Effect of electroacupuncture at "Zusanli" (ST 36) on duodenal mast cells, NGF and NTRK1 in rats with functional dyspepsia.
10.13703/j.0255-2930.20211230-k0003
- Author:
Jia-Zi DONG
1
,
2
;
Pei-Jing RONG
3
;
Xiao-Tong WANG
4
;
Dan WANG
4
;
Ming-Hui LENG
4
;
Lu-Jia XIAO
4
Author Information
1. College of Acupuncture-Moxibustion and Tuina, Liaoning University of TCM, Shenyang 110847, China
2. Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing 100700.
3. Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing 100700.
4. College of Acupuncture-Moxibustion and Tuina, Liaoning University of TCM, Shenyang 110847, China.
- Publication Type:Journal Article
- Keywords:
Point ST 36 (Zusanli);
duodenum;
electroacupuncture;
functional dyspepsia (FD);
mast cells;
nerve growth factor (NGF);
neurotrophic tyrosine kinase receptor type 1 (NTRK1)
- MeSH:
Acupuncture Points;
Animals;
Duodenum/metabolism*;
Dyspepsia/therapy*;
Electroacupuncture;
Ketotifen;
Mast Cells/metabolism*;
Nerve Growth Factor/metabolism*;
RNA, Messenger;
Rats;
Rats, Sprague-Dawley;
Receptor, trkA/genetics*
- From:
Chinese Acupuncture & Moxibustion
2022;42(7):767-772
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To observe the effect of electroacupuncture (EA) at "Zusanli" (ST 36) on duodenal mast cells, nerve growth factor (NGF) and neurotrophic tyrosine kinase receptor type 1 (NTRK1), and to explore the mechanism of electroacupuncture at Zusanli (ST 36) on functional dyspepsia (FD).
METHODS:Sixty SPF-grade 10-day-old SD rats were randomly divided into a normal group, a model group, a ketotifen group and an EA group, 15 rats in each group. The FD model was prepared by iodoacetamide combined with rat tail clamping method in the model group, the ketotifen group and the EA group. The rats in the ketotifen group were injected intraperitoneally with ketotifen (1 mg•kg-1•d-1) for 7 days; the rats in the EA group were treated with EA at bilateral "Zusanli" (ST 36), with disperse-dense wave, frequency of 2 Hz/50 Hz and intensity of 0.5 mA, 20 min each time, once a day for 14 days. The gastric emptying rate and small intestinal propulsion rate in each group were observed; the morphology of duodenal mucosa was observed by HE staining; the toluidine blue staining was used to observe the number and degranulation of mast cells in duodenal mucosa; the protein and mRNA expressions of NGF, NTRK1 in duodenum were detected by Western blot and real-time PCR; the level of interleukin-1β (IL-1β) in duodenum was measured by ELISA.
RESULTS:Compared with the normal group, the gastric emptying rate and small intestinal propulsion rate in the model group were decreased (P<0.01); compared with the model group, the gastric emptying rate and small intestinal propulsion rate in the ketotifen group and the EA group were increased (P<0.01); the small intestinal propulsion rate in the EA group was higher than that in the ketotifen group (P<0.01). In the model group, local defects in duodenal mucosa were observed with a small amount of inflammatory cell infiltration; no obvious abnormality was found in duodenal mucosa of the other groups. Compared with the normal group, the mast cells of duodenal mucosa in the model group were increased significantly with significant degranulation; compared with the model group, the mast cells of duodenal mucosa in the ketotifen group and the EA group were decreased significantly, and the degranulation was not obvious. Compared with the normal group, the protein and mRNA expressions of NGF, NTRK1 as well as the level of IL-1β in duodenum in the model group were increased (P<0.01); compared with the model group, the protein and mRNA expressions of NGF, NTRK1 as well as the levels of IL-1β in duodenum in the ketotifen group and the EA group were decreased (P<0.01, P<0.05); compared with the ketotifen group, the mRNA expression of NGF, as well as the protein and mRNA expressions of NTRK1 in duodenum in the EA group were decreased (P<0.05, P<0.01).
CONCLUSION:EA at "Zusanli" (ST 36) could inhibit the activation of duodenal mast cells and regulate the expressions of NGF and its receptor to improve the low-grade inflammatory response of duodenum, resulting in treatment effect on FD.
