• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肌肽在诱导的炎症性疼痛反应中具有抗伤害感受作用。

Carnosine has antinociceptive properties in the inflammation-induced nociceptive response in mice.

机构信息

Second Department of Pharmacology, School of Pharmaceutical Sciences, Kyushu University of Health and Welfare, 1714-1 Yoshino-machi, Nobeoka-shi, Miyazaki 882-8508 Japan.

出版信息

Eur J Pharmacol. 2012 May 5;682(1-3):56-61. doi: 10.1016/j.ejphar.2012.02.005. Epub 2012 Feb 17.

DOI:10.1016/j.ejphar.2012.02.005
PMID:22366199
Abstract

Carnosine is a biologically active dipeptide that is found in fish and chicken muscle. Recent studies have revealed that carnosine has neuroprotective activity in zinc-induced neural cell apoptosis and ischemic stroke. In the present study, we examined the expression of carnosine in the spinal cord, and the antinociceptive potency of carnosine in a mouse model of inflammation-induced nociceptive pain. Immunohistochemical studies with antiserum against carnosine showed an abundance of carnosine-immunoreactivity in the dorsal horn of the mouse spinal cord. Double-immunostaining techniques revealed that carnosine was expressed in the neurons and astrocytes in the spinal cord. Oral administration of carnosine attenuated the number of writhing behaviors induced by the intraperitoneal administration of 0.6% acetic acid. Treatment with carnosine also attenuated the second phase, but not the first phase, of the nociceptive response to formalin. Moreover, intrathecal, but not intraplanter, administration of carnosine attenuated the second phase of the nociceptive response to formalin. Our immunohistochemical and behavioral data suggest that carnosine has antinociceptive effects toward inflammatory pain, which may be mediated by the attenuation of nociceptive sensitization in the spinal cord.

摘要

肌肽是一种存在于鱼肉和鸡肉中的生物活性二肽。最近的研究表明,肌肽具有锌诱导的神经细胞凋亡和缺血性中风的神经保护活性。在本研究中,我们检测了肌肽在脊髓中的表达以及肌肽在炎症诱导的痛觉过敏疼痛的小鼠模型中的镇痛效力。用肌肽抗血清进行的免疫组织化学研究显示,肌肽在小鼠脊髓背角中大量存在。双免疫染色技术显示,肌肽在脊髓中的神经元和星形胶质细胞中表达。肌肽的口服给药可减轻 0.6%乙酸腹腔内给药引起的扭体行为的数量。肌肽治疗还可减轻对福尔马林的痛觉反应的第二阶段,但不减轻第一阶段。此外,鞘内但不是足底内给予肌肽可减轻对福尔马林的痛觉反应的第二阶段。我们的免疫组织化学和行为学数据表明,肌肽对炎症性疼痛具有镇痛作用,这可能是通过减轻脊髓中的伤害感受敏化来介导的。

