石菖蒲挥发油对炎性痛大鼠脊髓背角中胶质纤维酸性蛋白、c-Jun氨基末端蛋白激酶和肿瘤坏死因子α表达的影响

张润恒 杨翠珠 李诗琪 王姝涵 王欣 刘靖 马宇昕

解剖学报 ›› 2023, Vol. 54 ›› Issue (1) : 23-29.

PDF(3775 KB)
欢迎访问《解剖学报》官方网站!今天是 English
PDF(3775 KB)
解剖学报 ›› 2023, Vol. 54 ›› Issue (1) : 23-29. DOI: 10.16098/j.issn.0529-1356.2023.01.003
神经生物学

石菖蒲挥发油对炎性痛大鼠脊髓背角中胶质纤维酸性蛋白、c-Jun氨基末端蛋白激酶和肿瘤坏死因子α表达的影响

  • 张润恒 杨翠珠 李诗琪 王姝涵 王欣 刘靖 马宇昕*
作者信息 +

Effects of volatile oil from Acori graminei Rhizoma on glial fibrillary acidic protein, c-Jun N-terminal protein kinase and tumor necrosis factor-α expressions in the spinal cord dorsal horn of the inflammatory pain rats

  • ZHANG  Run-heng  YANG  Cui-zhu  LI  Shi-qi  WANG  Shu-han  WANG  Xin  LIU  Jing  MA  Yu-xin*
Author information +
文章历史 +

摘要

目的 探讨石菖蒲挥发油(VOA)对炎性痛大鼠脊髓背角中胶质纤维酸性蛋白(GFAP)、c-Jun氨基末端蛋白激酶(JNK)和肿瘤坏死因子α(TNF-α)表达的影响。  方法 36只雄性SD大鼠随机分为:对照组(control)、假手术组(sham)、完全弗氏佐剂组(CFA)、5 g/(kg·d)低剂量VOA + CFA组(VOA-L+CFA)、10 g/(kg·d) 中剂量VOA + CFA组(VOA-M+CFA)和20 g/(kg·d)高剂量VOA + CFA组(VOA-H+CFA),共6组,每组6只,于连续灌胃给药的第22天取材。利用免疫荧光染色和Western blotting技术检测各组大鼠脊髓背角中GFAP、JNK和TNF-α的表达情况。  结果 免疫荧光染色及Western blotting结果表明,与control和sham组相比,CFA组中大鼠脊髓背角中GFAP、JNK和TNF-α阳性表达均显著增多(P<0.01);与CFA组相比,不同剂量VOA处理组大鼠脊髓背角中GFAP、JNK和TNF-α阳性表达均减少,且VOA-H+CFA组大鼠脊髓背角中GFAP、JNK和TNF-α阳性表达减少更明显(P<0.05,P<0.01)。  结论 VOA可降低CFA诱导的炎性痛大鼠脊髓背角中GFAP、JNK和TNF-α的表达。

Abstract

Objective To investigate the influence of volatile oil from Acori graminei Rhizoma(VOA)on expressions of glial fibrillary acidic protein (GFAP), c-Jun N-terminal protein kainse (JNK) and tumour necrosis factor-α (TNF-α) in the spinal cord dorsal horn of imflammatory pain rats.   Methods Totally 36 male SD rats were randomly divided into control group (control), sham-operated group (sham), complete Freund’s adjuvant group (CFA), 5 g/(kg·d) low dose VOA+CFA group (VOA-L+CFA), 10 g/(kg·d) medium dose VOA + CFA group (VOA-M+CFA) and 20 g/(kg·d) high dose VOA + CFA group (VOA-H+CFA). All animals were sacrificed immediately after continuous gavage administration for 22 days. The expressions of GFAP, JNK and TNF-α in the spinal cord dorsal horn of rats in each group were detected by immunofluorescence and Western blotting methods.   Results The present results showed that the positive expressions of GFAP, JNK and TNF-α in the spinal cord dorsal horn of rats increased significantly in the CFA group, when compared to the control and sham groups (P< 0.01). The expressions of GFAP, JNK and TNF-α in the spinal cord dorsal horn of rats with VOA treatment reduced in the dose-dependent manner, when compared to the CFA group, the positive expressions of GFAP, JNK and TNF-α reduced significantly in the dorsal horn of the spinal cord of the VOA-H+CFA group (P<0.05, P<0.01).   Conclusion VOA reduces the expressions of GFAP, JNK and TNF-α in the spinal cord dorsal horn of rats of CFA-induced inflammatory pain.

