NEUROPATHIC PAIN; NMDA RECEPTORS; SPINAL-CORD; ACTIVATION; BRAIN;
D O I
10.1590/0004-282X20180099
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The neuropeptide orexin-A and its receptors are widely distributed in both hippocampal circuitry and pain transmission pathways. Objective: Involvement of the CA1 orexin 1 receptor (OX1R) on the modulation of orofacial pain and pain-induced changes in hippocampal expression of cyclooxygenase-2 (COX-2) and brain-derived neurotrophic factor (BDNF) was investigated. Methods: Orofacial pain was induced by an intra-lip injection of capsaicin (100 mu g). Reverse transcription polymerase chain reaction and immunoblot analysis were used to indicate changes in hippocampal BDNF and COX-2 expression, respectively. Results: Capsaicin induces a significant pain response, which is not affected by either orexin-A or SB-334867-A, an OX1R antagonist. However, an increased expression of COX-2 and decreased expression of BDNF was observed in the hippocampus of animals that received capsaicin or SB-334867-A (80 nM) plus capsaicin. Meanwhile, orexin-A (40 pM) attenuated the effects of capsaicin on the expression of COX-2 and BDNF. Conclusions: CA1 OX1R activation moderates capsaicin-induced neuronal inflammation and neurotrophic deficiency.
引用
收藏
页码:603 / 608
页数:6
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