Comparison of the effect between electroacupuncture and NSAIDs on pain memory based on cAMP/PKA/CREB pathway in anterior cingulate gyrus.
10.13703/j.0255-2930.20190130-k0002
- Author:
Jing SUN
1
,
2
;
Jian-Qiao FANG
1
,
2
;
Zui SHEN
1
,
2
;
Yi-Lin ZHU
3
;
Qin CHEN
1
,
2
;
Fang FANG
4
;
Jia-Ling WANG
5
;
Fei LI
6
;
Xiao-Mei SHAO
1
,
2
Author Information
1. Third Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou 310005, China
2. Zhejiang Key Laboratory of Acupuncture-Moxibustion and Neurology, Hangzhou 310053.
3. Third Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou 310005, China.
4. Department of Acupuncture-Moxibustion and Physiotherapy, Wenzhou Hospital of TCM.
5. Department of Rehabilitation, Zhenhai Refinind and Chemical Hospital of Ningbo.
6. Department of Acupuncture-Moxibustion and Tuina, First People's Hospital of Huzhou.
- Publication Type:Journal Article
- Keywords:
anterior cingulate gyrus (ACC);
cAMP/PKA/CREB pathway;
electroacupuncture (EA);
non-steroid anti-inflammatory drugs (NSAIDs);
pain memory
- MeSH:
Animals;
Anti-Inflammatory Agents, Non-Steroidal;
therapeutic use;
Cyclic AMP;
metabolism;
Cyclic AMP Response Element-Binding Protein;
metabolism;
Cyclic AMP-Dependent Protein Kinases;
metabolism;
Electroacupuncture;
Gyrus Cinguli;
metabolism;
Male;
Pain Threshold;
Random Allocation;
Rats;
Rats, Sprague-Dawley;
Signal Transduction
- From:
Chinese Acupuncture & Moxibustion
2020;40(4):397-404
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To observe the direct intervention effects of electroacupuncture (EA) and non-steroid anti-inflammatory drugs (NSAIDs) on pain memory, and to explore their effects on cAMP/PKA/cAMP pathway in anterior cingulate gyrus (ACC).
METHODS:Fifty clean healthy male SD rats were randomly divided into a control group, a model group, an indomethacin group, an EA group and a sham EA group, 10 rats in each group. Except the control group, the pain memory model was established in the remaining four groups by twice injection of carrageenan at foot; 0.1 mL of 2%λ-carrageenan was subcutaneously injected at the left foot of rats; 14 days later, when the pain threshold of rats of each group returned to the basic level, the second injection was performed with the same procedure. The rats in the EA group were treated with EA at bilateral "Zusanli" (ST 36) for 30 min; the rats in the indomethacin group was treated with indomethacin intragastric administration with the dose of 3 mg/kg; the rats in the sham EA group was treated with EA without electricity at the point 0.3 mm forward "Zusanli" (ST 36) with the depth of 2 mm for 30 min; the rats in the control group was not given any invention. All the above interventions were performed 5 h, 1 d, 2 d and 3 d after the second injection of 2% λ-carrageenan. The left-side paw withdrawal thresholds (PWT) were observed before the first injection, 4 h, 3 d, 5 d after the first injection, before the second injection and 4 h, 1 d, 2 d, 3 d after the second injection. Three days after the second injection, the number of positive cells of cAMP, p-PKA, p-CREB and the number of positive cells of protein co-expression in the right ACC brain area were detected by immunofluorescence, and the relative protein expression of p-PKA and p-CREB were detected by Western blot.
RESULTS:Compared with the control group, the PWTs in the model group decreased significantly 4 h, 3 d and 5 d after the first injection and 1 d, 2 d and 3 d after the second injection (<0.05); compared with the control group, the positive expression of cAMP, p-PKA and p-CREB in the right ACC brain area in the model group increased significantly (<0.05), and the number of positive cells of the co-expression of cAMP/p-PKA and p-PKA/p-CREB also increased significantly (<0.05). Compared with the model group, indomethacin group and sham EA group, the PWTs in the EA group were increased significantly 1 d, 2 d and 3 d after the second injection (<0.05); compared with the model group, indomethacin group and sham EA group, the positive expression of p-PKA and p-CREB in the right ACC brain area in the EA group decreased significantly (<0.05), and the number of positive cells of co-expression of cAMP/p-PKA and p-PKA/p-CREB was decreased significantly (<0.05). Compared with the model group and sham EA group, the positive expression of cAMP in the right ACC brain area was decreased in the EA group (<0.05).
CONCLUSION:EA have a direct intervention effect on pain memory, which have significant advantage over NSAIDs in the treatment of chronic pain. The advantage effect of EA on pain memory may be related to the inhibition of cAMP/PKA/CREB pathway in ACC area.