关键词

石菖蒲挥发油 / 炎性痛 / 胶质纤维酸性蛋白 / c-Jun氨基末端蛋白激酶 / 肿瘤坏死因子α / 免疫荧光 / 免疫印迹法 / 大鼠

Key words

Volatile oil from Acori graminei Rhizoma
/ Inflammatory pain / Glial fibrillary acidic protein / c-Jun N-terminal kinase / Tumour necrosis factor-α /   / Immunofluorescence / Western blotting / Rat 

引用本文

导出引用
张润恒 杨翠珠 李诗琪 王姝涵 王欣 刘靖 马宇昕. 石菖蒲挥发油对炎性痛大鼠脊髓背角中胶质纤维酸性蛋白、c-Jun氨基末端蛋白激酶和肿瘤坏死因子α表达的影响[J]. 解剖学报. 2023, 54(1): 23-29 https://doi.org/10.16098/j.issn.0529-1356.2023.01.003
ZHANG Run-heng YANG Cui-zhu LI Shi-qi WANG Shu-han WANG Xin LIU Jing MA Yu-xin.
Effects of volatile oil from Acori graminei Rhizoma on glial fibrillary acidic protein, c-Jun N-terminal protein kinase and tumor necrosis factor-α expressions in the spinal cord dorsal horn of the inflammatory pain rats
[J]. Acta Anatomica Sinica. 2023, 54(1): 23-29 https://doi.org/10.16098/j.issn.0529-1356.2023.01.003
中图分类号: R338.2+2   

