Analgesic Effect of Dehydrocorydaline on Chronic Constriction Injury-Induced Neuropathic Pain via Alleviating Neuroinflammation.
10.1007/s11655-024-3920-4
- Author:
Bai-Ling HOU
1
;
Chen-Chen WANG
2
;
Ying LIANG
2
;
Ming JIANG
2
;
Yu-E SUN
2
;
Yu-Lin HUANG
2
;
Zheng-Liang MA
3
Author Information
1. Department of Anaesthesiology, Nanjing Drum Tower Hospital, Nanjing Drum Tower Hospital Clinical College, Nanjing University of Chinese Medicine, Nanjing, 210008, China.
2. Department of Anaesthesiology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, 210008, China.
3. Department of Anaesthesiology, Nanjing Drum Tower Hospital, Nanjing Drum Tower Hospital Clinical College, Nanjing University of Chinese Medicine, Nanjing, 210008, China. mazhengliang1964@nju.edu.cn.
- Publication Type:Journal Article
- Keywords:
N-methyl-D-aspartate receptor subunit 2B;
dehydrocorydaline;
neuroinflammation;
neuropathic pain
- MeSH:
Animals;
Neuralgia/etiology*;
Mice, Inbred C57BL;
Analgesics/pharmacology*;
Neuroinflammatory Diseases/pathology*;
Constriction;
Male;
Receptors, N-Methyl-D-Aspartate/metabolism*;
Nitric Oxide Synthase Type II/metabolism*;
Mice, Inbred ICR;
Microglia/pathology*;
Spinal Cord/drug effects*;
Female;
Mice;
Tumor Necrosis Factor-alpha/metabolism*;
Disease Models, Animal;
Constriction, Pathologic/complications*;
Interleukin-6/metabolism*;
Astrocytes/metabolism*;
Chronic Disease;
Neurons/metabolism*
- From:
Chinese journal of integrative medicine
2025;31(6):499-505
- CountryChina
- Language:English
-
Abstract:
OBJECTIVE:To illustrate the role of dehydrocorydaline (DHC) in chronic constriction injury (CCI)-induced neuropathic pain and the underlying mechanism.
METHODS:C57BL/6J mice were randomly divided into 3 groups by using a random number table, including sham group (sham operation), CCI group [intrathecal injection of 10% dimethyl sulfoxide (DMSO)], and CCI+DHC group (intrathecal injection of DHC), 8 mice in each group. A CCI mouse model was conducted to induce neuropathic pain through ligating the right common sciatic nerve. On day 14 after CCI modeling or sham operation, mice were intrathecal injected with 5 µL of 10% DMSO or 10 mg/kg DHC (5 µL) into the 5th to 6th lumbar intervertebral space (L5-L6). Pregnant ICR mice were sacrificed for isolating primary spinal neurons on day 14 of embryo development for in vitro experiment. Pain behaviors were evaluated by measuring the paw withdrawal mechanical threshold (PWMT) of mice. Immunofluorescence was used to observe the activation of astrocytes and microglia in mouse spinal cord. Protein expressions of inducible nitric oxide synthase (iNOS), tumor necrosis factor alpha (TNF-α), interleukin 6 (IL-6), phosphorylation of N-methyl-D-aspartate receptor subunit 2B (p-NR2B), and NR2B in the spinal cord or primary spinal neurons were detected by Western blot.
RESULTS:In CCI-induced neuropathic pain model, mice presented significantly decreased PWMT, activation of glial cells, overexpressions of iNOS, TNF-α, IL-6, and higher p-NR2B/NR2B ratio in the spinal cord (P<0.05 or P<0.01), which were all reversed by a single intrathecal injection of DHC (P<0.05 or P<0.01). The p-NR2B/NR2B ratio in primary spinal neurons were also inhibited after DHC treatment (P<0.05).
CONCLUSION:An intrathecal injection of DHC relieved CCI-induced neuropathic pain in mice by inhibiting the neuroinflammation and neuron hyperactivity.
