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山矾叶水提物和醇提物对 CFA 诱导的慢性炎症痛的抗痛觉过敏活性。

Anti-hyperalgesic activity of the aqueous and methanol extracts of the leaves of Pittosporum mannii Hook on CFA-induced persistent inflammatory pain.

机构信息

Laboratory of Animal Physiology and Phytopharmacology, University of Dschang, P.O.Box 67, Dschang, Cameroon.

Laboratory of Applied and Environmental Chemistry, University of Dschang, P.O.Box 67, Dschang, Cameroon.

出版信息

Inflammopharmacology. 2018 Feb;26(1):197-205. doi: 10.1007/s10787-017-0376-6. Epub 2017 Aug 29.

Abstract

BACKGROUND

Previous study showed that aqueous (AEPM) and methanol (MEPM) extracts from the leaves of Pittosporum mannii have analgesic effects in acute pain models. The present study evaluates the acute and chronic anti-hypernociceptive and anti-inflammatory effects of AEPM and MEPM in a model of persistent inflammatory pain.

METHODS

The third day after induction of inflammatory pain by subplantar injection of 100 µL of CFA in Wistar rats, AEPM and MEPM were administered orally (75, 150 and 300 mg/kg/day) and their anti-hyperalgesic and anti-inflammatory effects were follow in acute (1-24 h) and chronic (for 14 days) treatments. At the end of the chronic treatment, oxidative stress and liver parameters were assessed. Effects of plant extracts were also evaluated on nociception induced by Phorbol 12-Myristate 13-Acetate (PMA) and 8-bromo 3',5'-cAMP (8-Br-cAMP) in mice.

RESULTS

AEPM and MEPM significantly reversed the mechanical hyperalgesia caused by CFA in acute and chronic treatment. Moreover, AEPM and MEPM also significantly reduced the nociception caused by PMA (60%) and 8-Br-cAMP (87%). Nevertheless, AEPM and MEPM failed to inhibit the paw edema caused by CFA. Plant extracts significantly reduced the nitric oxide content in the spinal cord and the plasmatic concentration of alanine aminotransferase. MEPM also significantly increased the glutathione content in the spinal cord.

CONCLUSION

AEPM and MEPM given orally are effective in inhibiting mechanical hyperalgesia in persistent inflammatory pain caused by CFA. Their mechanisms of action seem to involve an interaction with PKC, PKA and nitric oxide pathways. These extracts might be devoid of hepatotoxic effects.

摘要

背景

先前的研究表明,伯乐树叶片的水(AEPM)和甲醇(MEPM)提取物在急性疼痛模型中具有镇痛作用。本研究评估了 AEPM 和 MEPM 在持续性炎症性疼痛模型中的急性和慢性抗伤害感受和抗炎作用。

方法

在 Wistar 大鼠足底注射 100μL CFA 诱导炎症痛后的第 3 天,给予 AEPM 和 MEPM 口服(75、150 和 300mg/kg/天),并在急性(1-24 小时)和慢性(14 天)治疗中观察其抗伤害感受和抗炎作用。在慢性治疗结束时,评估氧化应激和肝参数。还评估了植物提取物对 Phorbol 12-Myristate 13-Acetate(PMA)和 8-bromo 3',5'-cAMP(8-Br-cAMP)诱导的小鼠疼痛的影响。

结果

AEPM 和 MEPM 在急性和慢性治疗中均显著逆转了 CFA 引起的机械性痛觉过敏。此外,AEPM 和 MEPM 还显著降低了 PMA(60%)和 8-Br-cAMP(87%)引起的疼痛。然而,AEPM 和 MEPM 未能抑制 CFA 引起的爪肿胀。植物提取物显著降低了脊髓中的一氧化氮含量和血浆丙氨酸氨基转移酶浓度。MEPM 还显著增加了脊髓中的谷胱甘肽含量。

结论

口服给予 AEPM 和 MEPM 可有效抑制 CFA 引起的持续性炎症性疼痛引起的机械性痛觉过敏。它们的作用机制似乎涉及与 PKC、PKA 和一氧化氮途径的相互作用。这些提取物可能没有肝毒性作用。

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