三七总皂苷预处理对炎性内脏痛大鼠脊髓背角谷氨酰胺合成酶表达的影响

张仁丽 万炜 刘红 曾杰 彭田红 刘政海*

解剖学报 ›› 2015, Vol. 46 ›› Issue (1) : 20-24.

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解剖学报 ›› 2015, Vol. 46 ›› Issue (1) : 20-24. DOI: 10.16098/j.issn.0529-1356.2015.01.004
神经生物学

三七总皂苷预处理对炎性内脏痛大鼠脊髓背角谷氨酰胺合成酶表达的影响

  • 张仁丽1 万炜1 刘红1 曾杰2 彭田红1 刘政海1*
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Panax notoginseng saponins pretreatment affects the inflammatory visceral pain via upregulation of the glutamine synthetase in the rat spinal dorsal horn

  • ZHANG Ren-li1 WAN Wei1 LIU Hong1 ZENG Jie2 PENG Tian-hong1 LIU Zheng-hai 1*
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摘要

目的 探讨三七总皂苷(PNS)预处理调节脊髓背角谷氨酰胺合成酶(GS)表达,进而影响大鼠炎性内脏痛的病理生理机制。方法 将27只SD大鼠随机分为正常对照组、PNS预处理组、溶媒对照组,给予相应处理15d后腹腔注射1%乙酸(10ml/kg)制作模型,每隔15min记录内脏痛指数;取小肠组织进行HE染色,光学显微镜下观察炎症反应;应用免疫组织化学技术检测胸段脊髓背角GS表达情况。结果 溶媒对照组内脏痛指数明显高于PNS预处理组;腹腔注射乙酸后小肠组织都有明显的炎症反应,但两实验组黏膜下层厚度无明显差异;两实验组脊髓背角GS表达较正常组明显降低,但PNS预处理组脊髓背角GS表达明显高于溶媒对照组。结论 PNS预处理能上调脊髓后角GS的表达,从而缓解乙酸所致炎性内脏痛。

Abstract

Objective To explore the effect of panax notoginseng saponins (PNS) pretreatment on the expression of glutamine synthetase (GS) in the inflammatory visceral pain in the rat spinal dorsal horn. Methods Twenty-seven SD rats were randomly divided into normal group, PNS pretreatment group, and vehicle control group. Fifteen days after pretreatment, the model of inflammatory visceral pain was made by intraperitoneal injection of 1% acetic. The visceral pain index of experimental rat was record every 15 minutes. The small intestine tissue was stained with HE. The thoracic spinal cord slices were immunostained with anti-glutamine-synthetase antibody, then observed and compared under an optical microscope. Results The score result of the vehicle control group was significantly higher than that of the PNS pretreatment group. Compared with the normal group, the small intestine tissues of the two experimental groups showed significantly inflammatory response with thickness submucosa, but there was no significantly difference among experimental comparison groups. Compared with the normal group, the GS expression of the two experimental groups was reduced apparently, but the group of PNS pretreatment was significantly higher than the vehicle control group. Conclusion PNS pretreatment may affect the acid-induced inflammatory visceral pain via promoting the experience of GS in the spinal dorsal horn.

关键词

炎性内脏痛 / 三七总皂苷 / 谷氨酰胺合成酶 / 内脏痛指数 / 免疫组织化学 / 大鼠

Key words

Inflammatory visceral pain / Panax notoginseng saponins / Glutamine synthetase / Visceral pain index / Immunohistochemistry / Rat

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导出引用
张仁丽 万炜 刘红 曾杰 彭田红 刘政海*. 三七总皂苷预处理对炎性内脏痛大鼠脊髓背角谷氨酰胺合成酶表达的影响[J]. 解剖学报. 2015, 46(1): 20-24 https://doi.org/10.16098/j.issn.0529-1356.2015.01.004
ZHANG Ren-li WAN Wei LIU Hong ZENG Jie PENG Tian-hong LIU Zheng-hai*. Panax notoginseng saponins pretreatment affects the inflammatory visceral pain via upregulation of the glutamine synthetase in the rat spinal dorsal horn[J]. Acta Anatomica Sinica. 2015, 46(1): 20-24 https://doi.org/10.16098/j.issn.0529-1356.2015.01.004

