The analgesic effects of β-elemene in rats with neuropathic pain by inhibition of spinal astrocytic ERK activation

Author:

Ma Li-Tian12ORCID,Bai Yang3,Cao Peng3,Ren Kai-Xi4,Chen Jing5,Zhang Ting5,Fan Bo-Yuan6,Qiao Yu7,Yan Hong-Yu8,Wang Jing-Jie2,Li Yun-Qing5910,Zheng Jin1

Affiliation:

1. Department of Traditional Chinese Medicine, Tangdu Hospital, Air Force Medical University, Xi’an, China

2. Department of Gastroenterology, Tangdu Hospital, Air Force Medical University, Xi'an, China

3. Department of Neurosurgery, General Hospital of Northern Theater Command, Shenyang, China

4. Department of Neurology, Tangdu Hospital, Air Force Medical University, Xi'an, China

5. Department of Anatomy, Histology and Embryology, Preclinical School of Medicine, Air Force Medical University, Xi’an, China

6. Department of Cardiology, The Second Affiliated Hospital of Xi’an Jiaotong University, Xi’an Jiaotong University, Xi’an, China

7. Laser Medical Center, Hainan Hospital, PLA General Hospital, Sanya, China

8. The First Affiliated Hospital of Dalian Medical University, Dalian, China

9. Department of Anatomy, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, China

10. Department of Anatomy, College of Basic Medicine, Dali University, Dali, China

Abstract

Neuropathic pain takes a heavy toll on individual well-being, while current therapy is far from desirable. Herein, we assessed the analgesic effect of β-elemene, a chief component in the traditional Chinese medicine Curcuma wenyujin, and explored the underlying mechanisms at the level of spinal dorsal horn (SDH) under neuropathic pain. A spared nerve injury (SNI)-induced neuropathic pain model was established in rats. Intraperitoneal injection (i.p.) of β-elemene was administered for 21 consecutive days. Mechanical allodynia was explored by von Frey filaments. The activation of the mitogen-activated protein kinase (MAPK) family (including ERK, p38, and JNK) in spinal neurons, astrocytes, and microglia was evaluated using immunostaining 29 days after SNI surgery. The expression of GFAP, Iba-1, p-ERK, p-JNK, and p-p38 within the SDH was measured using immunoblotting. The levels of proinflammatory cytokines (including TNF-α, IL-1β, and IL-6) were measured with ELISA. The levels of oxidative stress indicators (including MDA, SOD, and GSH-PX) were detected using biochemical tests. Consecutive i.p. administration of β-elemene relieved SNI-induced mechanical allodynia (with an EC50 of 16.40 mg/kg). SNI significantly increased the expression of p-ERK in spinal astrocytes but not microglia on day 29. β-elemene reversed spinal astrocytic ERK activation and subsequent upregulation of proinflammatory cytokines in SNI rats, with no effect on the expression of p38 and JNK in spinal glia. β-elemene also exerted antioxidative effects by increasing the levels of SOD and GSH-PX and decreasing the level of MDA. Our results suggest that SNI induces robust astrocytic ERK activation within the SDH in the late phase of neuropathic pain. β-elemene exerts remarkable analgesic effects on neuropathic pain, possibly by inhibiting spinal astrocytic ERK activation and subsequent neuroinflammatory processes. Our findings suggest that β-elemene might be a promising analgesic for the treatment of chronic pain.

Funder

Innovation and Development Plan project of the Fourth Military Medical University

National Natural Science Foundation of China

Publisher

SAGE Publications

Subject

Anesthesiology and Pain Medicine,Cellular and Molecular Neuroscience,Molecular Medicine

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