相似文献

1
Carnosine has antinociceptive properties in the inflammation-induced nociceptive response in mice.肌肽在诱导的炎症性疼痛反应中具有抗伤害感受作用。
Eur J Pharmacol. 2012 May 5;682(1-3):56-61. doi: 10.1016/j.ejphar.2012.02.005. Epub 2012 Feb 17.
2
Chemical stimulation of the ST36 acupoint reduces both formalin-induced nociceptive behaviors and spinal astrocyte activation via spinal alpha-2 adrenoceptors.电刺激 ST36 穴位可通过脊髓 α2 肾上腺素受体减少福尔马林诱导的伤害性行为和脊髓星形胶质细胞的激活。
Brain Res Bull. 2011 Nov 25;86(5-6):412-21. doi: 10.1016/j.brainresbull.2011.08.012. Epub 2011 Aug 26.
3
Antinociceptive profiles and mechanisms of centrally administered oxyntomodulin in various mouse pain models.中枢给予胰泌素在各种小鼠疼痛模型中的抗伤害作用特征和机制。
Neuropeptides. 2018 Apr;68:7-14. doi: 10.1016/j.npep.2018.01.002. Epub 2018 Feb 1.
4
The antinociceptive effect of intrathecal escin in the rat formalin test.鞘内七叶皂苷钠在大鼠福尔马林试验中的抗伤害作用。
Eur J Pharmacol. 2012 Jan 15;674(2-3):234-8. doi: 10.1016/j.ejphar.2011.10.025. Epub 2011 Oct 26.
5
N-antipyrine-3, 4-dichloromaleimide, an effective cyclic imide for the treatment of chronic pain: the role of the glutamatergic system.N- 安替比林-3,4-二氯马来酰亚胺,一种有效的用于治疗慢性疼痛的环状亚胺:谷氨酸能系统的作用。
Anesth Analg. 2010 Mar 1;110(3):942-50. doi: 10.1213/ANE.0b013e3181cbd7f6.
6
Manipulations of zinc in the spinal cord, by intrathecal injection of zinc chloride, disodium-calcium-EDTA, or dipicolinic acid, alter nociceptive activity in mice.通过鞘内注射氯化锌、乙二胺四乙酸二钠钙或二吡啶甲酸对脊髓中的锌进行调控,会改变小鼠的伤害性感受活动。
J Pharmacol Exp Ther. 1997 Sep;282(3):1319-25.
7
Ginsenoside Rb1 Attenuates Acute Inflammatory Nociception by Inhibition of Neuronal ERK Phosphorylation by Regulation of the Nrf2 and NF-κB Pathways.人参皂苷Rb1通过调节Nrf2和NF-κB信号通路抑制神经元ERK磷酸化,从而减轻急性炎性疼痛。
J Pain. 2016 Mar;17(3):282-97. doi: 10.1016/j.jpain.2015.10.007. Epub 2015 Nov 6.
8
Spinal vasopressin alleviates formalin-induced nociception by enhancing GABAA receptor function in mice.脊髓加压素通过增强小鼠体内GABAA受体功能减轻福尔马林诱导的伤害感受。
Neurosci Lett. 2015 Apr 23;593:61-5. doi: 10.1016/j.neulet.2015.03.023. Epub 2015 Mar 14.
9
Intrathecal landiolol inhibits nociception and spinal c-Fos expression in the mouse formalin test.鞘内注射兰地洛尔可抑制小鼠福尔马林试验中的伤害感受和脊髓c-Fos表达。
Can J Anaesth. 2007 Mar;54(3):201-7. doi: 10.1007/BF03022641.
10
Effect of spinally administered simvastatin on the formalin-induced nociceptive response in mice.鞘内给予辛伐他汀对小鼠福尔马林诱导的疼痛反应的影响。
J Pharmacol Sci. 2012;119(1):102-6. doi: 10.1254/jphs.12007sc. Epub 2012 Apr 18.

引用本文的文献

1
DNMT1 mediates the disturbed flow-induced endothelial to mesenchymal transition through disrupting β-alanine and carnosine homeostasis.DNMT1 通过破坏β-丙氨酸和肌肽内稳态介导紊乱流诱导的内皮细胞向间充质转化。
Theranostics. 2023 Aug 6;13(13):4392-4411. doi: 10.7150/thno.84427. eCollection 2023.
2
Carnosine Alleviates Knee Osteoarthritis and Promotes Synoviocyte Protection via Activating the Nrf2/HO-1 Signaling Pathway: An In-Vivo and In-Vitro Study.肌肽通过激活Nrf2/HO-1信号通路减轻膝骨关节炎并促进滑膜细胞保护:一项体内和体外研究
Antioxidants (Basel). 2022 Jun 20;11(6):1209. doi: 10.3390/antiox11061209.
3
Carnosine and Related Peptides: Therapeutic Potential in Age-Related Disorders.
肌肽及相关肽:在与年龄相关疾病中的治疗潜力
Aging Dis. 2015 Oct 1;6(5):369-79. doi: 10.14336/AD.2015.0616. eCollection 2015 Sep.
4
Neurorestorative targets of dietary long-chain omega-3 fatty acids in neurological injury.膳食长链ω-3脂肪酸在神经损伤中的神经修复靶点。
Mol Neurobiol. 2014 Aug;50(1):197-213. doi: 10.1007/s12035-014-8701-1. Epub 2014 Apr 17.
5
Carnosine: can understanding its actions on energy metabolism and protein homeostasis inform its therapeutic potential?肌肽:了解其对能量代谢和蛋白质稳态的作用能否揭示其治疗潜力?
Chem Cent J. 2013 Feb 25;7(1):38. doi: 10.1186/1752-153X-7-38.