参考文献

[1]Sengupta JN. Visceral Pain: The Neurophysiological Mechanism[M]. Berlin: Berlin Heidelberg Springer, 2009: 31-74.
[2]Sikandar S, Dickenson AH. Visceral pain: the ins and outs, the ups and downs[J]. Curr Opin Support Palliat Care, 2012, 6(1): 17-26.
[3]Liu QY, Zhu ChG. The somato-visceral divergent projections of peripheral process of substance P-containing spinal ganglionic neurons[J]. Acta Anatomica Sinica, 1989, 20(1):14-19, 106.(in Chinese)
刘庆莹, 朱长庚. 含P物质额脊神经节细胞周围突的躯体-内脏分支投射[J].解剖学报, 1989, 20(1):14-19,106.
[4]Hulsebosch CE, Hains BC, Crown ED, et al. Mechanisms of chronic central neuropathic pain after spinal cord injury[J]. Brain Res Rev, 2009, 60(1): 202-213.
[5]Wang XL, Li HL, Zhang YN, et al. The relationship between mGluR5 and C-fiber in the rat spinal dorsal horn-A immunohistochemical study at the level of light and electron microscopy[J]. Acta Anatomica Sinica, 2003, 34(3):261-264. (in Chinese)
王小丽, 李宏莲, 张亦农, 等. 大鼠脊髓后角内5型代谢型谷氨酸受体与C纤维的关系—免疫组织化学及电镜研究[J].解剖学报, 2003, 34(3):261-264.
[6]Doolen S, Blake CB, Smith BN, et al. Peripheral nerve injury increases glutamate-evoked calcium mobilization in adult spinal cord neurons[J]. Mol Pain, 2012, 8:56.
[7]Kant D, Tripathi IS, Qureshi MF, et al. The effect of glial glutamine synthetase inhibition on recognition and temporal memories in the rat[J]. Neurosci Lett, 2014, 560: 98-102.
[8]Hoshi A, Nakahara T, Kayama H, et al. Ischemic tolerance in chemical preconditioning: possible role of astrocytic glutamine synthetase buffering glutamate-mediated neurotoxicity[J]. J Neurosci Res, 2006, 84(1): 130-141.
[9]dos Santos AQ, Nardin P, Funchal C, et al. Resveratrol increases glutamate uptake and glutamine synthetase activity in C6 glioma cells[J]. Arch Biochem Biophys, 2006, 453(2): 161-167.
[10]Chow DH, Lai A, Tang FH, et al. Effects of panax ginseng-containing herbal plasters on compressed intervertebral discs in an in vivo rat tail model[J]. Chin Mede, 2013, 8(1): 4.
[11]Schmauss C, Yaksh T L. In vivo studies on spinal opiate receptor systems mediating antinociception. II. pharmacological profiles suggesting a differential association of mu, delta and kappa receptors with visceral chemical and cutaneous thermal stimuli in the rat[J]. J Pharmacol Exp Ther, 1984, 228(1): 1-12.
[12]Schmauss C, Shimohigashi Y, Jensen TS, et al. Studies on spinal opiate receptor pharmacology. III. analgetic effects of enkephalin dimers as measured by cutaneous-thermal and visceral-chemical evoked responses[J]. Brain Res, 1985, 337(2): 209-215.
[13]Koster R, Anderson M, DeBeer EJ. Acetic acid for analgesic Screening[J]. Federation Proc, 1959,18:412.
[14]Li H, Zhao ZJ, Pan D, et al. Protective effect of TSPN on spinal cord injury and its GFAP relative mechanism[J]. Progress in Modern Biomedicine, 2010, 10(10): 1825-1827,1835. (in Chinese)
李花,赵子进, 潘丁,等. 三七总皂苷对脊髓损伤后的保护作用及GFAP相关机制[J].现代生物医学进展,2010,10(10): 1825-1827,1835.
[15]Liu L, Zhu L, Zou Y, et al. Panax notoginseng saponins promotes stroke recovery by influencing expression of Nogo-A, NgR and p75NGF, in vitro and in vivo[J]. Biological and Pharmaceutical Bulletin, 2014, 37(4): 560-568.
[16]Wu Y, Sun B,  Xiao J, et al. Protective effect of Notoginesenoside R1 on lipopolysaccharide-induced myocardial dysfunction in mice[J].Chinese Pharmacological Bulletin, 2013, 29(2): 179-184.(in Chinese).
吴颖, 孙冰, 肖静, 等. 三七皂苷 R1 对 LPS 诱导的小鼠心肌损伤的保护作用[J]. 中国药理学通报, 2013, 29(2): 179-184.
[17]Guo YQ, Qi DM, Hao Y, et al. Regulation of sanchinoside R1 on inflammatory T lymphocytes in protecting vascular endothelium lesion in ApoE-/- mice[J].Chinese Pharmacological Bulletin, 2012, 28(2): 240-244, (in Chinese).
郭钰琪, 齐冬梅, 郝钰, 等. 三七皂苷 R1 调节炎性 T 细胞亚群保护血管内皮的实验研究[J]. 中国药理学通报, 2012, 28(2): 240-244.
[18]Ueda H. Molecular mechanisms of neuropathic pain-phenotypic switch and initiation mechanisms[J]. Pharmacol Ther, 2006, 109(1-2): 57-77.
[19]Fonseca LL, Monteiro MA, Alves PM, et al. Cultures of rat astrocytes challenged with a steady supply of glutamate: new model to study flux distribution in the glutamate-glutamine cycle[J]. Glia, 2005, 51(4): 286-296.
[20]Chiang CY, Wang J, Xie YF, et al. Astroglial glutamate-glutamine shuttle is involved in central sensitization of nociceptive neurons in rat medullary dorsal horn[J]. J Neurosci, 2007, 27(34): 9068-9076.

基金

湖南省教育厅科学研究项目;湖南省自然科学基金


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