参考文献

[1]Raja SN, Carr DB, Cohen M, et al. The revised International association for the study of pain definition of pain: concepts, challenges, and compromises [J]. Pain,2020, 161(9): 1976-1982.
[2]Vos T, Abajobir AA, Abate KH, et al. Global, regional, and national incidence, prevalence, and years lived with disability for 328 diseases and injuries for 195 countries, 1990-2016: a systematic analysis for the global burden of disease study 2016 [J]. Lancet,2017, 390(10100): 1211-1259.
[3]Cramer JD, Barnett ML, Anne S, et al. Nonopioid, Multimodal analgesia as first-line therapy after otolaryngology operations: primer on nonsteroidal anti-inflammatory drugs (NSAIDs) [J]. Otolaryngol Head   Neck Surg,2021, 164(4): 712-719.
[4]Herzberg DL, Sukumaran HP, Viscusi E. NSAIDs for analgesia in the era of COVID-19 [J]. Reg Anesth Pain Med, 2020, 45(9): 677-678.
[5]Ye F, Xu Y, Lin F, et al. TNF-α suppresses SHOX2 expression via NF-κB signaling pathway and promotes intervertebral disc degeneration and related pain in a rat model [J]. J Orthop Res, 2021, 39(8): 1745-1754.
[6]Liu X, He J, Gao J, et al. Fluorocitrate and neurotropin confer analgesic effects on neuropathic pain in diabetic rats via inhibition of astrocyte activation in the periaqueductal gray [J]. Neurosci Lett, 2022, 768: 136378.
[7]Oh SH, Kim SW, Kim DJ, et al. Sec-O-glucosylhamaudol mitigates inflammatory processes and autophagy via p38/JNK MAPK signaling in a rat neuropathic pain model [J]. Korean J Pain, 2021, 34(4): 405-416.
[8]Hu Y, Fang X, Wang J, et al. Astragalin attenuates AlCl3/D-galactose-induced aging-like disorders by inhibiting oxidative stress and neuroinflammation[J]. Neurotoxicology, 2022, 91:60-68.
[9]Wang N, Wang H, Li L, et al. β-asarone inhibits amyloid-β by promoting autophagy in a cell model of Alzheimer’s disease [J]. Front Pharmacol, 2020, 10:1529.
[10]Bushnell MC, Ceko M, Low LA. Cognitive and emotional control of pain and its disruption in chronic pain[J]. Nat Rev Neurosci, 2013, 14(7): 502-511.
[11]Wu L, Zhuo M. Targeting the NMDA receptor subunit NR2B for the treatment of neuropathic pain [J]. Neurotherapeutics, 2009, 6(4): 693-702.
[12]Gao Y, Ji R. Targeting astrocyte signaling for chronic pain [J]. Neurotherapeutics, 2010, 7(4): 482-493.
[13]Li ShQ, Yang CZh, Liu HQ, et al. Effect of volatile oil of acorus calamus on glial fibrillary acidic protein and immediate early gene expression in the basolateral amygdala of rats with inflammatory pain[J]. Acta Anatomica Sinica, 2021, 52(2): 189-195.(in Chinese)
李诗琪,杨翠珠,刘鸿庆,等. 石菖蒲挥发油对炎症痛大鼠基底外侧杏仁核中胶质纤维酸性蛋白和即刻早期基因表达的影响[J]. 解剖学报. 2021, 52(2): 189-195.
[14]Tian J, Song T, Wang H, et al. Thalidomide alleviates bone cancer pain by down-regulating expressions of NF-kappaB and GFAP in spinal astrocytes in a mouse model [J]. Int J Neurosci, 2019, 129(9): 896-903.
[15]Cai J, Yan Y, Zhang D, et al. Silencing oflncRNA Gm14461 alleviates pain in trigeminal neuralgia through inhibiting astrocyte activation [J]. IUBMB Life, 2020, 72(12): 2663-2671.
[16]Kwiatkowski K, Piotrowska A, Rojewska E, et al. The RS504393 influences the level of nociceptive factors and enhances opioid analgesic potency in neuropathic rats [J]. J Neuroimmune Pharmacol, 2017, 12(3): 402-419.
[17]Ni H, Yao M, Huang B, et al. Glial activation in the periaqueductal gray promotes descending facilitation of neuropathic pain through the p38 MAPK signaling pathway [J]. J Neurosci Res, 2016, 94(1): 50-61.
[18]Hu C, Lu K, Liu W. Exendin-4 attenuates inflammation-mediated endothelial cell apoptosis in varicose veins through inhibiting the MAPK-JNK signaling pathway [J]. J Recept Signal Transduct Res, 2020, 40(5): 464-470.
[19]Wang Y, Xu H, Tao M, et al. Ligustilide relieves complete freund’s adjuvant-induced mechanical hyperalgesia through inhibiting the activation of spinal c-jun n-terminal kinase/c-Jun pathway in rats [J]. Pharmacogn Mag, 2017, 13(52): 634-638.
[20]Zheng J, Dai Q, Han K, et al. JNK-IN-8, a c-Jun N-terminal kinase inhibitor, improves functional recovery through suppressing neuroinflammation in ischemic stroke[J]. J Cell Physiol, 2020, 235(3): 2792-2799.
[21]Huang X, Peng J, Pang J, et al. Peli1 contributions in microglial activation, neuroinflammatory responses and neurological deficits following experimental subarachnoid hemorrhage [J]. Front Mol Neurosci, 2017,10:398.
[22]Liu GX, Sun YY, Chen ZL, et al. Effects of inflammatory pain on inflammatory response and expression of TNF-α and MCP-1 in peripheral tissues of mice [J]. Journal of Xi’an Jiaotong University (Medical Edition), 2019, 40(1): 65-70.(in Chinese)
刘改霞,孙雨瑶,陈子璐,等. 炎性疼痛对小鼠外周组织炎症反应及TNF-α和MCP-1表达的影响[J]. 西安交通大学学报(医学版), 2019, 40(1): 65-70.
[23]Song X, Huang Z, Song WB, et al. Attenuation effect of spinal manipulation on neuropathic and postoperative pain through activating endogenous anti-inflammatory cytokine interleukin 10 in rat spinal cord [J]. J Manipulative Physiol Ther, 2016, 39(1): 42-53.
[24]Lamacchia ZM, Spengler RN, Jaffari M, et al. Perispinal injection of a TNF blocker directed to the brain of rats alleviates the sensory and affective components of chronic constriction injury-induced neuropathic pain [J]. Brain Behav Immun, 2019, 82: 93-105.

基金

广东省医学科学技术研究基金;广东省自然科学基金自由申请项目;国家自然科学基金青年项目

PDF(3775 KB)

Accesses

Citation

Detail

段落导航
相关文章

/